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

被引:17
|
作者
Pillai, S. G. [1 ]
Tang, Y. [1 ,2 ]
van den Oord, E. [3 ]
Klotsman, M. [1 ]
Barnes, K. [4 ,5 ]
Carlsen, K. [6 ]
Gerritsen, J. [7 ]
Lenney, W. [8 ]
Silverman, M. [9 ]
Sly, P. [10 ]
Sundy, J. [11 ]
Tsanakas, J. [12 ]
von Berg, A. [13 ]
Whyte, M. [14 ]
Ortega, H. G. [15 ]
Anderson, W. H. [1 ]
Helms, P. J. [16 ]
机构
[1] GlaxoSmithKline, Res Triangle Pk, NC 27709 USA
[2] Suny Downstate Med Ctr, Dept Psychiat, Brooklyn, NY 11203 USA
[3] Virginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Richmond, VA 23298 USA
[4] Johns Hopkins Univ, Dept Med, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD 21218 USA
[6] Ullevaal Univ Hosp, Oslo, Norway
[7] Univ Groningen, Univ Med Ctr Groningen, NL-9700 AB Groningen, Netherlands
[8] N Staffordshire Hosp, Acad Dept Pediat, Stoke On Trent, Staffs, England
[9] Univ Leicester, Div Child Hlth, Leicester LE1 7RH, Leics, England
[10] Univ Western Australia, Ctr Child Hlth Res, Perth, WA 6009, Australia
[11] Duke Univ, Med Ctr, Durham, NC 27706 USA
[12] Hippokrateion Hosp, Pediat Resp Unit, Thessaloniki, Greece
[13] Foschunginst Zur Praevent Allergien & Atemwegserk, Abt Fuer Kinderheilkunde, Wesel, Germany
[14] Univ Sheffield, Acad Unit Resp Med, Sheffield S10 2TN, S Yorkshire, England
[15] Glaxo SmithKline, Resp Med Dev Ctr, Res Triangle Pk, NC USA
[16] Univ Aberdeen, Royal Aberdeen Childrens Hosp, Dept Child Hlth, Aberdeen AB9 1FX, Scotland
关键词
atopy; FEV1; IgE; PC20; rhinitis;
D O I
10.1111/j.1365-2222.2007.02918.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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 (FEV1) 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 PC20, 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.
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收藏
页码:421 / 429
页数:9
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