Profound Perturbation of the Metabolome in Obesity Is Associated with Health Risk

被引:245
作者
Cirulli, Elizabeth T. [1 ]
Guo, Lining [2 ]
Swisher, Christine Leon [1 ]
Shah, Naisha [1 ]
Huang, Lei [1 ]
Napier, Lori A. [1 ]
Kirkness, Ewen F. [1 ]
Spector, Tim D. [3 ]
Caskey, C. Thomas [4 ]
Thorens, Bernard [5 ]
Venter, J. Craig [6 ]
Telenti, Amalio [7 ]
机构
[1] Human Longev Inc, San Diego, CA 92121 USA
[2] Metabolon Inc, Durham, NC USA
[3] Kings Coll London, Dept Twin Res & Genet Epidemiol, London, England
[4] Baylor Coll Med, Mol & Human Genet, Houston, TX 77030 USA
[5] Univ Lausanne, Ctr Integrat Genom, Lausanne, Switzerland
[6] J Craig Venter Inst, La Jolla, CA 92037 USA
[7] Scripps Res Inst, La Jolla, CA 92037 USA
基金
英国惠康基金;
关键词
BODY-MASS INDEX; METABOLICALLY HEALTHY; ANALYSIS REVEALS; CORTISOL; GLUCOSE; RESISTANCE; PROFILE; MEN;
D O I
10.1016/j.cmet.2018.09.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Obesity is a heterogeneous phenotype that is crudely measured by body mass index (BMI). There is a need for a more precise yet portable method of phenotyping and categorizing risk in large numbers of people with obesity to advance clinical care and drug development. Here, we used non-targeted metabolomics and whole-genome sequencing to identify metabolic and genetic signatures of obesity. We find that obesity results in profound perturbation of the metabolome; nearly a third of the assayed metabolites associated with changes in BMI. A metabolome signature identifies the healthy obese and lean individuals with abnormal metabolomes-these groups differ in health outcomes and underlying genetic risk. Specifically, an abnormal metabolome associated with a 2- to 5-fold increase in cardiovascular events when comparing individuals who were matched for BMI but had opposing metabolome signatures. Because metabolome profiling identifies clinically meaningful heterogeneity in obesity, this approach could help select patients for clinical trials.
引用
收藏
页码:488 / +
页数:15
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