Demographic and clinical characteristics of patients with α1-antitrypsin deficiency genotypes PI*ZZ and PI*SZ in the Spanish registry of EARCO

Author:

Torres-Durán María,López-Campos José LuisORCID,Rodríguez-Hermosa Juan Luis,Esquinas Cristina,Martínez-González CristinaORCID,Hernández-Pérez José MaríaORCID,Rodríguez Carlota,Bustamante AnaORCID,Casas-Maldonado Francisco,Barrecheguren Miriam,González CruzORCID,Miravitlles MarcORCID

Abstract

BackgroundThe Spanish registry of α1-antitrypsin deficiency (AATD) integrated in the European Alpha-1 Research Collaboration (EARCO) provides information about the characteristics of patients, in particular those with the PI*SZ genotype, which is frequent in Spain.MethodIndividuals with severe AATD defined as proteinase inhibitor (PI) genotypes PI*ZZ, PI*SZ and other rare deficient variants were included from February 1, 2020, to February 1, 2022. The analysis focused on a comparison of the characteristics of PI*ZZ and PI*SZ patients.Results409 patients were included (53.8% men) with a mean±sd age of 53.5±15.9 years. Genotypes were PI*ZZ in 181 (44.7%), PI*SZ in 163 (40.2%), PI*SS in 29 (7.2%) and other in 32 (7.9%). 271 (67.4%) had lung disease: 175 chronic obstructive pulmonary disease (43.5%), 163 emphysema (40.5%) and 83 bronchiectasis (20.6%). Patients with the PI*SZ genotype were younger, more frequently non-index cases and had a lower frequency of respiratory diseases except asthma compared with PI*ZZ patients. Among patients with respiratory diseases, PI*SZ individuals were significantly older both at onset of symptoms and at diagnosis; only asthma was more frequent in PI*SZ than in PI*ZZ individuals. Twelve PI*SZ patients (15.4%) received augmentation therapy compared with 94 PI*ZZ patients (66.2%; p<0.001).ConclusionsThere is a high prevalence of PI*SZ in Spain. Patients with the PI*SZ genotype were older at symptom onset and diagnosis and had less severe lung disease compared with PI*ZZ patients. The prevalence of asthma was higher in PI*SZ, and up to 15% of PI*SZ patients received augmentation therapy.

Funder

Grifols

Publisher

European Respiratory Society (ERS)

Subject

Pulmonary and Respiratory Medicine

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1. Nine controversial questions about augmentation therapy for alpha-1 antitrypsin deficiency: a viewpoint;European Respiratory Review;2023-12-06

2. Respuesta;Medicina Clínica;2023-12

3. Reply;Medicina Clínica (English Edition);2023-12

4. Alpha1-antitrypsin deficiency: An updated review;La Presse Médicale;2023-09

5. Recommendations for the Implementation of the Self-Administration of Alpha-1 Antitrypsin;International Journal of Chronic Obstructive Pulmonary Disease;2023-08

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