Chronic obstructive pulmonary disease (COPD) and diffuse panbronchiolitis (
DPB) are both characterized by chronic airflow limitation. Although the aet
iology of these diseases is under investigation, it is commonly hypothesize
d that neutrophils a major role in the disease pathogenesis. The variation
of the genes related to chemotaxis of neutrophils may confer a risk for the
development of both COPD and DPB.
In the present report, the authors investigated the association between gen
etic variation that codes for the 416th and 420th amino acid of Ge-globulin
, reported to be associated with chemotaxis of neutrophils, and susceptibil
ity to COPD and DPB. Blood samples obtained front patients with COPD (n=63)
, DPB (n=82), and control subjects (n=82) were used for the genotyping assa
y.
The proportion of GC*1F homozygotes was significantly higher in the COPD pa
tients than the control subjects (COPD 36.5% versus control 20.7%), and the
odds ratio for GC*1F homozygotes was 2.2 (95% confidence interval 1.1-4.6)
for the COPD group. There was no difference on the distribution of the oth
er genotypes (GC*1F-1S heterozygotes, GC*1S homozygotes, GC*2-1F heterozygo
tes, GC*2-1S heterozygotes and GC*2 homozygotes) or the allele frequencies
among these groups.
These findings suggest that the GC*1F gene polymorphism of Gc-globulin may
be one of the risk factors for chronic obstructive pulmonary disease. Howev
er, no association between this polymorphism of Ge-globulin and susceptibil
ity to diffuse panbronchiolitis was found.