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Trimethylamine-N-oxide (TMAO) as Novel Potential Biomarker of Early Predictors of Metabolic Syndrome
被引:210
作者:
Barrea, Luigi
[1
]
Annunziata, Giuseppe
[2
]
Muscogiuri, Giovanna
[1
]
Di Somma, Carolina
[3
]
Laudisio, Daniela
[1
]
Maisto, Maria
[2
]
de Alteriis, Giulia
[1
]
Tenore, Gian Carlo
[2
]
Colao, Annamaria
[1
]
Savastano, Silvia
[1
]
机构:
[1] Univ Naples Federico II, Med Sch Naples, Unit Endocrinol, Dipartimento Med Clin & Chirurg, Via Sergio Pansini 5, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Pharm, Via Domenico Montesano 49, I-80131 Naples, Italy
[3] IRCCS, SDN, Napoli Via Gianturco 113, I-80143 Naples, Italy
来源:
关键词:
trimethylamine N-oxide (TMAO);
obesity;
visceral adiposity index (VAI);
fatty liver index (FLI);
metabolic syndrome (MetS);
CLINICAL SEVERITY;
PROGNOSTIC VALUE;
GUT MICROBIOTA;
PLASMA;
CHOLINE;
BETAINE;
PHOSPHATIDYLCHOLINE;
CONSUMPTION;
POPULATION;
NUTRITION;
D O I:
10.3390/nu10121971
中图分类号:
R15 [营养卫生、食品卫生];
TS201 [基础科学];
学科分类号:
100403 ;
摘要:
There is a mechanistic link between the gut-derived metabolite trimethylamine-N-oxide (TMAO) and obesity-related diseases, suggesting that the TMAO pathway may also be linked to the pathogenesis of obesity. The Visceral Adiposity Index (VAI), a gender-specific indicator of adipose dysfunction, and the Fatty Liver Index (FLI), a predictor of non-alcoholic fatty liver disease (NAFLD), are early predictors of metabolic syndrome (MetS). In this cross-sectional observational study, we investigated TMAO levels in adults stratified according to Body Mass Index (BMI) and the association of TMAO with VAI and FLI. One hundred and thirty-seven adult subjects (59 males; 21-56 years) were enrolled. TMAO levels were detected using HPLC/MS analysis. Homeostatic Model Assessment of Insulin Resistance (HoMA-IR), VAI and FLI were included as cardio-metabolic indices. TMAO levels increased along with BMI and were positively associated with VAI and FLI, independently, on common potential covariates. The most sensitive and specific cut-offs for circulating levels of TMAO to predict the presence of NAFLD-FLI and MetS were 8.02 mu M and 8.74 mu M, respectively. These findings allow us to hypothesize a role of TMAO as an early biomarker of adipose dysfunction and NAFLD-FLI in all borderline conditions in which overt MetS is not present, and suggest that a specific cut-off of TMAO might help in identifying subjects at high risk of NAFLD.
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页数:19
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