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Prevalence of Cardiovascular Disease and Rate of Major Adverse Cardiovascular Events in Severe Alpha-1 Antitrypsin Deficiency COPD.
Ellis, Paul; Bailey, Emily; Choate, Radmila; Holm, Kristen E; Sandhaus, Robert A; Turner, Alice M; Newnham, Michael.
Afiliación
  • Ellis P; Institute of Applied Health Research, University of Birmingham, Birmingham, UK.
  • Bailey E; University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Choate R; University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Holm KE; University of Kentucky College of Public Health, Lexington, KY, USA.
  • Sandhaus RA; Division of Neurology and Behavioural Health, National Jewish Health, Denver, CO, USA.
  • Turner AM; AlphaNet, Kissimmee, FL, USA.
  • Newnham M; AlphaNet, Kissimmee, FL, USA.
Article en En | MEDLINE | ID: mdl-38249829
ABSTRACT

Aim:

Alpha-1 antitrypsin deficiency is an autosomal co-dominant condition that predisposes individuals to early-onset emphysema. As with COPD, AATD-COPD is associated with pulmonary exacerbations, which impacts on overall mortality and quality of life. Though there is evidence that COPD is associated with a higher prevalence of cardiovascular disease and major adverse cardiovascular events (MACE), it is unclear if this is true for patients with AATD-COPD.

Methods:

Prevalence of cardiovascular disease was determined in two separate severe AATD cohorts AlphaNet, USA and the Birmingham AATD registry, UK. All patients had preexisting lung disease. Cardiovascular disease was defined as presence of any of the following heart failure, ischaemic heart disease, atrial fibrillation, stroke, and myocardial infarction. A Cox proportional hazards model was used to assess the impact of prior cardiovascular disease and frequent exacerbator phenotype on risk of future MACE.

Results:

Out of 3493 patients with severe AATD, 14.7% had prior cardiovascular disease, including stroke (2.3%), myocardial infarction (2.2%), and heart failure (2.5%). Frequent exacerbators were more likely to have preexisting cardiovascular disease compared with those with one or no exacerbations in the preceding year (63% vs 44.8%, p = 0.001). There was increased risk of future MACE in frequent exacerbators (HR 1.85, 95% CI 1.24 to 2.75), former and current smokers (HR 1.80, 95% CI 1.07 to 3.02, p = 0.026, and HR 4.04, 95% CI 1.44 to 11.32, p = 0.008, respectively), and those with prior cardiovascular disease (HR 3.81, 95% CI 2.60 to 5.58, p < 0.001).

Conclusion:

In severe AATD-COPD, MACE are associated with an increased exacerbation frequency, previous cardiovascular disease, and a history of smoking.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Deficiencia de alfa 1-Antitripsina / Accidente Cerebrovascular / Enfermedad Pulmonar Obstructiva Crónica / Insuficiencia Cardíaca / Infarto del Miocardio Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Chron Obstruct Pulmon Dis Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Deficiencia de alfa 1-Antitripsina / Accidente Cerebrovascular / Enfermedad Pulmonar Obstructiva Crónica / Insuficiencia Cardíaca / Infarto del Miocardio Tipo de estudio: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Int J Chron Obstruct Pulmon Dis Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido