Frequency of genetic polymorphism for adrenergic receptor beta and cytochrome p450 2D6 enzyme, and effects on tolerability of beta-blocker therapy in heart failure with reduced ejection fraction patients: The Beta GenTURK study

被引:2
作者
Zoghi, Mehdi [1 ]
Kaya, Hakki [2 ]
Cavusoglu, Yuksel [3 ]
Aksakal, Enbiya [4 ]
Demir, Serafettin [5 ]
Yucel, Ceyhun [6 ]
Mutlu, Hasim [7 ]
Ergene, Oktay
Yilmaz, Mehmet Birhan [2 ,8 ]
机构
[1] Ege Univ, Dept Cardiol, Fac Med, Izmir, Turkey
[2] Cumhuriyet Univ, Fac Med, Dept Cardiol, Sivas, Turkey
[3] Osmangazi Univ, Fac Med, Dept Cardiol, Eskisehir, Turkey
[4] Ataturk Univ, Fac Med, Dept Cardiol, Erzurum, Turkey
[5] Cukurova Univ, Fac Med, Dept Cardiol, Adana, Turkey
[6] Cukurova Univ, Fac Med, Balcali Hosp, Dept Cardiol, Adana, Turkey
[7] Istanbul Univ, Fac Med, Dept Cardiol, Istanbul, Turkey
[8] Ataturk Training & Res Hosp, Dept Cardiol, Izmir, Turkey
来源
TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY | 2016年 / 44卷 / 06期
关键词
Functional capacity; heart failure; medical adherence; socioeconomic status;
D O I
10.5543/tkda.2016.10733
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The present objective was to determine frequency of Arginine389Glycine (Arg389Gly) and Cytochrome p450 2D6*10 (Cyp2D6*10) polymorphism in cases of heart failure-reduced ejection fraction (HFREF), and to evaluate the influence of the polymorphisms in response to beta-blocker (BB) therapy. Methods: A total of 206 HFREF patients and 90 healthy controls were prospectively enrolled. Genotypes for Arg389Gly and Cyp2D6*10 polymorphisms of the healthy controls and 162 of the 206 heart failure (HF) patients were measured, identified by polymerase-chain-reaction-and restriction-fragment-length-polymorphism analysis. HFREF patients and healthy controls were compared regarding Arg389Gly polymorphism. The HFREF patients were separated into 2 subgroups based on achievement of maximal target dose (MTD) of BB. Results: When comparing frequency of genotype distribution for Arg389Gly polymorphism in HFREF patients to the healthy controls, a statistically significant association was observed with CC genotype and Glisin-Glisin (GG) genotype (p<0.001, odds ratio [OR]=16, confidence interval [CI]: 3.8-67.9 and p<0.001, OR=0.3, CI: 0.2-0.6). Frequency of genotypes for Arg389Gly and Cyp2D6* 10 polymorphism were similar in patients who could or could not achieve BB MTD (p=0.13 and p=0.60, respectively). Conclusion: The frequency of Arg389Gly polymorphism in patients with HFREF in the present Turkish population differed from that of the healthy controls. However, neither Arg389Gly polymorphism nor Cyp2D6* 10 polymorphism was associated with dose tolerability of BB therapy.
引用
收藏
页码:457 / 465
页数:9
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