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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.评估α-1抗胰蛋白酶缺乏杂合性作为肺气肿病因中的一个风险因素。对来自随机人群的成年正常和杂合蛋白酶抑制剂表型受试者进行生理比较。
J Clin Invest. 1979 Feb;63(2):299-309. doi: 10.1172/JCI109303.
2
Effects of smoking and intermediate alpha 1-antitrypsin deficiency (PiMZ) on lung function.吸烟和中间型α1-抗胰蛋白酶缺乏症(PiMZ)对肺功能的影响。
Eur J Respir Dis. 1985 Oct;67(4):279-85.
3
Alpha-1-antitrypsin deficiency.α-1抗胰蛋白酶缺乏症
Clin Chest Med. 1983 Sep;4(3):359-75.
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Alpha-1 antitrypsin Null mutations and severity of emphysema.α-1抗胰蛋白酶基因无效突变与肺气肿严重程度
Respir Med. 2008 Jun;102(6):876-84. doi: 10.1016/j.rmed.2008.01.009. Epub 2008 Mar 18.
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A study on the lung function in alpha 1-antitrypsin-deficient (PiMZ) patients.一项关于α1-抗胰蛋白酶缺乏症(PiMZ型)患者肺功能的研究。
Hiroshima J Med Sci. 1993 Mar;42(1):41-5.
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Pulmonary abnormalities in intermediate alpha-1-antitrypsin deficiency.中间型α-1抗胰蛋白酶缺乏症的肺部异常
J Clin Invest. 1976 Nov;58(5):1069-77. doi: 10.1172/JCI108558.
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Longitudinal lung function study in heterozygous PiMZ phenotype subjects.PiMZ杂合表型受试者的纵向肺功能研究。
Eur Respir J. 1994 Dec;7(12):2199-204. doi: 10.1183/09031936.94.07122199.
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Chest. 2008 May;133(5):1095-100. doi: 10.1378/chest.07-2405. Epub 2008 Feb 8.
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Scand J Respir Dis. 1976;57(6):267-80.
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Family study of alpha 1-antitrypsin deficiency: effects of cigarette smoking, measured genotype, and their interaction on pulmonary function and biochemical traits.α1-抗胰蛋白酶缺乏症的家系研究:吸烟、测量基因型及其相互作用对肺功能和生化特征的影响。
Genet Epidemiol. 1992;9(5):317-31. doi: 10.1002/gepi.1370090504.

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Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis.α1-抗胰蛋白酶PI MZ杂合子中的慢性阻塞性肺疾病:一项荟萃分析。
Thorax. 2004 Oct;59(10):843-9. doi: 10.1136/thx.2004.022541.
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Genes, oxidative stress, and the risk of chronic obstructive pulmonary disease.基因、氧化应激与慢性阻塞性肺疾病风险
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3
Frequency and significance of phenotypes for alpha1-antitrypsin deficiency in type 1 autoimmune hepatitis.1型自身免疫性肝炎中α1抗胰蛋白酶缺乏症的表型频率及意义
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Replacement therapy of alpha 1-antitrypsin deficiency. Reversal of protease-antiprotease imbalance within the alveolar structures of PiZ subjects.α1-抗胰蛋白酶缺乏症的替代疗法。纠正PiZ型受试者肺泡结构内蛋白酶-抗蛋白酶失衡。
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Danazol-induced augmentation of serum alpha 1-antitrypsin levels in individuals with marked deficiency of this antiprotease.达那唑可使这种抗蛋白酶严重缺乏的个体血清α1-抗胰蛋白酶水平升高。
J Clin Invest. 1980 Jul;66(1):82-87. doi: 10.1172/JCI109838.
6
Lung distensibility and airway function in intermediate alpha 1-antitrypsin deficiency (Pi MZ).中间型α1-抗胰蛋白酶缺乏症(Pi MZ)患者的肺扩张性和气道功能
Thorax. 1979 Oct;34(5):637-46. doi: 10.1136/thx.34.5.637.

本文引用的文献

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IMPROVED TECHNIQUE FOR ESTIMATING PLEURAL PRESSURE FROM ESOPHAGEAL BALLOONS.通过食管气囊估计胸膜压力的改良技术
J Appl Physiol. 1964 Mar;19:207-11. doi: 10.1152/jappl.1964.19.2.207.
2
PULMONARY EMPHYSEMA AND ALPHA1-ANTITRYPSIN DEFICIENCY.肺气肿与α1-抗胰蛋白酶缺乏症
Acta Med Scand. 1964 Feb;175:197-205. doi: 10.1111/j.0954-6820.1964.tb00567.x.
3
A standardized breath holding technique for the clinical measurement of the diffusing capacity of the lung for carbon monoxide.一种用于临床测量肺一氧化碳弥散能力的标准化屏气技术。
J Clin Invest. 1957 Jan;36(1 Part 1):1-17. doi: 10.1172/JCI103402.
4
A rapid plethysmographic method for measuring thoracic gas volume: a comparison with a nitrogen washout method for measuring functional residual capacity in normal subjects.一种测量胸内气体容积的快速体积描记法:与氮洗出法测量正常受试者功能残气量的比较
J Clin Invest. 1956 Mar;35(3):322-6. doi: 10.1172/JCI103281.
5
Significance of the relationship between lung recoil and maximum expiratory flow.肺回缩与最大呼气流量之间关系的意义
J Appl Physiol. 1967 Jan;22(1):95-108. doi: 10.1152/jappl.1967.22.1.95.
6
A case of inherited deficiency of serum alpha-antitrypsin associated with pulmonary emphysema.一例与肺气肿相关的遗传性血清α-抗胰蛋白酶缺乏症病例。
Am Rev Respir Dis. 1966 Oct;94(4):529-39. doi: 10.1164/arrd.1966.94.4.529.
7
Elasticity of human lungs in relation to age.人类肺部弹性与年龄的关系。
J Appl Physiol. 1968 Dec;25(6):664-71. doi: 10.1152/jappl.1968.25.6.664.
8
Familial emphysema.家族性肺气肿
Am Rev Respir Dis. 1968 Oct;98(4):692-6. doi: 10.1164/arrd.1968.98.4.692.
9
The pattern of lung disease associated with alpha antitrypsin deficiency.与α-抗胰蛋白酶缺乏相关的肺部疾病模式。
Arch Intern Med. 1968 Sep;122(3):254-7.
10
Genetic and environmental determinants of chronic obstructive pulmonary disease.慢性阻塞性肺疾病的遗传和环境决定因素。
Ann Intern Med. 1970 May;72(5):627-32. doi: 10.7326/0003-4819-72-5-627.

评估α-1抗胰蛋白酶缺乏杂合性作为肺气肿病因中的一个风险因素。对来自随机人群的成年正常和杂合蛋白酶抑制剂表型受试者进行生理比较。

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.

作者信息

McDonagh D J, Nathan S P, Knudson R J, Lebowitz M D

出版信息

J Clin Invest. 1979 Feb;63(2):299-309. doi: 10.1172/JCI109303.

DOI:10.1172/JCI109303
PMID:311786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC371953/
Abstract

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.

摘要

为了进行肺力学的体积描记研究和肺弥散能力的测量,从随机选取的人群样本中抽取了62名受试者。将24名α-1抗胰蛋白酶缺乏杂合子表型(PiMZ)受试者的数据按年龄组与38名在性别、年龄和吸烟史方面匹配的正常(PiM)受试者的数据进行比较。按年龄组对肺容量、弥散能力、肺弹性回缩、最大呼气流量以及动态顺应性频率依赖性的发生率进行平均值比较,结果显示表型组之间没有差异。与正常受试者相比,没有证据表明PiMZ受试者存在加速衰老的效应,也没有证据表明吸烟的影响增加。从这些数据来看,PiMZ表型本身似乎不是肺气肿发生发展的危险因素。