[Genetics of bronchial asthma with reference to allergy].

Kinderarztliche Praxis Pub Date : 1993-10-01
L Ritter, W Thal, J Gedschold, S Kropf
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Abstract

No uniform opinion exists to date in respect of the transmission of a genetic disposition to asthma bronchiale and atopy. Literature references discuss both monogenic, autosomal dominant or recessive and multifactorial-polygenic heredity. The following contribution discusses the results of an own study on the occurrence of atopy and asthma bronchiale in 153 families. Multifactorial-polygenic heredity with threshold value range is most suitable for the interpretation of our findings, even though an autosomal dominant heredity with reduced penetrance and variable expressivity might well be the basis for the transmission of a disposition to atopy and asthma bronchiale. In multifactorial-polygenic heredity with threshold value range, empirical risk data are important for predicting the disease risk. Such data can be obtained only on the basis of extensive family research and apply only to the population for which they were obtained. The risk of occurrence of atopy or asthma bronchiale in families already affected by the increases, in our experience, with the number of the patients already suffering from the disease and with the closeness of relationship with the patients concerned. We found a recurrence risk for further children of 40-45% for atopy and of 5-10% for asthma bronchiale in those marriages where both one parent and already one child are suffering from the disease.

[与过敏相关的支气管哮喘遗传学]。
关于支气管哮喘和特应性哮喘的遗传倾向的传递,迄今尚无统一的意见。文献文献讨论了单基因遗传、常染色体显性或隐性遗传和多因素多基因遗传。下面的文章讨论了153个家庭中特应性和支气管哮喘发生的研究结果。具有阈值范围的多因子-多基因遗传最适合解释我们的发现,即使外显率降低和表达性可变的常染色体显性遗传可能是特应性和支气管哮喘倾向传播的基础。在具有阈值范围的多因素多基因遗传中,经验风险数据是预测疾病风险的重要依据。这种数据只能在广泛的家庭研究的基础上获得,并且只适用于获得这些数据的人口。根据我们的经验,在已经受该病影响的家庭中,发生特应性或支气管哮喘的风险随着已经患有该病的患者人数的增加以及与有关患者关系的密切而增加。我们发现,在父母一方和已经有一个孩子患有该病的婚姻中,后代的特应性疾病复发风险为40-45%,哮喘支气管疾病复发风险为5-10%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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