Effects of the menstrual cycle on lung function variables in women with asthma

Am J Respir Crit Care Med. 2009 Aug 15;180(4):304-10. doi: 10.1164/rccm.200904-0497OC. Epub 2009 Jun 11.

Abstract

Rationale: Angiogenesis is a defining pathologic feature of airway remodeling and contributes to asthma severity. Women experience changes in asthma control over the menstrual cycle, a time when vessels routinely form and regress under the control of angiogenic factors. One vital function modulated over the menstrual cycle in healthy women is gas transfer, and this has been related to angiogenesis and cyclic expansion of the pulmonary vascular bed.

Objectives: We hypothesized that changes in gas transfer and the pulmonary vascular bed occur in women with asthma over the menstrual cycle and are associated with worsening airflow obstruction.

Methods: Twenty-three women, 13 with asthma and 10 healthy control subjects, were evaluated over the menstrual cycle with weekly measures of spirometry, gas transfer, nitric oxide, hemoglobin, factors affecting hemoglobin binding affinity, and proangiogenic factors.

Measurements and main results: Airflow and lung diffusing capacity varied over the menstrual cycle with peak levels during menses that subsequently declined to nadir in early luteal phase. In contrast to healthy women, changes in lung diffusing capacity (DL(CO)) were associated with changes in membrane diffusing capacity and DL(CO) was not related to proangiogenic factors. DL(CO) did not differ between the two groups, although methemoglobin and carboxyhemoglobin were higher in women with asthma than in healthy women.

Conclusions: Women with asthma experience cyclic changes in airflow as well as gas transfer and membrane diffusing capacity supportive of a hormonal effect on lung function.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Airway Resistance / physiology
  • Asthma / diagnosis
  • Asthma / physiopathology*
  • Bronchial Provocation Tests
  • Carbon Dioxide / blood
  • Carboxyhemoglobin / metabolism
  • Female
  • Forced Expiratory Volume / physiology
  • Humans
  • Hydrogen-Ion Concentration
  • Lung / blood supply
  • Menstrual Cycle / physiology*
  • Methemoglobin / metabolism
  • Neovascularization, Physiologic / physiology
  • Oxygen / blood
  • Pulmonary Diffusing Capacity / physiology*
  • Pulmonary Gas Exchange / physiology*
  • Pulmonary Ventilation / physiology
  • Stem Cell Factor / blood
  • Vascular Endothelial Growth Factor A / blood
  • Vital Capacity / physiology

Substances

  • Stem Cell Factor
  • Vascular Endothelial Growth Factor A
  • Carbon Dioxide
  • Methemoglobin
  • Carboxyhemoglobin
  • Oxygen