Genome screen for asthma and bronchial hyperresponsiveness: Interactions with passive smoke exposure

被引:88
作者
Meyers, DA
Postma, DS
Stine, OC
Koppelman, GH
Ampleford, EJ
Jongepier, H
Howard, TD
Bleecker, ER
机构
[1] Wake Forest Univ, Sch Med, Ctr Human Genom, Dept Pediat, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Sch Med, Dept Med, Winston Salem, NC USA
[3] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC USA
[4] Univ Hosp, Dept Pulmonol, Groningen, Netherlands
[5] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Baltimore, MD 21201 USA
关键词
smoking; bronchial hyperresponsiveness; asthma; lung function; linkage; genome-wide sereen;
D O I
10.1016/j.jaci.2005.01.070
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Asthma is a common respiratory disease caused by the interaction of genetic susceptibility and exposure to various environmental factors. Passive smoke exposure, characterized by parental smoking, has been shown to be a risk factor for the development of atopy and asthma. Objective: We sought to perform a genome-wide linkage screen for asthma and bronchial hyperresponsiveness (BHR) and to determine the influence of passive tobacco smoke exposure during childhood on the results of genetic linkage studies to investigate gene-environment interactions. Methods: A genome-wide linkage screen for asthma and BHR was performed in 200 families ascertained through a parent with asthma. Analyses were performed separately for the entire sample and for the smoking-exposed and nonexposed families. Results: For asthma and BHR, the strongest evidence for linkage was observed for chromosomes 3p and 5q. The families in which the children were exposed to passive smoking accounted for the evidence for linkage of BHR to 5q (P < .001), but evidence for linkage to 3p was found in both sets of families. Similar results were observed for asthma. However, there was no observed difference in the frequency of asthma or BHR in the offspring from the smoke-exposed compared with the nonexposed families. Conclusion: The results from this study demonstrate that the influence of susceptibility genes for a common disease such as asthma might not be apparent unless there is the appropriate exposure to environmental stimuli, such as passive exposure to cigarette smoke. This approach should be useful for identification of asthma susceptibility genes.
引用
收藏
页码:1169 / 1175
页数:7
相关论文
共 40 条
[1]   RELATIONSHIPS OF BRONCHIAL RESPONSIVENESS ASSESSED BY METHACHOLINE TO SERUM IGE, LUNG-FUNCTION, SYMPTOMS, AND DIAGNOSES IN 11-YEAR-OLD NEW-ZEALAND CHILDREN [J].
BURROWS, B ;
SEARS, MR ;
FLANNERY, EM ;
HERBISON, GP ;
HOLDAWAY, MD .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 90 (03) :376-385
[2]   Airways responsiveness, wheeze onset, and recurrent asthma episodes in young adolescents - The East Boston childhood respiratory disease cohort [J].
Carey, VJ ;
Weiss, ST ;
Tager, IB ;
Leeder, SR ;
Speizer, FE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (01) :356-361
[3]   Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure [J].
Colilla, S ;
Nicolae, D ;
Pluzhnikov, A ;
Blumenthal, MN ;
Beaty, TH ;
Bleecker, ER ;
Lange, EM ;
Rich, SS ;
Meyers, DA ;
Ober, C ;
Cox, NJ .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 111 (04) :840-846
[4]   A genome-wide search for quantitative trait loci underlying asthma [J].
Daniels, SE ;
Bhattacharrya, S ;
James, A ;
Leaves, NI ;
Young, A ;
Hill, MR ;
Faux, JA ;
Ryan, GF ;
leSouef, PN ;
Lathrop, GM ;
Musk, AW ;
Cookson, WOCM .
NATURE, 1996, 383 (6597) :247-250
[5]  
DEVRIES K, 1962, INT ARCH ALLERGY, V20, P63
[6]   Genome screen for asthma and related phenotypes in the French EGEA study [J].
Dizier, MH ;
Besse-Schmittler, C ;
Guilloud-Bataille, M ;
Annesi-Maesano, I ;
Boussaha, M ;
Bousquet, J ;
Charpin, D ;
Degioanni, A ;
Gormand, F ;
Grimfeld, A ;
Hochez, J ;
Hyne, G ;
Lockhart, A ;
Luillier-Lacombe, M ;
Matran, R ;
Meunier, F ;
Neukirch, F ;
Pacheco, Y ;
Parent, V ;
Paty, E ;
Pin, I ;
Pison, C ;
Scheinmann, P ;
Thobie, N ;
Vervloet, D ;
Kauffmann, F ;
Feingold, J ;
Lathrop, M ;
Demenais, F .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (05) :1812-1818
[7]  
Ehrlich F, 1906, BIOCHEM Z, V1, P8
[8]   Environmental tobacco smoke and absenteeism related to respiratory illness in schoolchildren [J].
Gilliland, FD ;
Berhane, K ;
Islam, T ;
Wenten, M ;
Rappaport, E ;
Avol, E ;
Gauderman, WJ ;
McConnell, R ;
Peters, JM .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2003, 157 (10) :861-869
[9]   Effects of maternal smoking during pregnancy and environmental tobacco smoke on asthma and wheezing in children [J].
Gilliland, FD ;
Li, YF ;
Peters, JM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (02) :429-436
[10]   A major susceptibility gene for asthma maps to chromosome 14q24 [J].
Hakonarson, H ;
Bjornsdottir, US ;
Halapi, E ;
Palsson, S ;
Adalsteinsdottir, E ;
Gislason, D ;
Finnbogason, G ;
Gislason, T ;
Kristjansson, K ;
Arnason, T ;
Birkisson, I ;
Frigge, ML ;
Kong, A ;
Gulcher, JR ;
Stefansson, K .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (03) :483-491