4.7 Article

Plasma concentration of trimethylamine-N-oxide and risk of gestational diabetes mellitus

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 108, Issue 3, Pages 603-610

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ajcn/nqy116

Keywords

trimethylamine-N-oxide; gestational diabetes mellitus; nested case-control study; nutrition; metabolite

Funding

  1. Integrated Innovative Team for Major Human Diseases Program of Tongji Medical College, HUST, Sanming Project of Medicine in Shenzhen [SZSM201511007]
  2. National Program on Basic Research Project of China [2013FY114200]
  3. NIH [R21 HD091458]
  4. University of Iowa Fraternal Order of Eagles Diabetes Research Center
  5. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [R21HD091458] Funding Source: NIH RePORTER

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Background: The microbiota-dependent metabolite trimethylamine-N-oxide (TMAO) has been reported as a novel and independent risk factor for the development of cardiovascular and metabolic diseases, but the association with gestational diabetes mellitus (GDM) remains unclear. Objective: The aim of this study was to investigate the association between plasma TMAO concentration and GDM in a 2-phase study. Design: A 2-phase design was used in the current study. An initial phase included 866 participants (433 GDM cases and 433 matched controls) with fasting blood samples collected at the time of GDM screening (24-32 wk of gestation). An independent-phase study, with 276 GDM cases and 552 matched controls who provided fasting blood samples before 20 wk of gestation and who had GDM screened during 24-32 wk of gestation, was nested within a prospective cohort study. These 2 studies were both conducted in Wuhan, China, and the incidence of GDM in the cohort study was 10.8%. Plasma TMAO concentrations were determined by stable isotope dilution liquid chromatography-tandem mass spectrometry. GDM was diagnosed according to the American Diabetes Association criteria by using an oral-glucose-tolerance test. Results: In the initial case-control study, the adjusted OR of GDM comparing the highest TMAO quartile with the lowest quartile was 1.94 (95% CI: 1.28, 2.93). Each SD increment of ln-transformed plasma TMAO was associated with 22% (95% CI: 5%, 41%) higher odds of GDM. In the nested case-control study, women in the highest quartile also had increased odds of GDM (adjusted OR: 2.06; 95% CI: 1.28, 3.31) compared with women in the lowest quartile, and the adjusted OR for GDM per SD increment of ln-transformed plasma TMAO was 1.26 (95% CI: 1.08, 1.47). Conclusions: Consistent findings from this 2-phase study indicate a positive association between plasma TMAO concentrations and GDM. Future studies are warranted to elucidate the underlying mechanisms.

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