The DOI matches its Crossref record; 46 of the 48 references it cites were found in a registry or an index, and 1 are not checked yet.
Obesity in Pregnancy Stimulates Macrophage Accumulation and Inflammation in the Placenta
Open accessAbstract
Obesity and pregnancy are associated with a combination of insulin resistance and inflammatory changes which exacerbate in combination. Based on the similarity between the inflammatory transcriptomes of adipose tissue and placenta, we hypothesized that the placenta develops exaggerated inflammation in response to obesity. The aim of this study was to characterize placental inflammatory mediators and macrophage accumulation in relation to peripheral inflammation in obesity. Placental macrophages and maternal peripheral blood mononuclear cells (PBMC) from 20 obese and 15 lean women were functionally and phenotypically characterized using immunohistochemistry, flow cytometry and expression for macrophage markers and inflammatory cytokines. The number of resident CD68+ and CD14+ cells was increased 2-3 fold in the placenta of obese as compared to lean women. The macrophage population was characterized by a marked phenotypic heterogeneity with complex subsets of CD14+, CD68+ and CD11b+ (mac-1) cells and by an increased expression of the pro-inflammatory cytokines IL-1, TNF-alpha, IL-6. Placental inflammation was associated with an activation of PBMC gene expression with an increase in the monocyte differentiation and maturation markers CD14 and CD68 in maternal but not fetal PBMC. The inflammatory changes were associated with higher plasma concentrations of C-reactive protein and IL-6 in obese compared to lean women. In conclusion, the chronic inflammation state of pre-gravid obesity is extending to in utero life with accumulation of a heterogeneous macrophage population and pro-inflammatory mediators in the placenta. The resulting inflammatory milieu in which the fetus develops may have critical consequences for short and long term programming of obesity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Increased oxidative stress and inflammation markers have been found in the placenta of obese mothers, suggesting a decisive role of an abnormal intrauterine environment in modulating fetal programming [76,79].”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [79]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Therefore, fetuses of obese mothers are exposed to an imbalance of cytokines, as well as nutrients that can negatively affect fetal programming, leading to adverse long-term effects in the offspring.”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [79]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The negative effect of maternal obesity on offspring health might be mediated by an alteration in the inflammatory state and an increase in oxidative stress due to excess adipose tissue.”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [79]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Pregnancy is normally an inflammatory state caused by the remodeling of immunological system to allow embryo implantation, growth and life, regulated by a delicate balance of pro-inflammatory and anti-inflammatory cytokines; in pregnancies complicated by obesity, this balance is shifted mainly towards a pro-inflammatory state.”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [79]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Evidence of a key role of inflammation in fetal programming was provided by Reynolds et al. in 2015, thanks to a study where supplementation with an anti-inflammatory molecule, the conjugated linoleic acid, led to a reduction in the expression of pro-inflammatory cytokines such as TNF-α and IL-1β and metabolic dysfunction in offspring [76,79].”
From Maternal Overnutrition and Fetal Programming: Long-Term Metabolic, Cognitive, and Epigenetic Consequences (2026) · cites this paper as [79]
Experimental — accuracy not yet measured
In the citing paper
“A number of maternal conditions, both infectious and non-infectious, have been linked to placental inflammation (102, 453).”
From Placental Origins of Chronic Disease (2016) · cites this paper as [102]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
Chirgwin, J. M., Przybyla, A., MacDonald, R. J., & Rutter, W. J. (1979) · Biochemistry · doi:10.1021/bi00591a005 · Cited by 21,460
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
Inflammation and metabolic disorders
Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199
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
Monocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Local and systemic insulin resistance resulting from hepatic activation of IKK-β and NF-κB
Cai, D., Yuan, M., Frantz, D. F., Melendez, P. A., Hansen, L., Lee, J., & Shoelson, S. E. (2005) · Nature Medicine · doi:10.1038/nm1166 · Cited by 2,245
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 2,032
Criteria for screening tests for gestational diabetes
Carpenter, M. W., & Coustan, D. R. (1982) · American Journal of Obstetrics and Gynecology · doi:10.1016/0002-9378(82)90349-0 · Cited by 1,924
Preeclampsia: An excessive maternal inflammatory response to pregnancy
Redman, C. W. G., Sacks, G. P., & Sargent, I. L. (1999) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(99)70239-5 · Cited by 1,838
Obesity-induced inflammatory changes in adipose tissue
Wellen, K. E., & Hotamisligil, G. S. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200320514 · Cited by 1,823
Flagged first, then by citations
1 of the 48 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 201–300 of 710
Obesity and High-Fat Diet Induce Distinct Changes in Placental Gene Expression and Pregnancy Outcome
Mahany, E. B., Han, X., Borges, B. C., Cruz‐Machado, S. D. S., Allen, S. J., García-Galiano, D., Hoenerhoff, M. J., Bellefontaine, N., & Elias, C. F. (2018) · Endocrinology · doi:10.1210/en.2017-03053 · Cited by 52
Yu, J., Zhou, Y., Gui, J., Li, A.-Z., Su, X., & Feng, L. (2013) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-013-1187-7 · Cited by 51
Kosa, J. L., Guendelman, S., Pearl, M., Graham, S., Abrams, B. F., & Kharrazi, M. (2010) · Maternal and Child Health Journal · doi:10.1007/s10995-010-0633-4 · Cited by 51
“macrophages has been found in the placenta of obese pregnant women [ 35 ].”
BackgroundDiabesity-associated oxidative and inflammatory stress signalling in the early human placenta
Hoch, D., Gauster, M., Mouzon, S. H., & Desoyé, G. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.11.002 · Cited by 56
Kim, D. W., Glendining, K. A., Grattan, D. R., & Jasoni, C. L. (2016) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2016.06.005 · Cited by 50
Musillo, C., Berry, A., & Cirulli, F. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104624 · Cited by 49
“In particular, leptin acts as a pro-inflammatory factor on immune cells leading to a release of cytokines, supporting the hypothesis that high levels of leptin, that are observed in stressed and obese mothers, could represent a primer for placental inflammation (Challier et al., 2008; Tessier et al., 2013).”
Yang, X., Li, M., Haghiac, M., Catalano, P. M., O’Tierney-Ginn, P., & Mouzon, S. H. (2016) · Diabetologia · doi:10.1007/s00125-016-4073-6 · Cited by 50
“Lowgrade inflammation encompasses the placenta [13], suggesting that maternal obesity exposes the developing fetus to an inflammatory environment.”
Self-citationLazarides, C., Epel, E. S., Lin, J., Blackburn, E. H., Voelkle, M. C., Buß, C., Simhan, H. N., Wadhwa, P. D., & Entringer, S. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.04.021 · Cited by 51
Perinatal factors in neonatal and pediatric lung diseases
Britt, R. D., Faksh, A., Vogel, E. R., Martin, R. J., Pabelick, C. M., & Prakash, Y. S. (2013) · Expert Review of Respiratory Medicine · doi:10.1586/17476348.2013.838020 · Cited by 46
Impaired Treg and NK cells profile in overweight women with gestational diabetes mellitus
Lobo, T. F., Borges, C. D. M., Mattar, R., Gomes, C. P., Angelo, A. G. S., Pendeloski, K. P. T., & Daher, S. (2018) · American Journal of Reproductive Immunology · doi:10.1111/aji.12810 · Cited by 49
Perinatal inflammation: a common factor in the early origins of cardiovascular disease?
Nguyen, M. U., Wallace, M. J., Pepe, S., Menheniott, T. R., Moss, T. J. M., & Burgner, D. P. (2015) · Clinical Science · doi:10.1042/cs20150045 · Cited by 49
Wankhade, U. D., Thakali, K. M., & Shankar, K. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.07.001 · Cited by 51
Influence of Maternal Body Mass Index and Macrophage Activation on Asthma Exacerbations in Pregnancy
Murphy, V. E., Jensen, M. E., Powell, H. A., & Gibson, P. G. (2017) · The Journal of Allergy and Clinical Immunology In Practice · doi:10.1016/j.jaip.2017.03.040 · Cited by 48
“Toll-like receptor activation by fatty acids induces cleavage of the macrophage surface marker CD-163, which results in increased circulating soluble CD-163 (sCD-163), a marker of macrophage activation.11 In addition, macrophages have an important role in the placenta, with significantly more placental macrophages in…”
BackgroundTorricelli, M., Voltolini, C., Bloise, E., Biliotti, G., Giovannelli, A., Bonis, M. D., Imperatore, A., & Petraglia, F. (2009) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2009.00729.x · Cited by 47
Sen, S., Carpenter, A. H., Hochstadt, J., Huddleston, J. Y., Kustanovich, V., Reynolds, A. A., & Roberts, S. B. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.04.014 · Cited by 48
Effect of maternal obesity on pregnancy outcomes and long-term metabolic consequences
Valsamakis, G., Kyriazi, E., Mouslech, Z., Siristatidis, C. S., & Mastorakos, G. P. (2015) · HORMONES · doi:10.14310/horm.2002.1590 · Cited by 47
Cytokine and adipokine are biofactors can act in blood and colostrum of obese mothers
Fujimori, M., França, E. L., Morais, T. C., Fiorin, V., de Abreu, L. C., & Honório‐França, A. C. (2016) · BioFactors · doi:10.1002/biof.1339 · Cited by 48
“The course of pregnancy and postpartum is characterized by major changes in inflammatory mediators, and in obese women these modifications include increased levels of inflammatory markers in serum [6,24–28] amniotic fluid [29], placenta [18,30], fetal blood [31], and newborns [6,32].”
BackgroundInfluentialNogues, P., Santos, E. D., Couturier‐Tarrade, A., Berveiller, P., Arnould, L., Lamy, E., Grassin‐Delyle, S., Vialard, F., & Dieudonné, M. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa660 · Cited by 47
Maternal Obesity and Gut Microbiota Are Associated with Fetal Brain Development
Basak, S., Das, R. K., Banerjee, A., Paul, S., Pathak, S., & Duttaroy, A. K. (2022) · Nutrients · doi:10.3390/nu14214515 · Cited by 55
“An increase in total lipid content characterizes the placentas of obese women at term, infiltrated neutrophils, foam-loaded macrophages and increased levels of pro-inflammatory mediators [68,69].”
BackgroundMann, J., McDermott, S., Hardin, J. W., Pan, C., & Zhang, Z. (2012) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.12052 · Cited by 46
de Fante, T., Simino, L. A. D. P., Reginato, A., Payolla, T. B., Vitoréli, D. C. G., de Souza, M., Torsoni, M. A., Milanski, M., & Torsoni, A. S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160184 · Cited by 48
“During pregnancy, consumption of a HFD may exacerbate the inflammatory response by stimulating macrophage infiltration, inflammatory signalling pathways and the production of inflammatory markers [20, 21].”
BackgroundPlacental fatty acid transport in maternal obesity
Cetin, I., Parisi, F., Berti, C., Mandò, C., & Desoye, G. (2012) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174412000414 · Cited by 45
Kandadi, M. R., Hua, Y., Zhu, M. J., Turdi, S., Nathanielsz, P. W., Ford, S. P., Nair, S., & Ren, J. T. (2013) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2013.07.003 · Cited by 45
“A number of studies from humans and animal models have demonstrated an overt elevation in proinflammatory mediators including TLR4, IL-6, circulating C-reactive protein (CRP), expression of CD-14 and CD-64 in liver, gut, adipose tissue, skeletal muscle and placenta [21,29–31].”
BackgroundRetractedProinflammatory Diets during Pregnancy and Neonatal Adiposity in the Healthy Start Study
Moore, B. F., Sauder, K. A., Starling, A. P., Hébert, J. R., Shivappa, N., Ringham, B. M., Glueck, D. H., & Dabelea, D. (2017) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2017.10.030 · Cited by 49
Diet-induced obesity in mice reduces placental efficiency and inhibits placental mTOR signaling
Lager, S., Samulesson, A.-M., Taylor, P. D., Poston, L., Powell, T. L., & Jansson, T. (2014) · Physiological Reports · doi:10.1002/phy2.242 · Cited by 44
“Obese pregnant women also have elevated circulating levels of inflammatory markers (Challier et al. 2008; Roberts et al. 2011) such as interleukin (IL)-6, which stimulates amino acid uptake in PHTs (Jones et al. 2009).”
BackgroundResultInfluentialEaston, Z. J. W., & Regnault, T. R. H. (2020) · Nutrients · doi:10.3390/nu12103031 · Cited by 49
Desforges, M., Ditchfield, A., Hirst, C., Pegorie, C., Martyn-Smith, K., Sibley, C. P., & Greenwood, S. L. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-6093-0_9 · Cited by 43
Racial and Ethnic Health Disparities in Reproductive Medicine: An Evidence-Based Overview
Owen, C. M., Goldstein, E. H., Clayton, J. A., & Segars, J. H. (2013) · Seminars in Reproductive Medicine · doi:10.1055/s-0033-1348889 · Cited by 45
van der Burg, J. W., Allred, E. N., McElrath, T. F., Fichorova, R. N., Kuban, K., O’Shea, T. M., Dammann, O., & Leviton, A. (2013) · Early Human Development · doi:10.1016/j.earlhumdev.2013.09.014 · Cited by 43
“Compared to their leaner peers, obese women tend to have higher blood concentrations of proinflammatory proteins when not pregnant [11–14] and when pregnant [11–15].”
BackgroundBari, M. F., Weickert, M. O., Sivakumar, K., James, S. G., Snead, D. R. J., Tan, B. K., Randeva, H. S., Bastie, C. C., & Vatish, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0101327 · Cited by 43
Reynés, B., Priego, T., Cifre, M., Oliver, P., & Palou, A. (2018) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12363 · Cited by 42
Brouwers, L., Franx, A., Vogelvang, T. E., Houben, M. L., van Rijn, B. B., & Nikkels, P. G. J. (2018) · Pediatric and Developmental Pathology · doi:10.1177/1093526618785838 · Cited by 42
Leptin and Adiponectin as markers for preeclampsia in obese pregnant women, a cohort study
Thagaard, I. N., Hedley, P. L., Holm, J., Lange, T., Larsen, T., Krebs, L., & Christiansen, M. (2018) · Pregnancy Hypertension · doi:10.1016/j.preghy.2018.12.002 · Cited by 44
Srugo, S. A., Bloise, E., Nguyen, T. T.-T. N., & Connor, K. L. (2019) · Nutrients · doi:10.3390/nu11061375 · Cited by 48
Panda, B., Panda, A., Ueda, I., Abrahams, V. M., Norwitz, E. R., Stanic, A. K., Young, B. C., Ecker, J. L., Altfeld, M. A., Shaw, A. C., et al. (2012) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2012.01.008 · Cited by 43
Maternal obesity and risk of cerebral palsy in children: a systematic review and meta‐analysis
Zhang, J., Peng, L., Chang, Q., Xu, R., Zhong, N. A., Huang, Q., Zhong, M., & Yu, Y. (2018) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.13982 · Cited by 44
Sun, M., Sun, B. H., Shicong, Q., Feng, X., Li, Y., Zhang, S., Lin, Y., & Hou, L. (2020) · Fertility and Sterility · doi:10.1016/j.fertnstert.2020.02.005 · Cited by 41
Prescott, S. L. (2016) · Nestlé Nutrition Institute Workshop series · doi:10.1159/000439477 · Cited by 43
Prince, C. S., Maloyan, A., & Myatt, L. (2016) · Placenta · doi:10.1016/j.placenta.2016.11.010 · Cited by 42
“The increasing prevalence of obesity [2] in women of reproductive age presents a major challenge to placental and fetal development as it increases the risk for placental hypoxia [3], increases placental inflammation [4, 5], decreases placental cellular respiration [6], and dysregulates the placental transcriptome [6-…”
BackgroundImpact of pregravid obesity on maternal and fetal immunity: Fertile grounds for reprogramming
Sureshchandra, S., Marshall, N., & Messaoudi, I. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ri0619-181r · Cited by 38
“Free fatty acids CRP IL6 Leptin Insulin CCL2 IL-8 [166] Altered placental structure [64, 121-123] Oxidative Stress [125] Disrupted nutrient transport [114-117] Inflammation [109, 124-126] Increased frequencies of decidual macrophages [121, 144] Phenotypic shift of macrophages [66, 145, 146] Early (first trimester) dro…”
BackgroundSegovia, S. A., Vickers, M. H., Zhang, X. D., Gray, C. L., & Reynolds, C. M. (2015) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2015.07.013 · Cited by 44
“In the setting of maternal obesity, this inflammatory state extends to the placenta, which has negative implications for placental function and fetal development [7,8].”
BackgroundEdlow, A. G., Hui, L., Wick, H., Fried, I., & Bianchi, D. W. (2015) · BJOG An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.13795 · Cited by 42
Varghese, M., Griffin, C. A., McKernan, K. E., Eter, L., Abrishami, S., & Singer, K. (2020) · Aging · doi:10.18632/aging.102709 · Cited by 40
“Contrary to a mouse model inhabited in regulated conditions, in humans, other stressors may play a part in increasing disease risk such as maternal programming of offspring obesity by HFD exposure and childhood obesity [48, 49].”
BackgroundObesity impairs cell-mediated immunity during the second trimester of pregnancy
Sen, S., Iyer, C., Klebenov, D., Histed, A., Aviles, J. A., & Meydani, S. N. (2012) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2012.11.004 · Cited by 41
Human supraphysiological gestational weight gain and fetoplacental vascular dysfunction
Pardo, F., Silva, L., Sáez, T., Salsoso, R., Gutiérrez, J., Sanhueza, C., Leiva, A., & Sobrevía, L. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.57 · Cited by 40
Bar, J., Schreiber, L., Saruhanov, E., Ben‐Haroush, A., Golan, A., & Kovo, M. (2012) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-012-2450-z · Cited by 39
“This finding may be at least partly attributable to overproduction by maternal peripheral blood mononuclear cells [10].”
BackgroundLager, S., Ramirez, V. I., Acosta, O. M., Meireles, C. L., Miller, E., Gaccioli, F., Rosario, F. J., Gelfond, J. A. L., Hakala, K. W., Weintraub, S. T., et al. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-01384 · Cited by 39
Johns, E. C., Denison, F. C., & Reynolds, R. M. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.12.025 · Cited by 42
Effects of pregnancy on obesity-induced inflammation in a mouse model of fetal programming
Ingvorsen, C., Thysen, A. H., Fernandez‐Twinn, D. S., Nordby, P., Nielsen, K. F., Ozanne, S. E., Brix, S., & Hellgren, L. I. (2014) · International Journal of Obesity · doi:10.1038/ijo.2014.69 · Cited by 40
Crew, R. C., Waddell, B. J., & Mark, P. J. (2016) · Placenta · doi:10.1016/j.placenta.2016.01.002 · Cited by 41
Uteroplacental Circulation and Fetal Vascular Function and Development
Thornburg, K. L. R., & Louey, S. (2013) · Current Vascular Pharmacology · doi:10.2174/1570161111311050012 · Cited by 38
“These molecules may be the basis for diseases ranging from preeclampsia to obesity-related placental inflammation [60, 61].”
BackgroundObesity and Maternal-Placental-Fetal Immunology and Health
Monaco-Brown, M., & Lawrence, D. A. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.859885 · Cited by 39
The Effect of Maternal Obesity on Pregnancy Outcome in Correlation With Placental Pathology
Kovo, M., Zion-Saukhanov, E., Schreiber, L., Zussman, N. M., Divon, M. Y., Ben‐Haroush, A., & Bar, J. (2015) · Reproductive Sciences · doi:10.1177/1933719115592712 · Cited by 38
“Third, in the current study we have not looked for inflammatory cytokine or specific key regulators of the inflammatory response in obese versus nonobese placentas, though it is well known that proinflammatory cytokines are considered landmarks of obesity and in the placenta.(21,26) The present study is unique in seve…”
BackgroundFetal Programming of the Neuroendocrine-Immune System and Metabolic Disease
Fisher, R. E., Steele, M. A., & Karrow, N. A. (2012) · Journal of Pregnancy · doi:10.1155/2012/792934 · Cited by 43
“Additionally, obese woman have an increase in the expression of CD14+ and CD68+ cells; two markers that define macrophages, and support the observed increase in proinflammatory cytokines [48].”
BackgroundOverweight and Obesity before, during and after Pregnancy
Stupin, J. H., & Arabin, B. (2014) · Geburtshilfe und Frauenheilkunde · doi:10.1055/s-0034-1368486 · Cited by 41
Zgutka, K., Tkacz, M., Tomasiak, P., Piotrowska, K., Ustianowski, P., Pawlik, A., & Tarnowski, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111409 · Cited by 45
“It is known that obesity is one of the most important risk factors for developing GDM, and increased production of pro-inflammatory cytokines in the placenta of obese women is observed [21].”
BackgroundChemerin expression in Chinese pregnant women with and without gestational diabetes mellitus
Li, X., Ji, H., Li, C., Wang, P., Yu, P., & Yu, D. M. (2014) · Annales d Endocrinologie · doi:10.1016/j.ando.2014.10.001 · Cited by 37
Dias, C. T., Curi, H. T., Payolla, T. B., Lemes, S. F., Pavan, I. C. B., Torsoni, M. A., Simabuco, F. M., Lambertucci, R. H., & da Silva, C. M. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104781 · Cited by 39
Barker, G., Lim, R., Rice, G. E., & Lappas, M. (2012) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2012.686540 · Cited by 36
“Obesity during pregnancy and GDM are both associated with insulin resistance [19,20] and enhanced inflammation [21,22].”
BackgroundCifuentes‐Zúñiga, F., Arroyo‐Jousse, V., Soto‐Carrasco, G., Casanello, P. C., Uauy, R. D., Krause, B. J., & Castro-Rodríguez, J. A. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25845 · Cited by 36
Diabetes Mellitus Complicating Pregnancy
Landon, M. B., Catalano, P. M., & Gabbe, S. G. (2007) · Elsevier eBooks · doi:10.1016/b978-0-443-06930-7.50039-6 · Cited by 36
Self-citationNelson, B. N., & Friedman, J. E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115951 · Cited by 39
“The normal cellular population of the placenta is also altered under obese conditions; an increased accumulation of CD68 + macrophages and a reduced number of M1 (proinflammatory) polarized macrophages have been reported [51,52].”
BackgroundMaternal obesity and immune dysregulation in mother and infant: A review of the evidence
Rizzo, G. S., & Sen, S. (2014) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2014.10.005 · Cited by 35
“This enhanced inflammatory response results in an increase of inflammatory factors in the fetal environment, such as CD14+ and CD68+ macrophages [37,45].”
BackgroundSano, M., Shimazaki, S., Kaneko, Y., Karasawa, T., Takahashi, M., Ohkuchi, A., Takahashi, H., Kurosawa, A., Torii, Y., Iwata, H., et al. (2020) · Journal of Reproduction and Development · doi:10.1262/jrd.2020-007 · Cited by 36
Vanishing Twins Conceived Through Fresh In Vitro Fertilization
Harris, A. L., Sacha, C. R., Basnet, K. M., James, K. E., Freret, T. S., Kaimal, A. J., Yeh, J., Souter, I. C., Roberts, D. J., & Toth, T. L. (2020) · Obstetrics and Gynecology · doi:10.1097/aog.0000000000003888 · Cited by 35
Phillips, E. A., Hendricks, N., Bucher, M., & Maloyan, A. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.893848 · Cited by 34
“org 2 mitochondrial respiration and excessive production of reactive oxygen species (16), accumulation of inflammation (19), dysregulated autophagy (17), and changes in miRNA expression (20) and epigenetic modifications (21).”
BackgroundMicrobiome and pregnancy: focus on microbial dysbiosis coupled with maternal obesity
Beckers, K. F., Flanagan, J. P., & Sones, J. L. (2023) · International Journal of Obesity · doi:10.1038/s41366-023-01438-7 · Cited by 35
“[109].”
Thakali, K. M., Saben, J. L., Faske, J. B., Lindsey, F., Gómez-Acevedo, H., Lowery, C. L., Badger, T. M., Andres, A., & Shankar, K. (2014) · Pediatric Research · doi:10.1038/pr.2014.72 · Cited by 34
Diet, behavior and immunity across the lifespan
Hale, M. W., Spencer, S. J., Conti, B., Jasoni, C. L., Kent, S., Radler, M. E., Reyes, T. M., & Sominsky, L. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.009 · Cited by 34
Endocrine and metabolic adaptations to pregnancy; impact of obesity
Mouzon, S. H., & Lassance, L. (2015) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2015-0042 · Cited by 34
The influence of maternal obesity on macrophage subsets in the human decidua
Laskewitz, A., van Benthem, K. L., Kieffer, T. E. C., Faas, M. M., Verkaik‐Schakel, R. N., Plösch, T., Scherjon, S. A., & Prins, J. R. (2019) · Cellular Immunology · doi:10.1016/j.cellimm.2019.01.002 · Cited by 34
Sharps, M. C., Baker, B., Guevara, T., Bischof, H., Jones, R. L., Greenwood, S. L., & Heazell, A. E. P. (2020) · American Journal of Reproductive Immunology · doi:10.1111/aji.13267 · Cited by 34
Santos-Rosendo, C., Bugatto, F., González‐Domínguez, Á., Lechuga-Sancho, A. M., Mateos, R. M., & Visiedo, F. (2020) · Antioxidants · doi:10.3390/antiox9090794 · Cited by 36
Sivakumar, K., Bari, M. F., Adaikalakoteswari, A., Guller, S. M., Weickert, M. O., Randeva, H. S., Grammatopoulos, D. K., Bastie, C. C., & Vatish, M. (2013) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2012-4293 · Cited by 34
Multimodal profiling of term human decidua demonstrates immune adaptations with pregravid obesity
Sureshchandra, S., Doratt, B. M., True, H., Mendoza, N., Rincon, M. P., Marshall, N., & Messaoudi, I. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112769 · Cited by 30
“30 In line with these observations, higher transcript levels of proinflammatory genes IL6, CCL2, IL8, and TLR4 were detected in a baboon model of high-fat diet-induced obesity, 31,32 suggesting potential immune cell adaptations with obesity at the maternal-fetal interface.”
Salati, J., Roberts, V. H. J., Schabel, M. C., Lo, J. O.-T., Kroenke, C. D., Lewandowski, K. S., Lindner, J. R., Grove, K. L., & Frias, A. E. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0145-7 · Cited by 33
Early Life Origins of Low-Grade Inflammation and Atherosclerosis Risk in Children and Adolescents
Labayen, I., Ortega, F. B., Sjöstróm, M., & Ruiz, J. R. (2009) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2009.04.056 · Cited by 34
Second-Trimester Amniotic Fluid Proinflammatory Cytokine Levels in Normal and Overweight Women
Bugatto, F., Fernández‐Deudero, Á., Bailén, Á., Fernández-Macías, R., Hervías‐Vivancos, B., & Bartha, J. L. (2009) · Obstetrics and Gynecology · doi:10.1097/aog.0b013e3181c5367f · Cited by 32
Maternal Obesity and Offspring Long-Term Infectious Morbidity
Gutvirtz, G., Wainstock, T., Landau, D., & Sheiner, E. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8091466 · Cited by 32
“Studies show that placentas of obese women exhibit alterations in immune cell populations compared to placentas of non-obese women [28], but these were aimed to explain the inflammatory state leading to metabolic changes in the offspring and not the infectious outcome.”
BackgroundNguyen‐Ngo, C., Willcox, J. C., & Lappas, M. (2020) · Placenta · doi:10.1016/j.placenta.2020.08.002 · Cited by 32
Placental morphology in pregnancies associated with pregravid obesity
Loardi, C., Falchetti, M., Prefumo, F., Facchetti, F., & Frusca, T. (2015) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.3109/14767058.2015.1094792 · Cited by 32
“[10] who reported that obesity exacerbates the basal inflammatory state of pregnancy, paralleling findings at the molecular level [11,12].”
BackgroundBrocato, B. E., Zoerner, A. A., Janjetović, Z., Skobowiat, C., Gupta, S., Moore, B. M., II, Slominski, A. T., Zhang, J., Schenone, M., Phinehas, R., et al. (2013) · Placenta · doi:10.1016/j.placenta.2013.08.007 · Cited by 31
“ECB hydrolysis could lead to a described in maternal obesity placental inflammatory response (macrophages and neutrophils accumulation) [20,44] through the formation of AA and COX-2 [45].”
BackgroundFunctional and genomic adaptations of blood monocytes to pregravid obesity during pregnancy
Sureshchandra, S., Marshall, N., Mendoza, N., Jankeel, A., Zulu, M. Z., & Messaoudi, I. (2021) · iScience · doi:10.1016/j.isci.2021.102690 · Cited by 30
Iozzo, P., Holmes, M. C., Schmidt, M. V., Cirulli, F., Guzzardi, M. A., Berry, A., Balsevich, G., Andreassi, M. G., Wesselink, J., Liistro, T., et al. (2014) · Obesity Facts · doi:10.1159/000362656 · Cited by 32
Lindsay, K. L., Buß, C., Wadhwa, P. D., & Entringer, S. (2018) · Nutrients · doi:10.3390/nu10091252 · Cited by 36
Capobianco, V., Caterino, M., Iaffaldano, L., Nardelli, C., Sirico, A., del Vecchio, L., Martinelli, P., Pastore, L., Pucci, P., & Sacchetti, L. (2016) · Scientific Reports · doi:10.1038/srep25270 · Cited by 30
Obesity downregulates lipid metabolism genes in first trimester placenta
Rasool, A., Mahmoud, T. G., Mathyk, B. A., Kaneko-Tarui, T., Roncari, D., White, K. O., & O’Tierney-Ginn, P. (2022) · Scientific Reports · doi:10.1038/s41598-022-24040-9 · Cited by 30
Woolner, A., & Bhattacharya, S. (2014) · Best Practice & Research Clinical Obstetrics & Gynaecology · doi:10.1016/j.bpobgyn.2014.07.025 · Cited by 32
Guerra, S., Sartini, C., Méndez, M. A., Morales, E., Guxens, M., Basterrechea, M., Arranz, L., & Sunyer, J. (2012) · Paediatric and Perinatal Epidemiology · doi:10.1111/ppe.12013 · Cited by 29
The Effects of Maternal Obesity on Porcine Placental Efficiency and Proteome
Li, J.-W., Hu, J., Wei, M., Guo, Y., & Yan, P. (2019) · Animals · doi:10.3390/ani9080546 · Cited by 29
Tinius, R. A., Cahill, A. G., Strand, E. A., & Cade, W. T. (2015) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2015-0316 · Cited by 29
“Interestingly, maternal inflammatory changes during pregnancy are believed to extend into the placenta, suggesting that the fetus of a woman with excessive inflammation is exposed to an inflammatory environment during development (Challier et al. 2008).”
BackgroundSantangelo, C., Varı́, R., Scazzocchio, B., Filesi, C., & Masella, R. (2013) · BioFactors · doi:10.1002/biof.1126 · Cited by 30
“TNF-a Impaired levels in FF correlate with oocytes quality [111] and reduced fertilization rate [112] in ART; " levels in PCOS obesity-correlated [114] " during pregnancy [116]; "" in obese pregnancy [117]; " in PE [118]”
BackgroundPalmitate induces apoptotic cell death and inflammasome activation in human placental macrophages
Rogers, L. M., Serezani, C. H., Eastman, A. J., Hasty, A. H., Englund‐Ögge, L., Jacobsson, B., Vickers, K. C., & Aronoff, D. M. (2019) · Placenta · doi:10.1016/j.placenta.2019.12.009 · Cited by 32
Can adipokine visfatin be a novel marker of pregnancy‐related disorders in women with obesity?
Wnuk, A., Stangret, A., Wątroba, M., Platek, A. E., Skoda, M., Cendrowski, K., Sawicki, W., & Szukiewicz, D. (2020) · Obesity Reviews · doi:10.1111/obr.13022 · Cited by 32
The Emerging Spectrum of Early Life Exposure-Related Inflammation and Epigenetic Therapy
Yang, Q., Ali, M. K., Andaloussi, A. E., & Al-Hendy, A. A. (2018) · Cancer Studies and Molecular Medicine - Open Journal · doi:10.17140/csmmoj-4-125 · Cited by 28
Lee, S., Shin, J., Hong, Y.-J., Shin, S. M., Shin, H. W., Shin, J., Lee, S. K., & Park, H. (2020) · American Journal of Reproductive Immunology · doi:10.1111/aji.13222 · Cited by 28
Inhibition of IL-1beta improves Glycaemia in a Mouse Model for Gestational Diabetes
Schulze, F., Wehner, J., Kratschmar, D. V., Makshana, V., Meier, D. T., Häuselmann, S. P., Dalmas, É., Thienel, C., Dror, E., Wiedemann, S. J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-59701-0 · Cited by 32
Maternal obesity in females born small: Pregnancy complications and offspring disease risk
Mahizir, D., Briffa, J. F., Hryciw, D. H., Wadley, G. D., Moritz, K. M., & Wlodek, M. E. (2015) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500289 · Cited by 29
Zhong, X., Jiang, Y.-Z., Liu, P., He, W., Xiong, Z., Chang, W., Zhu, J., & Cui, Q. (2016) · Oncotarget · doi:10.18632/oncotarget.11987 · Cited by 28
Nikolova, V., Papacleovoulou, G., Bellafante, E., Manna, L. B., Jansen, E. H. J. M., Baron, S., Abu‐Hayyeh, S., Parker, M. G., & Williamson, C. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00449.2016 · Cited by 29
Metadata
- Authors
- Challier, J. C., Basu, S., Bintein, T., Minium, J., Hotmire, K., Catalano, P. M., & Hauguel-de Mouzon, S.
- Affiliations
- Université Pierre-et-Marie-Curie (FR)
- MetroHealth (US)
- ORCID
- Catalano, P.M.
- Venue
- Placenta
- Publisher
- Elsevier BV
- Published
- 2008-03
- Volume
- 29
- Issue
- 3
- Pages
- 274-281
- ISSN
- 0143-4004 (ISSN-L)
- PMC
- PMC4284075
- OpenAlex
- W1975136933
- Cited by
- 712
- References
- 48
- Citations by year
- 2026: 18 · 2025: 32 · 2024: 25 · 2023: 47 · 2022: 57 · 2021: 30 · 2020: 66 · 2019: 33 · 2018: 44 · 2017: 48 · 2016: 51 · 2015: 67 · 2014: 53 · 2013: 46 · 2012: 34
- FWCI
- 22.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Placenta (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Deutsches Krebsforschungszentrum
- National Institutes of Health
- National Center for Research Resources (M01RR000080, RR 00080)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD022965, HD-22965)
- Topics
- Health Sciences › Medicine › Obstetrics and Gynecology › Gestational Diabetes Research and Management
- Health Sciences › Medicine › Obstetrics and Gynecology › Pregnancy and preeclampsia studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- maternal obesity, placental inflammation, placental macrophages, macrophage heterogeneity, CD68, CD14, CD11b, inflammatory cytokines, interleukin-6, TNF-α, interleukin-1, C-reactive protein, insulin resistance, fetal programming
- MeSH terms
- CD68 Molecule, Adult, Calcium-Binding Proteins, Cell Count, Cells, Cultured, Female, Fetal Blood, Humans, Inflammation, Leukocytes, Mononuclear, Macrophages, Membrane Glycoproteins, Mucins, Obesity, Placenta, Pregnancy, Pregnancy Complications, Tumor Necrosis Factor-alpha, Antigens, Differentiation, Myelomonocytic, Antigens, CD, Interleukin-6, Lipopolysaccharide Receptors, Receptors, G-Protein-Coupled
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review