{"title":"Growth differentiation factor-15 and body roundness index in relation to cardiometabolic risk in young adults with obesity.","authors":"Omar Jasim Mohammed, Hassanain K Mehdi","doi":"10.1007/s12020-026-04784-4","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Cardiometabolic risk in young adults is often subclinical. This cross-sectional study evaluated Growth Differentiation Factor-15 (GDF-15) and Body Roundness Index (BRI) in relation to cardiometabolic risk in young adults.</p><p><strong>Methods: </strong>Ninety adults aged 18-35 years were classified into control, low-risk, and high-risk groups using predefined criteria. Anthropometric, glycemic, and lipid parameters, hs-CRP, GDF-15, leptin, and adiponectin were analyzed using ANCOVA, partial correlation, regression, and ROC analysis.</p><p><strong>Results: </strong>GDF-15 rose progressively across groups (control 337.7 ± 82.6, low-risk 865.8 ± 76.9, high-risk 1130.7 ± 79.2 pg/mL; p < 0.001). Leptin, the leptin-to-adiponectin ratio, and adiponectin were higher in both risk groups than controls (p < 0.001), with no difference between risk groups. GDF-15 showed high discriminatory ability for controls versus obese groups (AUC 0.939-0.954), reflecting phenotypic separation, but only modest discrimination between low-risk and high-risk groups (AUC = 0.677, 95% CI 0.535-0.819; p = 0.024), the clinically relevant comparison. In exploratory subgroup regression, adiponectin was associated with GDF-15 in low-risk (β = 0.465, p = 0.011) and high-risk groups (β = 0.551, p = 0.038). Combining GDF-15 with waist-to-hip ratio gave a numerically higher AUC (0.708), although the difference was not formally tested.</p><p><strong>Conclusion: </strong>GDF-15 levels increased progressively across the study groups and remained significantly different across groups after adjustment for age. GDF-15 and adiponectin showed very high discrimination between obese participants and controls but only modest discrimination between risk groups. These exploratory, cross-sectional findings identify GDF-15 as a candidate biomarker of cardiometabolic risk in young adults, requiring confirmation in larger prospective cohorts.</p>","PeriodicalId":49211,"journal":{"name":"Endocrine","volume":"91 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12020-026-04784-4","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Cardiometabolic risk in young adults is often subclinical. This cross-sectional study evaluated Growth Differentiation Factor-15 (GDF-15) and Body Roundness Index (BRI) in relation to cardiometabolic risk in young adults.
Methods: Ninety adults aged 18-35 years were classified into control, low-risk, and high-risk groups using predefined criteria. Anthropometric, glycemic, and lipid parameters, hs-CRP, GDF-15, leptin, and adiponectin were analyzed using ANCOVA, partial correlation, regression, and ROC analysis.
Results: GDF-15 rose progressively across groups (control 337.7 ± 82.6, low-risk 865.8 ± 76.9, high-risk 1130.7 ± 79.2 pg/mL; p < 0.001). Leptin, the leptin-to-adiponectin ratio, and adiponectin were higher in both risk groups than controls (p < 0.001), with no difference between risk groups. GDF-15 showed high discriminatory ability for controls versus obese groups (AUC 0.939-0.954), reflecting phenotypic separation, but only modest discrimination between low-risk and high-risk groups (AUC = 0.677, 95% CI 0.535-0.819; p = 0.024), the clinically relevant comparison. In exploratory subgroup regression, adiponectin was associated with GDF-15 in low-risk (β = 0.465, p = 0.011) and high-risk groups (β = 0.551, p = 0.038). Combining GDF-15 with waist-to-hip ratio gave a numerically higher AUC (0.708), although the difference was not formally tested.
Conclusion: GDF-15 levels increased progressively across the study groups and remained significantly different across groups after adjustment for age. GDF-15 and adiponectin showed very high discrimination between obese participants and controls but only modest discrimination between risk groups. These exploratory, cross-sectional findings identify GDF-15 as a candidate biomarker of cardiometabolic risk in young adults, requiring confirmation in larger prospective cohorts.
期刊介绍:
Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology.
Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted.
Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.