Association of Metabolically Healthy and Unhealthy Obesity Phenotypes with Oxidative Stress Parameters and Telomere Length in Healthy Young Adult Men. Analysis of the MAGNETIC Study
Open accessAbstract
Obesity is a significant factor related to metabolic disturbances that can lead to metabolic syndrome (MetS). Metabolic dysregulation causes oxidative stress, which affects telomere structure. The current study aimed to evaluate the relationships between telomere length, oxidative stress and the metabolically healthy and unhealthy phenotypes in healthy young men. Ninety-eight participants were included in the study (49 healthy slim and 49 obese patients). Study participants were divided into three subgroups according to body mass index and metabolic health. Selected oxidative stress markers were measured in serum. Relative telomere length (rTL) was measured using quantitative polymerase chain reaction. The analysis showed associations between laboratory markers, oxidative stress markers and rTL in metabolically healthy and unhealthy participants. Total oxidation status (TOS), total antioxidant capacity (TAC) and rTL were significantly connected with metabolically unhealthy obesity. TAC was associated with metabolically healthy obesity. Telomeres shorten in patients with metabolic dysregulation related to oxidative stress and obesity linked to MetS. Further studies among young metabolically healthy and unhealthy individuals are needed to determine the pathways related to metabolic disturbances that cause oxidative stress that leads to MetS.
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
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?
Telomeres are shorter especially in obesity accompanied by metabolic abnormalities leading to metabolic syndrome.
“Increased visceral adipose tissue is further associated with oxidative stress and it has been shown that telomeres are shorter especially in obesity that is accompanied by metabolic abnormalities leading to metabolic syndrome [21].”
From Mediterranean Diet as an Antioxidant: The Impact on Metabolic Health and Overall Wellbeing (2021) · cites this paper as [21]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction
Ohkawa, H., Ohishi, N., & Yagi, K. (1979) · Analytical Biochemistry · doi:10.1016/0003-2697(79)90738-3 · Cited by 29,460 · see citing works
Grundy, S. M., Bilheimer, D. W., Chait, A., Clark, L. T., Denke, M. A., Havel, R. J., Hazzard, W. R., Hulley, S. B., Hunninghake, D. B., Kreisberg, R. A., et al. (1993) · JAMA · doi:10.1001/jama.269.23.3015 · Cited by 27,944 · see citing works
Expert Panel on Detection, E. (2001) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.285.19.2486 · Cited by 26,011 · see citing works
Alberti, K. G. M. M., Eckel, R. H., Grundy, S. M., Zimmet, P. Z., Cleeman, J. I., Donato, K. A., Fruchart, J.-C., James, W. P. T., Loria, C. M., & Smith, S. C. (2009) · Circulation · doi:10.1161/circulationaha.109.192644 · Cited by 14,860 · see citing works
MissForest—Non-parametric missing value imputation for mixed-type data
Stekhoven, D. J., & Bühlmann, P. (2012) · Bioinformatics · doi:10.1093/bioinformatics/btr597 · Cited by 6,156 · see citing works
Increased oxidative stress in obesity and its impact on metabolic syndrome
Furukawa, S., Fujita, T., Shimabukuro, M., Iwaki, M., Yamada, Y., Nakajima, Y., Nakayama, O., Makishima, M., Matsuda, M., & Shimomura, I. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21625 · Cited by 5,508 · see citing works
The Pathobiology of Diabetic Complications
Brownlee, M. (2005) · Diabetes · doi:10.2337/diabetes.54.6.1615 · Cited by 5,339 · see citing works
Obesity: global epidemiology and pathogenesis
Blüher, M. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0176-8 · Cited by 5,126 · see citing works
Oxidative stress, aging, and diseases
Liguori, I., Russo, G., Curcio, F., Bulli, G., Aran, L., Della-Morte, D., Gargiulo, G., Testa, G., Cacciatore, F., Bonaduce, D., et al. (2018) · Clinical Interventions in Aging · doi:10.2147/cia.s158513 · Cited by 3,979 · see citing works
Role of Oxidative Stress in Development of Complications in Diabetes
Baynes, J. (1991) · Diabetes · doi:10.2337/diab.40.4.405 · Cited by 3,791 · see citing works
A new automated colorimetric method for measuring total oxidant status
Erel, Ö. (2005) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2005.08.008 · Cited by 3,747 · see citing works
Structure and function of telomeres
Blackburn, E. H. (1991) · Nature · doi:10.1038/350569a0 · Cited by 3,596 · see citing works
Bilirubin Is an Antioxidant of Possible Physiological Importance
Stocker, R., Yamamoto, Y., McDonagh, A. F., Glazer, A. N., & Ames, B. N. (1987) · Science · doi:10.1126/science.3029864 · Cited by 3,502 · see citing works
Telomere measurement by quantitative PCR
Cawthon, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.10.e47 · Cited by 3,492 · see citing works
Erel, Ö. (2004) · Clinical Biochemistry · doi:10.1016/j.clinbiochem.2003.11.015 · Cited by 2,940 · see citing works
Reactive oxygen species have a causal role in multiple forms of insulin resistance
Houstis, N., Rosen, E. D., & Lander, E. S. (2006) · Nature · doi:10.1038/nature04634 · Cited by 2,525 · see citing works
Role of oxidative stress in diabetic complications: a new perspective on an old paradigm.
Baynes, J. W., & Thorpe, S. R. (1999) · Diabetes · doi:10.2337/diabetes.48.1.1 · Cited by 2,441 · see citing works
Ceriello, A., & Motz, E. (2004) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000122852.22604.78 · Cited by 1,378 · see citing works
Dandona, P., Aljada, A., Chaudhuri, A., Mohanty, P., & Garg, R. (2005) · Circulation · doi:10.1161/01.cir.0000158483.13093.9d · Cited by 1,263 · see citing works
Oxidative stress in obesity: A critical component in human diseases
Marseglia, L., Manti, S., D’Angelo, G., Nicotera, A., Parisi, E., Di Rosa, G., Gitto, E., & Arrigo, T. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms16010378 · Cited by 933 · see citing works
Reevaluation of assay methods and establishment of kit for superoxide dismutase activity
Ōyanagui, Y. (1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90467-6 · Cited by 917 · see citing works
Oxidative stress and metabolic syndrome
Roberts, C. K., & Sindhu, K. K. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.02.026 · Cited by 865 · see citing works
Dandona, P., Aljada, A., Mohanty, P., Ghanim, H., Hamouda, W., Assian, E., & Ahmad, S. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.7.7623 · Cited by 695 · see citing works
Characterizing the profile of obese patients who are metabolically healthy
Primeau, V., Coderre, L., Karelis, A. D., Brochu, M., Lavoie, M.-È., Messier, V., SLADEK, R. M., & RABASA-LHORET, R. P. R. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.216 · Cited by 630 · see citing works
Yu, M.-A., Sánchez-Lozada, L. G., Johnson, R. J., & Kang, D.-H. (2010) · Journal of Hypertension · doi:10.1097/hjh.0b013e328337da1d · Cited by 626 · see citing works
Metabolically Healthy Obesity and Risk of All-Cause and Cardiovascular Disease Mortality
Hamer, M., & Stamatakis, E. A. (2012) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-3475 · Cited by 565 · see citing works
Telomere length assessment: Biomarker of chronic oxidative stress?
Houben, J. M. J., Moonen, H. J. J., van Schooten, F., & Hageman, G. J. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.10.001 · Cited by 562 · see citing works
Oxidative stress and glycemic regulation
Ceriello, A. (2000) · Metabolism · doi:10.1016/s0026-0495(00)80082-7 · Cited by 550 · see citing works
Mechanism of telomere shortening by oxidative stress
KAWANISHI, S., & OIKAWA, S. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.047 · Cited by 522 · see citing works
Therapeutic potentials of superoxide dismutase.
Younus, H. (2018) · PubMed · Cited by 516 · see citing works
Determinants of telomere length across human tissues
Demanelis, K., Jasmine, F., Chen, L. S., Chernoff, M., Tong, L., Delgado, D., Zhang, C., Shinkle, J., Sabarinathan, M., Lin, H., et al. (2020) · Science · doi:10.1126/science.aaz6876 · Cited by 515 · see citing works
Mitochondrial dysfunction in obesity
de Mello, A. H., Costa, A. B., Engel, J. D. G., & Rezin, G. T. (2018) · Life Sciences · doi:10.1016/j.lfs.2017.11.019 · Cited by 508 · see citing works
Cell aging in relation to stress arousal and cardiovascular disease risk factors
Epel, E. S., Lin, J., Wilhelm, F. H., Wolkowitz, O. M., Cawthon, R., Adler, N. E., Dolbier, C., Mendes, W. B., & Blackburn, E. H. (2006) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2005.08.011 · Cited by 450 · see citing works
Pathogenesis of Chronic Hyperglycemia: From Reductive Stress to Oxidative Stress
Yan, L. (2014) · Journal of Diabetes Research · doi:10.1155/2014/137919 · Cited by 403 · see citing works
Rise in Insulin Resistance Is Associated With Escalated Telomere Attrition
Gardner, J. P., Li, S., Srinivasan, S. R., Chen, W., Kimura, M., Lu, X., Berenson, G. S., & Aviv, A. (2005) · Circulation · doi:10.1161/01.cir.0000163550.70487.0b · Cited by 361 · see citing works
Syndromes of Telomere Shortening
Armanios, M. (2009) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082908-150046 · Cited by 317 · see citing works
Speakman, J. R., Levitsky, D. A., Allison, D. B., Bray, M. S., de Castro, J. M., Clegg, D. J., Clapham, J. C., Dulloo, A. G., Gruer, L. D., Haw, S. J., et al. (2011) · Disease Models & Mechanisms · doi:10.1242/dmm.008698 · Cited by 316 · see citing works
Rey-López, J. P., Rezende, L. F. M., Pastor‐Valero, M., & Tess, B. H. (2014) · Obesity Reviews · doi:10.1111/obr.12198 · Cited by 311 · see citing works
Willeit, P., Willeit, J., Kloss‐Brandstätter, A., Ehrlenbach, S., Mayr, A., Gasperi, A., Weger, S., Oberhollenzer, F., Reindl, M., Kronenberg, F., et al. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.205492 · Cited by 289 · see citing works
Can we identify metabolically healthy but obese individuals (MHO)?
Karelis, A. D., Brochu, M., & RABASA-LHORET, R. P. R. (2004) · Diabetes & Metabolism · doi:10.1016/s1262-3636(07)70156-8 · Cited by 269 · see citing works
Body fat distribution, relative weight, and liver enzyme levels: A population-based study
Stranges, S., Dorn, J. M., Muti, P. C., et al. (2004) · Hepatology · doi:10.1002/hep.20149 · Cited by 235 · see citing works
Lim, J.-S., Yang, J.-H., Chun, B.-Y., Kam, S., Jacobs, D. R., & Lee, D. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.06.032 · Cited by 218 · see citing works
Intracellular and extracellular sulphydryl levels in rheumatoid arthritis.
Koster, J. F., Biemond, P., & Swaak, A. J. G. (1986) · Annals of the Rheumatic Diseases · doi:10.1136/ard.45.1.44 · Cited by 205 · see citing works
Metabolically healthy and unhealthy obese – the 2013 S tock C onference report
Samocha‐Bonet, D., Dixit, V. D., Kahn, C. R., Leibel, R. L., Lin, X., Nieuwdorp, M., Pietiläinen, K. H., RABASA-LHORET, R. P. R., Roden, M., Scherer, P. E., et al. (2014) · Obesity Reviews · doi:10.1111/obr.12199 · Cited by 169 · see citing works
Tan, C. Y., & Vidal‐Puig, A. (2008) · Biochemical Society Transactions · doi:10.1042/bst0360935 · Cited by 169 · see citing works
Plasma lipid hydroperoxides measurement by an automated xylenol orange method
Arab, K., & Steghens, J. (2003) · Analytical Biochemistry · doi:10.1016/j.ab.2003.10.022 · Cited by 161 · see citing works
Fluorescent substances in mouse and human sera as a parameter of in vivo lipid peroxidation
Masako, T., Toshiyuki, M., Kaoru, M., & AIBARA, K. (1985) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(85)90156-0 · Cited by 143 · see citing works
Phagocytic NADPH Oxidase Overactivity Underlies Oxidative Stress in Metabolic Syndrome
Fortuño, A., San José, G., Moreno, M. U., Beloqui, O., Díez, J., & Zalba, G. (2006) · Diabetes · doi:10.2337/diabetes.55.01.06.db05-0751 · Cited by 128 · see citing works
André, P., Balkau, B., Born, C., Charles, M.-A. A., Eschwège, É., & D.E.S.I.R. study group (2006) · Diabetologia · doi:10.1007/s00125-006-0418-x · Cited by 97 · see citing works
Oxidative stress is associated with the number of components of metabolic syndrome: LIPGENE study
Yubero‐Serrano, E. M., Delgado‐Lista, J., Peña‐Orihuela, P. J., Pérez‐Martínez, P., Fuentes, F. J., Marı́n, C., Túnez, I., Tinahones, F. J., Pérez‐Jiménez, F., Roche, H. M., et al. (2013) · Experimental & Molecular Medicine · doi:10.1038/emm.2013.53 · Cited by 96 · see citing works
Can metabolically healthy obesity be explained by diet, genetics, and inflammation?
Navarro, E., Funtikova, A. N., Fitó, M., & Schröder, H. (2014) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201400521 · Cited by 91 · see citing works
Chen, J., Pan, W., Hsu, C., Yeh, W., Chuang, S., Chen, P., Chen, H., Chang, C., & Huang, W. (2012) · Arthritis Care & Research · doi:10.1002/acr.21824 · Cited by 89 · see citing works
Han, T., Meng, X., Shan, R., Zi, T., Li, Y., Ma, H., Zhao, Y., Shi, D., Qu, R., Guo, X., et al. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0074-5 · Cited by 80 · see citing works
Metabolically healthy obese individuals: Key protective factors
Gonçalves, C. G., Glade, M. J., & Meguid, M. M. (2015) · Nutrition · doi:10.1016/j.nut.2015.07.010 · Cited by 75 · see citing works
Rospleszcz, S., Dermyshi, D., Müller‐Peltzer, K., Strauch, K., Bamberg, F., & Peters, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-57459-z · Cited by 64 · see citing works
Kim, M., Paik, J. K., Kang, R., Kim, S. Y., Lee, S., & Lee, J. H. (2012) · Metabolism · doi:10.1016/j.metabol.2012.10.006 · Cited by 63 · see citing works
Giral, P., Ratziu, V., Couvert, P., et al. (2009) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2009.12.026 · Cited by 61 · see citing works
Telomere length and cardiovascular disease risk
Zhan, Y., & Hägg, S. (2019) · Current Opinion in Cardiology · doi:10.1097/hco.0000000000000613 · Cited by 57 · see citing works
Giral, P., Jacob, N., Dourmap, C., Hansel, B., Carrié, A., Bruckert, É., Girerd, X. J., & Chapman, M. J. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.157891 · Cited by 56 · see citing works
Proinflammatory and lipid biomarkers mediate metabolically healthy obesity: A proteomics study
Doumatey, A. P., Zhou, J., Zhou, M., Prieto, D. A., Rotimi, C. N., & Adeyemo, A. (2016) · Obesity · doi:10.1002/oby.21482 · Cited by 52 · see citing works
Marital status, telomere length and cardiovascular disease risk in a Swedish prospective cohort
Chen, R., Zhan, Y., Pedersen, N. L., Fall, K., Valdimarsdóttir, U. A., Hägg, S., & Fang, F. (2019) · Heart · doi:10.1136/heartjnl-2019-315629 · Cited by 52 · see citing works
Abolnezhadian, F., Hosseini, S. A., Alipour, M., Zakerkish, M., Cheraghian, B., Ghandil, P., & Cheraghpour, M. (2020) · Vascular Health and Risk Management · doi:10.2147/vhrm.s251927 · Cited by 52 · see citing works
Osadnik, K., Osadnik, T., Lonnie, M., Lejawa, M., Reguła, R., Fronczek, M., Gawlita, M., Wądołowska, L., Gąsior, M., & Pawlas, N. (2020) · Nutrition Journal · doi:10.1186/s12937-020-00532-0 · Cited by 41 · see citing works
Self-citationTian, R., Zhang, L.-N., Zhang, T., et al. (2017) · Medical Science Monitor · doi:10.12659/msm.902106 · Cited by 37 · see citing works
Metabolic syndrome, endothelial function and lifestyle modification
Aizawa, K., Shoemaker, J. K., Overend, T. J., & Petrella, R. J. (2009) · Diabetes and Vascular Disease Research · doi:10.1177/1479164109336375 · Cited by 29 · see citing works
Oxidative Stress, Telomere Length, and Frailty in an Old Age Population
Martínez‐Ezquerro, J. D., Rodríguez-Castañeda, A., Ortiz‐Ramírez, M., et al. (2019) · Revista de investigaci�n Cl�nica · doi:10.24875/ric.19003116 · Cited by 25 · see citing works
Molli, A. E. I., Panero, J., Santos, P. C. D., González, C. D., Vilarino, J. F., Sereday, M., Cerrone, G. E., Slavutsky, I. R., & Frechtel, G. D. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174945 · Cited by 23 · see citing works
Osadnik, T., Osadnik, K., Pawlas, N., Strzelczyk, J. K., Kasperczyk, J., Poloński, L., & Gąsior, M. (2019) · Archives of Medical Science · doi:10.5114/aoms.2018.75895 · Cited by 16 · see citing works
Self-citationOsadnik, K., Osadnik, T., Delijewski, M., Lejawa, M., Fronczek, M., Reguła, R., Gąsior, M., & Pawlas, N. (2020) · Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy · doi:10.2147/dmso.s232497 · Cited by 15 · see citing works
Self-citationZhang, X., Lü, Q., Zhang, Z., Chen, Y., Wang, Y., Wang, Y., Zheng, L., & Jiang, L. (2018) · Clinical Rheumatology · doi:10.1007/s10067-018-4132-0 · Cited by 11 · see citing works
Długość telomerów – nowy biomarker w medycynie
Kozłowska, A., Mikołajczyk, A., & Pawlas, N. (2015) · Medycyna Środowiskowa - Environmental Medicine · Cited by 1 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Mediterranean Diet as an Antioxidant: The Impact on Metabolic Health and Overall Wellbeing
Gantenbein, K. V., & Kanaka-Gantenbein, C. (2021) · Nutrients · doi:10.3390/nu13061951 · Cited by 288 · see citing works
- Authors
- Lejawa, M., Osadnik, K., Osadnik, T., & Pawlas, N.
- Affiliations
- Medical University of Silesia (PL)
- Corresponding author
- Lejawa, Mateusz
- Venue
- Antioxidants
- Publisher
- MDPI AG
- Published
- 2021-01-11
- Volume
- 10
- Issue
- 1
- Pages
- 93
- ISSN
- 2076-3921 (ISSN-L)
- PMC
- PMC7826733
- OpenAlex
- W3118332550
- Cited by
- 30
- References
- 71
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 6 · 2023: 8 · 2022: 6 · 2021: 4
- FWCI
- 3.77
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Antioxidants (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Narodowe Centrum Nauki (UMO-2014113IBINZ5/03166)
- Śląski Uniwersytet Medyczny (KNW-1-039/N/8/K)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Keywords
- metabolically healthy obesity, metabolically unhealthy obesity, oxidative stress, telomere length, metabolic syndrome, total antioxidant capacity, young men, obesity phenotypes, body mass index
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