Science and Research

Cardiovascular risk in pulmonary alveolar proteinosis

We hypothesized that cardiovascular events and/or indices of cardiac dysfunction may be increased in pulmonary alveolar proteinosis (PAP). Systemic and pulmonary arterial hypertension, arrhythmias, pulmonary embolism, stroke and ischemic heart attack were reported. Patients underwent serum anti-GM-CSF antibodies, disease severity score (DSS), Doppler transthoracic echocardiograph, glucose, thyroid hormones, lipids, troponin and pro-Brain natriuretic peptide (BNP) examination. Thirteen patients (8 female) were studied, median age of 47. Pro-BNP inversely related to DLCO% and TLC%; troponin directly related to DSS, age, P(A-a)O2, left atrium-, left ventricle-end-diastole diameter and BMI. On multiple regression analysis DSS was the only parameter significantly and strongly related with troponin (R(2) = 0.776, p = 0.007). No cardiovascular event was reported during follow-up. In PAP cardiovascular risk indices relate to lung disease severity. Therefore, PAP patients could be at increased risk for cardiovascular events. Quantitation of its magnitude and potential links to lungs' physiologic derangement will be addressed in future studies.

  • Manali, E. D.
  • Papadaki, G.
  • Konstantonis, D.
  • Tsangaris, I.
  • Papaioannou, A. I.
  • Kolilekas, L.
  • Schams, A.
  • Kagouridis, K.
  • Karakatsani, A.
  • Orfanos, S.
  • Griese, M.
  • Papiris, S. A.

Keywords

  • Cardiovascular Diseases/*etiology
  • Echocardiography, Doppler
  • Female
  • Humans
  • Male
  • Middle Aged
  • Prospective Studies
  • Pulmonary Alveolar Proteinosis/*complications
  • Risk Assessment
  • Severity of Illness Index
  • Troponin/blood
  • Pulmonary alveolar proteinosis
  • autoimmune pulmonary alveolar proteinosis
  • cardiovascular events
  • disease severity
  • inhaled GM-CSF
  • pro-BNP
  • pulmonary arterial hypertension
  • serum lipids
  • troponin
Publication details
DOI: 10.1586/17476348.2016.1116389
Journal: Expert Rev Respir Med
Pages: 235-40 
Number: 2
Work Type: Original
Location: CPC-M
Disease Area: General Lung and Other
Partner / Member: KUM, LMU
Access-Number: 26558331
See publication on PubMed


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