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Factor analysis in the Genetics of Asthma International Network family study identifies five major quantitative asthma phenotypes.

机译:哮喘遗传学国际网络家族研究中的因子分析确定了五种主要的定量哮喘表型。

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BACKGROUND: Asthma is a clinically heterogeneous disease caused by a complex interaction between genetic susceptibility and diverse environmental factors. In common with other complex diseases the lack of a standardized scheme to evaluate the phenotypic variability poses challenges in identifying the contribution of genes and environments to disease expression. OBJECTIVE: To determine the minimum number of sets of features required to characterize subjects with asthma which will be useful in identifying important genetic and environmental contributors. Methods Probands aged 7-35 years with physician diagnosed asthma and symptomatic siblings were identified in 1022 nuclear families from 11 centres in six countries forming the Genetics of Asthma International Network. Factor analysis was used to identify distinct phenotypes from questionnaire, clinical, and laboratory data, including baseline pulmonary function, allergen skin prick test (SPT). RESULTS: Five distinct factors were identified:(1) baseline pulmonary function measures [forced expiratory volume in 1 s (FEV(1)) and forced vital capacity (FVC)], (2) specific allergen sensitization by SPT, (3) self-reported allergies, (4) symptoms characteristic of rhinitis and (5) symptoms characteristic of asthma. Replication in symptomatic siblings was consistent with shared genetic and/or environmental effects, and was robust across age groups, gender, and centres. Cronbach's alpha ranged from 0.719 to 0.983 suggesting acceptable internal scale consistencies. Derived scales were correlated with serum IgE, methacholine PC(20), age and asthma severity (interrupted sleep). IgE correlated with all three atopy-related factors, the strongest with the SPT factor whereas severity only correlated with baseline lung function, and with symptoms characteristic of rhinitis and of asthma. CONCLUSION: In children and adolescents with established asthma, five distinct sets of correlated patient characteristics appear to represent important aspects of the disease. Factor scores as quantitative traits may be better phenotypes in epidemiological and genetic analyses than those categories derived from the presence or absence of combinations of +ve SPTs and/or elevated IgE.
机译:背景:哮喘是一种临床异质性疾病,由遗传易感性和各种环境因素之间的复杂相互作用引起。与其他复杂疾病一样,缺乏评估表型变异性的标准化方案对确定基因和环境对疾病表达的贡献提出了挑战。目的:确定特征性哮喘患者所需的最少特征集,这将有助于识别重要的遗传和环境因素。方法从构成哮喘国际网络的六个国家的11个中心的1022个核心家庭中,鉴定了7-35岁的经医生诊断为哮喘和有症状兄弟姐妹的先证者。因子分析用于从问卷,临床和实验室数据中识别不同的表型,包括基线肺功能,过敏原皮肤点刺试验(SPT)。结果:确定了五个不同的因素:(1)基线肺功能测量[1秒钟呼气量(FEV(1))和强制肺活量(FVC)],(2)SPT对特定过敏原致敏,(3)自我-过敏,(4)鼻炎的症状和(5)哮喘的症状。有症状的同胞中的复制与遗传和/或环境的共同影响一致,并且在不同年龄段,性别和中心的人群中均表现良好。 Cronbach的alpha值介于0.719至0.983之间,表明可接受的内部量表一致性。推导的量表与血清IgE,乙酰甲胆碱PC(20),年龄和哮喘严重程度(睡眠中断)相关。 IgE与所有三种与特应性相关的因子相关,最强与SPT因子相关,而严重程度仅与基线肺功能以及鼻炎和哮喘特征性症状相关。结论:在患有哮喘的儿童和青少年中,五组不同的相关患者特征似乎代表了该疾病的重要方面。在流行病学和遗传学分析中,因子分数作为定量性状可能比源自+ ve SPT和/或升高的IgE组合存在或不存在的那些类别更好。

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