Division of General Internal Medicine, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
National Phenome Centre, Imperial College London, Hammersmith Hospital Campus, London, UK.
Diabet Med. 2021 Feb;38(2):e14494. doi: 10.1111/dme.14494. Epub 2020 Dec 25.
South Asians are at higher risk for diabetes (DM) than many other racial/ethnic groups. Circulating metabolites are measurable products of metabolic processes that may explain the aetiology of elevated risk. We characterized metabolites associated with prevalent DM and glycaemic measures in South Asians.
We included 717 participants from the Mediators of Atherosclerosis in South Asians Living in America (MASALA) study, aged 40-84 years. We used baseline fasting serum for metabolomics and demographic, behavioural, glycaemic data from baseline and at 5 years. We performed LC-MS untargeted metabolomic and lipidomic analysis with targeted integration of known signals. Individual linear and ordinal logistic regression models were adjusted for age, sex, BMI, diet, exercise, alcohol, smoking and family history of DM followed by elastic net regression to identify metabolites most associated with the outcome.
There were 258 metabolites with detectable signal in >98% of samples. Thirty-four metabolites were associated with prevalent DM in an elastic net model. Predominant metabolites associated with DM were sphingomyelins, proline (OR 15.86; 95% CI 4.72, 53.31) and betaine (OR 0.03; 0.004, 0.14). Baseline tri- and di-acylglycerols [DG (18:0/16:0) (18.36; 11.79, 24.92)] were positively associated with fasting glucose and long-chain acylcarnitines [CAR 26:1 (-0.40; -0.54, -0.27)] were inversely associated with prevalent DM and HbA at follow-up.
A metabolomic signature in South Asians may help determine the unique aetiology of diabetes in this high-risk ethnic group. Future work will externally validate our findings and determine the effects of modifiable risk factors for DM.
南亚人患糖尿病(DM)的风险高于许多其他种族/族裔群体。循环代谢物是代谢过程的可测量产物,可能可以解释风险升高的病因。我们描述了与南亚人现患 DM 和血糖测量值相关的代谢物。
我们纳入了 MASALA 研究中的 717 名参与者,年龄在 40-84 岁之间。我们使用基线空腹血清进行代谢组学和人口统计学、行为学、血糖数据的检测,这些数据来自基线和 5 年后的数据。我们使用 LC-MS 进行非靶向代谢组学和脂质组学分析,并对已知信号进行靶向整合。个体线性和有序逻辑回归模型在调整年龄、性别、BMI、饮食、运动、酒精、吸烟和 DM 家族史后,通过弹性网络回归来识别与结果最相关的代谢物。
在 >98%的样本中可检测到 258 种具有可检测信号的代谢物。34 种代谢物与弹性网络模型中的现患 DM 相关。与 DM 相关的主要代谢物是神经鞘磷脂、脯氨酸(OR 15.86;95%CI 4.72,53.31)和甜菜碱(OR 0.03;0.004,0.14)。基线三酰基和二酰基甘油[DG(18:0/16:0)(18.36;11.79,24.92)]与空腹血糖呈正相关,长链酰基肉碱[CAR 26:1(-0.40;-0.54,-0.27)]与现患 DM 和随访时的 HbA 呈负相关。
南亚人的代谢组学特征可能有助于确定该高风险族裔群体中糖尿病的独特病因。未来的工作将对外验证我们的发现,并确定 DM 的可改变风险因素的影响。