» Articles » PMID: 25003824

The Natural History of Lung Function After Lung Transplantation for α(1)-antitrypsin Deficiency

Overview
Specialty Critical Care
Date 2014 Jul 9
PMID 25003824
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Rationale: Lung transplantation (LT) is an established treatment for end-stage lung diseases, including chronic obstructive pulmonary disease (COPD) associated with α1-antitrypsin deficiency (AATD).

Objectives: We sought to compare the post-transplantation course of patients with AATD and AAT-replete COPD.

Methods: Between June 1991 and January 2008, a total of 231 patients with AAT-replete COPD and 45 with AATD underwent LT at Cleveland Clinic. Data reviewed included baseline recipient, donor, and surgical data; all spirometry evaluations; acute cellular rejection (ACR) events; and survival data. Endpoints included temporal change in FEV1, severity of ACR, and survival. A longitudinal temporal decomposition model was used for analysis.

Measurements And Main Results: Comparison of overall rates of FEV1 decline in AATD and AAT-replete patients with COPD showed no significant differences (P > 0.09). However, although the single LT patients had similar trends in FEV1 in both groups, patients with AATD with double LT declined faster (P < 0.002) than the AAT-replete patients. No differences in the frequency or severity of ACR episodes were observed (P = 0.32). Furthermore, there was no difference in early or late mortality between patients with AATD and patients with AAT-replete COPD (P > 0.09).

Conclusions: Although overall the post-LT FEV1 slope, severity of ACR, and survival among patients with AATD is similar to that of AAT-replete patients with COPD, patients with AATD with double LT have a faster rate of FEV1 decline. These findings support the eligibility of patients with AATD for LT, and suggest the need for additional studies to better understand the difference between single and double LT in AATD.

Citing Articles

Recommendations for the diagnosis and treatment of alpha-1 antitrypsin deficiency.

Feitosa P, Castellano M, Costa C, Cardoso A, Pereira L, Fernandes F J Bras Pneumol. 2024; 50(5):e20240235.

PMID: 39661838 PMC: 11601085. DOI: 10.36416/1806-3756/e20240235.


Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint.

Miravitlles M, Anzueto A, Barrecheguren M Eur Respir Rev. 2023; 32(170).

PMID: 38056890 PMC: 10698548. DOI: 10.1183/16000617.0170-2023.


Graft dysfunction and rejection of lung transplant, a review on diagnosis and management.

Sun H, Deng M, Chen W, Liu M, Dai H, Wang C Clin Respir J. 2022; 16(1):5-12.

PMID: 35080130 PMC: 9060084. DOI: 10.1111/crj.13471.


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

Zamora M, Ataya A Ther Adv Chronic Dis. 2021; 12_suppl:20406223211002988.

PMID: 34408830 PMC: 8367211. DOI: 10.1177/20406223211002988.


[Predictors for the Bronchiolitis Obliterans Syndrome in Lung Transplant Patient].

Yang S, Abuduwufuer A, Lv W, Bao F, Hu J Zhongguo Fei Ai Za Zhi. 2020; 23(6):496-502.

PMID: 32517455 PMC: 7309540. DOI: 10.3779/j.issn.1009-3419.2020.101.03.