Association of clinical features with HLA in chronic pulmonary thromboembolism

Eur Respir J. 2005 Jan;25(1):131-8. doi: 10.1183/09031936.04.00042304.

Abstract

The aetiology of chronic thromboembolic pulmonary hypertension (CTEPH) is largely unknown and may be heterogeneous, because there are several ethnic differences in the clinical characteristics of CTEPH. Female predominance and a higher ratio of chronic to acute pulmonary thromboembolism have been reported in Japan as compared with the USA. Because such ethnic differences may be controlled by genetic factors, the current study investigated HLA polymorphisms in Japanese patients with CTEPH. HLA typing by serological and/or DNA typing methods was performed (for HLA-A, B, DPB1, DRB1) in 80 patients and 678 controls, and the association of clinical characteristics with HLA alleles was studied. The frequencies of HLA-B*5201 (40 versus 24%) and DPB1*0202 (19 versus 6%) were significantly higher in the patients. HLA-B*5201 positive patients showed a significant female predominance. Total pulmonary vascular resistance and mixed venous oxygen tension were better in the HLA-B*5201 positive patients. In contrast, cardiac index and gas exchange parameters were worse in the HLA-DPB1*0202 positive patients. In the patients carrying HLA-B*5201 and/or -DPB1*0202, the frequency of deep vein thrombosis was significantly lower than the other patients. These observations suggested that both the susceptibility and clinical characteristics of chronic thromboembolic pulmonary hypertension were controlled in part by the HLA-B and -DPB1 loci.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Distribution
  • Aged
  • Alleles
  • Case-Control Studies
  • Chronic Disease
  • Female
  • Genetic Predisposition to Disease*
  • HLA Antigens / genetics*
  • Humans
  • Hypertension, Pulmonary / epidemiology
  • Hypertension, Pulmonary / genetics*
  • Incidence
  • Japan / epidemiology
  • Male
  • Middle Aged
  • Odds Ratio
  • Polymorphism, Genetic*
  • Probability
  • Pulmonary Embolism / epidemiology
  • Pulmonary Embolism / genetics*
  • Risk Assessment
  • Severity of Illness Index
  • Sex Distribution

Substances

  • HLA Antigens