Eosinophilia is associated with increased all-cause mortality after a follow-up of 30 years in a general population sample

Citation
Jj. Hospers et al., Eosinophilia is associated with increased all-cause mortality after a follow-up of 30 years in a general population sample, EPIDEMIOLOG, 11(3), 2000, pp. 261-268
Citations number
34
Categorie Soggetti
Envirnomentale Medicine & Public Health","Medical Research General Topics
Journal title
EPIDEMIOLOGY
ISSN journal
10443983 → ACNP
Volume
11
Issue
3
Year of publication
2000
Pages
261 - 268
Database
ISI
SICI code
1044-3983(200005)11:3<261:EIAWIA>2.0.ZU;2-W
Abstract
We investigated whether allergy is associated with increased all-cause mort ality. Two allergy markers, peripheral blood eosinophilia (greater than or equal to 275 eosinophilic cells per mm(3)) and positive skin tests (sum sco re greater than or equal to 3), were available for 5,383 subjects of a coho rt study on asthma and chronic obstructive pulmonary disease in general pop ulation samples of Vlagtwedde and Vlaardingen, the Netherlands, in 1965-197 2. During 30 years of follow-up, 1,135 subjects died. In a Cox regression a nalysis, eosinophilia was associated with an increased risk (relative risk = 1.4; 95% confidence interval = 1.2-1.7) of all-cause mortality, independe nt of gender, age, smoking habits, percentage predicted forced expiratory v olume in 1 second (FEV1 % predicted), and positive skin tests at the start of the study. Subjects with positive skin tests had only an increased risk of all-cause mortality in the subgroup of subjects with FEV1 <80% of predic ted (relative risk = 1.7; 95% confidence interval = 1.0-2.8). These results remained essentially unchanged after exclusion of subjects with asthma. We conclude that eosinophilia is associated with increased all-cause mortalit y. An increased number of peripheral blood eosinophils may reflect an incre ased inflammatory response, resulting in tissue injury. It is possible that the association between a low FEV1 % predicted and all-cause mortality is partly mediated by an atopic constitution.