Erbakan Ayşe N, Mutlu H Hicran, Uzunlulu Mehmet, Caştur Lütfullah, Akbaş Muhammet Mikdat, Kaya Fatoş N, Erbakan Mehmet, İşman Ferruh K, Oğuz Aytekin
Department of Internal Medicine, Istanbul Medeniyet University, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, 34722 Istanbul, Turkey.
Department of Family Medicine, Istanbul Medeniyet University, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, 34722 Istanbul, Turkey.
J Pers Med. 2024 May 3;14(5):487. doi: 10.3390/jpm14050487.
Metabolically healthy obesity (MHO) refers to obese individuals with a favorable metabolic profile, without severe metabolic abnormalities. This study aimed to investigate the potential of follistatin, a regulator of metabolic balance, as a biomarker to distinguish between metabolically healthy and unhealthy obesity. This cross-sectional study included 30 metabolically healthy and 32 metabolically unhealthy individuals with obesity. Blood samples were collected to measure the follistatin levels using an enzyme-linked immunosorbent assay (ELISA). While follistatin did not significantly differentiate between metabolically healthy (median 41.84 [IQR, 37.68 to 80.09]) and unhealthy (median 42.44 [IQR, 39.54 to 82.55]) individuals with obesity ( = 0.642), other biochemical markers, such as HDL cholesterol, triglycerides, C-peptide, and AST, showed significant differences between the two groups. Insulin was the most significant predictor of follistatin levels, with a coefficient of 0.903, followed by C-peptide, which exerted a negative influence at -0.624. Quantile regression analysis revealed nuanced associations between the follistatin levels and metabolic parameters in different quantiles. Although follistatin may not serve as a biomarker for identifying MHO and metabolically unhealthy obesity, understanding the underlying mechanisms that contribute to metabolic dysfunction could provide personalized strategies for managing obesity and preventing associated complications.
代谢健康型肥胖(MHO)是指具有良好代谢特征、无严重代谢异常的肥胖个体。本研究旨在探讨代谢平衡调节剂卵泡抑素作为区分代谢健康型肥胖和代谢不健康型肥胖生物标志物的潜力。这项横断面研究纳入了30名代谢健康的肥胖个体和32名代谢不健康的肥胖个体。采集血样,采用酶联免疫吸附测定法(ELISA)检测卵泡抑素水平。虽然卵泡抑素在代谢健康的肥胖个体(中位数41.84 [四分位间距,37.68至80.09])和代谢不健康的肥胖个体(中位数42.44 [四分位间距,39.54至82.55])之间没有显著差异(P = 0.642),但其他生化标志物,如高密度脂蛋白胆固醇、甘油三酯、C肽和谷草转氨酶,在两组之间显示出显著差异。胰岛素是卵泡抑素水平最显著的预测因子,系数为0.903,其次是C肽,其影响系数为-0.624,呈负相关。分位数回归分析揭示了卵泡抑素水平与不同分位数下代谢参数之间的细微关联。虽然卵泡抑素可能无法作为识别MHO和代谢不健康型肥胖的生物标志物,但了解导致代谢功能障碍的潜在机制可为管理肥胖和预防相关并发症提供个性化策略。