Effect of ADRB2 polymorphisms on response to longacting β2-agonist therapy:: a pharmacogenetic analysis of two randomised studies

被引:166
作者
Bleecker, Eugene R. [1 ]
Postma, Dirkje S. [2 ]
Lawrance, Rachael M. [4 ]
Meyers, Deborah A. [1 ]
Ambrose, Helen J. [3 ]
Goldman, Mitch [4 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC 27157 USA
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol, Groningen, Netherlands
[3] AstraZeneca, Macclesfield, Cheshire, England
[4] AstraZeneca, Wilmington, DE USA
关键词
D O I
10.1016/S0140-6736(07)61906-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background New evidence has suggested that people with asthma who are homozygous for arginine at aminoacid 16 of the beta(2)-adrenergic receptor (ADRB2) might not benefit from longacting beta(2)-agonist therapy. We, therefore, investigated whether ADRB2 polymorphisms affect response to longacting beta(2)-agonists in combination with inhaled corticosteroids. Methods Asthmatics were stratified by ADRB2 genotype in two studies to assess the effects of inhaled corticosteroids plus longacting beta(2)-agonists on asthma exacerbations. In study 1 (double-blind), 2250 asthmatics were randomly assigned to budesonide plus formoterol maintenance and reliever therapy, fixed-dose budesonide plus formoterol, or fixed-dose fluticasone plus salmeterol for 6 months. Study 2 (open-label) consisted of 405 asthmatics and compared an adjustable regimen of budesonide plus formoterol with fixed-dose budesonide plus formoterol and fixed-dose fluticasone plus salmeterol for 7 months. The relation between ADRB2 polymorphism, severe asthma exacerbations, and other asthma outcomes was analysed. Primary endpoints for studies 1 and 2 were severe asthma exacerbation and asthma control as assessed by measures of exacerbations, respectively. Findings In study 1, Gly16Arg genotype had no effect on the percentage of participants with severe exacerbations across all treatment groups (99 [12%] of 833 Gly/Gly, 110 [11%] of 1028 Gly/Arg, and 32 [9%] of 361 Arg/Arg participants). Secondary endpoints, including forced expiratory volume in 1 s, peak expiratory flow, use of as-needed medication, and number of nights with awakenings were similar between genotype groups. No relation was recorded between ADRB2 haplotype and primary and secondary endpoints. In study 2, the frequency of asthma exacerbations (15 [9%] of 168 Gly/Gly, 13 [8%] of 169 Gly/Arg, and 6 [9%] of 67 Arg/Arg participants) and other study endpoints were closely similar for all ADRB2 genotypes. Interpretation Since we showed no pharmacogenetic effect of ADRB2 variation on therapeutic response in asthma, patients, irrespective of their genotype, can continue to receive inhaled corticosteroids plus longacting beta(2)-agonists.
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页码:2118 / 2125
页数:8
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共 32 条
  • [1] [Anonymous], 1987, AM REV RESPIR DIS, V136, P225
  • [2] [Anonymous], 2006, GLOB STRAT ASTHM MAN
  • [3] Becker A., 2005, CAN MED ASSOC J, V173, pS3
  • [4] Salmeterol response is not affected by β2-adrenergic receptor genotype in subjects with persistent asthma
    Bleecker, Eugene R.
    Yancey, Steven W.
    Baitinger, Leslie A.
    Edwards, Lisa D.
    Klotsman, Michael
    Anderson, Wayne H.
    Dorinsky, Paul M.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (04) : 809 - 816
  • [5] British Thoracic Society and Scottish Intercollegiate Guidelines Network (SIGN), British guideline on the management of asthma. A national clinical guideline
  • [6] Asthma guidelines: A changing paradigm to improve asthma care
    Busse, WW
    Lenfant, C
    Lemanske, RF
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (05) : 703 - 705
  • [7] BUSSE WW, 2007, COMPARISON ASTHMA EX
  • [8] Asthma variability in patients previously treated with β2-agonists alone
    Calhoun, WJ
    Sutton, LB
    Emmett, A
    Dorinsky, PM
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 112 (06) : 1088 - 1094
  • [9] Meta-analysis of the association of β2-adrenergic receptor polymorphisms with asthma phenotypes
    Contopoulos-Ioannidis, DG
    Manoli, EN
    Ioannidis, JPA
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 115 (05) : 963 - 972
  • [10] CROW JF, 1988, GENETICS, V119, P473