TY - JOUR
T1 - Metabolic effects of betaine
T2 - A randomized clinical trial of betaine supplementation in prediabetes
AU - Grizales, Ana Maria
AU - Patti, Mary Elizabeth
AU - Lin, Alexander P.
AU - Beckman, Joshua A.
AU - Sahni, V. Anik
AU - Cloutier, Emilie
AU - Fowler, Kristen M.
AU - Dreyfuss, Jonathan M.
AU - Pan, Hui
AU - Kozuka, Chisayo
AU - Lee, Adrienne
AU - Basu, Rita
AU - Pober, David M.
AU - Gerszten, Robert E.
AU - Goldfine, Allison B.
N1 - Funding Information:
Sunstar Foundation Postdoctoral Fellowship; The Harvard Catalyst, The Harvard Clinical and Translational Science Center (National Center for Research Resources and the National Center for Advancing Translational Sciences, NIH Award UL1 TR001102); and financial contributions from Harvard University and its affiliated academic health care centers. We also acknowledge support of the Joslin Clinical Research Center.
Funding Information:
Financial Support: This work was supported by American Diabetes Association Grant 7-13-CE-17 (Bedside to Bench and Back: Cardiometabolic Effects of Betaine Supplementation, to A.B.G.); American Diabetes Association Mentor-Based Minority Postdoctoral Fellowship (Grant 1-15-MI-05 to A.B.G.); National Institutes of Health (NIH; Grants P30 DK036836 and R01 DK 029953 to R.B. and R01DK1081572, DK108159, and DK08157209 to R.E.G.);
Publisher Copyright:
© 2018 Endocrine Society.
PY - 2018
Y1 - 2018
N2 - Context: Plasma betaine correlates with insulin sensitivity in humans. Betaine supplementation improves metabolic effects in mice fed a high-fat diet. Objective: To assess metabolic effects of oral betaine in obese participants with prediabetes. Design: A 12-week, parallel arm, randomized, double-masked, placebo-controlled trial. Setting: University-affiliated hospital. Participants and Interventions: Persons with obesity and prediabetes (N = 27) were randomly assigned to receive betaine 3300 mg orally twice daily for 10 days, then 4950 mg twice daily for 12 weeks, or placebo. Main Outcome Measures: Changes from baseline in insulin sensitivity, glycemia, hepatic fat, and endothelial function. Results: There was a 16.5-fold increase in plasma dimethylglycine [dimethylglycine (DMG); P , 0.0001] levels, but modest 1.3- and 1.5-fold increases in downstream serine and methionine levels, respectively, in the betaine vs placebo arm. Betaine tended to reduce fasting glucose levels (P = 0.08 vs placebo) but had no other effect on glycemia. Insulin area under curve after oral glucose was reduced for betaine treatment compared with placebo (P = 0.038). Insulin sensitivity, assessed by euglycemic hyperinsulinemic clamp, was not improved. Serum total cholesterol levels increased after betaine treatment compared with placebo (P = 0.032). There were no differences in change in intrahepatic triglyceride or endothelial function between groups. Conclusion: DMG accumulation supports DMG dehydrogenase as rate limiting for betaine metabolism in persons with prediabetes. Betaine had little metabolic effect. Additional studies may elucidate mechanisms contributing to differences between preclinical and human responses to betaine, and whether supplementation of metabolites downstream of DMG improves metabolism.
AB - Context: Plasma betaine correlates with insulin sensitivity in humans. Betaine supplementation improves metabolic effects in mice fed a high-fat diet. Objective: To assess metabolic effects of oral betaine in obese participants with prediabetes. Design: A 12-week, parallel arm, randomized, double-masked, placebo-controlled trial. Setting: University-affiliated hospital. Participants and Interventions: Persons with obesity and prediabetes (N = 27) were randomly assigned to receive betaine 3300 mg orally twice daily for 10 days, then 4950 mg twice daily for 12 weeks, or placebo. Main Outcome Measures: Changes from baseline in insulin sensitivity, glycemia, hepatic fat, and endothelial function. Results: There was a 16.5-fold increase in plasma dimethylglycine [dimethylglycine (DMG); P , 0.0001] levels, but modest 1.3- and 1.5-fold increases in downstream serine and methionine levels, respectively, in the betaine vs placebo arm. Betaine tended to reduce fasting glucose levels (P = 0.08 vs placebo) but had no other effect on glycemia. Insulin area under curve after oral glucose was reduced for betaine treatment compared with placebo (P = 0.038). Insulin sensitivity, assessed by euglycemic hyperinsulinemic clamp, was not improved. Serum total cholesterol levels increased after betaine treatment compared with placebo (P = 0.032). There were no differences in change in intrahepatic triglyceride or endothelial function between groups. Conclusion: DMG accumulation supports DMG dehydrogenase as rate limiting for betaine metabolism in persons with prediabetes. Betaine had little metabolic effect. Additional studies may elucidate mechanisms contributing to differences between preclinical and human responses to betaine, and whether supplementation of metabolites downstream of DMG improves metabolism.
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U2 - 10.1210/jc.2018-00507
DO - 10.1210/jc.2018-00507
M3 - Article
C2 - 29860335
AN - SCOPUS:85055258193
SN - 0021-972X
VL - 103
SP - 3038
EP - 3049
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 8
ER -