Pallister T, Jackson M A, Martin T C, Glastonbury C A, Jennings A, Beaumont M, Mohney R P, Small K S, MacGregor A, Steves C J, Cassidy A, Spector T D, Menni C, Valdes A M
Department of Twin Research and Genetic Epidemiology, Kings College London, London, UK.
Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, UK.
Int J Obes (Lond). 2017 Jul;41(7):1106-1113. doi: 10.1038/ijo.2017.70. Epub 2017 Mar 15.
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.
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 × 10), VFM (0.057 (0.019), P=2.73 × 10) 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).
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.
背景/目的:较高的内脏脂肪量(VFM)与发生心血管代谢疾病的风险增加相关。不健康的饮食模式可能影响内脏脂肪(VF)发育的机制尚未通过前沿的多组学方法进行研究。因此,我们的目标是研究饮食对VFM的影响,并确定将食物摄入与VFM联系起来的肠道微生物群和代谢物谱。
受试者/方法:在2218名有VFM数据的双胞胎中,我们在50%的样本中确定了与VFM最密切相关的食物摄入,然后在其余样本中构建并测试了“VFM饮食评分”。使用线性回归(对协变量进行调整,包括体重指数和总脂肪量),我们研究了VFM饮食评分、血液代谢组学谱和粪便微生物群(n = 889)之间的关联,并证实了这些与VFM的关联。我们在VFM不一致(相差⩾1个标准差)、年龄、性别和基线基因序列匹配的同卵(MZ)双胞胎中重复了主要发现。
四种代谢物与VFM饮食评分和VFM相关:马尿酸盐、α-羟基异戊酸盐、胆红素(Z,Z)和丁酰肉碱。我们在VFM不一致的MZ双胞胎中重复了VFM与饮食评分(β(标准误):0.281(0.091);P = 0.002)、丁酰肉碱(0.199(0.087);P = 0.023)和马尿酸盐(-0.297(0.095);P = 0.002)之间的关联。我们确定了单一物种多形真杆菌与VFM饮食评分(0.042(0.011),P = 8.47×10)、VFM(0.057(0.019),P = 2.73×10)和马尿酸盐(-0.075(0.032),P = 0.021)相关。此外,较高的血液马尿酸盐与脂肪组织中神经球蛋白表达升高相关,神经球蛋白在细胞氧稳态中起作用(0.016(0.004),P = 9.82×10)。
我们将饮食VFM评分和VFM与多形真杆菌和血液中的四种代谢物联系起来。特别是,源自膳食多酚微生物代谢的代谢物马尿酸盐与降低的VFM、微生物群以及脂肪组织中神经球蛋白表达增加之间的关系,为饮食对VFM的影响提供了潜在的机制性见解。