Suppr超能文献

具有不同表型特征的ΔF508纯合囊性纤维化双胞胎和同胞对的类别。

Categories of deltaF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics.

作者信息

Mekus F, Ballmann M, Bronsveld I, Bijman J, Veeze H, Tümmler B

机构信息

Department of Pediatrics, Medizinische Hochschule Hannover, Germany.

出版信息

Twin Res. 2000 Dec;3(4):277-93. doi: 10.1375/136905200320565256.

Abstract

Cystic fibrosis (CF), the most common severe autosomal recessive trait among Caucasians, is caused by molecular lesions in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The course of the multi-organ disease CF is highly variable, suggesting the influence of environmental factors and/or modulating genes other than CFTR on the disease phenotype. To evaluate the cause of CF disease variability, the European CF Twin and Sibling Study collected data on two clinical parameters most sensitive for the course and prognosis of CF, ie weight predicted for height (wfh)% (representative for the nutritional status) and FEVPerc (representative for the pulmonary status) for a cohort of 277 sibling pairs, 12 pairs of dizygous twins and 29 pairs of monozygous twins. Of these 318 CF twin and sib pairs, 114 were reported to be homozygous for the most frequent CF disease-causing lesion, deltaF508. Intra-pair discordance was assessed by the intra-pair differences with wfh% and FEVPerc and by DELTA, a composite parameter defined by linear combination of wfh% and FEVPerc in order to describe discordance with respect to the overall disease severity. Monozygous twins had a significantly lower DELTA than dizygous twins (P = 0.05) indicating that CF disease severity is modulated by an inherited component in addition to the CFTR gene itself. Extreme phenotypes are considered to be more informative for the analysis of any quantitative trait. Thus, we aimed to quantify disease severity and intra-pair discordance in order to select pairs with the extreme phenotypes DIS (discordant patient pairs), CON+ (concordant and mildy affected patient pairs) and CON- (concordant and severely affected patient pairs). The algorithm reliably discriminated between pairs DIS, CON+ and CON- among the cohort of deltaF508 homozygotes. The selected pairs from these categories demonstrated non-overlapping properties for wfh%, FEVPerc and the intra-pair difference of both parameters.

摘要

囊性纤维化(CF)是白种人中最常见的严重常染色体隐性遗传病,由囊性纤维化跨膜传导调节因子基因(CFTR)的分子病变引起。多器官疾病CF的病程高度可变,提示环境因素和/或CFTR以外的调节基因对疾病表型有影响。为评估CF疾病变异性的原因,欧洲CF双胞胎和同胞研究收集了277对同胞、12对异卵双胞胎和29对同卵双胞胎队列中两个对CF病程和预后最敏感的临床参数的数据,即身高预期体重(wfh)%(代表营养状况)和FEVPerc(代表肺部状况)。在这318对CF双胞胎和同胞对中,114对被报告为最常见的CF致病病变deltaF508的纯合子。通过wfh%和FEVPerc的配对内差异以及DELTA(一个由wfh%和FEVPerc线性组合定义的综合参数,用于描述总体疾病严重程度的不一致性)评估配对内不一致性。同卵双胞胎的DELTA显著低于异卵双胞胎(P = 0.05),表明除CFTR基因本身外,CF疾病严重程度还受遗传成分调节。极端表型被认为对任何数量性状的分析更具信息性。因此,我们旨在量化疾病严重程度和配对内不一致性,以选择具有极端表型DIS(不一致患者对)、CON+(一致且轻度受影响患者对)和CON-(一致且重度受影响患者对)的对。该算法在deltaF508纯合子队列中可靠地区分了DIS、CON+和CON-对。从这些类别中选择的对在wfh%、FEVPerc以及两个参数的配对内差异方面表现出不重叠的特性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验