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乳糜泻相关肝损伤:对相关病症及潜在发病机制的见解

Celiac disease-related hepatic injury: Insights into associated conditions and underlying pathomechanisms.

作者信息

Marciano Francesca, Savoia Marcella, Vajro Pietro

机构信息

Department of Molecular Medicine and Medical Biotechnology, University of Naples "Federico II", Naples, Italy.

Department of Medicine and Surgery, Pediatrics Section, University of Salerno, Baronissi, Italy; ELFID, University of Naples "Federico II", Naples, Italy.

出版信息

Dig Liver Dis. 2016 Feb;48(2):112-9. doi: 10.1016/j.dld.2015.11.013. Epub 2015 Nov 24.

Abstract

BACKGROUND

Celiac disease (CD) is the most common autoimmune enteropathy. Clinical manifestations may range from a typical malabsorption syndrome to several apparently unrelated extra-intestinal symptoms.

AIM

Here we specifically focus on the spectrum of CD-related liver disorders and the underlying pathomechanisms.

METHODS

A computer-based search up to August 2015 was completed using appropriate keywords. References from selected papers were also reviewed and used if relevant.

RESULTS

An unexplained hypertransaminasemia with nonspecific histologic hepatic changes is the most common hepatic presentation. CD however can coexist with a number of liver disorders such as Autoimmune Hepatitis, Autoimmune Cholangitis, Primary Biliary Cirrhosis and Primary Sclerosing Cholangitis requiring a specific treatment in addition to gluten-free diet. CD has also been associated with Viral Hepatitis, Fatty Liver, Non-Alcoholic Steatohepatitis and some severe cryptogenic hepatopaties in the liver transplantation list. Pathomechanisms underlying hepatic injury in CD are multiple, appear still not completely defined and may probably co-occur.

CONCLUSIONS

An ever-increasing number of CD-related liver injuries exist, probably representing a continuum of a same disorder where genetic predisposition, timing, and duration of previous gluten exposure might influence the reversibility of liver damage. Evidences, although not conclusive, support therefore testing for CD also in cryptogenic hepatobiliary conditions where the relationship with CD has not yet been fully investigated.

摘要

背景

乳糜泻(CD)是最常见的自身免疫性肠病。其临床表现范围从典型的吸收不良综合征到一些明显不相关的肠外症状。

目的

在此我们特别关注CD相关肝脏疾病的范围及其潜在病理机制。

方法

使用适当的关键词完成了截至2015年8月的基于计算机的检索。还对所选论文的参考文献进行了审查,并在相关时加以使用。

结果

无法解释的高转氨酶血症伴非特异性肝脏组织学改变是最常见的肝脏表现。然而,CD可与多种肝脏疾病共存,如自身免疫性肝炎、自身免疫性胆管炎、原发性胆汁性肝硬化和原发性硬化性胆管炎,除无麸质饮食外还需要特定治疗。CD还与病毒性肝炎、脂肪肝、非酒精性脂肪性肝炎以及肝移植名单中的一些严重原因不明的肝病有关。CD肝损伤的潜在病理机制是多方面的,似乎仍未完全明确,可能会同时发生。

结论

存在越来越多与CD相关的肝损伤,可能代表同一疾病的连续谱,其中遗传易感性、先前麸质暴露的时间和持续时间可能会影响肝损伤的可逆性。因此,尽管证据不确凿,但支持在与CD的关系尚未充分研究的原因不明的肝胆疾病中也进行CD检测。

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