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本文引用的文献

1
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis.一项全基因组关联研究证实了 PNPLA3 基因,并确定了 TM6SF2 和 MBOAT7 基因是与酒精性肝硬化相关的风险基因。
Nat Genet. 2015 Dec;47(12):1443-8. doi: 10.1038/ng.3417. Epub 2015 Oct 19.
2
Altered Bile Acid Metabolome in Patients with Nonalcoholic Steatohepatitis.非酒精性脂肪性肝炎患者胆汁酸代谢组的改变
Dig Dis Sci. 2015 Nov;60(11):3318-28. doi: 10.1007/s10620-015-3776-8. Epub 2015 Jul 3.
3
Moderate alcohol consumption diminishes the development of non-alcoholic fatty liver disease (NAFLD) in ob/ob mice.适度饮酒可减少ob/ob小鼠非酒精性脂肪性肝病(NAFLD)的发生。
Eur J Nutr. 2016 Apr;55(3):1153-64. doi: 10.1007/s00394-015-0929-7. Epub 2015 May 24.
4
Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease.跨膜 6 超家族成员 2 基因突变可将非酒精性脂肪性肝炎与心血管疾病区分开。
Hepatology. 2015 Feb;61(2):506-14. doi: 10.1002/hep.27490.
5
TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease.TM6SF2基因的rs58542926位点影响非酒精性脂肪性肝病患者肝纤维化的进展。
Nat Commun. 2014 Jun 30;5:4309. doi: 10.1038/ncomms5309.
6
Modest alcohol consumption and carotid plaques or carotid artery stenosis in men with non-alcoholic fatty liver disease.非酒精性脂肪性肝病男性适度饮酒与颈动脉斑块或颈动脉狭窄
Atherosclerosis. 2014 Jun;234(2):270-5. doi: 10.1016/j.atherosclerosis.2014.03.001. Epub 2014 Mar 21.
7
Colonic inflammation and secondary bile acids in alcoholic cirrhosis.酒精性肝硬化中的结肠炎症和次级胆汁酸。
Am J Physiol Gastrointest Liver Physiol. 2014 Jun 1;306(11):G929-37. doi: 10.1152/ajpgi.00315.2013. Epub 2014 Apr 3.
8
Association of adiponectin with hepatic steatosis: a study of 1,349 subjects in a random population sample.脂联素与肝脂肪变性的关联:一项针对1349名随机人群样本受试者的研究。
BMC Res Notes. 2014 Apr 3;7:207. doi: 10.1186/1756-0500-7-207.
9
Carriage of the PNPLA3 rs738409 C >G polymorphism confers an increased risk of non-alcoholic fatty liver disease associated hepatocellular carcinoma.载脂蛋白基因 PNPLA3 rs738409C>G 多态性增加非酒精性脂肪性肝病相关肝细胞癌的风险。
J Hepatol. 2014 Jul;61(1):75-81. doi: 10.1016/j.jhep.2014.02.030. Epub 2014 Mar 6.
10
Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease.外显子组关联研究鉴定出一个 TM6SF2 变异,该变异赋予非酒精性脂肪性肝病易感性。
Nat Genet. 2014 Apr;46(4):352-6. doi: 10.1038/ng.2901. Epub 2014 Feb 16.

非酒精性脂肪性肝病中适度饮酒是好是坏?一项批判性综述。

Is moderate alcohol use in nonalcoholic fatty liver disease good or bad? A critical review.

作者信息

Ajmera Veeral H, Terrault Norah A, Harrison Stephen A

机构信息

Division of Gastroenterology, Department of Medicine, University of California, San Francisco, San Francisco, CA.

Division of Gastroenterology, Department of Medicine, San Antonio Military Medical Center, Fort Sam Houston, TX.

出版信息

Hepatology. 2017 Jun;65(6):2090-2099. doi: 10.1002/hep.29055. Epub 2017 Apr 28.

DOI:10.1002/hep.29055
PMID:28100008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5444963/
Abstract

Moderate alcohol consumption in patients with nonalcoholic fatty liver disease (NAFLD) is common, yet the effects on cardiovascular and liver health are unclear. Moderate alcohol use is associated with improved insulin sensitivity and decreased cardiovascular mortality in the general population, but whether similar benefits would be observed in persons with NAFLD remains largely unstudied. There is significant overlap in the pathogenesis of alcoholic liver disease (ALD) and NAFLD, although studies of ALD have focused on pathological alcohol intake and few mechanistic studies of moderate alcohol use in NAFLD exist. We undertook a critical review of the effect of moderate alcohol use on cardiovascular and liver disease in patients with NAFLD. A total of seven observational studies met the criteria for inclusion (one for cardiovascular endpoints and six for liver endpoints). Insufficient studies have assessed the association of moderate alcohol use with cardiovascular outcomes. There was a positive association between moderate alcohol use and decreased NASH and fibrosis; however, heavy episodic drinking may accelerate fibrosis progression and moderate alcohol use may increase the risk of hepatocellular carcinoma in patients with advanced fibrosis. Significant methodological limitations were present, including incomplete adjustment for confounding factors and failure to measure lifetime use or the pattern of alcohol intake. Thus, a strong recommendation of benefit of moderate alcohol use in NAFLD cannot be made. There remains a need for additional high-quality longitudinal studies that evaluate both cardiovascular and liver outcomes among NAFLD patients with moderate or lesser degrees of alcohol use. (Hepatology 2017;65:2090-2099).

摘要

非酒精性脂肪性肝病(NAFLD)患者中适度饮酒很常见,但其对心血管和肝脏健康的影响尚不清楚。在一般人群中,适度饮酒与胰岛素敏感性改善和心血管死亡率降低有关,但NAFLD患者是否也有类似益处仍大多未被研究。酒精性肝病(ALD)和NAFLD的发病机制有显著重叠,尽管ALD的研究主要集中在病理性饮酒量,而关于NAFLD患者适度饮酒的机制研究很少。我们对NAFLD患者适度饮酒对心血管和肝脏疾病的影响进行了批判性综述。共有7项观察性研究符合纳入标准(1项针对心血管终点,6项针对肝脏终点)。评估适度饮酒与心血管结局之间关联的研究不足。适度饮酒与非酒精性脂肪性肝炎(NASH)和纤维化程度降低呈正相关;然而,大量暴饮可能会加速纤维化进展,而适度饮酒可能会增加晚期纤维化患者患肝细胞癌的风险。研究存在显著的方法学局限性,包括对混杂因素的不完全调整以及未测量终生饮酒量或饮酒模式。因此,不能强烈推荐NAFLD患者适度饮酒有益。仍需要更多高质量的纵向研究来评估饮酒适度或较少的NAFLD患者的心血管和肝脏结局。(《肝脏病学》2017年;65:2090 - 2099)