Metabolite profiles of diabetes incidence and intervention response in the Diabetes Prevention Program

Publication Description
Identifying novel biomarkers of type 2 diabetes risk may improve prediction and prevention among individuals at high risk of the disease and elucidate new biological pathways relevant to diabetes development. We performed plasma metabolite profiling in the Diabetes Prevention Program (DPP), a completed trial that randomized high-risk individuals to lifestyle, metformin, or placebo interventions. Previously reported markers, branched chain and aromatic amino acids and glutamine/glutamate, were associated with incident diabetes (P<0.05 for all), but these associations were attenuated upon adjustment for clinical and biochemical measures. By contrast, baseline levels of betaine (also known as glycine betaine, HR 0.84 per SD log metabolite level, P=0.02) and three other metabolites were associated with incident diabetes even after adjustment. Moreover, betaine was increased by the lifestyle intervention, which was the most effective approach to preventing diabetes, and increases in betaine at 2 years were also associated with lower diabetes incidence (P=0.01). Our findings indicate betaine is a marker of diabetes risk among high-risk individuals both at baseline and during preventive interventions, and complement animal models demonstrating a direct role for betaine in modulating metabolic health.

Primary Author
Walford,G. A.
Ma,Y.
Clish,C.
Florez,J. C.
Wang,T. J.
Gerszten,R. E.
Diabetes Prevention Program Research Group

Author Address
Center for Human Genetic Research; Massachusetts General Hospital; Boston, MA, 02114; USA Diabetes Clinical and Research Center (Diabetes Unit); Department of Medicine; Massachusetts General Hospital; Boston, MA, 02114, USA Harvard Medical Schoo(TRUNCATED)

Volume
Epub ahead of print

Publisher
by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered

Author Address
Center for Human Genetic Research; Massachusetts General Hospital; Boston, MA, 02114; USA Diabetes Clinical and Research Center (Diabetes Unit); Department of Medicine; Massachusetts General Hospital; Boston, MA, 02114, USA Harvard Medical Schoo(TRUNCATED)

PMID
26861782

PMCID
PMC4839205



Reference Type
Journal Article

Periodical Full
Diabetes

Publication Year
2016

Publication Date
9-Feb

ISSN/ISBN
1939-327X

Document Object Index
b151063 [pii]

Accession Number
PMID: 26861782