Abstract

Many studies suggest that trimethylamine-N-oxide (TMAO), a gut-flora-dependent metabolite of choline, contributes to the risk of cardiovascular diseases, but little is known for non-alcoholic fatty liver disease (NAFLD). We examined the association of circulating TMAO, choline and betaine with the presence and severity of NAFLD in Chinese adults. We performed a hospital-based case-control study (CCS) and a cross-sectional study (CSS). In the CCS, we recruited 60 biopsy-proven NAFLD cases and 35 controls (18–60 years) and determined serum concentrations of TMAO, choline and betaine by HPLC-MS/MS. For the CSS, 1,628 community-based adults (40-75 years) completed the blood tests and ultrasonographic NAFLD evaluation. In the CCS, analyses of covariance showed adverse associations of ln-transformed serum levels of TMAO, choline and betaine/choline ratio with the scores of steatosis and total NAFLD activity (NAS) (all P-trend <0.05). The CSS revealed that a greater severity of NAFLD was independently correlated with higher TMAO but lower betaine and betaine/choline ratio (all P-trend <0.05). No significant choline-NAFLD association was observed. Our findings showed adverse associations between the circulating TMAO level and the presence and severity of NAFLD in hospital- and community-based Chinese adults, and a favorable betaine-NAFLD relationship in the community-based participants.

Highlights

  • Many studies suggest that trimethylamine-N-oxide (TMAO), a gut-flora-dependent metabolite of choline, contributes to the risk of cardiovascular diseases, but little is known for non-alcoholic fatty liver disease (NAFLD)

  • The ln-transformed levels of TMAO were positively associated with the corresponding values of choline (pearson correlation coefficient (r) = 0.487, 0.203) and betaine (r = 0.294, 0.159) in the case-control study (CCS) and cross-sectional study (CSS)

  • Our findings suggest that TMAO, an intestinal microbiota-dependent metabolite of phosphatidylcholine (PC)/choline, may be an independent risk marker for Non-alcoholic fatty liver disease (NAFLD)

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Summary

Introduction

Many studies suggest that trimethylamine-N-oxide (TMAO), a gut-flora-dependent metabolite of choline, contributes to the risk of cardiovascular diseases, but little is known for non-alcoholic fatty liver disease (NAFLD). Several human studies have shown that an elevated level of TMAO may increase the risk of cardiovascular disease (CVD) and exacerbate the effects of high choline and betaine levels on the risk of MACEs in a large-scale clinical cohort[14,18]. These studies have suggested that high circulating TMAO, a gut-flora-dependent choline metabolite, may increase the risk of cardiometabolic disease. To our knowledge, no study has examined the association between TMAO and NAFLD in humans to date, and few studies have determined the relationship between blood betaine and NAFLD in humans either

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