Genotype-Guided Hydralazine Therapy

被引:19
作者
Collins, Kimberly S. [1 ]
Raviele, Anthony L. J. [1 ]
Elchynski, Amanda L. [2 ]
Woodcock, Alexander M. [1 ]
Zhao, Yang [2 ]
Cooper-DeHoff, Rhonda M. [2 ]
Eadon, Michael T. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Med, 950 W Walnut St E202, Indianapolis, IN 46202 USA
[2] Univ Florida, Dept Pharmacotherapy & Translat Res, Gainesville, FL USA
关键词
Hydralazine; N-acetyltransferase; 2; Pharmacogenetics; Resistant hypertension; ARYLAMINE N-ACETYLTRANSFERASE; N-ACETYLTRANSFERASE-2; NAT2; POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISMS; ACETYLATOR PHENOTYPE; ANTIHYPERTENSIVE RESPONSE; PLASMA-CONCENTRATION; BLOOD-PRESSURE; SLOW; ASSOCIATION; CONCORDANCE;
D O I
10.1159/000510433
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Despite its approval in 1953, hydralazine hydrochloride continues to be used in the management of resistant hypertension, a condition frequently managed by nephrologists and other clinicians. Hydralazine hydrochloride undergoes metabolism by the N-acetyltransferase 2 (NAT2) enzyme. NAT2 is highly polymorphic as approximately 50% of the general population are slow acetylators. In this review, we first evaluate the link between NAT2 genotype and phenotype. We then assess the evidence available for genotype-guided therapy of hydralazine, specifically addressing associations of NAT2 acetylator status with hydralazine pharmacokinetics, antihypertensive efficacy, and toxicity. Summary: There is a critical need to use hydralazine in some patients with resistant hypertension. Available evidence supports a significant link between genotype and NAT2 enzyme activity as 29 studies were identified with an overall concordance between genotype and phenotype of 92%. The literature also supports an association between acetylator status and hydralazine concentration, as fourteen of fifteen identified studies revealed significant relationships with a consistent direction of effect. Although fewer studies are available to directly link acetylator status with hydralazine antihypertensive efficacy, the evidence from this smaller set of studies is significant in 7 of 9 studies identified. Finally, 5 studies were identified which support the association of acetylator status with hydralazine-induced lupus. Clinicians should maintain vigilance when prescribing maximum doses of hydralazine. Key Messages: NAT2 slow acetylator status predicts increased hydralazine levels, which may lead to increased efficacy and adverse effects. Caution should be exercised in slow acetylators with total daily hydralazine doses of 200 mg or more. Fast acetylators are at risk for inefficacy at lower doses of hydralazine. With appropriate guidance on the usage of NAT2 genotype, clinicians can adopt a personalized approach to hydralazine dosing and prescription, enabling more efficient and safe treatment of resistant hypertension.
引用
收藏
页码:764 / 776
页数:13
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