Revisiting the Dutch hypothesis

Dirkje S. Postma*, Scott T. Weiss, Maarten van den Berge, Huib A. M. Kerstjens, Gerard H. Koppelman

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

61 Citations (Scopus)

Abstract

The Dutch hypothesis was first articulated in 1961, when many novel and advanced scientific techniques were not available, such as genomics techniques for pinpointing genes, gene expression, lipid and protein profiles, and the microbiome. In addition, computed tomographic scans and advanced analysis techniques to dissect (small) airways disease and emphysema were not available. At that time, the group of researchers under the visionary guidance of Professor N. G. M. Orie put forward that both genetic and environmental factors can determine whether one would have airway obstructive diseases, such as asthma and chronic obstructive pulmonary disease (COPD). Moreover, they stipulated that the phenotype of obstructive airway disease could be affected by sex and changes with aging. Orie and colleagues' call to carefully phenotype patients with obstructive airways diseases has been adopted by many current researchers in an attempt to determine the heterogeneity of both asthma andCOPD to better define these diseases and optimize their treatment. The founders of the Dutch hypothesis were far ahead of their time, and we can learn from their insights. We should fully characterize all patients in our clinical practice and not just state that they have asthma, COPD, or asthma and COPD overlap syndrome. This detailed phenotyping can help in understanding these obstructive airway diseases and provide guidance for disease management.

Original languageEnglish
Pages (from-to)521-529
Number of pages9
JournalJournal of Allergy and Clinical Immunology
Volume136
Issue number3
DOIs
Publication statusPublished - Sept-2015

Keywords

  • Asthma
  • chronic obstructive pulmonary disease
  • Dutch hypothesis
  • allergy
  • hyperresponsiveness
  • OBSTRUCTIVE PULMONARY-DISEASE
  • AIR-FLOW OBSTRUCTION
  • RANDOMIZED CONTROLLED-TRIAL
  • INHALED CORTICOSTEROID TREATMENT
  • LONG-TERM TREATMENT
  • RESPIRATORY SYMPTOMS
  • BRONCHIAL HYPERRESPONSIVENESS
  • LUNG-FUNCTION
  • RISK-FACTOR
  • ADENOSINE 5'-MONOPHOSPHATE

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