AI Article Synopsis

  • This study investigates exacerbations in patients with alpha-1 antitrypsin deficiency (AATD) lung disease using data from the Portuguese EARCO registry.
  • Out of 137 enrolled patients, 123 were analyzed, revealing that 22% experienced exacerbations, with those having the Pi*ZZ phenotype being three times more likely to have exacerbations compared to others.
  • The study found that factors such as the BODE index, BODEx, and DLCO were significant predictors of exacerbations, highlighting their importance in managing AATD-related lung disease.

Article Abstract

Introduction: Exacerbations are common in individuals with alpha-1 antitrypsin deficiency (AATD)-related lung disease. This study intended to identify independent predictive factors for exacerbations in AATD using the Portuguese European Alpha-1 Research Collaboration (EARCO) registry.

Methods: This study includes patients from the Portuguese EARCO registry, a prospective multicenter cohort (NCT04180319). From October 2020 to April 2023, this registry enrolled 137 patients, 14 of whom were excluded for analysis for either missing 12 months of follow-up or baseline pulmonary function.

Results: Among the 123 AATD patients, 27 (22.0%) had at least one exacerbation in the last 12 months of follow-up. Patients with Pi*ZZ phenotype were three times more likely than the rest of the population to experience any exacerbation (32.7 vs. 14.1%, p = 0.014; OR 3.0). BODE index was significantly higher in exacerbators than in non-exacerbators (3.9 ± 2.4 vs. 1.3 ± 1.2; p < 0.001), including on multivariate analysis (p = 0.002). Similar results were found for BODEx (multivariate p < 0.001). DLCO was the only functional parameter independently associated with exacerbations (p = 0.024).

Conclusions: DLCO, BODE, and BODEx were independent predictors of exacerbations at 12 months in AATD patients. Understanding these risk factors can aid decision-making on AATD-related lung disease management and improve patient outcomes.

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http://dx.doi.org/10.1159/000537759DOI Listing

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