Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland

被引:75
作者
Hakonarson, H
Bjornsdottir, US
Ostermann, E
Arnason, T
Adalsteinsdottir, AE
Halapi, E
Shkolny, D
Kristjansson, K
Gudnadottir, SA
Frigge, ML
Gislason, D
Gislason, T
Kong, A
Gulcher, J
Stefansson, K
机构
[1] deCODE Genet Inc, IS-110 Reykjavik, Iceland
[2] Vifilstadir Univ Hosp, Reykjavik, Iceland
关键词
asthma; atopy; genetic variations; linkage; single-nucleotide polymorphism;
D O I
10.1164/ajrccm.164.11.2101086
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Numerous asthma and atopy loci have been reported in studies demonstrating associations of the asthma-related phenotypes atopy, elevated IgE levels, and bronchial hyperresponsiveness with alleles of microsatellite markers and single-nucleotide polymorphisms (SNPs) within specific cytokine/chemokine and IgE-regulating genes. Although the studies reporting these observations are compelling, most of them lack statistical power. We assessed the nature, pattern, and frequency of SNPs in 24 candidate genes in Iceland and looked for associations with asthma and atopy. We Identified 42 SNPs with an average minor allele frequency of 20.3% (asthma) and 20.7% (control). Twenty SNPs (48%) were within coding sequences and 90% of those led to a predicted change in protein sequence. No differences were detected in the allelic frequencies of SNPs in any of these candidate genes between control subjects and the patients with atopic asthma. Moreover, linkage analysis that included 269 patients with atopic asthma uncovered no evidence of linkage to markers associated with these genes. We conclude that this study has failed to produce evidence in support of the notion that variations within these 24 candidate atopy and asthma genes significantly influence the expression of the atopic asthmatic phenotype or contribute to the susceptibility of atopic asthma.
引用
收藏
页码:2036 / 2044
页数:9
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共 82 条
  • [1] ABRAHAM LJ, 1991, IMMUNOGENETICS, V33, P50
  • [2] Albuquerque RV, 1998, CLIN EXP ALLERGY, V28, P578
  • [3] Amelung PJ, 1999, AM J RESP CRIT CARE, V159, pA646
  • [4] A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13
    Arngrímsson, R
    Siguróardóttir, S
    Frigge, ML
    Bjarnadóttir, RI
    Jónsson, T
    Stefánsson, H
    Baldursdóttir, A
    Einarsdóttir, AS
    Palsson, B
    Snorradóttir, S
    Lachmeijer, AMA
    Nicolae, D
    Kong, A
    Bragason, BT
    Gulcher, JR
    Geirsson, RT
    Stefánsson, K
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (09) : 1799 - 1805
  • [5] A polymorphism* in the 5′ flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E
    Baldini, M
    Lohman, IC
    Halonen, M
    Erickson, RP
    Holt, PG
    Martinez, FD
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (05) : 976 - 983
  • [6] Barnes KC, 1999, CLIN EXP ALLERGY, V29, P47
  • [7] Pathophysiology of asthma
    Barnes, PJ
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 42 (01) : 3 - 10
  • [8] Evidence for multiple genetic susceptibility loci for asthma
    Bleecker, ER
    Postma, DS
    Meyers, DA
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 156 (04) : S113 - S116
  • [9] SSC POLYMORPHISMS IN INTERLEUKIN GENES
    BORISH, L
    MASCALI, JJ
    KLINNERT, M
    LEPPERT, M
    ROSENWASSER, LJ
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (09) : 1710 - 1710
  • [10] Brauer JE, 1999, AM J RESP CRIT CARE, V159, pA650