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肝功能检查结果无法诊断 α(1)-抗胰蛋白酶缺乏症成人的肝病。

Liver test results do not identify liver disease in adults with α(1)-antitrypsin deficiency.

机构信息

Division of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Florida, Gainesville, Florida 32610-0214, USA.

出版信息

Clin Gastroenterol Hepatol. 2012 Nov;10(11):1278-83. doi: 10.1016/j.cgh.2012.07.007. Epub 2012 Jul 24.

Abstract

BACKGROUND & AIMS: Liver disease is a significant cause of death among adults with α(1)-antitrypsin (A-AT) deficiency. Age and male sex are reported risk factors for liver disease. In the absence of adequate risk stratification, current recommendations are to intermittently test A-AT-deficient adults for liver function. We evaluated this recommendation in a large group of adults with A-AT deficiency to determine the prevalence of increased levels of alanine aminotransferase (ALT) and identify risk factors for liver disease.

METHODS

We used the Alpha-1 Foundation DNA and Tissue Bank to identify a cross section of A-AT-deficient adults (n = 647) with and without liver disease; individuals without A-AT deficiency were used as controls (n = 152). Results from ALT tests were compared between groups.

RESULTS

The prevalence of liver disease among individuals with A-AT deficiency was 7.9%; an increased level of ALT was observed in 7.8% of A-AT-deficient individuals, which did not differ significantly from controls. Mean levels of ALT fell within normal range for all groups. An increased level of ALT identified patients with liver disease with 11.9% sensitivity. The level of only γ-glutamyl transpeptidase was significantly higher in the A-AT-deficient group than in controls (43 vs 30 IU/mL; P < .003). A childhood history of liver disease and male sex were risk factors for adult liver disease in the multivariate analysis.

CONCLUSIONS

An increased level of ALT does not identify adults with A-AT deficiency who have liver disease. Male sex and liver disease during childhood might help identify those at risk.

摘要

背景与目的

肝脏疾病是导致 α(1)-抗胰蛋白酶(A-AT)缺乏症成年人死亡的重要原因。年龄和男性是报告的肝脏疾病危险因素。在缺乏充分风险分层的情况下,目前的建议是间歇性地对 A-AT 缺乏症成年人进行肝功能检测。我们在一大组 A-AT 缺乏症成年人中评估了这一建议,以确定丙氨酸氨基转移酶(ALT)升高的患病率,并确定肝脏疾病的危险因素。

方法

我们使用 Alpha-1 基金会 DNA 和组织库来鉴定有和没有肝脏疾病的 A-AT 缺乏症成年人的横断面(n = 647);无 A-AT 缺乏症的个体作为对照(n = 152)。比较各组之间 ALT 检测结果。

结果

A-AT 缺乏症个体的肝脏疾病患病率为 7.9%;7.8%的 A-AT 缺乏症个体的 ALT 水平升高,与对照组无显著差异。所有组的 ALT 均值均在正常范围内。ALT 水平升高可识别出 11.9%的肝脏疾病患者。A-AT 缺乏症组的 γ-谷氨酰转肽酶水平仅显著高于对照组(43 比 30 IU/mL;P <.003)。在多变量分析中,儿童期肝脏疾病史和男性是成年期肝脏疾病的危险因素。

结论

ALT 水平升高不能识别出患有肝脏疾病的 A-AT 缺乏症成年人。男性和儿童期肝脏疾病可能有助于识别高危人群。

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