Disparities in α 1 -Antitrypsin Deficiency Testing and Treatment in US Adults - Summary - MDSpire
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Differences in α1-Antitrypsin Deficiency Testing and Treatment Among US Adults

  • By

  • Arianne K. Baldomero

  • Lisa Smith

  • Amy Gravely

  • Vickram Tejwani

  • Chris H. Wendt

  • October 15, 2026

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Objective:

To assess how often adults receiving Veterans Affairs care for COPD and/or asthma were tested for α1-antitrypsin deficiency (AATD), and to examine factors associated with testing and augmentation therapy.

Approach:
  • Design and population: Retrospective cohort study using national VA electronic health records. The cohort included patients with at least two documented encounters for COPD, asthma, asthma-COPD overlap, or spirometry-confirmed airflow obstruction from January 2000 through December 2…
  • Measures: AATD testing was defined as at least one serum α1-antitrypsin measurement and/or genotype test. AATD was classified by serum concentration below 100 mg/dL, ZZ, SZ, or SS genotype, or an augmentation therapy prescription.
  • Analyses: The study evaluated testing frequency and sociodemographic and geographic factors associated with testing; among patients classified as having AATD, it assessed augmentation therapy prescriptions and associated characteristics.
Interpretation:

The supplied context describes the study rationale, design, population, and outcome definitions but does not provide study results.

Limitations:
  • The supplied article context ends before the results and does not report testing rates, treatment rates, or associations.
  • AATD classification included serum AAT below 100 mg/dL even without a qualifying genotype, so the study definition was broader than severe deficiency.
Sources:

Original Source(s)

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