首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Assessment of alpha-1-antitrypsin deficiency heterozygosity as a risk factor in the etiology of emphysema. Physiological comparison of adult normal and heterozygous protease inhibitor phenotype subjects from a random population.
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Assessment of alpha-1-antitrypsin deficiency heterozygosity as a risk factor in the etiology of emphysema. Physiological comparison of adult normal and heterozygous protease inhibitor phenotype subjects from a random population.

机译:评估α-1-抗胰蛋白酶缺乏杂合性是肺气肿病因中的危险因素。随机人群中成人正常和杂合蛋白酶抑制剂表型受试者的生理比较。

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摘要

For plethysmographic studies of lung mechanics and measurement of pulmonary diffusing capacity, 62 subjects were drawn from a randomly selected population sample. Data obtained from the 24 subjects of heterozygous phenotype for alpha-1-antitrypsin deficiency (PiMZ) were compared by age group with data from 38 normal (PiM) subjects matched for sex, age, and smoking history. Comparison of mean values by age group for lung volumes, diffusing capacity, lung elastic recoil, maximum expiratory flow, and the occurrence of frequency dependence of dynamic compliance revealed no differences between phenotype groups. There was no evidence of an accelerated effect of aging among PiMZ subjects when compared with normal counterparts nor was there evidence of an increased effect of smoking. From these data it appears that the PiMZ phenotype per se is not a risk factor in the development of emphysema.
机译:对于肺力学的体积描记研究和肺扩散能力的测量,从随机选择的人群样本中抽取了62名受试者。将按年龄组从24位杂合子表型的α-1-抗胰蛋白酶缺乏症(PiMZ)获得的数据与来自38位正常(PiM)受试者的性别,年龄和吸烟史相匹配的数据进行比较。比较按年龄组划分的肺容量,扩散能力,肺弹性后坐力,最大呼气流量和动态依从性频率依赖性的平均值,表明表型组之间没有差异。与正常人相比,没有证据表明PiMZ受试者中有加速衰老的迹象,也没有证据表明吸烟效果有所提高。从这些数据看来,PiMZ表型本身不是肺气肿发生的危险因素。

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