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本文引用的文献

1
Interactions between chronic liver disease and inflammatory bowel disease.慢性肝病与炎症性肠病之间的相互作用。
Inflamm Bowel Dis. 1997 Winter;3(4):288-302.
2
European evidence-based Consensus on the diagnosis and management of ulcerative colitis: Definitions and diagnosis.欧洲溃疡性结肠炎诊断与管理循证共识:定义与诊断
J Crohns Colitis. 2008 Mar;2(1):1-23. doi: 10.1016/j.crohns.2007.11.001. Epub 2008 Jan 18.
3
Hepatopancreatobiliary manifestations and complications associated with inflammatory bowel disease.炎症性肠病相关的肝胆胰管表现和并发症。
Inflamm Bowel Dis. 2010 Sep;16(9):1598-619. doi: 10.1002/ibd.21219.
4
Changes in liver biochemistry during methotrexate use for inflammatory bowel disease.甲氨蝶呤治疗炎症性肠病过程中肝生化指标的变化。
Am J Gastroenterol. 2010 Jul;105(7):1620-6. doi: 10.1038/ajg.2010.21. Epub 2010 Feb 16.
5
Primary sclerosing cholangitis, autoimmune hepatitis and overlap syndromes in inflammatory bowel disease.炎症性肠病中的原发性硬化性胆管炎、自身免疫性肝炎及重叠综合征
World J Gastroenterol. 2008 Jan 21;14(3):331-7. doi: 10.3748/wjg.14.331.
6
Liver injury in inflammatory bowel disease: long-term follow-up study of 786 patients.炎症性肠病中的肝损伤:786例患者的长期随访研究
Inflamm Bowel Dis. 2007 Sep;13(9):1106-14. doi: 10.1002/ibd.20160.
7
Thiopurine-induced liver injury in patients with inflammatory bowel disease: a systematic review.硫唑嘌呤诱导的炎症性肠病患者肝损伤:一项系统评价。
Am J Gastroenterol. 2007 Jul;102(7):1518-27. doi: 10.1111/j.1572-0241.2007.01187.x. Epub 2007 Mar 27.
8
Abnormal hepatic biochemistries in patients with inflammatory bowel disease.炎症性肠病患者的肝脏生化指标异常。
Am J Gastroenterol. 2007 Feb;102(2):344-50. doi: 10.1111/j.1572-0241.2006.00947.x. Epub 2006 Nov 13.
9
Serious liver disease induced by infliximab.英夫利昔单抗诱发的严重肝脏疾病。
Clin Rheumatol. 2007 Apr;26(4):578-81. doi: 10.1007/s10067-005-0169-y. Epub 2006 Mar 18.
10
Extraintestinal manifestations in inflammatory bowel disease.炎症性肠病的肠外表现
World J Gastroenterol. 2005 Dec 14;11(46):7227-36. doi: 10.3748/wjg.v11.i46.7227.

炎症性肠病患者的肝功能检查异常:一项基于医院的调查。

Liver Function Test Abnormalities in Patients with Inflammatory Bowel Diseases: A Hospital-based Survey.

作者信息

Cappello Maria, Randazzo Claudia, Bravatà Ivana, Licata Anna, Peralta Sergio, Craxì Antonio, Almasio Piero Luigi

机构信息

Gastroenterology and Hepatology Section, Dipartimento Biomedico di Medicina Interna e Specialistica, Università di Palermo, Palermo, Italy.

出版信息

Clin Med Insights Gastroenterol. 2014 Jun 17;7:25-31. doi: 10.4137/CGast.S13125. eCollection 2014.

DOI:10.4137/CGast.S13125
PMID:24966712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4069044/
Abstract

BACKGROUND AND AIMS

Inflammatory bowel diseases (IBD) are frequently associated with altered liver function tests (LFTs). The causal relationship between abnormal LFTs and IBD is unclear. The aim of our study was to evaluate the prevalence and etiology of LFTs abnormalities and their association with clinical variables in a cohort of IBD patients followed up in a single center.

MATERIALS AND METHODS

A retrospective review was undertaken of all consecutive IBD in- and outpatients routinely followed up at a single referral center. Clinical and demographic parameters were recorded. Subjects were excluded if they had a previous diagnosis of chronic liver disease. LFT abnormality was defined as an increase in aspartate aminotransferase, (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), gamma-glutamyl transpeptidase (GGT), or total bilirubin.

RESULTS

A cohort of 335 patients (179 males, mean age 46.0 ± 15.6 years) was analyzed. Abnormal LFTs were detected in 70 patients (20.9%). In most cases, the alterations were mild and spontaneously returned to normal values in about 60% of patients. Patients with abnormal LFTs were less frequently on treatment with aminosalicylates (22.8 vs. 36.6%, P = 0.04). The most frequent cause for transient abnormal LFTs was drug-induced cholestasis (34.1%), whereas fatty liver was the most frequent cause of persistent liver damage (65.4%). A cholestatic pattern was found in 60.0% of patients and was mainly related to older age, longer duration of disease, and hypertension.

CONCLUSIONS

The prevalence of LFT abnormalities is relatively high in IBD patients, but the development of severe liver injury is exceptional. Moreover, most alterations of LFTs are mild and spontaneously return to normal values. Drug-induced hepatotoxicity and fatty liver are the most relevant causes of abnormal LFTs in patients with IBD.

摘要

背景与目的

炎症性肠病(IBD)常伴有肝功能检查(LFTs)异常。LFTs异常与IBD之间的因果关系尚不清楚。我们研究的目的是评估在单一中心随访的IBD患者队列中LFTs异常的患病率、病因及其与临床变量的关联。

材料与方法

对在单一转诊中心常规随访的所有连续IBD门诊和住院患者进行回顾性研究。记录临床和人口统计学参数。如果患者先前被诊断为慢性肝病,则将其排除。LFT异常定义为天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、γ-谷氨酰转肽酶(GGT)或总胆红素升高。

结果

分析了335例患者(179例男性,平均年龄46.0±15.6岁)的队列。70例患者(20.9%)检测到LFTs异常。在大多数情况下,这些改变是轻微的,约60%的患者会自发恢复到正常水平。LFTs异常的患者使用氨基水杨酸盐治疗的频率较低(22.8%对36.6%,P=0.04)。短暂性LFTs异常最常见的原因是药物性胆汁淤积(34.1%),而脂肪肝是持续性肝损伤最常见的原因(65.4%)。60.0%的患者出现胆汁淤积模式,主要与年龄较大、病程较长和高血压有关。

结论

IBD患者中LFT异常的患病率相对较高,但严重肝损伤的发生较为罕见。此外,大多数LFTs改变是轻微的,会自发恢复到正常水平。药物性肝毒性和脂肪肝是IBD患者LFTs异常的最相关原因。