INFLAMMATION, AUTONOMIC DYSFUNCTION AND AIRWAY DISEASE
INFLAMMATION, AUTONOMIC DYSFUNCTION AND AIRWAY DISEASE
批准号:
3363982
负责人:
DAVID W. SPARROW
金额:
$14.5万
依托单位国家:
美国
项目类别:
财政年份:
1990
资助国家:
美国
项目状态:
已结题
起止时间:
1990-07-01 至 1993-06-30
关键词:
allergens asthma autonomic disorder bronchial mucus bronchoconstrictors bronchodilators case history catecholamines chromatography electrocardiography emphysema heart rate histamine human middle age (35-64) human old age (65+) human subject immunoglobulin E inflammation isoproterenol leukotrienes methacholine neural information processing parasympathetic nervous system respiratory disorder diagnosis respiratory disorder epidemiology secretion serotonin sign /symptom sympathetic nervous system tobacco abuse urinalysis
中文摘要
中老年哮喘和慢性支气管炎的发病机制
英文摘要
The pathogenesis of asthma and chronic bronchitis among middle-aged and
older adults remains obscure. We hypothesize that both airway inflammation
(secondary to inhalation of specific allergens and other environmental
agents) and functional imbalance of the autonomic nervous system play
important roles in functional alterations that characterize these diseases
(increased bronchodilator responsiveness, increased responsiveness to
nonspecific bronchoconstricting stimuli bronchial mucus hypersecretion).
Airway hyperresponsiveness and/or mucus hypersecretion may be especially
likely to occur in the setting of coexisting airway inflammation and
disordered neural regulation. The goal of this study is to evaluate this
hypothesis in a well-characterized cohort of middle-aged and elderly men.
The study will use the VA Normative Aging Study (NAS) population which
consists of approximately 1800 community-dwelling men who return for
examination every three years. Data on the occurrence of outcomes of
interest (heightened responsiveness to inhaled isoproterenol, methacholine
airway hyperresponsiveness, reported bronchial mucus hypersecretion) are
already being collected in this cohort. We propose collecting new data on
indices of inflammation (inflammatory mediators in urine), autonomic
activity (urinary catecholamine excretion, heart rate variations induced by
deep breathing), and autonomic responsiveness pupillary alpha-adrenergic
and cholinergic responses) from those NAS participants returning for
examination over a 1/2 year period. The proposed study would be the first
investigation of a human population which examines the interrelationships
between inflammation, autonomic activity, and autonomic responsiveness, and
explores the hypothesis that both inflammation and autonomic nervous system
alterations are necessary for the occurrence of airway hyperresponsiveness
and mucus hypersecretion.
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