TY - JOUR
T1 - Coffee consumption and nonalcoholic fatty liver onset
T2 - A prospective study in the general population
AU - Zelber-Sagi, Shira
AU - Salomone, Federico
AU - Webb, Muriel
AU - Lotan, Roni
AU - Yeshua, Hanny
AU - Halpern, Zamir
AU - Santo, Erwin
AU - Oren, Ran
AU - Shibolet, Oren
N1 - Publisher Copyright:
© 2015 Elsevier Inc. All rights reserved.
PY - 2015/3/1
Y1 - 2015/3/1
N2 - Retrospective studies suggest that coffee consumption may exert beneficial effects in patients with nonalcoholic fatty liver; however, prospective data supporting a protective role on liver steatosis development are lacking. In this study, we aimed to evaluate the association between coffee consumption and fatty liver onset in the general population. The analysis was performed both in a cross-sectional cohort (n = 347) and, prospectively, in a subcohort of patients without fatty liver at baseline and followed-up for 7 years (n = 147). Fatty liver was diagnosed with abdominal ultrasound and liver steatosis was quantified noninvasively by hepatorenal index (HRI) and SteatoTest, whereas FibroTest was used to assess fibrosis degree. A structured questionnaire on coffee consumption was administrated during a face-to-face interview. Neither the incidence nor the prevalence of fatty liver according to ultrasonography, SteatoTest, and the HRI was associated with coffee consumption. In the cross-sectional study, high coffee consumption was associated with a lower proportion of clinically significant fibrosis ≥F2 (8.8% vs 16.3%; P = 0.038); consistently, in multivariate logistic regression analysis, high coffee consumption was associated with lower odds for significant fibrosis (odds ratio = 0.49, 95% confidence interval, 0.25-0.97; P = 0.041) and was the strongest predictor for significant fibrosis. No association was demonstrated between coffee consumption and the new onset of nonalcoholic fatty liver, but coffee intake may exert beneficial effects on fibrosis progression.
AB - Retrospective studies suggest that coffee consumption may exert beneficial effects in patients with nonalcoholic fatty liver; however, prospective data supporting a protective role on liver steatosis development are lacking. In this study, we aimed to evaluate the association between coffee consumption and fatty liver onset in the general population. The analysis was performed both in a cross-sectional cohort (n = 347) and, prospectively, in a subcohort of patients without fatty liver at baseline and followed-up for 7 years (n = 147). Fatty liver was diagnosed with abdominal ultrasound and liver steatosis was quantified noninvasively by hepatorenal index (HRI) and SteatoTest, whereas FibroTest was used to assess fibrosis degree. A structured questionnaire on coffee consumption was administrated during a face-to-face interview. Neither the incidence nor the prevalence of fatty liver according to ultrasonography, SteatoTest, and the HRI was associated with coffee consumption. In the cross-sectional study, high coffee consumption was associated with a lower proportion of clinically significant fibrosis ≥F2 (8.8% vs 16.3%; P = 0.038); consistently, in multivariate logistic regression analysis, high coffee consumption was associated with lower odds for significant fibrosis (odds ratio = 0.49, 95% confidence interval, 0.25-0.97; P = 0.041) and was the strongest predictor for significant fibrosis. No association was demonstrated between coffee consumption and the new onset of nonalcoholic fatty liver, but coffee intake may exert beneficial effects on fibrosis progression.
KW - ALT
KW - Abbreviations
KW - BMI
KW - FFQ
KW - HOMA
KW - HRI
KW - NAFLD
KW - NASH
KW - US
KW - alanine aminotransferase
KW - body mass index
KW - food-frequency questionnaire
KW - hepatorenal index
KW - homeostasis model assessment
KW - nonalcoholic fatty liver disease
KW - nonalcoholic steatohepatitis
KW - ultrasonography
UR - http://www.scopus.com/inward/record.url?scp=84924500492&partnerID=8YFLogxK
U2 - 10.1016/j.trsl.2014.10.008
DO - 10.1016/j.trsl.2014.10.008
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C2 - 25468486
AN - SCOPUS:84924500492
SN - 1931-5244
VL - 165
SP - 428
EP - 436
JO - Translational Research
JF - Translational Research
IS - 3
M1 - 843
ER -