Effects of the Menstrual Cycle on Lung Function Variables in Women with Asthma

被引:78
作者
Farha, Samar [1 ]
Asosingh, Kewal [2 ]
Laskowski, Daniel [1 ,2 ]
Hammel, Jeffrey [2 ]
Dweik, Raed A. [1 ,2 ]
Wiedemann, Herbert P. [1 ]
Erzurum, Serpil C. [1 ,2 ]
机构
[1] Cleveland Clin, Resp Inst, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Pathobiol, Lerner Res Inst, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
gas transfer; angiogenesis; asthma; menstrual cycle; proangiogenic progenitor cell; PULMONARY DIFFUSING-CAPACITY; AIRWAY RESPONSIVENESS; CARBON-MONOXIDE; NITRIC-OXIDE; CARBOXYHEMOGLOBIN CONCENTRATIONS; CHILDHOOD ASTHMA; ANGIOGENESIS; FLOW; SEX; PERMEABILITY;
D O I
10.1164/rccm.200904-0497OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Anglogenesis 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 (DLCO) were associated with changes in membrane diffusing capacity and DLCO was not related to proangiogenic factors. DLCO 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.
引用
收藏
页码:304 / 310
页数:7
相关论文
共 50 条
[1]   Oxidative and nitrosative events in asthma [J].
Andreadis, AA ;
Hazen, SL ;
Comhair, SAA ;
Erzurum, SC .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (03) :213-225
[2]  
[Anonymous], 1999, Am J Respir Crit Care Med, V160, P2104
[3]  
[Anonymous], 2006, R LANG ENV STAT COMP
[4]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[5]   Th1- and Th2-dependent endothelial progenitor cell recruitment and angiogenic switch in asthma [J].
Asosingh, Kewal ;
Swaidani, Shadi ;
Aronica, Mark ;
Erzurum, Serpil C. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (10) :6482-6494
[6]   Myeloid lineage progenitors give rise to vascular endothelium [J].
Bailey, Alexis S. ;
Willenbring, Holger ;
Jiang, Shuguang ;
Anderson, Daniel A. ;
Schroeder, David A. ;
Wong, Melissa H. ;
Grompe, Markus ;
Fleming, William H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (35) :13156-13161
[7]   Gender differences in airway behaviour over the human life span [J].
Becklake, MR ;
Kauffmann, F .
THORAX, 1999, 54 (12) :1119-1138
[8]   Essential role of nitric oxide in VEGF-induced, asthma-like angiogenic, inflammatory, mucus, and physiologic responses in the lung [J].
Bhandari, Vineet ;
Choo-Wing, Rayman ;
Chapoval, Svetlana P. ;
Lee, Chun G. ;
Tang, C. ;
Kim, Y. K. ;
Ma, Bing ;
Baluk, Peter ;
Lin, Michelle I. ;
McDonald, Donald M. ;
Homer, Robert J. ;
Sessa, William C. ;
Elias, Jack A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (29) :11021-11026
[9]  
BORLAND CDR, 1989, EUR RESPIR J, V2, P56
[10]  
CLAUDE F, 1938, PRESSE MED, V38, P755