4.6 Article

Inflammatory markers and longitudinal lung function decline in the elderly

Journal

AMERICAN JOURNAL OF EPIDEMIOLOGY
Volume 168, Issue 6, Pages 602-610

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/aje/kwn174

Keywords

aged; biological markers; C-reactive protein; fibrinogen; forced expiratory volume; inflammation; spirometry; vital capacity

Funding

  1. National Heart, Lung, and Blood Institute, Bethesda, Maryland [N01-HC-35129, N01-HC-45133, N01-HC-75150, N01-HC-85079, N01HC85086, N01-HC-15103, N01-HC-55222, R01-HL77612, R01-HL-75476, R01-AG-23629, U01-HL80295]

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Longitudinal studies examining associations of the inflammatory markers fibrinogen and C-reactive protein (CRP) with lung function decline are sparse. The authors examined whether elevated fibrinogen and CRP levels were associated with greater longitudinal lung function decline in the elderly. The Cardiovascular Health Study measured fibrinogen and CRP in 5,790 Whites and African Americans from four US communities aged 65 years or older in 1989-1990 or 1992-1993. Spirometry was performed in 1989-1990 and 4, 7, and 16 years later. Fibrinogen and CRP were inversely associated with lung function at baseline after adjustment for multiple potential confounders. In mixed models, the rate of decline in forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) ratio with increasing age was faster among those with higher baseline fibrinogen (-0.032%/year per standard deviation higher fibrinogen (95% confidence interval: -0.057, -0.0074)) but not among those with higher CRP (-0.0037%/year per standard deviation higher CRP (95% confidence interval: -0.013, 0.0056)). Longitudinal analyses for FEV1 and FVC yielded results in the direction opposite of that hypothesized, possibly because of the high mortality rate and strong inverse association of FEV1 and FVC but not FEV1/FVC with mortality. An alternative approach to missing data yielded similar results. In conclusion, higher levels of fibrinogen, but not CRP, independently predicted greater FEV1/FVC decline in the elderly.

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