4.5 Article

Untangling the relationship between diet and visceral fat mass through blood metabolomics and gut microbiome profiling

期刊

INTERNATIONAL JOURNAL OF OBESITY
卷 41, 期 7, 页码 1106-1113

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NATURE PUBLISHING GROUP
DOI: 10.1038/ijo.2017.70

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资金

  1. FP7 project HEALS (Health and Environment-wide Associations based on Large population Surveys) of the European Union's Seventh Framework Programme [603946]
  2. Wellcome Trust European Community's Seventh Framework Programme
  3. National Institute for Health Research (NIHR) Clinical Research Facility at Guy's and St Thomas' NHS Foundation Trust and NIHR Biomedical Research Centre based at Guy's and St Thomas' NHS Foundation Trust and King's College London
  4. MRC [MR/L01999X/1] Funding Source: UKRI

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BACKGROUND/OBJECTIVES: Higher visceral fat mass (VFM) is associated with an increased risk for developing cardio-metabolic diseases. The mechanisms by which an unhealthy diet pattern may influence visceral fat (VF) development has yet to be examined through cutting-edge multi-omic methods. Therefore, our objective was to examine the dietary influences on VFM and identify gut microbiome and metabolite profiles that link food intakes to VFM. SUBJECTS/METHODS: In 2218 twins with VFM, food intake and metabolomics data available we identified food intakes most strongly associated with VFM in 50% of the sample, then constructed and tested the 'VFM diet score' in the remainder of the sample. Using linear regression (adjusted for covariates, including body mass index and total fat mass), we investigated associations between the VFM diet score, the blood metabolomics profile and the fecal microbiome (n = 889), and confirmed these associations with VFM. We replicated top findings in monozygotic (MZ) twins discordant (>= 1 s.d. apart) for VFM, matched for age, sex and the baseline genetic sequence. RESULTS: Four metabolites were associated with the VFM diet score and VFM: hippurate, alpha-hydroxyisovalerate, bilirubin (Z,Z) and butyrylcarnitine. We replicated associations between VFM and the diet score (beta (s.e.): 0.281 (0.091); P = 0.002), butyrylcarnitine (0.199 (0.087); P = 0.023) and hippurate (-0.297 (0.095); P = 0.002) in VFM-discordant MZ twins. We identified a single species, Eubacterium dolichum to be associated with the VFM diet score (0.042 (0.011), P = 8.47 x 10(-5)), VFM (0.057 (0.019), P = 2.73 x 10(-3)) and hippurate (-0.075 (0.032), P = 0.021). Moreover, higher blood hippurate was associated with elevated adipose tissue expression neuroglobin, with roles in cellular oxygen homeostasis (0.016 (0.004), P = 9.82x10(-6)). CONCLUSIONS: We linked a dietary VFM score and VFM to E. dolichum and four metabolites in the blood. In particular, the relationship between hippurate, a metabolite derived from microbial metabolism of dietary polyphenols, and reduced VFM, the microbiome and increased adipose tissue expression of neuroglobin provides potential mechanistic insight into the influence of diet on VFM.

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