Histamine airway hyper-responsiveness and mortality from chronic obstructive pulmonary disease: a cohort study

JJ Hospers, DS Postma, B Rijcken, ST Weiss, JP Schouten*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

185 Citations (Scopus)

Abstract

Background Smoking and airway lability, which is expressed by histamine airway hyper-responsiveness, are known risk factors for development of respiratory symptoms. Smoking is also associated with increased mortality risks. We studied whether airway hyper-responsiveness is associated with increased mortality, and whether this risk was independent of smoking and reduced lung function.

Methods We followed up 2008 inhabitants of the communities of Vlagtwedde, Vlaardingen, and Meppel (Netherlands), who had histamine challenge test data, from 1964-72 for 30 years. Follow-up was 99% successful (29 patients lost to follow-up) with 1453 participants alive and 526 deaths (246 died from cardiovascular disease, 54 from lung cancer, and 21 from chronic obstructive pulmonary disease [COPD]).

Findings Mortality from COPD increased with more severe hyper-responsiveness; relative risks of 3.83 (95% CI 0.97-15.1), 4.40 (1.16-16.7), 4.78 (1.27-18.0), 6.69 (1.71-26.1), and 15.8 (3.72-67.1) were associated with histamine thresholds of 32 g/L, 16 g/L, 8 g/L, 4 g/L, and 1 g/L, respectively, compared with no hyper-responsiveness. These risks were adjusted for sex, age, smoking, lung function, body-mass index, positive skin tests, eosinophilia, asthma, and city of residence.

Interpretation Increased histamine airway hyperresponsiveness predicts mortality from COPD. Although this trend was more pronounced in smokers, an increasing proportion of COPD deaths with increasing hyperresponsiveness was also present among individuals who had never smoked.

Original languageEnglish
Pages (from-to)1313-1317
Number of pages5
JournalLANCET
Volume356
Issue number9238
DOIs
Publication statusPublished - 14-Oct-2000

Keywords

  • NONSPECIFIC BRONCHIAL RESPONSIVENESS
  • COMMUNITY-BASED POPULATION
  • SKIN-TEST REACTIVITY
  • RESPIRATORY SYMPTOMS
  • HYPERRESPONSIVENESS
  • DECLINE
  • EOSINOPHILIA
  • ATOPY
  • ADULTS
  • ASTHMA

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