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IJE Advance Access originally published online on March 22, 2006
International Journal of Epidemiology 2006 35(4):1001-1008; doi:10.1093/ije/dyl049
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Published by Oxford University Press on behalf of the International Epidemiological Association

Respiratory Disease

Plasma fibrinogen and lung function: the CARDIA Study

Bharat Thyagarajan1, David R Jacobs1,2,*, George G Apostol1, Lewis J Smith3, Cora E Lewis4 and O Dale Williams4

1 Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis, MN, USA.
2 Department of Nutrition, University of Oslo, Oslo, Norway.
3 Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
4 Division of Preventive Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

* Corresponding author. Division of Epidemiology, School of Public Health, University of Minnesota, 1300 South 2nd Street, Suite 300, Minneapolis, MN 55454, USA. E-mail: Jacobs{at}epi.umn.edu.

Background We hypothesized that fibrinogen, as a marker of chronic inflammation, is inversely associated with forced vital capacity (FVC) and forced expiratory volume in 1 s (FEV1) in healthy persons.

Methods The CARDIA cohort started in 1985 and included black and white men and women, aged 18–30, from the general population. Spirometry testing conducted at years 5 and 10 [FVC, FEV1, and their ratio (FEV1/FVC)] was studied relative to plasma fibrinogen levels measured at year 5 (cross-sectional n = 4040) and at year 7 (longitudinal n = 3001), controlling for race, sex, age, height, smoking, asthma, body mass index, physical activity, birth control pill use, and alcohol intake.

Results In cross-sectional analyses, FVC at year 5 was lower by 166 ml (95% confidence interval 116–216 ml) in the highest vs lowest year 5 fibrinogen quartile. At year 10, holding year 5 FVC and change in fibrinogen (year 7–year 5) constant, the difference in FVC between the highest and the lowest year 5 fibrinogen quartiles widened by 67 ml (95% CI 31–103 ml). The corresponding differences for FEV1 were 166 ml (95% CI 146–253 ml) at year 5 and 45 ml (95% CI 11–80 ml) widening by year 10. The FEV1/FVC ratio was unrelated to plasma fibrinogen.

Conclusion These findings are consistent with the hypothesis that fibrinogen, possibly as a marker for chronic low-grade inflammation, is associated with modest deterioration of lung function in healthy young adults.


Keywords Fibrinogen, FEV1, FVC, FEV1/FVC ratio, lung function, inflammation, smoking, asthma, BMI

Accepted 2 March 2006


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