Emory University Medical Center Atlanta GA USA.
Advanced Analytics Division SAS Institute Inc Cary NC USA.
Endocrinol Diabetes Metab. 2021 Apr 1;4(3):e00250. doi: 10.1002/edm2.250. eCollection 2021 Jul.
Insulin resistance in adolescents with obesity associates with a sex-dependent metabolic 'signature' comprising branched-chain amino acids (BCAAs), glutamate and C3/C5 acylcarnitines (C3/C5), implicating altered flux through BCAA catabolic pathways. Here, we investigated the effects of lifestyle intervention on BCAA catabolism and insulin sensitivity. We hypothesized (1) weight reduction and improved insulin sensitivity associate with enhanced BCAA catabolism; (2) baseline BCAAs and their metabolic by-products predict changes in weight and insulin sensitivity during lifestyle intervention.
A 33 adolescents with obesity were studied before and after 6 months of lifestyle intervention. Principal component analysis and multiple linear regression models were used to correlate changes in metabolic factors with changes in weight and insulin sensitivity assessed by HOMA-IR, adiponectin and ratio of triglyceride (TG) to HDL. Baseline metabolic factors were used as explanatory variables in prediction models.
Weight reduction was associated with reductions in BCAA, glutamate, and C3/C5 ( = .002) and increases in urea cycle AA ( = .029), suggesting an increase in BCAA catabolism. Increases in urea cycle AA during weight reduction were associated with increases in adiponectin, a marker of insulin sensitivity. Markers of insulin resistance (high BCAA, glutamate, and C3/C5 and low urea cycle AA) at baseline predicted increases in metrics of insulin sensitivity (decreased TG/HDL and increased adiponectin) during lifestyle intervention.
Weight reduction in adolescents is associated with increases in BCAA catabolism and improvements in insulin sensitivity. Our study underscores the therapeutic potential of manipulating BCAA catabolism to treat obesity-associated insulin resistance in adolescents and prevent progression to T2D.
肥胖青少年的胰岛素抵抗与性别依赖的代谢“特征”相关,该特征包括支链氨基酸 (BCAA)、谷氨酸和 C3/C5 酰基辅酶 A (C3/C5),表明支链氨基酸分解代谢途径的通量发生改变。在这里,我们研究了生活方式干预对支链氨基酸分解代谢和胰岛素敏感性的影响。我们假设:(1)体重减轻和胰岛素敏感性改善与增强的支链氨基酸分解代谢相关;(2)基线支链氨基酸及其代谢产物可预测生活方式干预期间体重和胰岛素敏感性的变化。
研究了 33 名肥胖青少年在生活方式干预前后的情况。采用主成分分析和多元线性回归模型,将代谢因子的变化与通过 HOMA-IR、脂联素和甘油三酯 (TG) 与高密度脂蛋白 (HDL) 比值评估的体重和胰岛素敏感性的变化相关联。将基线代谢因素用作预测模型中的解释变量。
体重减轻与支链氨基酸、谷氨酸和 C3/C5 的减少有关(r =.002),与尿素循环 AA 的增加有关(r =.029),这表明支链氨基酸分解代谢增加。在体重减轻期间,尿素循环 AA 的增加与胰岛素敏感性的标志物(脂联素)的增加相关。基线时的胰岛素抵抗标志物(高支链氨基酸、谷氨酸和 C3/C5 以及低尿素循环 AA)预测生活方式干预期间胰岛素敏感性指标(TG/HDL 降低和脂联素增加)的增加。
青少年体重减轻与支链氨基酸分解代谢增加和胰岛素敏感性改善相关。我们的研究强调了操纵支链氨基酸分解代谢治疗肥胖相关胰岛素抵抗和预防 T2D 进展的治疗潜力。