4.7 Article

Plasma metabolomics identified novel metabolites associated with risk of type 2 diabetes in two prospective cohorts of Chinese adults

Journal

INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
Volume 45, Issue 5, Pages 1507-1516

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ije/dyw221

Keywords

Type 2 diabetes; targeted metabolomics; nested case-control study; Chinese population

Funding

  1. Natural National Scientific Foundation of China [81230069, 81390542, 81390543]
  2. National Key Basic Research and Development Program (973 project) [2011CB503806]
  3. 111 Project
  4. Program for Changjiang Scholars and Innovative Research Team in University
  5. Fundamental Research Funds for the Central Universities, HUST
  6. Priority Academic Program for the Development of Jiangsu Higher Education Institutions (Public Health and Preventive Medicine)
  7. Flagship Major Development of Jiangsu Higher Education Institutions

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Background: Metabolomics studies in Caucasians have identified a number of novel metabolites in association with the risk of type 2 diabetes (T2D). However, few prospective metabolomic studies are available in Chinese populations. In the present study, we sought to identify novel metabolites consistently associated with incident T2D in two independent cohorts of Chinese adults. Methods: We performed targeted metabolomics (52 metabolites) of fasting plasma samples by liquid chromatography-mass spectrometry in two prospective case-control studies nested within the Dongfeng-Tongji (DFTJ) cohort and Jiangsu Non-communicable Disease (JSNCD) cohort. After following for 4.61 +/- 0.15 and 7.57 +/- 1.13 years, respectively, 1039 and 520 eligible participants developed incident T2D in these two cohorts, and controls were 1: 1 matched with cases by age (+/- 5 years) and sex. Multivariate conditional logistic regression models were constructed to identify metabolites associated with future T2D risk in both cohorts. Results: We identified four metabolites consistently associated with an increased risk of developing T2D in the two cohorts, including alanine, phenylalanine, tyrosine and palmitoylcarnitine. In the meta-analysis of two cohorts, the odds ratios (95% confidence intervals, CIs) comparing extreme quartiles were 1.79 (1.32-2.42) for alanine, 1.91 (1.41-2.60) for phenylalanine, 1.85 (1.37-2.48) for tyrosine and 1.63 (1.21-2.20) for palmitoylcarnitine ( all P-trend <= 0.01). Conclusions: We confirmed the association of alanine, phenylalanine and tyrosine with future T2D risk and further identified palmitoylcarnitine as a novel metabolic marker of incident T2D in two prospective cohorts of Chinese adults. Our findings might provide new aetiological insight into the development of T2D.

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