Pulmonary Function Decline in Alpha-1 Antitrypsin Deficiency: A Systematic Review and Meta-Analysis

Background: Limited data exist on pulmonary function decline in patients with alpha-1 antitrypsin deficiency (AATD)-associated lung and/or liver disease. This study aimed to conduct a systematic literature review (SLR) and meta-analysis of pulmonary function decline and associated risk factors, clinical outcomes, and health-related quality of life (HRQoL) in patients with AATD-associated lung and/or liver disease. Methods: Following PRISMA guidelines, studies were identified from MEDLINE/Embase (2003– 2023) using Population, Intervention, Comparison, Outcomes, and Study criteria; key congresses were hand-searched (2021– 2023). For each publication, two independent reviewers determined eligibility for inclusion and quality was assessed using relevant JBI tools. Meta-analyses were conducted on select outcomes that were deemed appropriate. Results: Overall, 77 publications were included in the SLR and 32 reported pulmonary function decline in patients with AATD-associated lung and/or liver disease. Eight publications that evaluated forced expiratory volume in 1 second (FEV1) in mL, five that evaluated FEV1% predicted and four that evaluated HRQoL (as measured by St. George’s Respiratory Questionnaire [SGRQ]) were deemed eligible for meta-analysis. In patients with AATD-associated lung disease, based on the random effects model, annualized change (95% confidence interval) in FEV1 was – 39.1 (– 45.2, – 32.9) mL/year and – 1.1 (– 1.2, – 0.9) %/year, and there was a slight worsening in SGRQ score (1.3 [0.6, 1.9] points/year). Data in patients with AATD-associated liver disease with or without comorbid lung disease were too limited to calculate an annualized rate of decline in pulmonary function or SGRQ. Conclusion: This comprehensive SLR and meta-analysis provides an estimate for annual pulmonary function decline in patients with AATD-associated lung disease and highlights an evidence gap in patients with AATD-associated liver disease with or without comorbid lung disease. Further insights into risk factors or potential biomarkers of pulmonary function decline may support clinical strategies for optimizing treatment. Keywords: alpha-1 antitrypsin deficiency, chronic obstructive pulmonary disease, emphysema, meta-analysis, respiratory function test, quality of life

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Journal
International Journal of COPD
Published
2026-01-01
DOI
https://doi.org/10.2147/copd.s552227
Primary Topic
Protease and Inhibitor Mechanisms
Type
article
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article

Pulmonary Function Decline in Alpha-1 Antitrypsin Deficiency: A Systematic Review and Meta-Analysis

Lisi Wang, Anne E. Wyman, May Hagiwara, Suna Park et al.
International Journal of COPD
Protease and Inhibitor Mechanisms
article

Pulmonary Function Decline in Alpha-1 Antitrypsin Deficiency: A Systematic Review and Meta-Analysis

Lisi Wang, Anne E. Wyman, May Hagiwara, Suna Park, Ed G. Marins, Priscilla Geraldine Wittkopf, Mariana Farraia, Caroline von Wilamowitz-Moellendorff, Alice Turner, Kyle Fahrbach
article en

Abstract

Background: Limited data exist on pulmonary function decline in patients with alpha-1 antitrypsin deficiency (AATD)-associated lung and/or liver disease. This study aimed to conduct a systematic literature review (SLR) and meta-analysis of pulmonary function decline and associated risk factors, clinical outcomes, and health-related quality of life (HRQoL) in patients with AATD-associated lung and/or liver disease. Methods: Following PRISMA guidelines, studies were identified from MEDLINE/Embase (2003– 2023) using Population, Intervention, Comparison, Outcomes, and Study criteria; key congresses were hand-searched (2021– 2023). For each publication, two independent reviewers determined eligibility for inclusion and quality was assessed using relevant JBI tools. Meta-analyses were conducted on select outcomes that were deemed appropriate. Results: Overall, 77 publications were included in the SLR and 32 reported pulmonary function decline in patients with AATD-associated lung and/or liver disease. Eight publications that evaluated forced expiratory volume in 1 second (FEV1) in mL, five that evaluated FEV1% predicted and four that evaluated HRQoL (as measured by St. George’s Respiratory Questionnaire [SGRQ]) were deemed eligible for meta-analysis. In patients with AATD-associated lung disease, based on the random effects model, annualized change (95% confidence interval) in FEV1 was – 39.1 (– 45.2, – 32.9) mL/year and – 1.1 (– 1.2, – 0.9) %/year, and there was a slight worsening in SGRQ score (1.3 [0.6, 1.9] points/year). Data in patients with AATD-associated liver disease with or without comorbid lung disease were too limited to calculate an annualized rate of decline in pulmonary function or SGRQ. Conclusion: This comprehensive SLR and meta-analysis provides an estimate for annual pulmonary function decline in patients with AATD-associated lung disease and highlights an evidence gap in patients with AATD-associated liver disease with or without comorbid lung disease. Further insights into risk factors or potential biomarkers of pulmonary function decline may support clinical strategies for optimizing treatment. Keywords: alpha-1 antitrypsin deficiency, chronic obstructive pulmonary disease, emphysema, meta-analysis, respiratory function test, quality of life

International Journal of COPDVol. Volume 21
Ithaka Harbors (US), Birmingham City University (GB), Institut de Biologie systémique et synthétique (FR), Evides (Netherlands) (NL), Takeda (United States) (US), University of Birmingham (GB)
Reduced inequalities
Openalex Percentile: Top 93%
Protease and Inhibitor Mechanisms
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