A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity

被引:22
作者
Blumenthal, MN
Langefeld, CD
Barnes, KC
Ober, C
Meyers, DA
King, RA
Beaty, TH
Beck, SR
Bleecker, ER
Rich, SS
机构
[1] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, MRI Ctr 310, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Ctr Human Genom, Winston Salem, NC 27157 USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[4] Johns Hopkins Univ, Dept Epidemiol, Bloomberg Sch Publ Hlth, Baltimore, MD USA
[5] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
genome scan; seasonal pollen sensitivity; asthma; atopy; linkage;
D O I
10.1016/j.jaci.2005.09.038
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Asthma and atopy represent complex traits for which genetic predisposition has been demonstrated. Pollen sensitivity, whether seasonal or chronic, appears to be a major contributor to the asthmatic phenotype. Objective: Regions of the genome contributing to skin test reactivity to 5 seasonal allergens are to be identified in a genome-wide scan. These regions may be distinct from those contributing to risk for asthma and/or atopy. Methods: In the Collaborative Study on the Genetics of Asthma, 4 sites collected 287 families with 2 or more members with asthma. Reactivity to individual pollens were determined on all family members. A genome scan was performed at 9-centiMorgan intervals, and skin test reactivity to 5 seasonal allergens was the focus of nonparametric genetic linkage analysis. Results: Chromosomal regions that exhibited suggestive linkage (logarithm of the odds > 1.18; P < .01) to seasonal pollen reactivity were identified on chromosomes 13q34, 20p12, and 21q21. Evidence of ethnic differences in linkage to seasonal allergens was demonstrated, with support for linkage in African American subjects on chromosomes 8, 10, and 12, in European American subjects on chromosomes 14, 19, 20, and 22, and in Hispanics on chromosome 21. In all families, evidence for linkage of skin test reactivity for Betula, Lolium, and Artemisia was strongest in a region on chromosome 21 that contained the candidate gene, A Disintegrin And Metalloprotease domain 33 (ADAM33). Conclusion: These results suggest both substantial genetic overlap and extensive heterogeneity in the genetic basis for the allergic response to seasonal allergens.
引用
收藏
页码:79 / 85
页数:7
相关论文
共 31 条
  • [1] BLUMENTHAL M, 1992, J IMMUNOL, V148, P411
  • [2] Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA)
    Blumenthal, MN
    Ober, C
    Beaty, TH
    Bleecker, ER
    Langefeld, CD
    King, RA
    Lester, L
    Cox, N
    Barnes, K
    Togias, A
    Mathias, R
    Meyers, DA
    Oetting, W
    Rich, SS
    [J]. GENES AND IMMUNITY, 2004, 5 (03) : 226 - 231
  • [3] A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma
    Blumenthal, MN
    Langefeld, CD
    Beaty, TH
    Bleecker, ER
    Ober, C
    Lester, L
    Lange, E
    Barnes, KC
    Wolf, R
    King, RA
    Solway, J
    Oetting, W
    Meyers, DA
    Rich, SS
    [J]. HUMAN GENETICS, 2004, 114 (02) : 157 - 164
  • [4] Absence of linkage between 5q markers and serum IgE levels in four large atopic families
    Blumenthal, MN
    Wang, Z
    Weber, JL
    Rich, SS
    [J]. CLINICAL AND EXPERIMENTAL ALLERGY, 1996, 26 (08) : 892 - 896
  • [5] Polymorphisms in ADAM33 are associated with allergic rhinitis due to Japanese cedar pollen
    Cheng, L
    Enomoto, T
    Hirota, T
    Shimizu, M
    Takahashi, N
    Akahoshi, M
    Matsuda, A
    Dake, Y
    Doi, S
    Enomoto, K
    Yamasaki, A
    Fukuda, S
    Mao, XQ
    Hopkin, JM
    Tamari, M
    Shirakawa, T
    [J]. CLINICAL AND EXPERIMENTAL ALLERGY, 2004, 34 (08) : 1192 - 1201
  • [6] Cooke RA, 1916, J IMMUNOL, V1, P201
  • [7] A genome-wide search for quantitative trait loci underlying asthma
    Daniels, SE
    Bhattacharrya, S
    James, A
    Leaves, NI
    Young, A
    Hill, MR
    Faux, JA
    Ryan, GF
    leSouef, PN
    Lathrop, GM
    Musk, AW
    Cookson, WOCM
    [J]. NATURE, 1996, 383 (6597) : 247 - 250
  • [8] Genome screen for asthma and related phenotypes in the French EGEA study
    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
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (05) : 1812 - 1818
  • [9] ADAM 33 and its association with airway remodeling and hyperresponsiveness in asthma
    Holgate, ST
    Davies, DE
    Rorke, S
    Cakebread, J
    Murphy, G
    Powell, RM
    Holloway, JW
    [J]. CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2004, 27 (01) : 23 - 34
  • [10] Holloway John W., 2004, Expert Reviews in Molecular Medicine, V6, P1, DOI 10.1017/S1462399404007963