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α-1抗胰蛋白酶缺乏症患者的肺和肝移植

Lung and liver transplantation in patients with alpha-1 antitrypsin deficiency.

作者信息

Zamora Martin R, Ataya Ali

机构信息

Lung Transplant Program, Division of Pulmonary Sciences and Critical Care Medicine, University of Colorado, Aurora, CO, USA.

Division of Pulmonary, Critical Care and Sleep Medicine, University of Florida, Gainesville, FL, USA.

出版信息

Ther Adv Chronic Dis. 2021 Jul 29;12_suppl:20406223211002988. doi: 10.1177/20406223211002988. eCollection 2021.

Abstract

Alpha-1 antitrypsin (AAT) augmentation is effective in slowing the progression of emphysema due to AAT deficiency (AATD) but cannot prevent eventual progression to end-stage lung disease and complete respiratory failure, which is the leading cause of death for individuals with severe AATD. When patients develop end-stage lung disease, lung transplantation is the only treatment option available, and this can improve lung physiology and patient health status. The available data suggest that survival rates for lung transplantation are significantly higher for patients with AATD-related chronic obstructive pulmonary disease (COPD) compared with non-AATD-related COPD, but, conversely, there is a higher risk of common post-lung transplant complications in patients with AATD non-AATD COPD. Nevertheless, lung transplantation (single and bilateral) is favorable for patients with AATD. After respiratory failure, the second leading cause of death in patients with AATD is liver disease, for example, cirrhosis and hepatocellular carcinoma, caused by the accumulation of mutant forms of AAT retained within the liver. As with lung disease, the only treatment option for end-stage liver disease is liver transplantation. Survival rates for patients with AATD undergoing liver transplantation are also favorable, and patients, particularly pediatric patients, have benefitted from advancements in peri-/post-surgical care. As the majority of AAT is produced by the liver, the AAT phenotype of the recipient becomes that of the donor, meaning that AAT serum levels should be normalized (if the donor is AAT-replete), halting further lung and liver disease progression. However, post-liver transplant respiratory function may continue to decline in line with normal age-related lung function decline. In the most severe cases, where patients have simultaneous end-stage lung and liver disease, combined lung and liver transplantation is a treatment option with favorable outcomes. However, there is very little information available on this procedure in patients with AATD.

摘要

α-1抗胰蛋白酶(AAT)替代疗法对于减缓因AAT缺乏症(AATD)导致的肺气肿进展有效,但无法阻止最终发展为终末期肺病和完全呼吸衰竭,而这是重度AATD患者的主要死因。当患者发展为终末期肺病时,肺移植是唯一可用的治疗选择,这可以改善肺生理功能和患者健康状况。现有数据表明,与非AATD相关的慢性阻塞性肺疾病(COPD)相比,AATD相关COPD患者的肺移植存活率显著更高,但相反,AATD患者发生肺移植常见并发症的风险高于非AATD COPD患者。尽管如此,肺移植(单肺和双肺)对AATD患者是有利的。在呼吸衰竭之后,AATD患者的第二大死因是肝脏疾病,例如由肝脏内蓄积的突变形式AAT引起的肝硬化和肝细胞癌。与肺病一样,终末期肝病的唯一治疗选择是肝移植。接受肝移植的AATD患者的存活率也很可观,患者,尤其是儿科患者,已从围手术期/术后护理的进展中受益。由于大多数AAT由肝脏产生,受者的AAT表型变为供者的表型,这意味着AAT血清水平应恢复正常(如果供者AAT充足),从而阻止肺和肝脏疾病的进一步进展。然而,肝移植后的呼吸功能可能会随着与年龄相关的正常肺功能下降而继续下降。在最严重的情况下,患者同时患有终末期肺病和肝病,联合肺和肝移植是一种有良好疗效的治疗选择。然而,关于AATD患者进行此手术的信息非常少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/528c/8367211/fbf899568dfe/10.1177_20406223211002988-fig1.jpg

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