Duke Molecular Physiology Institute, Durham, NC, USA.
Sarah W. Stedman Nutrition and Metabolism Center, Durham, NC, USA.
Nutr Diabetes. 2021 Feb 24;11(1):10. doi: 10.1038/s41387-021-00151-6.
There is marked heterogeneity in the response to weight loss interventions with regards to weight loss amount and metabolic improvement. We sought to identify biomarkers predictive of type 2 diabetes remission and amount of weight loss in individuals with severe obesity enrolled in the Longitudinal Assessment of Bariatric Surgery (LABS) and the Look AHEAD (Action for Health in Diabetes) studies. Targeted mass spectrometry-based profiling of 135 metabolites was performed in pre-intervention blood samples using a nested design for diabetes remission over five years (n = 93 LABS, n = 80 Look AHEAD; n = 87 remitters), and for extremes of weight loss at five years (n = 151 LABS; n = 75 with high weight loss). Principal components analysis (PCA) was used for dimensionality reduction, with PCA-derived metabolite factors tested for association with both diabetes remission and weight loss. Metabolic markers were tested for incremental improvement to clinical models, including the DiaRem score. Two metabolite factors were associated with diabetes remission: one primarily composed of branched chain amino acids (BCAA) and tyrosine (odds ratio (95% confidence interval) [OR (95% CI)] = 1.4 [1.0-1.9], p = 0.045), and one with betaine and choline (OR [95% CI] = 0.7 [0.5-0.9], p = 0.02).These results were not significant after adjustment for multiple tests. Inclusion of these two factors in clinical models yielded modest improvements in model fit and performance: in a constructed clinical model, the C-statistic improved from 0.87 to 0.90 (p = 0.02), while the net reclassification index showed improvement in prediction compared to the DiaRem score (NRI = 0.26, p = 0.0013). No metabolite factors associated with weight loss at five years. Baseline levels of metabolites in the BCAA and trimethylamine-N-oxide (TMAO)-microbiome-related pathways are independently and incrementally associated with sustained diabetes remission after weight loss interventions in individuals with severe obesity. These metabolites could serve as clinically useful biomarkers to identify individuals who will benefit the most from weight loss interventions.
在减肥干预措施对减肥量和代谢改善的反应方面存在明显的异质性。我们试图确定生物标志物,以预测在严重肥胖的个体中进行减肥手术(LABS)和前瞻性糖尿病研究(Look AHEAD)的 2 型糖尿病缓解和减肥量。使用嵌套设计,对五年内糖尿病缓解(n=93LABS,n=80Look AHEAD;n=87 缓解者)和五年内体重减轻的极端情况(n=151LABS;n=75 体重减轻量高)的预干预血样进行基于靶向质谱的 135 种代谢物的分析。使用主成分分析(PCA)进行降维,使用 PCA 衍生的代谢物因子测试其与糖尿病缓解和减肥的关联。测试代谢标志物对临床模型的增量改善,包括 DiaRem 评分。两个代谢物因子与糖尿病缓解相关:一个主要由支链氨基酸(BCAA)和酪氨酸组成(优势比(95%置信区间)[OR(95%CI)]1.4[1.0-1.9],p=0.045),另一个由甜菜碱和胆碱组成(OR[95%CI]0.7[0.5-0.9],p=0.02)。这些结果在经过多次测试调整后并不显著。将这两个因素纳入临床模型可适度提高模型拟合度和性能:在构建的临床模型中,C 统计量从 0.87 提高到 0.90(p=0.02),而净重新分类指数显示与 DiaRem 评分相比,预测有所改善(NRI=0.26,p=0.0013)。没有与五年后体重减轻相关的代谢物因子。在严重肥胖的个体中,减肥干预后持续糖尿病缓解与基线时支链氨基酸(BCAA)和三甲胺-N-氧化物(TMAO)-微生物组相关途径中的代谢物水平独立且呈递增相关。这些代谢物可以作为临床上有用的生物标志物,以识别最能从减肥干预中受益的个体。