The insertion/deletion variation in the α2B-adrenoceptor does not seem to modify the risk for acute myocardial infarction, but may modify the risk for hypertension in sib-pairs from families with type 2 diabetes

被引:15
作者
Snapir, Amir [1 ]
Scheinin, Mika [1 ]
Groop, Leif C. [2 ]
Orho-Melander, Marju [2 ]
机构
[1] Univ Turku, Dept Pharmacol & Clin Pharmacol, FIN-20520 Turku, Finland
[2] Lund Univ, Dept Endocrinol, Malmo Univ Hosp, Wallenberg Lab,Univ Hosp MAS, S-20502 Malmo, Sweden
关键词
Adrenergic; Alpha; 2; Genetics; Hypertension; Myocardial infarction; Polymorphism; Receptors;
D O I
10.1186/1475-2840-2-15
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: An insertion/deletion polymorphism in the alpha(2B)-adrenoceptor (AR) has been associated with the risk for acute myocardial infarction (AMI) and sudden cardiac death. In this study we tested whether this polymorphism is associated with the risk for AMI among members of families with type 2 diabetes. Methods: 154 subjects with a history of AMI were matched for age and sex with one of their siblings who did not have a history of AMI. The prevalence of the genotypes of the alpha(2B)-AR insertion/deletion polymorphism was compared between the siblings using McNemar's test. We also explored the data to see whether this genetic variation affects the risk for hypertension by using logistic regression models in the two subpopulations of subjects, with and without a history of AMI. Results: Among all study subjects, 73 (24%) carried the alpha(2B)-AR deletion/deletion genotype, 103 (33%) carried the insertion/insertion genotype, and 132 (43%) were heterozygous. The distribution of genotypes of the alpha(2B)-AR insertion/deletion variation in the group of subjects with a history of AMI and their phenotype-discordant siblings did not statistically significantly differ from that expected by random distribution (p = 0.52): the deletion/deletion genotype was carried by 34 subjects with AMI (22%), and by 39 subjects without AMI (25%). Neither did we observe any significant difference in deletion allele frequencies of the alpha(2B)-AR insertion/deletion polymorphism between patients with a history of AMI (0.44) and their sib-pair controls (0.46, p = 0.65). In an exploratory analysis, the alpha(2B)-AR deletion/deletion genotype was associated with increased odds for hypertension compared with subjects carrying any of the other genotypes. Conclusions: The deletion/deletion genotype of the alpha(2B)-AR does not emerge in this study as a risk factor for AMI among members of families with type 2 diabetes; however, it might be involved in the development of hypertension.
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页数:6
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