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年龄影响天冬氨酸-丙氨酸转氨酶比值预测非酒精性脂肪性肝病进展期肝纤维化的能力。

Age impacts ability of aspartate-alanine aminotransferase ratio to predict advanced fibrosis in nonalcoholic Fatty liver disease.

作者信息

Goh George Boon-Bee, Pagadala Mangesh R, Dasarathy Jaividhya, Unalp-Arida Aynur, Pai Rish K, Yerian Lisa, Khiyami Amer, Sourianarayanane Achuthan, Sargent Ruth, Hawkins Carol, Dasarathy Srinivasan, McCullough Arthur J

机构信息

Department of Gastroenterology, Cleveland Clinic Foundation, 9500 Euclid Avenue/A30, Cleveland, OH, 44195, USA,

出版信息

Dig Dis Sci. 2015 Jun;60(6):1825-31. doi: 10.1007/s10620-015-3529-8. Epub 2015 Feb 24.

Abstract

BACKGROUND AND AIM

While histological differences have been reported between pediatric and adult nonalcoholic fatty liver disease (NAFLD), potential age-related changes in serum transaminases and liver histology remain largely unexplored. Our study sought to investigate the clinical and histological characteristics of NAFLD across age.

METHODS

This was a prospective cross-sectional study of 502 biopsy-proven NAFLD patients. Clinical data were evaluated and compared among different age groups; group A (ages 18-44), B (ages 45-64), and C (≥ ages 65).

RESULTS

34.9, 56.0, and 9.1 % of the cohort were distributed among group A, B, and C, respectively. While the prevalence of nonalcoholic steatohepatitis (NASH) was comparable across age groups, the prevalence of advanced fibrosis increased with age (p = 0.000). Although the mean ALT progressively decreased with age; 87, 64, 56 U/L in group A, B, and C, respectively (p = 0.000), there was no difference in mean AST (p = 0.939) across age. The AST:ALT ratio (AAR) progressively increased from 0.7, 0.9, and 1.1 in group A, B, and C, respectively (p = 0.000). In group C, an AAR ≥ 1 was found in 74 and 40 % of patients with and without advanced fibrosis.

CONCLUSION

With advancing age, ALT levels progressively declined while AST levels remained stable, leading to a higher AAR. Although higher AAR is often used as a surrogate measure of advanced fibrosis, advancing age can also contribute to increased AAR. In fact, an AAR ≥ 1 was found in significant number of elderly patients without advanced fibrosis. Consequently, an increased AAR may be a function of decreasing ALT with age in addition to progressive fibrosis.

摘要

背景与目的

虽然已有报道称儿童和成人非酒精性脂肪性肝病(NAFLD)存在组织学差异,但血清转氨酶和肝脏组织学中潜在的年龄相关变化在很大程度上仍未得到探索。我们的研究旨在调查不同年龄段NAFLD的临床和组织学特征。

方法

这是一项对502例经活检证实的NAFLD患者进行的前瞻性横断面研究。对不同年龄组(A组:18 - 44岁;B组:45 - 64岁;C组:≥65岁)的临床数据进行评估和比较。

结果

该队列中分别有34.9%、56.0%和9.1%分布在A组、B组和C组。虽然非酒精性脂肪性肝炎(NASH)的患病率在各年龄组中相当,但晚期纤维化的患病率随年龄增加而升高(p = 0.000)。尽管平均谷丙转氨酶(ALT)随年龄逐渐降低,A组、B组和C组分别为87、64、56 U/L(p = 0.000),但各年龄组的平均谷草转氨酶(AST)无差异(p = 0.939)。AST与ALT比值(AAR)分别从A组的0.7、B组的0.9和C组的1.1逐渐升高(p = 0.000)。在C组中,有和没有晚期纤维化的患者中分别有74%和40%的AAR≥1。

结论

随着年龄增长,ALT水平逐渐下降而AST水平保持稳定,导致AAR升高。虽然较高的AAR常被用作晚期纤维化的替代指标,但年龄增长也会导致AAR升高。事实上,在大量无晚期纤维化的老年患者中发现AAR≥1。因此,AAR升高可能是年龄导致ALT降低以及进行性纤维化共同作用的结果。

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