Abou-Samra Murielle, Venema Koen, Ayoub Moubareck Carole, Karavetian Mirey
Faculty of Health, Medicine and Life Sciences, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, 6200 MD Maastricht, The Netherlands.
Centre for Healthy Eating & Food Innovation, Faculty of Science & Engineering, Maastricht University Campus Venlo, 5928 SZ Venlo, The Netherlands.
Metabolites. 2022 Nov 1;12(11):1051. doi: 10.3390/metabo12111051.
Peptide-hormones, including pancreatic peptide-YY(PYY), glucagon-like peptide-1 (GLP-1), cholecystokinin (CCK), insulin, and leptin function as satiety signals, while ghrelin promotes hunger. These hormones are also involved in glucose homeostasis and body-weight regulation. The aim of this cross-sectional analysis was to examine the association of these peptide-hormones with obesity-markers, insulin-resistance, and dyslipidemia (total-cholesterol (TC), low-density-lipoprotein-cholesterol (LDL-C), high-density-lipoprotein-cholesterol (HDL-C), triglyceride (TG)). Sixteen-obese (OB) adults and 21 normal-weight (NW) age-and gender-matched counterparts were recruited. OB-participants showed significantly higher levels of leptin, insulin, Homeostatic-Model Assessment of Insulin Resistance (HOMA-IR), and TG. NW participants had significantly higher levels of ghrelin. GLP-1 was positively correlated with insulin, HOMA-IR, and obesity-markers except percent body fat. Leptin was positively correlated with all markers (except glucose and dyslipidemia). PYY was positively correlated with BMI, insulin and HOMA-IR. Ghrelin was inversely correlated with all of the markers except glucose, TC, and LDL-C. In the regression analysis model, leptin was positively associated with obesity markers and insulin resistance. Our results indicate a significant difference in peptide hormones among OB and NW Lebanese individuals. Since there is controversial evidence regarding body-weight and peptide-hormones in the literature, this study highlights a step forward towards finding ethnic based strategies to treat obesity and its consequences.
肽类激素,包括胰多肽(PYY)、胰高血糖素样肽-1(GLP-1)、胆囊收缩素(CCK)、胰岛素和瘦素,发挥饱腹感信号的作用,而胃饥饿素则促进饥饿感。这些激素还参与葡萄糖稳态和体重调节。本横断面分析的目的是研究这些肽类激素与肥胖标志物、胰岛素抵抗和血脂异常(总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)、甘油三酯(TG))之间的关联。招募了16名肥胖(OB)成年人和21名年龄及性别匹配的正常体重(NW)对照者。OB参与者的瘦素、胰岛素、胰岛素抵抗稳态模型评估(HOMA-IR)和TG水平显著更高。NW参与者的胃饥饿素水平显著更高。GLP-1与胰岛素、HOMA-IR以及除体脂百分比之外的肥胖标志物呈正相关。瘦素与所有标志物(葡萄糖和血脂异常除外)呈正相关。PYY与BMI、胰岛素和HOMA-IR呈正相关。胃饥饿素与除葡萄糖、TC和LDL-C之外的所有标志物呈负相关。在回归分析模型中,瘦素与肥胖标志物和胰岛素抵抗呈正相关。我们的结果表明,黎巴嫩肥胖和正常体重个体之间的肽类激素存在显著差异。由于文献中关于体重和肽类激素的证据存在争议,本研究朝着寻找基于种族的肥胖及其后果治疗策略迈出了重要一步。