Inflammatory markers and bariatric surgery: a meta-analysis

Meta-analysis of Observational Studies in Epidemiology<SUBTITLE>A Proposal for Reporting</SUBTITLE>

Stroup, D. F. (2000) · JAMA · doi:10.1001/jama.283.15.2008 · Cited by 20,623 · see citing works

Obesity is associated with macrophage accumulation in adipose tissue

Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041 · see citing works

Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance

Xu, H., Barnes, G. T., Yang, Q., Tan, G., Yang, D., Chou, C. J., Sole, J., Nichols, A., Ross, J. S., Tartaglia, L. A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319451 · Cited by 6,760 · see citing works

TLR4 links innate immunity and fatty acid-induced insulin resistance

Shi, H., Kokoeva, M. V., Inouye, K., Tzameli, I., Yin, H., & Flier, J. S. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28898 · Cited by 3,690 · see citing works

Elevated C-reactive protein levels in overweight and obese adults

Visser, M. (1999) · JAMA · doi:10.1001/jama.282.22.2131 · Cited by 2,494 · see citing works

Subcutaneous Adipose Tissue Releases Interleukin-6, But Not Tumor Necrosis Factor-α,in Vivo1

Mohamed‐Ali, V., Goodrick, S., Rawesh, A., Katz, D. R., Miles, J. M., Yudkin, J. S., Klein, S., & Coppack, S. W. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.12.4450 · Cited by 2,012 · see citing works

Omental and Subcutaneous Adipose Tissues of Obese Subjects Release Interleukin-6: Depot Difference and Regulation by Glucocorticoid 1

Fried, S. K., Bunkin, D. A., & Greenberg, A. S. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.3.4660 · Cited by 1,528 · see citing works

Visceral fat adipokine secretion is associated with systemic inflammation in obese humans

Fontana, L., Eagon, J. C., Trujillo, M. E., Scherer, P. E., & Klein, S. (2007) · Diabetes · doi:10.2337/db06-1656 · Cited by 1,417 · see citing works

Interleukin-6 in Biology and Medicine

Akira, S., Taga, T., & Kishimoto, T. (1993) · Advances in immunology · doi:10.1016/s0065-2776(08)60532-5 · Cited by 1,384 · see citing works

NIDDM as a disease of the innate immune system: association of acute-phase reactants and interleukin-6 with metabolic syndrome X

Pickup, J. C., Mattock, M. B., Chusney, G. D., & Burt, D. J. (1997) · Diabetologia · doi:10.1007/s001250050822 · Cited by 1,241 · see citing works

Interleukin-6-deficient mice develop mature-onset obesity

Wallenius, V., Wallenius, K., Ahrén, B., Rudling, M., Carlsten, H., Dickson, S. L., Ohlsson, C., & Jansson, J.-O. (2002) · Nature Medicine · doi:10.1038/nm0102-75 · Cited by 1,213 · see citing works

Reduction of Macrophage Infiltration and Chemoattractant Gene Expression Changes in White Adipose Tissue of Morbidly Obese Subjects After Surgery-Induced Weight Loss

Cancello, R., Henegar, C., Viguerie, N., Taleb, S., Poitou, C., Rouault, C., Coupaye, M., Pelloux, V., Hugol, D., Bouillot, J.-L., et al. (2005) · Diabetes · doi:10.2337/diabetes.54.8.2277 · Cited by 1,164 · see citing works

Omental and Subcutaneous Adipose Tissues of Obese Subjects Release Interleukin-6: Depot Difference and Regulation by Glucocorticoid

Fried, S. K. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.83.3.847 · Cited by 1,146 · see citing works

Elevated Levels of Interleukin 6 Are Reduced in Serum and Subcutaneous Adipose Tissue of Obese Women after Weight Loss

Bastard, J., Jardel, C., Bruckert, É., Blondy, P., Capeau, J., Laville, M., Vidal, H., & Hainque, B. (2000) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.85.9.6839 · Cited by 1,102 · see citing works

Interleukin-6 (IL-6) Induces Insulin Resistance in 3T3-L1 Adipocytes and Is, Like IL-8 and Tumor Necrosis Factor-α, Overexpressed in Human Fat Cells from Insulin-resistant Subjects

Rotter, V., Nagaev, I., & Smith, U. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301977200 · Cited by 1,062 · see citing works

Appetite control: methodological aspects of the evaluation of foods

Blundell, J. E., de Graaf, C., Hulshof, T. G., Jebb, S. A., Livingstone, B., Lluch, A., Mela, D. J., Salah, S., Schuring, E. A. H., van der Knaap, H. C. M., et al. (2010) · Obesity Reviews · doi:10.1111/j.1467-789x.2010.00714.x · Cited by 1,010 · see citing works

Visfatin, an Adipocytokine with Proinflammatory and Immunomodulating Properties

Moschen, A. R., Kaser, A., Enrich, B., Mosheimer, B. A., Theurl, M., Niederegger, H., & Tilg, H. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.3.1748 · Cited by 938 · see citing works

Interleukin-6 Increases Insulin-Stimulated Glucose Disposal in Humans and Glucose Uptake and Fatty Acid Oxidation In Vitro via AMP-Activated Protein Kinase

Carey, A. L., Steinberg, G. R., Macaulay, S. L., Thomas, W. G., Holmes, A. G., Ramm, G., Prelovsek, O., Hohnen-Behrens, C., Watt, M. J., James, D. E., et al. (2006) · Diabetes · doi:10.2337/db05-1404 · Cited by 898 · see citing works

Reciprocal Association of C-Reactive Protein With Adiponectin in Blood Stream and Adipose Tissue

Ouchi, N., Kihara, S., Funahashi, T., Nakamura, T., Nishida, M., Kumada, M., Okamoto, Y., Ohashi, K., Nagaretani, H., Kishida, K., et al. (2003) · Circulation · doi:10.1161/01.cir.0000055188.83694.b3 · Cited by 850 · see citing works

Subcutaneous Adipose Tissue Releases Interleukin-6, But Not Tumor Necrosis Factor- , in Vivo

Mohamed-Ali, V. (1997) · Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.82.12.4196 · Cited by 717 · see citing works

Association between C-reactive protein and features of the metabolic syndrome: a population-based study.

Fröhlich, M., Imhof, A., Berg‐Beckhoff, G., Hutchinson, W. L., Pepys, M. B., Boeing, H., Muche, R., Brenner, H., & Köenig, W. (2000) · Diabetes Care · doi:10.2337/diacare.23.12.1835 · Cited by 683 · see citing works

Tumor Necrosis Factor-α Induces Skeletal Muscle Insulin Resistance in Healthy Human Subjects via Inhibition of Akt Substrate 160 Phosphorylation

Plomgaard, P., Bouzakri, K., Krogh-Madsen, R., Mittendorfer, B., Zierath, J. R., & Pedersen, B. K. (2005) · Diabetes · doi:10.2337/diabetes.54.10.2939 · Cited by 627 · see citing works

Increased Infiltration of Macrophages in Omental Adipose Tissue Is Associated With Marked Hepatic Lesions in Morbid Human Obesity

Cancello, R., Tordjman, J., Poitou, C., Guilhem, G., Bouillot, J. L., Hugol, D., Coussieu, C., Basdevant, A., Hen, A. B., Bedossa, P., et al. (2006) · Diabetes · doi:10.2337/db06-0133 · Cited by 607 · see citing works

Weight Loss Reduces C-Reactive Protein Levels in Obese Postmenopausal Women

Tchernof, A., Nolan, A., Sites, C. K., Ades, P. A., & Poehlman, E. T. (2002) · Circulation · doi:10.1161/hc0502.103331 · Cited by 541 · see citing works

Low vitamin D status: a contributing factor in the pathogenesis of congestive heart failure?

Zittermann, A., Schleithoff, S. S., Tenderich, G., Berthold, H. K., Körfer, R., & Stehle, P. (2002) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(02)02624-4 · Cited by 535 · see citing works

Adiponectin gene expression and secretion is inhibited by interleukin-6 in 3T3-L1 adipocytes

Faßhauer, M., Kralisch, S., Klier, M., Lössner, U., Blüher, M., Klein, J. C., & Paschke, R. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00090-1 · Cited by 534 · see citing works

Effects of an Engineered Human Anti–TNF-α Antibody (CDP571) on Insulin Sensitivity and Glycemic Control in Patients With NIDDM

Ofei, F., Hurel, S. J., Newkirk, J., Sopwith, M., & Taylor, R. (1996) · Diabetes · doi:10.2337/diab.45.7.881 · Cited by 510 · see citing works

Chronic Exposure to Interleukin-6 Causes Hepatic Insulin Resistance in Mice

Klover, P. J., Zimmers, T. A., Koniaris, L. G., & Mooney, R. A. (2003) · Diabetes · doi:10.2337/diabetes.52.11.2784 · Cited by 488 · see citing works

Insulin resistance associated to obesity: the link TNF-alpha

Nieto-Vázquez, I., Fernández‐Veledo, S., Kramer, D., Vila‐Bedmar, R., García‐Guerra, L., & Lorenzo, M. (2008) · Archives of Physiology and Biochemistry · doi:10.1080/13813450802181047 · Cited by 475 · see citing works

Insulin Resistance in Morbid Obesity

Greco, A. V., Mingrone, G., Giancaterini, A., Manco, M., Morroni, M., Cinti, S., Granzotto, M., Vettor, R., Camastra, S., & Ferrannini, E. (2002) · Diabetes · doi:10.2337/diabetes.51.1.144 · Cited by 442 · see citing works

The adipocyte in insulin resistance: key molecules and the impact of the thiazolidinediones

Arner, P. (2003) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(03)00024-9 · Cited by 423 · see citing works

Mechanisms of TNF-α-induced insulin resistance

Hotamışlıgil, G. S. (2009) · Experimental and Clinical Endocrinology & Diabetes · doi:10.1055/s-0029-1212086 · Cited by 420 · see citing works

Chronic interleukin-6 (IL-6) treatment increased IL-6 secretion and induced insulin resistance in adipocyte: prevention by rosiglitazone

Lagathu, C., Bastard, J.-P., Auclair, M., Maachi, M., Capeau, J., & Caron, M. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.10.013 · Cited by 385 · see citing works

Energy Restriction and Weight Loss on Very-Low-Fat Diets Reduce C-Reactive Protein Concentrations in Obese, Healthy Women

Heilbronn, L. K., Noakes, M., & Clifton, P. M. (2001) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.21.6.968 · Cited by 331 · see citing works

Induction of leptin resistance through direct interaction of C-reactive protein with leptin

Chen, K., Li, F., Li, J., Cai, H., Strom, S., Bisello, A., Kelley, D. E., Friedman-Einat, M., Skibinski, G. A., McCrory, M. A., et al. (2006) · Nature Medicine · doi:10.1038/nm1372 · Cited by 325 · see citing works

Anti-tumor necrosis factor-alpha blockade improves insulin resistance in patients with rheumatoid arthritis.

González-Gay, M. Á., Matias, J. M. D., González‐Juanatey, C., Garcı́a-Porrúa, C., Sanchez-Andrade, A., Martin, J. J., & Llorca, J. (2006) · PubMed · Cited by 313 · see citing works

Impaired glucose tolerance is associated with increased serum concentrations of interleukin 6 and co-regulated acute-phase proteins but not TNF-α or its receptors

Müller, S., Martin, S., Koenig, W., Hanifi-Moghaddam, P., Rathmann, W., Haastert, B., Giani, G., Illig, T., Thorand, B., & Kolb, H. (2002) · Diabetologia · doi:10.1007/s00125-002-0829-2 · Cited by 311 · see citing works

Role of hepatic STAT3 in brain-insulin action on hepatic glucose production

Inoue, H., Ogawa, W., Asakawa, A., Okamoto, Y., Nishizawa, A., Matsumoto, M., Teshigawara, K., Matsuki, Y., Watanabe, E., Hiramatsu, R., et al. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.02.009 · Cited by 294 · see citing works

Human C-reactive protein and the metabolic syndrome

Devaraj, S., Singh, U. S., & Jialal, I. (2009) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32832ac03e · Cited by 291 · see citing works

Release of Inflammatory Mediators by Human Adipose Tissue Is Enhanced in Obesity and Primarily by the Nonfat Cells: A Review

Fain, J. N. (2010) · Mediators of Inflammation · doi:10.1155/2010/513948 · Cited by 286 · see citing works

Interleukin-6 depletion selectively improves hepatic insulin action in obesity.

Klover, P. J., Clementi, A. H., & Mooney, R. A. (2005) · Endocrinology · doi:10.1210/en.2004-1468 · Cited by 273 · see citing works

Benefits of massive weight loss on symptoms, systemic inflammation and cartilage turnover in obese patients with knee osteoarthritis

Richette, P., Poitou, C., Garnero, P., Vicaut, É., Bouillot, J., Lacorte, J., Basdevant, A., Clément, K., Bardin, T., & Chevalier, X. (2010) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2010.134015 · Cited by 254 · see citing works

Functional Analysis of Tumor Necrosis Factor (TNF) Receptors in TNF-α-Mediated Insulin Resistance in Genetic Obesity**This work is supported in part by a grant from the NIH (DK-52539).

Uysal, K. T., Wiesbrock, S. M., & Hotamışlıgil, G. S. (1998) · Endocrinology · doi:10.1210/endo.139.12.6337 · Cited by 247 · see citing works

Metformin Reduces Serum C-Reactive Protein Levels in Women with Polycystic Ovary Syndrome

Morin-Papunen, L. C., Rautio, K., Ruokonen, A., Hedberg, P. S. M., Puukka, M., & Tapanainen, J. S. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2002-021688 · Cited by 245 · see citing works

Increased leptin concentrations correlate with increased concentrations of inflammatory markers in morbidly obese individuals

van Dielen, F., Veer, C. V. ′., Schols, A. M. W. J., Soeters, P. B., Buurman, W. A., & Greve, J.-W. M. (2001) · International Journal of Obesity · doi:10.1038/sj.ijo.0801825 · Cited by 231 · see citing works

Chapter 21 Interleukin‐6 and Insulin Resistance

Kim, J., Bachmann, R. A., & Chen, J. (2009) · Vitamins & Hormones · doi:10.1016/s0083-6729(08)00621-3 · Cited by 224 · see citing works

Serum 25-hydroxyvitamin D levels are inversely associated with systemic inflammation in severe obese subjects

Bellia, A., Garcovich, C., D’Adamo, M., Lombardo, M., Tesauro, M., Donadel, G., Gentileschi, P., Lauro, D., Federici, M., Lauro, R., et al. (2013) · Internal and Emergency Medicine · doi:10.1007/s11739-011-0559-x · Cited by 206 · see citing works

Effects of Changes in Body Weight and Insulin Resistance on Inflammation and Endothelial Function in Morbid Obesity after Bariatric Surgery

Vázquez, L. A., Pazos, F., de Berrazueta, J. R., Fernández-Escalante, C., García‐Unzueta, M. T., Freijanes, J., & Amado, J. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-032059 · Cited by 205 · see citing works

The effects of rosiglitazone, a peroxisome proliferator-activated receptor-gamma agonist, on markers of endothelial cell activation, C-reactive protein, and fibrinogen levels in non-diabetic coronary artery disease patients

Sidhu, J. S., Cowan, D., & Kaski, J. C. (2003) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2003.04.001 · Cited by 197 · see citing works

Impact of TNF inhibition on insulin resistance and lipids levels in patients with rheumatoid arthritis

Tam, L.-S., Tomlinson, B., Chu, T. T., Li, T. K., & Li, E. K. (2007) · Clinical Rheumatology · doi:10.1007/s10067-007-0539-8 · Cited by 197 · see citing works

Adipose and Liver Expression of Interleukin (IL)-1 Family Members in Morbid Obesity and Effects of Weight Loss

Moschen, A. R., Molnar, C., Enrich, B., Geiger, S., Ebenbichler, C. F., & Tilg, H. (2011) · Molecular Medicine · doi:10.2119/molmed.2010.00108 · Cited by 185 · see citing works

Obesity and diabetes in TNF-alpha receptor- deficient mice.

Schreyer, S. A., Chua, S. C., & LeBoeuf, R. C. (1998) · Journal of Clinical Investigation · doi:10.1172/jci2849 · Cited by 172 · see citing works

Constitutive and IL‐6‐induced nuclear factors that interact with the human C‐reactive protein promoter.

Majello, B., Arcone, R., Toniatti, C., & Ciliberto, G. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb08131.x · Cited by 172 · see citing works

A randomized study comparing the effects of a low-carbohydrate diet and a conventional diet on lipoprotein subfractions and C-reactive protein levels in patients with severe obesity

Seshadri, P., Iqbal, N., Stern, L., Williams, M., Chicano, K. L., Daily, D. A., McGrory, J., Gracely, E. J., Rader, D. J., & Samaha, F. F. (2004) · The American Journal of Medicine · doi:10.1016/j.amjmed.2004.04.009 · Cited by 169 · see citing works

Effect of Massive Weight Loss on Inflammatory Adipocytokines and the Innate Immune System in Morbidly Obese Women

Manco, M., Fernández‐Real, J. M., Equitani, F., Vendrell, J. J., Mora, M. E. V., Nanni, G., Tondolo, V., Calvani, M., Ricart, W., Castagneto, M., et al. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0960 · Cited by 162 · see citing works

Leptin-Induced IL-6 Production Is Mediated by Leptin Receptor, Insulin Receptor Substrate-1, Phosphatidylinositol 3-Kinase, Akt, NF-κB, and p300 Pathway in Microglia

Tang, C., Lu, D.-Y., Yang, R., Tsai, H.-Y., Kao, M., Fu, W., & Chen, Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.2.1292 · Cited by 160 · see citing works

Lipid and carbohydrate metabolism in mice with a targeted mutation in the IL-6 gene: absence of development of age-related obesity

Gregorio, G. B. D., Hensley, L. L., Lü, T., Ranganathan, G., & Kern, P. A. (2004) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00189.2003 · Cited by 160 · see citing works

Interleukin-6 is a negative regulator of visfatin gene expression in 3T3-L1 adipocytes

Kralisch, S., Klein, J. C., Lössner, U., Blüher, M., Paschke, R., Stümvoll, M., & Faßhauer, M. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00090.2005 · Cited by 158 · see citing works

Short-term Treatment of RAW264.7 Macrophages with Adiponectin Increases Tumor Necrosis Factor-α (TNF-α) Expression via ERK1/2 Activation and Egr-1 Expression

Park, P., McMullen, M. R., Huang, H., Thakur, V., & Nagy, L. E. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701419200 · Cited by 148 · see citing works

Partial Reversibility of Hypothalamic Dysfunction and Changes in Brain Activity After Body Mass Reduction in Obese Subjects

van de Sande‐Lee, S., Pereira, F., Cintra, D. E., Fernandes, P. T., Cardoso, A. R., Garlipp, C. R., Chaim, É. A., Pareja, J. C., Geloneze, B., Li, L. M., et al. (2011) · Diabetes · doi:10.2337/db10-1614 · Cited by 148 · see citing works

Interleukin-6 and insulin sensitivity: friend or foe?

Carey, A. L., & Febbraio, M. A. (2004) · Diabetologia · doi:10.1007/s00125-004-1447-y · Cited by 140 · see citing works

Serial changes in inflammatory biomarkers after Roux-en-Y gastric bypass surgery

Miller, G. D., Nicklas, B. J., & Fernandez, A. (2011) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2011.03.006 · Cited by 130 · see citing works

Longitudinal changes in pancreatic and adipocyte hormones following Roux-en-Y gastric bypass surgery

Swarbrick, M. M., Stanhope, K. L., Austrheim-Smith, I. T., Loan, M. D. V., Ali, M. R., Wolfe, B. M., & Havel, P. J. (2008) · Diabetologia · doi:10.1007/s00125-008-1118-5 · Cited by 125 · see citing works

Nutritional Management of Weight Regain After Bariatric Surgery

Faria, S. L., Kelly, E. D. O., Lins, R. D., & Faria, O. P. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9610-z · Cited by 116 · see citing works

Gastric Bypass Surgery Reduces Plasma Ceramide Subspecies and Improves Insulin Sensitivity in Severely Obese Patients

Huang, H., Kasumov, T., Gatmaitan, P., Heneghan, H., Kashyap, S. R., Schauer, P. R., Brethauer, S. A., & Kirwan, J. P. (2011) · Obesity · doi:10.1038/oby.2011.107 · Cited by 113 · see citing works

Moderate-intensity regular exercise decreases serum tumor necrosis factor-α and HbA1c levels in healthy women

Tsukui, S., Kanda, T., Nara, M., Nishino, M., KONDO, T., & Kobayashi, I. (2000) · International Journal of Obesity · doi:10.1038/sj.ijo.0801373 · Cited by 109 · see citing works

Decreased serum hepcidin and improved functional iron status 6 months after restrictive bariatric surgery

Tussing‐Humphreys, L. M., Nemeth, E., Fantuzzi, G., Freels, S., Holterman, A. L., Galvani, C., Ayloo, S., Vitello, J., & Braunschweig, C. (2010) · Obesity · doi:10.1038/oby.2009.490 · Cited by 105 · see citing works

Impact of Laparoscopic Sleeve Gastrectomy on Iron Indices: 1 Year Follow-Up

Hakeam, H. A., O’Regan, P. J., Salem, A. M., Bamehriz, F. Y., & Eldali, A. (2009) · Obesity Surgery · doi:10.1007/s11695-009-9919-2 · Cited by 102 · see citing works

Changes in tumor necrosis factor-alpha system and insulin sensitivity during an exercise training program in obese women with normal and impaired glucose tolerance

Strączkowski, M., Kowalska, I., Dzienis-Straczkowska, S., Stępień, A., Skibinska, E., Szelachowska, M., & Kinalska, I. (2001) · European Journal of Endocrinology · doi:10.1530/eje.0.1450273 · Cited by 101 · see citing works

Effects of an engineered human anti-TNF-alpha antibody (CDP571) on insulin sensitivity and glycemic control in patients with NIDDM

Ofei, F., Hurel, S. J., Newkirk, J., Sopwith, M., & Taylor, R. (1996) · Diabetes · doi:10.2337/diabetes.45.7.881 · Cited by 101 · see citing works

Acute Effect of Roux-En-Y Gastric Bypass on Whole-Body Insulin Sensitivity: A Study with the Euglycemic-Hyperinsulinemic Clamp

Lima, M. M. D. O., Pareja, J. C., Alegre, S. M., Geloneze, S. R., Kahn, S. E., Astiarraga, B., Chaim, É. A., & Geloneze, B. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2010-0085 · Cited by 99 · see citing works

Osteoprotegerin in relation to body weight, lipid parameters insulin sensitivity, adipocytokines, and C-reactive protein in obese and non-obese young individuals: results from both cross-sectional and interventional study

Gannagé‐Yared, M., Yaghi, C., Habre, B., Khalifé, S., Noun, R. J., Germanos-Haddad, M., & Trak-Smayra, V. E. (2008) · European Journal of Endocrinology · doi:10.1530/eje-07-0797 · Cited by 93 · see citing works

Effect of bariatric surgery on circulating chemerin levels

Ress, C., Tschoner, A., Engl, J., Klaus, A., Tilg, H., Ebenbichler, C. F., Patsch, J. R., & Kaser, S. (2010) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2010.02255.x · Cited by 90 · see citing works

Serum C-Reactive Protein and White Blood Cell Count in Morbidly Obese Surgical Patients

Chen, S.-B., Lee, Y.-C., Ser, K., Chen, J., Chen, S. C., Hsieh, H., & Lee, W. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9619-3 · Cited by 82 · see citing works

Increases in Adiponectin Predict Improved Liver, but Not Peripheral, Insulin Sensitivity in Severely Obese Women During Weight Loss

Lin, E., Phillips, L. S., Ziegler, T. R., Schmotzer, B. J., Wu, K., Gu, L. H., Khaitan, L., Lynch, S. A., Torres, W. E., Smith, C. D., et al. (2007) · Diabetes · doi:10.2337/db06-1161 · Cited by 80 · see citing works

C-reactive protein impairs hepatic insulin sensitivity and insulin signaling in rats: Role of mitogen-activated protein kinases

Liang, X., Xiao, C., Bandsma, R., Naples, M., Adeli, K., & Lewis, G. F. (2010) · Hepatology · doi:10.1002/hep.24011 · Cited by 77 · see citing works

Bariatric Surgery Reduces Visceral Adipose Inflammation and Improves Endothelial Function in Type 2 Diabetic Mice

Zhang, H., Wang, Y., Zhang, J., Potter, B. J., Sowers, J. R., & Zhang, C. (2011) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.225870 · Cited by 76 · see citing works

Tumor necrosis factor (TNF)-α induces leptin production through the p55 TNF receptor

Finck, B. N., & Johnson, R. W. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.278.2.r537 · Cited by 76 · see citing works

Functional Analysis of Tumor Necrosis Factor (TNF) Receptors in TNF- -Mediated Insulin Resistance in Genetic Obesity

Uysal, K. T. (1998) · Endocrinology · doi:10.1210/en.139.12.4832 · Cited by 74 · see citing works

CRP reduction following gastric bypass surgery is most pronounced in insulin-sensitive subjects

Holdstock, C., Lind, L., Engstrom, B. E., Ohrvall, M., Sundbom, M., Larsson, A., & Karlsson, F. A. (2005) · International Journal of Obesity · doi:10.1038/sj.ijo.0803000 · Cited by 73 · see citing works

Increased Colorectal Epithelial Cell Proliferation and Crypt Fission Associated with Obesity and Roux-en-Y Gastric Bypass

Sainsbury, A., Goodlad, R. A., Perry, S., Pollard, S. G., Robins, G. G., & Hull, M. A. (2008) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-07-2874 · Cited by 70 · see citing works

Only C-Reactive Protein, but not TNF-α or IL6, Reflects the Improvement in Inflammation after Bariatric Surgery

Pardina, E., Ferrer, R., Baena‐Fustegueras, J. A., Déniz, J. R., Lecube, A., Fort, J. M., Vargas, V., Catalán, R., & Peinado‐Onsurbe, J. (2011) · Obesity Surgery · doi:10.1007/s11695-011-0546-3 · Cited by 69 · see citing works

Relation between degree of weight loss after bariatric surgery and reduction in albuminuria and C-reactive protein

Agrawal, V., Krause, K. R., Chengelis, D. L., Zalesin, K. C., Rocher, L. L., & McCullough, P. A. (2008) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2008.07.011 · Cited by 68 · see citing works

Increased visceral adipose tissue mass is associated with increased C-reactive protein in patients with manifest vascular diseases

Faber, D. R., van der Graaf, Y., Westerink, J., & Visseren, F. L. J. (2010) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2010.04.029 · Cited by 67 · see citing works

Systemic Blockade of TNF-α does not Improve Insulin Resistance in Humans

Ferraz‐Amaro, I., Arce‐Franco, M., Muñiz, J., López‐Fernández, J., Hernández-Hernández, V., Franco, A., Quevedo-Abeledo, J. C., Martínez-Martín, J., & Díaz‐González, F. (2011) · Hormone and Metabolic Research · doi:10.1055/s-0031-1287783 · Cited by 63 · see citing works

Variations in plasma soluble tumour necrosis factor receptors after diet‐induced weight loss in obesity

Bastard, J., Jardel, C., Bruckert, É., Vidal, H., & Hainque, B. (2000) · Diabetes Obesity and Metabolism · doi:10.1046/j.1463-1326.2000.00090.x · Cited by 61 · see citing works

Globular adiponectin decreases leptin-induced tumor necrosis factor-α expression by murine macrophages: Involvement of cAMP-PKA and MAPK pathways

Zhao, T., Hou, M., Xia, M., Wang, Q., Zhu, H., Xiao, Y., Tang, Z., Ma, J., & Ling, W. (2005) · Cellular Immunology · doi:10.1016/j.cellimm.2005.12.002 · Cited by 60 · see citing works

One Year Improvements in Cardiovascular Risk Factors: a Comparative Trial of Laparoscopic Roux-en-Y Gastric Bypass vs. Adjustable Gastric Banding

Woodard, G. A., Peraza, J., Bravo, S., Toplosky, L., Hernandez‐Boussard, T., & Morton, J. M. (2010) · Obesity Surgery · doi:10.1007/s11695-010-0088-0 · Cited by 58 · see citing works

Adipocyte Fatty Acid‐binding Protein as a Determinant of Insulin Sensitivity in Morbid‐obese Women

Simón, I., Escoté, X., Vilarrasa, N., Gómez, J. M., Fernández‐Real, J. M., Megía, A., Gutiérrez, C., Gallart, L., Noguera, C. M., & Vendrell, J. J. (2009) · Obesity · doi:10.1038/oby.2008.665 · Cited by 54 · see citing works

Association of Retinol-Binding Protein-4 (RBP4) with Lipid Parameters in Obese Women

Broch, M., Gómez, J. M., Auguet, T., Vilarrasa, N., Pastor, R., Elío, I., Olona, M., García‐España, A., & Richart, C. (2010) · Obesity Surgery · doi:10.1007/s11695-010-0200-5 · Cited by 50 · see citing works

Inhibition of C-Reactive Protein in Morbidly Obese Patients After Laparoscopic Sleeve Gastrectomy

Hakeam, H. A., O’Regan, P. J., Salem, A. M., Bamehriz, F. Y., & Jomaa, L. F. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9729-y · Cited by 50 · see citing works

Visceral Adipose Tissue Loss and Insulin Resistance 6 Months after Laparoscopic Gastric Banding Surgery: A Preliminary Study

Carroll, J. F., Franks, S. F., Smith, A. B., & Phelps, D. R. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9642-4 · Cited by 48 · see citing works

Significant Correlation Between Visceral Adiposity and High-sensitivity C-reactive Protein (hs-CRP) in Japanese Subjects

Tsuriya, D., Morita, H., Morioka, T., Takahashi, N., Ito, T., Oki, Y., & Nakamura, H. (2011) · Internal Medicine · doi:10.2169/internalmedicine.50.5908 · Cited by 48 · see citing works

Human serum levels of fetal antigen 1 (FA1/Dlk1) increase with obesity, are negatively associated with insulin sensitivity and modulate inflammation in vitro

Chacón, M. R., Miranda, M., Jensen, C. H., Fernández‐Real, J. M., Vilarrasa, N., Gutiérrez, C., Näf, S., Gómez, J. M., & Vendrell, J. J. (2008) · International Journal of Obesity · doi:10.1038/ijo.2008.40 · Cited by 47 · see citing works

Longterm anti-tumor necrosis factor-alpha treatment in patients with refractory rheumatoid arthritis: relationship between insulin resistance and disease activity.

SERIOLO, B., Ferrone, C., & Cutolo, M. (2008) · PubMed · Cited by 45 · see citing works

Renal cytokines improve early after bariatric surgery

Bueter, M., Dubb, S. S., Gill, A., Joannou, L., Ahmed, A. R., Frankel, A., Tam, F. W. K., & le Roux, C. W. (2010) · British journal of surgery · doi:10.1002/bjs.7264 · Cited by 42 · see citing works

The effect of weight loss after gastric bypass on C-reactive protein levels

Zagorski, S. M., Papa, N., & Chung, M. H. (2005) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2005.01.001 · Cited by 40 · see citing works

Roux-en-Y Bypass Gastroplasty: Markers of Oxidative Stress 6 Months After Surgery

Boesing, F., Moreira, E. A. M., Wilhelm-Filho, D., Vigil, S. V. G., Parizottto, E. B., Inácio, D. B., Portari, G. V., Trindade, E. B. S. D. M., Jordão, A. A., & Fröde, T. S. (2010) · Obesity Surgery · doi:10.1007/s11695-010-0196-x · Cited by 39 · see citing works

Effects of Two Variants of Roux-en-Y Gastric Bypass on Metabolism Behaviour: Focus on Plasma Ghrelin Concentrations Over a 2-Year Follow-up

Pérez, N., Serra, A., Granada, M. L., Rull, M., Alastrué, A., Navarro-Díaz, M., Romero, R., & Fernández-Llamazares, J. (2009) · Obesity Surgery · doi:10.1007/s11695-009-0035-0 · Cited by 36 · see citing works

Nitric oxide production is paradoxically decreased after weight reduction surgery in morbid obesity patients

Lin, L., Lee, W.-J., Shen, H.-N., Yang, W., Pai, N.-H., Su, T., & Liau, C. (2006) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2006.02.033 · Cited by 32 · see citing works

Increase of Osteopontin Plasma Concentrations After Bariatric Surgery Independent from Inflammation and Insulin Resistance

Schaller, G., Aso, Y., Schernthaner, G.-H., Kopp, H.-P., Inukai, T., Kriwanek, S., & Schernthaner, G. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9532-9 · Cited by 32 · see citing works

Adjustable Gastric Banding

Arata, J., & Perry, A. (1991) · Obesity Surgery · doi:10.1381/096089291765561565 · Cited by 31 · see citing works

Relationship of Androgens to Insulin Resistance and Chronic Inflammation in Morbidly Obese Premenopausal Women: Studies before and after Vertical Banded Gastroplasty

Kopp, H.-P., Krzyżanowska, K., Schernthaner, G.-H., Kriwanek, S., & Schernthaner, G. (2006) · Obesity Surgery · doi:10.1381/096089206778392130 · Cited by 30 · see citing works

Effect of laparoscopic sleeve gastrectomy on elevated C-reactive protein and atherogenic dyslipidemia in morbidly obese patients

Wong, A. T. Y., Chan, D. C., Armstrong, J., & Watts, G. F. (2010) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2010.12.004 · Cited by 29 · see citing works

Systemic blood osteopontin, endostatin, and E-selectin concentrations after vertical banding surgery in severely obese adults

Komorowski, J., Jankiewicz-Wika, J., Kołomecki, K., Cywiński, J. B., Piestrzeniewicz, K., Świętosławski, J., & Stepien, H. (2011) · Cytokine · doi:10.1016/j.cyto.2011.03.020 · Cited by 28 · see citing works

C-Reactive Protein, Insulin Resistance, and Metabolic Syndrome in a Population With a High Burden of Subclinical Infection

Howard, B. V., Best, L. G., Comuzzie, A. G., Ebbesson, S. O. E., Epstein, S. E., Fabsitz, R. R., Howard, W. J., Silverman, A., Wang, H., Zhu, J., et al. (2008) · Diabetes Care · doi:10.2337/dc08-0815 · Cited by 28 · see citing works

Augmentation of Pulmonary Epithelial Cell IL-8 Expression and Permeability by Pre-B-cell Colony Enhancing Factor

Li, H., Liu, P., Cepeda, J., Fang, D., Easley, R. B., Simon, B. A., Zhang, L. Q., & Ye, S. Q. (2008) · Journal of Inflammation · doi:10.1186/1476-9255-5-15 · Cited by 27 · see citing works

Leptin as an Acute Phase Reactant after Non-Adjustable Laparoscopic Gastric Banding

Maruna, P., Gürlich, R., Fried, M., Fraško, R., Chachkhiani, I., & Haluzı́k, M. (2001) · Obesity Surgery · doi:10.1381/09608920160556814 · Cited by 26 · see citing works

Body composition changes after laparoscopic adjustable gastric banding: what is the role of −174G>C interleukin-6 promoter gene polymorphism in the therapeutic strategy?

Renzo, L. D., Carbonelli, M. G., Bianchi, A., Iacopino, L., Fiorito, R., Daniele, N. D., & LORENZO, A. D. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.132 · Cited by 25 · see citing works

Plasma visfatin and tumor necrosis factor-alpha (TNF-α) levels in metabolic syndrome.

Olszanecka‐Glinianowicz, M., Kocełak, P., Janowska, J., Skorupa, A. J., Nylec, M., & Zahorska‐Markiewicz, B. (2011) · PubMed · Cited by 25 · see citing works

Sleep Apnea Determines Soluble TNF-α Receptor 2 Response to Massive Weight Loss

Pallayová, M., Steele, K. E., Magnuson, T. H., Schweitzer, M., Smith, P. L., Patil, S. P., Bevans‐Fonti, S., Polotsky, V. Y., & Schwartz, A. R. (2011) · Obesity Surgery · doi:10.1007/s11695-011-0359-4 · Cited by 24 · see citing works

PGC1α gene Gly482Ser polymorphism predicts improved metabolic, inflammatory and vascular outcomes following bariatric surgery

Geloneze, S. R., Geloneze, B., Morari, J., Matos‐Souza, J. R., Lima, M. M. D. O., Chaim, É. A., Pareja, J. C., & Velloso, L. A. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.176 · Cited by 23 · see citing works

The decrease in serum IL-18 levels after bariatric surgery in morbidly obese women is a time-dependent event

Botella-Carretero, J. I., Álvarez‐Blasco, F., Martínez-García, M. Á., Luque‐Ramírez, M., Millán, J. L. S., & Escobar-Morreale, H. F. (2007) · Obesity Surgery · doi:10.1007/s11695-007-9202-3 · Cited by 19 · see citing works

Suppressed cytokine production in whole blood cultures may be related to iron status and hepcidin and is partially corrected following weight reduction in morbidly obese pre-menopausal women

Tussing-Humphreys, L. M., Pini, M., Ponemone, V., Braunschweig, C. L., & Fantuzzi, G. (2010) · Cytokine · doi:10.1016/j.cyto.2010.11.008 · Cited by 18 · see citing works

Effect of weight loss on serum pigment epithelium-derived factor levels

Tschoner, A., Sturm, W., Ress, C., Engl, J., Kaser, S., Laimer, M. W., Laimer, E., Klaus, A., Tilg, H., Patsch, J. R., et al. (2011) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2011.02482.x · Cited by 13 · see citing works

Influence of G308A Polymorphism of Tumor Necrosis Factor Alpha Gene on Surgical Results of Biliopancreatic Diversion

de Luis, D. A., Pacheco, D., Aller, R., Sagrado, M. G., Izaola, O., Terroba, M. C., Cuéllar, L., Conde, R., & Martin, T. (2008) · Obesity Surgery · doi:10.1007/s11695-008-9591-y · Cited by 12 · see citing works

SUBCUTANEOUS SMALL RESISTANCE ARTERY MORPHOLOGY AND CIRCULATING INDICES OF INFLAMMATION/OXIDATIVE STRESS IN OBESE PATIENTS BEFORE AND AFTER BARIATRIC SURGERY AND CONSISTENT WEIGHT LOSS

Ciuceis, C. D., PORTERI, E., Boria, E. L., Boari, G. E. M., Mittempergher, F., Casella, C., Rosei, C. A., Ruggeri, G., & Rizzoni, G. (2011) · Journal of Hypertension · doi:10.1097/00004872-201106001-00043 · Cited by 1 · see citing works

Abstract 5550: C-reactive Protein (CRP) Causes Insulin Resistance in Mice Through Fc γ RIIB-mediated Inhibition of Insulin Signaling

Tanigaki, K., Mineo, C., Longoria, C., Vongpatanasin, W., & Shaul, P. W. (2009) · Circulation · doi:10.1161/circ.120.suppl_18.s1114-c · Cited by 1 · see citing works

The Role of Inflammation in Diabetes: Current Concepts and Future Perspectives

Tsalamandris, S., Antonopoulos, A. S., Oikonomou, E., Papamikroulis, G.-A., Vogiatzi, G., Papaioannou, S., Deftereos, S., & Tousoulis, D. (2019) · European Cardiology Review · doi:10.15420/ecr.2018.33.1 · Cited by 1,381 · see citing works

Epigenomics, gestational programming and risk of metabolic syndrome

Desai, M., Jellyman, J. K., & Ross, M. G. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.13 · Cited by 277 · see citing works

Immune aging, dysmetabolism, and inflammation in neurological diseases

Deleidi, M., Jäggle, M., & Rubino, G. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00172 · Cited by 260 · see citing works

Role of Adiposity-Driven Inflammation in Depressive Morbidity

Capuron, L., Lasselin, J., & Castanon, N. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.123 · Cited by 182 · see citing works

Role of neuroinflammation in the emotional and cognitive alterations displayed by animal models of obesity

Castanon, N., Luheshi, G. N., & Layé, S. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00229 · Cited by 179 · see citing works

Therapeutic approaches targeting inflammation for diabetes and associated cardiovascular risk

Goldfine, A. B., & Shoelson, S. E. (2017) · Journal of Clinical Investigation · doi:10.1172/jci88884 · Cited by 172 · see citing works

Obesity, adipokines and neuroinflammation

Aguilar‐Valles, A., Inoue, W., Rummel, C. D., & Luheshi, G. N. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.12.023 · Cited by 166 · see citing works

Chronic Low-Grade Inflammation in Metabolic Disorders: Relevance for Behavioral Symptoms

Lasselin, J., & Capuron, L. (2014) · NeuroImmunoModulation · doi:10.1159/000356535 · Cited by 129 · see citing works

Effect of bariatric surgery on serum inflammatory factors of obese patients: a systematic review and meta-analysis

Askarpour, M., Khani, D., Sheikhi, A., Ghaedi, E., & Alizadeh, S. (2019) · Obesity Surgery · doi:10.1007/s11695-019-03926-0 · Cited by 120 · see citing works

Changes in inflammation, oxidative stress and adipokines following bariatric surgery among adolescents with severe obesity

Kelly, A. S., Ryder, J. R., Marlatt, K. L., Rudser, K. D., Jenkins, T. M., & Inge, T. H. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.174 · Cited by 113 · see citing works

Depression and Obesity: Analysis of Common Biomarkers

Milano, W., Ambrosio, P., Carizzone, F., Biasio, V. D., Munzio, W. D., Foia, M. G., & Capasso, A. (2020) · Diseases · doi:10.3390/diseases8020023 · Cited by 107 · see citing works

PYY plays a key role in the resolution of diabetes following bariatric surgery in humans

Guida, C., Stephen, S. D., Watson, M., Dempster, N. J., Larraufie, P., Marjot, T., Cargill, T. N., Rickers, L., Pavlides, M., Tomlinson, J., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2018.12.040 · Cited by 97 · see citing works

The Effects of Bariatric Surgery on Colorectal Cancer Risk: Systematic Review and Meta-analysis

Afshar, S., Kelly, S. B., Seymour, K., Lara, J., Woodcock, S., & Mathers, J. C. (2014) · Obesity Surgery · doi:10.1007/s11695-014-1359-y · Cited by 96 · see citing works

Healthy lifestyles and wellbeing reduce neuroinflammation and prevent neurodegenerative and psychiatric disorders

Kip, E., & Parr‐Brownlie, L. C. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1092537 · Cited by 96 · see citing works

Sclerostin Levels and Changes in Bone Metabolism After Bariatric Surgery

Muschitz, C., Kocijan, R., Marterer, C., Nia, A., Muschitz, G. K., Resch, H., & Pietschmann, P. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-3367 · Cited by 90 · see citing works

The influence of bariatric surgery on oral drug bioavailability in patients with obesity: A systematic review

Angeles, P. C., Robertsen, I., Seeberg, L. T., Krogstad, V., Skattebu, J., Sandbu, R., Åsberg, A., & Hjelmesaeth, J. S. (2019) · Obesity Reviews · doi:10.1111/obr.12869 · Cited by 87 · see citing works

Diet and depression: A systematic review of whole dietary interventions as treatment in patients with depression

Swainson, J., Reeson, M., Malik, U., Stefanuk, I., Cummins, M., & Sivapalan, S. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.01.094 · Cited by 87 · see citing works

Effects of bariatric surgery on markers of subclinical atherosclerosis and endothelial function: a meta-analysis of literature studies

Lupoli, R., Minno, M. N. D. D., Guidone, C., CEFALO, C. M. A., Capaldo, B., Riccardi, G., & Mingrone, G. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.187 · Cited by 83 · see citing works

FNDC4, a novel adipokine that reduces lipogenesis and promotes fat browning in human visceral adipocytes

Frühbeck, G., Fernández-Quintana, B., Paniagua, M., Hernández‐Pardos, A. W., Valentí, V., Moncada, R., Catalán, V., Becerril, S., Gómez‐Ambrosi, J., Portincasa, P., et al. (2020) · Metabolism · doi:10.1016/j.metabol.2020.154261 · Cited by 80 · see citing works

Changes in Bile Acid Profile After Laparoscopic Sleeve Gastrectomy are Associated with Improvements in Metabolic Profile and Fatty Liver Disease

Belgaumkar, A. P., Vincent, R. P., Carswell, K. A., Hughes, R. D., Alaghband-Zadeh, J., Mitry, R. R., le Roux, C. W., & Patel, A. G. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1878-1 · Cited by 79 · see citing works

Leptin Increases: Physiological Roles in the Control of Sympathetic Nerve Activity, Energy Balance, and the Hypothalamic–Pituitary–Thyroid Axis

Martelli, D., & Brooks, V. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032684 · Cited by 75 · see citing works

Evaluation of the biochemical, inflammatory and oxidative profile of obese patients given clinical treatment and bariatric surgery

Schmatz, R., Bitencourt, M. R., Patias, L. D., Beck, M. D. O., Alvarez, G. D. C., Zanini, D., Gutierres, J. M., Dallazem, L. N. D., Pereira, L. B., Leal, C. A. M., et al. (2016) · Clinica Chimica Acta · doi:10.1016/j.cca.2016.12.012 · Cited by 70 · see citing works

The Pharmacokinetics of the CYP3A Substrate Midazolam in Morbidly Obese Patients Before and One Year After Bariatric Surgery

Brill, M. J. E., van Rongen, A., van Dongen, E. P., van Ramshorst, B., Hazebroek, E. J., Darwich, A. S., Rostami‐Hodjegan, A., & Knibbe, C. A. J. (2015) · Pharmaceutical Research · doi:10.1007/s11095-015-1752-9 · Cited by 68 · see citing works

Methylation and Expression of Immune and Inflammatory Genes in the Offspring of Bariatric Bypass Surgery Patients

Guénard, F., Tchernof, A., Deshaies, Y., Cianflone, K., Kral, J. G., Marceau, P., & Vohl, M. (2013) · Journal of Obesity · doi:10.1155/2013/492170 · Cited by 66 · see citing works

The Impact of Obesity on Gallstone Disease, Acute Pancreatitis, and Pancreatic Cancer

Cruz‐Monserrate, Z., Conwell, D. L., & Krishna, S. G. (2016) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.07.010 · Cited by 65 · see citing works

LP(a): Structure, Genetics, Associated Cardiovascular Risk, and Emerging Therapeutics

Tasdighi, E., Adhikari, R., Almaadawy, O., Leucker, T. M., & Blaha, M. J. (2023) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-031023-100609 · Cited by 63 · see citing works

Attenuated improvements in adiponectin and fat loss characterize type 2 diabetes non‐remission status after bariatric surgery

Malin, S. K., Bena, J., Abood, B., Pothier, C. E., Bhatt, D. L., Nissen, S. E., Brethauer, S. A., Schauer, P. R., Kirwan, J. P., & Kashyap, S. R. (2014) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12376 · Cited by 60 · see citing works

Lipids and bariatric procedures part 1 of 2: Scientific statement from the National Lipid Association, American Society for Metabolic and Bariatric Surgery, and Obesity Medicine Association: FULL REPORT

Bays, H. E., Jones, P. H., Jacobson, T. A., Cohen, D. E., Orringer, C. E., Kothari, S. N., Azagury, D. E., Morton, J. M., Nguyen, N. T., Westman, E. C., et al. (2015) · Journal of clinical lipidology · doi:10.1016/j.jacl.2015.12.002 · Cited by 57 · see citing works

Whole-body cryostimulation as an effective method of reducing low-grade inflammation in obese men

Ziemann, E., Olek, R. A., Grzywacz, T., Antosiewicz, J., Kujach, S., Łuszczyk, M., Smaruj, M., Śledziewska, E., & Laskowski, R. (2013) · The Journal of Physiological Sciences · doi:10.1007/s12576-013-0269-4 · Cited by 56 · see citing works

Whole-body cryostimulation as an effective way of reducing exercise-induced inflammation and blood cholesterol in young men-->

Ziemann, E., Olek, R. A., Grzywacz, T., Kaczor, J. J., Antosiewicz, J., Skrobot, W. R., Kujach, S., & Laskowski, R. (2014) · European Cytokine Network · doi:10.1684/ecn.2014.0349 · Cited by 56 · see citing works

Obesity and weight loss could alter the properties of adipose stem cells?

Baptista, L. S. (2015) · World Journal of Stem Cells · doi:10.4252/wjsc.v7.i1.165 · Cited by 55 · see citing works

The immune remodel: Weight loss-mediated inflammatory changes to obesity

Phillips, C. L., & Grayson, B. E. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370219900185 · Cited by 56 · see citing works

Differential methylation in inflammation and type 2 diabetes genes in siblings born before and after maternal bariatric surgery

Berglind, D., Müller, P., Willmer, M., Sinha, I., Tynelius, P., Näslund, E. B., Dahlman‐Wright, K., & Rasmussen, F. E. (2015) · Obesity · doi:10.1002/oby.21340 · Cited by 54 · see citing works

Effect of Roux-en-Y Bariatric Surgery on Lipoproteins, Insulin Resistance, and Systemic and Vascular Inflammation in Obesity and Diabetes

Yadav, R., Hama, S., Liu, Y., Siahmansur, T. J., Schofield, J. D., Syed, A. A., France, M. W., Pemberton, P. W., Adam, S., Ho, J. H., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01512 · Cited by 54 · see citing works

Changes in inflammatory markers after sleeve gastrectomy in patients with impaired glucose homeostasis and type 2 diabetes

Mallipedhi, A., Prior, S. L., Barry, J. D., Caplin, S., BAXTER, J. N., & Stephens, J. W. (2014) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2014.04.019 · Cited by 52 · see citing works

Effects of Bariatric Surgery Versus Medical Therapy on the 24-Hour Ambulatory Blood Pressure and the Prevalence of Resistant Hypertension

Schiavon, C. A., Ikeoka, D., Santucci, E. V., Santos, R. N., Damiani, L. P., Bueno, P. R. T., de Oliveira, J. D., Torreglosa, C. R., Bersch-Ferreira, Â. C., Miranda, T. A., et al. (2019) · Hypertension · doi:10.1161/hypertensionaha.118.12290 · Cited by 51 · see citing works

Effects of bariatric surgery on pericardial ectopic fat depositions and cardiovascular function

van Schinkel, L. D., Sleddering, M. A., Lips, M. A., Jonker, J. T., Roos, A., Lamb, H. J., Jazet, I. M., Pijl, H., & Smit, J. W. A. (2014) · Clinical Endocrinology · doi:10.1111/cen.12402 · Cited by 50 · see citing works

The effect of bariatric surgery on renal function and disease: a focus on outcomes and inflammation

Neff, K., Frankel, A., Tam, F. W. K., Sadlier, D. M., Godson, C., & le Roux, C. W. (2013) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gft262 · Cited by 47 · see citing works

Systemic Inflammation in Severe Obese Patients Undergoing Surgery for Obesity and Weight-Related Diseases

de Freitas, W. R., de Oliveira, L. V. F., Perez, E. A., Ilias, E. J., Lottenberg, C. P., Silva, A. S., Urbano, J. J., Oliveira‐Junior, M. C., Vieira, R. P., Alves, M. R., et al. (2018) · Obesity Surgery · doi:10.1007/s11695-017-3104-9 · Cited by 46 · see citing works

Changes in Pain Sensitization After Bariatric Surgery

Stefanik, J. J., Felson, D. T., Apovian, C. M., Niu, J., Clancy, M. M., LaValley, M. P., & Neogi, T. (2018) · Arthritis Care & Research · doi:10.1002/acr.23513 · Cited by 45 · see citing works

The Impact of Obesity and Metabolic Surgery on Chronic Inflammation

Chiappetta, S., Schaack, H. M., Wölnerhannsen, B., Stier, C. K., Squillante, S., & Weiner, R. A. (2018) · Obesity Surgery · doi:10.1007/s11695-018-3320-y · Cited by 43 · see citing works

Impact of bariatric surgery on cardiovascular and renal complications of diabetes: a focus on clinical outcomes and putative mechanisms

Martin, W. P., Docherty, N. G., & le Roux, C. W. (2018) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2018.1518130 · Cited by 44 · see citing works

Influence of weight loss on pulmonary function and levels of adipokines among asthmatic individuals with obesity: One-year follow-up

Baltieri, L., Cazzo, E., de Souza, A. L., Alegre, S. M., Vieira, R. P., Antunes, E., de Mello, G. C., Martins, L. C., & Chaim, É. A. (2018) · Respiratory Medicine · doi:10.1016/j.rmed.2018.10.017 · Cited by 43 · see citing works

Immune Dysregulation in Obesity

Jiang, Z., Tabuchi, C., Gayer, S. G., & Bapat, S. P. (2025) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-051222-015350 · Cited by 42 · see citing works

Effects of gastric bypass surgery followed by supervised physical training on inflammation and endothelial function: A randomized controlled trial

Stolberg, C. R., Mundbjerg, L. H., Funch-Jensen, P. M., Gram, B., Bladbjerg, E., & Juhl, C. B. (2018) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2018.04.002 · Cited by 42 · see citing works

Change in Levels of C-Reactive Protein (CRP) and Serum Cortisol in Morbidly Obese Patients After Laparoscopic Sleeve Gastrectomy

Ruíz-Tóvar, J., Oller, I., Galindo, I., Llavero, C., Antonio Arroyo, S., Calero, A., Diez, M., Zubiaga, L., & Calpena, R. (2013) · Obesity Surgery · doi:10.1007/s11695-013-0865-7 · Cited by 41 · see citing works

Computed Tomography‐Based Assessment of Abdominal Adiposity Changes and Their Impact on Metabolic Alterations Following Bariatric Surgery

Galanakis, C., Daskalakis, M., Manios, A. G., Xyda, A., Karantanas, A. H., & Melissas, J. (2014) · World Journal of Surgery · doi:10.1007/s00268-014-2826-2 · Cited by 41 · see citing works

Short‐ and long‐term effects of body weight, calorie restriction and gastric bypass on CYP1A2, CYP2C19 and CYP2C9 activity

Kvitne, K. E., Krogstad, V., Wegler, C., Johnson, L. K., Kringen, M. K., Hovd, M. H., Hertel, J. K., Heijer, M., Sandbu, R., Skovlund, E., et al. (2022) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.15349 · Cited by 40 · see citing works

‘Adiposopathy’ and cardiovascular disease

Appachi, S., & Kashyap, S. R. (2013) · Current Opinion in Cardiology · doi:10.1097/hco.0b013e3283642a33 · Cited by 40 · see citing works

Biomarkers of Colorectal Cancer Risk Decrease 6 months After Roux-en-Y Gastric Bypass Surgery

Afshar, S., Malcomson, F. C., Kelly, S. B., Seymour, K., Woodcock, S., & Mathers, J. C. (2017) · Obesity Surgery · doi:10.1007/s11695-017-2953-6 · Cited by 40 · see citing works

PYY, a Therapeutic Option for Type 2 Diabetes?

Guida, C., & Ramracheya, R. D. (2020) · Clinical Medicine Insights Endocrinology and Diabetes · doi:10.1177/1179551419892985 · Cited by 38 · see citing works

Serum SPARC and Matrix Metalloproteinase-2 and Metalloproteinase-9 Concentrations after Bariatric Surgery in Obese Adults

Lee, Y. J., Heo, Y., Park, H. S., Lee, S. H., Lee, S. K., & Jang, Y. J. (2013) · Obesity Surgery · doi:10.1007/s11695-013-1111-z · Cited by 38 · see citing works

Impact of Bariatric Surgery on White Adipose Tissue Inflammation

Labrecque, J., Laforest, S., Michaud, A., Biertho, L. D., & Tchernof, A. (2017) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2016.12.003 · Cited by 36 · see citing works

Reduction in Thyroid-Stimulating Hormone Correlated with Improved Inflammation Markers in Chinese Patients with Morbid Obesity Undergoing Laparoscopic Sleeve Gastrectomy

Zhu, C., Gao, J., Mei, F., Lu, L., Zhou, D., & Qu, S. (2019) · Obesity Surgery · doi:10.1007/s11695-019-04063-4 · Cited by 35 · see citing works

Short‐ and long‐term effects of body weight loss following calorie restriction and gastric bypass on CYP3A‐activity – a non‐randomized three‐armed controlled trial

Kvitne, K. E., Robertsen, I., Skovlund, E., Christensen, H., Krogstad, V., Wegler, C., Angeles, P. C., Wollmann, B. M., Hole, K., Johnson, L. K., et al. (2021) · Clinical and Translational Science · doi:10.1111/cts.13142 · Cited by 34 · see citing works

The Effect of Bariatric Surgery on Circulating Levels of Lipoprotein (a): A Meta‐analysis

Jamialahmadi, T., Reiner, Ž., Alidadi, M., Kroh, M., Almahmeed, W. A., Ruscica, M., Sirtori, C. R., Rizzo, M., Santos, R. D., & Sahebkar, A. (2022) · BioMed Research International · doi:10.1155/2022/8435133 · Cited by 33 · see citing works

The role of obesity and bariatric surgery-induced weight loss in breast cancer

Bohm, M. S., Sipe, L. M., Pye, M. E., Davis, M. J., Pierre, J. F., & Makowski, L. (2022) · Cancer and Metastasis Reviews · doi:10.1007/s10555-022-10050-6 · Cited by 31 · see citing works

Fatty acids role on obesity induced hypothalamus inflammation: From problem to solution – A review

Salsinha, A. S., Rodríguez-Alcalá, L. M., Relvas, J. B., & Pintado, M. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.03.042 · Cited by 29 · see citing works

Glomerular hyperfiltration in morbid obesity: Role of the inflammasome signalling

Moriconi, D., Antonioli, L., Masi, S., Bellini, R., Pellegrini, C., Rebelos, E., Taddei, S., & Nannipieri, M. (2022) · Nephrology · doi:10.1111/nep.14077 · Cited by 29 · see citing works

Weight Loss Associated with Bariatric Surgery Does Not Restore Short Telomere Length of Severe Obese Patients After 1 Year

Formichi, C., Cantara, S., Ciuoli, C., Neri, O., Chiofalo, F., Selmi, F., Tirone, A., Colasanto, G., Cosmo, L. D., Vuolo, G., et al. (2014) · Obesity Surgery · doi:10.1007/s11695-014-1300-4 · Cited by 29 · see citing works

Corneal Keratocyte Density and Corneal Nerves Are Reduced in Patients With Severe Obesity and Improve After Bariatric Surgery

Iqbal, Z., Kalteniece, A., Ferdousi, M., Adam, S., D’Onofrio, L., Ho, J. H., Rao, A. P., Dhage, S. S., Azmi, S., Liu, Y., et al. (2021) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.62.1.20 · Cited by 28 · see citing works

Potential mechanisms by which bariatric surgery improves systemic metabolism

Koshy, A. A., Bobe, A. M., & Brady, M. (2012) · Translational research · doi:10.1016/j.trsl.2012.09.004 · Cited by 26 · see citing works

Effects of Bariatric Surgery on Outcomes of Patients With Acute Pancreatitis

Krishna, S. G., Behzadi, J., Hinton, A. M., El-Dika, S. S., Groce, J. R., Hussan, H., Hart, P. A., & Conwell, D. L. (2016) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2016.02.015 · Cited by 27 · see citing works

Relationship between the Plasma Proteome and Changes in Inflammatory Markers after Bariatric Surgery

Fachim, H., Iqbal, Z., Gibson, M., Baričević-Jones, I., Campbell, A. E., Geary, B., Syed, A. A., Whetton, A. D., Soran, H., Donn, R. P., et al. (2021) · Cells · doi:10.3390/cells10102798 · Cited by 26 · see citing works

Microvascular complications of obesity and diabetes—Role of bariatric surgery

Bashir, B., Iqbal, Z., Adam, S., Ferdousi, M., Chick, W., Hussein, H. A., Syed, A. A., le Roux, C. W., COHEN, R. V., Malik, R. A., et al. (2023) · Obesity Reviews · doi:10.1111/obr.13602 · Cited by 25 · see citing works

Differential Impact of Weight Loss and Glycemic Control on Inflammasome Signaling

Antonioli, L., Moriconi, D., Masi, S., Bottazzo, D., Pellegrini, C., Fornai, M., Anselmino, M., Ferrannini, E., Blandizzi, C., Taddei, S., et al. (2020) · Obesity · doi:10.1002/oby.22734 · Cited by 23 · see citing works

Lipids and bariatric procedures part 1 of 2: Scientific statement from the National Lipid Association, American Society for Metabolic and Bariatric Surgery, and Obesity Medicine Association: EXECUTIVE SUMMARY

Bays, H. E., Jones, P. H., Jacobson, T. A., Cohen, D. E., Orringer, C. E., Kothari, S. N., Azagury, D. E., Morton, J. M., Nguyen, N. T., Westman, E. C., et al. (2015) · Journal of clinical lipidology · doi:10.1016/j.jacl.2015.12.003 · Cited by 23 · see citing works

Bariatric surgery is independently associated with a decrease in the development of colorectal lesions

Kwak, M., Mehaffey, J. H., Hawkins, R. B., Hedrick, T. L., Slingluff, C. L., Schirmer, B. D., Hallowell, P. T., & Friel, C. M. (2019) · Surgery · doi:10.1016/j.surg.2019.03.013 · Cited by 22 · see citing works

COVID‐19 and its Severity in Bariatric Surgery‐Operated Patients

Lassen, P. B., Poitou, C., Genser, L., Marchelli, F., Aron‐Wisnewsky, J., Ciangura, C., Jacques, F., Moreau, P., NutriOmics investigators, Oppert, J., et al. (2020) · Obesity · doi:10.1002/oby.23026 · Cited by 22 · see citing works

A proteomic analysis of excreted and circulating proteins from obese patients following two different weight-loss strategies

Alfadda, A. A., Turjoman, A. A., Moustafa, A. S., Al-Naami, M. Y., Chishti, M. A., Sallam, R. M., Gibson, D. S., & Duncan, M. W. (2014) · Experimental Biology and Medicine · doi:10.1177/1535370214523894 · Cited by 21 · see citing works

Serum biomarkers of inflammation and adiposity in the LABS cohort: associations with metabolic disease and surgical outcomes

O’Rourke, R. W., Johnson, G., Purnell, J. Q., Courcoulas, A. P., Dakin, G. F., Garcia, L., Hinojosa, M. W., Mitchell, J. E., Pomp, A., Pories, W. J., et al. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0088-z · Cited by 22 · see citing works

Sleeve Gastrectomy and Roux-en-Y Gastric Bypass Attenuate Pro-inflammatory Small Intestinal Cytokine Signatures

Subramaniam, R., Aliakbarian, H., Bhutta, H. Y., Harris, D. A., Tavakkoli, A., & Sheu, E. G. (2019) · Obesity Surgery · doi:10.1007/s11695-019-04059-0 · Cited by 21 · see citing works

Endocannabinoid receptor blockade increases vascular endothelial growth factor and inflammatory markers in obese women with polycystic ovary syndrome

Sathyapalan, T., Javed, Z., Kilpatrick, E. S., Coady, A., & Atkin, S. L. (2016) · Clinical Endocrinology · doi:10.1111/cen.13239 · Cited by 20 · see citing works

C-Reactive protein level in morbidly obese patients before and after bariatric surgery

Rojano‐Rodriguez, M., Valenzuela-Salazar, C., Cárdenas-Lailson, L. E., Loera, L. S. R., Torres-Olalde, M. E., & Moreno-Portillo, M. (2014) · Revista de Gastroenterología de México (English Edition) · doi:10.1016/j.rgmxen.2013.11.002 · Cited by 19 · see citing works

Effects of Roux-en-Y gastric bypass on the metabolic profile and systemic inflammatory status of women with metabolic syndrome: randomized controlled clinical trial

Felipe, L. A., Bachi, A. L. L., Oliveira, M. C., Moreira, S. M. B. P., Afonso, J. P. R., Lino, M. E. M., Paixão, V., Silva, C. H. M., Vieira, R. P., Vencio, S. A. C., et al. (2023) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-023-00986-2 · Cited by 17 · see citing works

Effect of bariatric surgery on flow mediated dilation and carotid intima-media thickness in patients with morbid obesity: 1-year follow-up study

Elitok, A. (2019) · The Anatolian Journal of Cardiology · doi:10.14744/anatoljcardiol.2019.85249 · Cited by 16 · see citing works

Weight Reduction for Obesity-Induced Heart Failure with Preserved Ejection Fraction

Ayinapudi, K., Samson, R., Jemtel, T. H. L., MARROUCHE, N. F., & Oparil, S. (2020) · Current Hypertension Reports · doi:10.1007/s11906-020-01074-w · Cited by 16 · see citing works

Nivel de proteína C reactiva en pacientes con obesidad mórbida antes y después de cirugía bariátrica

Rojano‐Rodriguez, M., Valenzuela-Salazar, C., Cárdenas-Lailson, L. E., Loera, L. S. R., Torres-Olalde, M. E., & Moreno-Portillo, M. (2014) · Revista de Gastroenterología de México · doi:10.1016/j.rgmx.2013.11.002 · Cited by 16 · see citing works

Vertical sleeve gastrectomy induces distinctive transcriptomic responses in liver, fat and muscle

Ahn, C. H., Choi, E. H., Lee, H.-J., Lee, W., Kim, J., & Cho, Y. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-81866-5 · Cited by 16 · see citing works

Six Months of Treatment with the Endoscopic Duodenal-Jejunal Bypass Liner Does Not Lead to Decreased Systemic Inflammation in Obese Patients with Type 2 Diabetes

de Jonge, C., Rensen, S. S., D‘Agnolo, H. M. A., Bouvy, N. D., Buurman, W. A., & Greve, J. W. M. (2013) · Obesity Surgery · doi:10.1007/s11695-013-1154-1 · Cited by 15 · see citing works

Premorbid obesity and metabolic disturbances as promising clinical targets for the prevention and early screening of bipolar disorder

Gálvez, J. F., Sanches, M., Bauer, I. E., Sharma, A. N., Hamilton, J. E., Mwangi, B., Quevedo, J., Zunta‐Soares, G. B., & Soares, J. C. (2015) · Medical Hypotheses · doi:10.1016/j.mehy.2015.01.016 · Cited by 15 · see citing works

Long-term Impact of Mini-Gastric Bypass on Inflammatory Cytokines in Cohort of Morbidly Obese Patients: a Prospective Study

Salman, M. A., Abdallah, A., Mikhail, H. M. S., Abdelsalam, A., Ibrahim, A. H., Sultan, A. A. E. A., El‐ghobary, M., Ismail, A. A. M., Abouelregal, T. E., Omar, M. G., et al. (2020) · Obesity Surgery · doi:10.1007/s11695-020-04471-x · Cited by 15 · see citing works

Therapeutic effects of the gold nanoparticle on obesity-triggered neuroinflammation: a review

Abel, J. D. S., da Silva, M. R., Costa, A. B., de Oliveira, M. P., da Silva, L. E., Vedova, L. M. D., Mendes, T. F., Tartari, G., Possato, J. C., Ferreira, G. K., et al. (2022) · Journal of drug targeting · doi:10.1080/1061186x.2022.2120613 · Cited by 14 · see citing works

Bariatric surgery for diabetic comorbidities: A focus on hepatic, cardiac and renal fibrosis

Ding, H., Zhang, Y., Ma, X., Zhang, Z., Xu, Q., Liu, C., Li, B., Dong, S., Li, L., Zhu, J., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1016635 · Cited by 15 · see citing works

Bariatric surgery and its impact on depressive symptoms, cognition, brain and inflammation

Kotačková, L., Mareček, R., Mouraviev, A., Tang, A., Brázdil, M., Čierny, M., Paus, T., Pausová, Z., & Marečková, K. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1171244 · Cited by 13 · see citing works

The Burden of Systemic Adiposity on Pancreatic Disease: Acute Pancreatitis, Non-Alcoholic Fatty Pancreas Disease, and Pancreatic Cancer.

Malli, A. H., Li, F., Conwell, D. L., Cruz‐Monserrate, Z., Hussan, H., & Krishna, S. G. (2017) · PubMed · Cited by 13 · see citing works

Nutrition, epigenetics and health through life

Malcomson, F. C., & Mathers, J. C. (2017) · Nutrition Bulletin · doi:10.1111/nbu.12281 · Cited by 13 · see citing works

Potential associations between alterations in gut microbiome and obesity‐related traits after the bariatric surgery

Özdemir, A., Yozgat, A., Işgın‐Atıcı, K., Avcı, E., Yıldız, B. D., Gündoğdu, A., Nalbantoğlu, U., Turhan, T., Al, F. D., & Büyüktuncer, Z. (2022) · Journal of Human Nutrition and Dietetics · doi:10.1111/jhn.13087 · Cited by 12 · see citing works

The effect of bariatric surgery on reducing the risk of colorectal cancer: a meta-analysis of 3,233,044 patients

Janik, M. R., Clapp, B. L., Sroczyński, P., & Ghanem, O. M. (2022) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2022.10.003 · Cited by 12 · see citing works

Temporal effects of laparoscopic sleeve gastrectomy on adipokines, inflammation, and oxidative stress in patients with impaired glucose homeostasis

Stephens, J. W., Min, T., Dunseath, G. J., Churm, R., Barry, J. D., & Prior, S. L. (2019) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2019.04.006 · Cited by 12 · see citing works

Effect of Sleeve Gastrectomy on Buprenorphine Pharmacokinetics: A Planned Case Observation

Krabseth, H., Strømmen, M., Spigset, O., & Helland, A. (2020) · Clinical Therapeutics · doi:10.1016/j.clinthera.2020.08.016 · Cited by 12 · see citing works

Decreased Long-Term Respiratory Infection Risk After Bariatric Surgery: a Comprehensive National Cohort Study

Chen, J., Wei, Y.-F., Chen, C. O., Su, Y., Tsai, R. S. F., Chin, W.-L., & Lee, H.-S. (2020) · Obesity Surgery · doi:10.1007/s11695-020-05001-5 · Cited by 11 · see citing works

Roux-en-Y gastric bypass potentially improved intestinal permeability by regulating gut innate immunity in diet-induced obese mice

Jin, Z., Chen, K., Zhou, Z., Peng, W., & Liu, W. (2021) · Scientific Reports · doi:10.1038/s41598-021-94094-8 · Cited by 11 · see citing works

Effect of Bariatric Surgery on Intima Media Thickness: A Systematic Review and Meta-Analysis

Jamialahmadi, T., Reiner, Ž., Alidadi, M., Almahmeed, W. A., Kesharwani, P., Al‐Rasadi, K., Eid, A. H., Rizzo, M., & Sahebkar, A. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11206056 · Cited by 11 · see citing works

Roux-en-Y Gastric Bypass Improves Adiponectin to Leptin Ratio and Inflammatory Profile in Severely Obese Women with and without Metabolic Syndrome: A Randomized Controlled Trial

Moreira, S. M. B. P., Bachi, A. L. L., Ilias, E. J., Malheiros, C. A., Vencio, S. A. C., Alves, V. L. D. S., de Sousa, A. R. T., Felipe, L. A., Perez, E. A., Lino, M. E. M., et al. (2023) · Nutrients · doi:10.3390/nu15153312 · Cited by 11 · see citing works

Roux-en-Y Esophagojejunostomy Ameliorates Renal Function Through Reduction of Renal Inflammatory and Fibrotic Markers in Diabetic Nephropathy

Wang, C., He, B., Piao, D., & Han, P. (2015) · Obesity Surgery · doi:10.1007/s11695-015-1947-5 · Cited by 11 · see citing works

Adipokine Pattern After Bariatric Surgery: Beyond the Weight Loss

Adami, G. F., Scopinaro, N., & Cordera, R. (2016) · Obesity Surgery · doi:10.1007/s11695-016-2347-1 · Cited by 12 · see citing works

Impact of serum uric acid on renal function after bariatric surgery: a retrospective study

Hung, K., Ho, C., Chen, I., Chu, C., Sun, C., & Soong, T. (2019) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2019.10.029 · Cited by 11 · see citing works

Ileal Transposition Increases Pancreatic β Cell Mass and Decreases β Cell Senescence in Diet-Induced Obese Rats

Ahn, C. H., Choi, E. H., Oh, T. J., & Cho, Y. M. (2020) · Obesity Surgery · doi:10.1007/s11695-020-04406-6 · Cited by 11 · see citing works

Effect of bariatric surgery on serum inflammatory factors of obese patients: a systematic review and meta-analysis

Askarpour, M., Khani, D., Sheikhi, A., Ghaedi, E., & Alizadeh, S. (2019) · Obesity Surgery · doi:10.1007/s11695-019-03926-0 · Cited by 120 · see citing works

Short-term Changes in Tnf-alpha, Il-6 and Adiponectin Following Bariatric Surgery in Romanian Obese Adults – an Observational Case-control StudyPreprint

Ion, R. M., Huţanu, A., Sala, D. T., Constantin, C., Fodor, S. R., Voidăzan, S. T., Muresan, M. G., & Neagoe, R. M. (2024) · Research Square · doi:10.21203/rs.3.rs-4263046/v1

Short-Term Changes in TNF-Alpha, IL-6 and Adiponectin Following Bariatric Surgery in Caucasian Obese Adults: An Observational Case–Control Study

Ion, R.-M., Huţanu, A., Sala, D. T., Muresan, M. G., Fodor, S. R., Voidăzan, S. T., Beresescu, G. F., & Neagoe, R. M. (2024) · Medicina · doi:10.3390/medicina60111789 · Cited by 8 · see citing works

Variation of modulation and expression of biomarkers associated with inflammation in bariatric surgery patients: A systematic review and meta-analysis

Machado, C. R., Braun, A. M., Ceolin, J., Richter, S. A., Ribeiro, M. C., Santos, L. D., Rigo, M., de Souza, A. P. D., Padoin, A. V., Alves, L. B., et al. (2023) · Surgery · doi:10.1016/j.surg.2023.07.002 · Cited by 7 · see citing works

Only C-Reactive Protein, but not TNF-α or IL6, Reflects the Improvement in Inflammation after Bariatric Surgery

Pardina, E., Ferrer, R., Baena‐Fustegueras, J. A., Déniz, J. R., Lecube, A., Fort, J. M., Vargas, V., Catalán, R., & Peinado‐Onsurbe, J. (2011) · Obesity Surgery · doi:10.1007/s11695-011-0546-3 · Cited by 69 · see citing works