Department of Pathology, University of Washington School of Medicine, Seattle, WA.
Department of Laboratory Medicine, University of Washington School of Medicine, Seattle, WA.
Liver Transpl. 2020 Jan;26(1):17-24. doi: 10.1002/lt.25652. Epub 2019 Nov 25.
Cirrhotic explanted livers occasionally have unexpected periodic acid-Schiff-diastase (PASD)-positive globules within the hepatocyte cytoplasm. It is often unclear whether this finding is a nonspecific consequence of cirrhosis or is indicative of an underlying alpha-1-antitrypsin deficiency (A1ATD) contributing to the cirrhosis. In this study, explanted livers were retrospectively evaluated for histopathology (including PASD status with confirmatory alpha-1-antitrypsin [A1AT] immunohistochemistry [IHC]), and chart review provided etiology of liver failure and general clinical parameters. Real-time polymerase chain reaction was used to detect A1AT genotype (SERPINA1 S and Z alleles) by melting curve analysis on liver explant tissue from selected cases. Of 196 explanted livers, 21 (11%) had PASD+ globules, which were significantly enriched in patients with a clinical diagnosis of nonalcoholic steatohepatitis (NASH; 47%) compared with other causes (P < 0.001). IHC confirmed all PASD+ globules were A1AT+, with 20 of 21 cases demonstrating diffuse A1AT staining. In an expanded NASH cohort, 42% (14/33) of explants had PASD+ globules, 92% of which were homozygous (n = 1) or heterozygous (n = 11) for the SERPINA1 Z allele, corresponding to nearly 40% of all NASH patients. Overall, the Z allele was present in 10% of all tested liver explants, with 85% of PASD+ cases genotyping homozygous (n = 2) or heterozygous (n = 20), which is far in excess of the estimated 2% in the general population. These results indicate PASD+ A1AT globules (with confirmatory genotyping showing at least 1 Z allele) are commonly observed in NASH, suggesting a synergistic relationship toward liver fibrosis. In addition, the high frequency of SERPINA1 Z alleles in liver transplantation patients supports the utility of pretransplant genotyping.
肝硬化患者的被移植肝脏偶尔会在肝细胞细胞质中出现意外的过碘酸-Schiff-二淀粉酶(PASD)阳性小球。通常不清楚这种发现是肝硬化的非特异性后果,还是表明潜在的α-1-抗胰蛋白酶缺乏症(A1ATD)导致了肝硬化。在这项研究中,回顾性评估了被移植肝脏的组织病理学(包括 PASD 状态和确认的α-1-抗胰蛋白酶[A1AT]免疫组织化学[IHC]),并通过图表审查提供了肝衰竭的病因和一般临床参数。使用实时聚合酶链反应通过对选定病例的肝组织进行融解曲线分析来检测 A1AT 基因型(SERPINA1 S 和 Z 等位基因)。在 196 例被移植的肝脏中,有 21 例(11%)有 PASD+小球,在有非酒精性脂肪性肝炎(NASH;47%)临床诊断的患者中明显富集,与其他原因相比(P <0.001)。IHC 确认所有 PASD+小球均为 A1AT+,21 例中有 20 例显示弥漫性 A1AT 染色。在扩大的 NASH 队列中,有 42%(14/33)的肝组织有 PASD+小球,其中 92%(n=1)或杂合子(n=11)为 SERPINA1 Z 等位基因,几乎占所有 NASH 患者的 40%。总体而言,Z 等位基因存在于 10%的所有测试肝组织中,其中 PASD+病例的 85%(n=2)或杂合子(n=20)的基因型为纯合子,远远超过一般人群中估计的 2%。这些结果表明,PASD+A1AT 小球(通过确认的基因分型显示至少 1 个 Z 等位基因)在 NASH 中很常见,这表明它们与肝纤维化有协同关系。此外,肝移植患者中 SERPINA1 Z 等位基因的高频率支持移植前基因分型的实用性。