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(Circulation. 2002;106:2555.)
© 2002 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Departments of Community Medicine (G.E., B.H., L.J.), Internal Medicine (P.L., L.S.), Vascular Diseases (F.L.), and Clinical Physiology (P.W.), Malmö University Hospital, Malmö, Sweden.
Correspondence to Gunnar Engström, Department of Community Medicine, Malmö University Hospital, S-20502 Malmö, Sweden. E-mail Gunnar.Engstrom{at}smi.mas.lu.se
Background The inverse relationship between pulmonary function and incidence of cardiovascular disease remains largely unexplained. This prospective study explored the hypothesis of a relationship with inflammation-sensitive plasma proteins.
Methods and Results Forced vital capacity (FVC) and plasma levels of fibrinogen,
1-antitrypsin, haptoglobin, ceruloplasmin, and orosomucoid were determined in 5064 healthy men aged 28 to 61 years. All-cause mortality, cardiovascular mortality, and incidence of myocardial infarction were monitored over a mean follow-up period of 18.4 years. Low FVC (fourth quartile) was associated with higher protein levels and with increased incidences of myocardial infarction and cardiovascular death. Adjustments for protein levels reduced the age-adjusted relative risks (RRs) for myocardial infarction (from 1.99, 95% CI 1.5 to 2.6, to 1.70, 95% CI 1.3 to 2.2) and cardiovascular death (from 2.71, 95% CI 1.9 to 3.9, to 2.28, 95% CI 1.6 to 3.3) among men with low FVC, corresponding to
25% of the excess risk. The risk factoradjusted RRs were reduced from 1.45 (95% CI 1.1 to 1.9) to 1.38 (95% CI 1.1 to 1.8) and from 1.96 (95% CI 1.4 to 2.8) to 1.85 (95% CI 1.3 to 2.7) for myocardial infarction and cardiovascular death, respectively, corresponding to
10% to 15% of the excess risk. Among men with low FVC, the risk factoradjusted RR for myocardial infarction was 2.5 (95% CI 1.7 to 3.6) for those with high protein levels (
2 proteins in top quartile) and 1.7 (95% CI 1.1 to 2.4) for those with low protein levels (
1 protein in top quartile; reference, top quartile of FVC and low protein levels).
Conclusions FVC is significantly and inversely associated with plasma levels of inflammation-sensitive plasma proteins. This relationship contributes to but cannot fully explain the increased cardiovascular risk among men with low FVC.
Key Words: forced vital capacity epidemiology inflammation
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