Ramsay L E, Silas J H, Ollerenshaw J D, Tucker G T, Phillips F C, Freestone S
Eur J Clin Pharmacol. 1984;26(1):39-42. doi: 10.1007/BF00546706.
The role of acetylator phenotype in determining the response to hydralazine when it was added to diuretic and beta-blocker at doses not exceeding 200 mg daily was examined in 57 hypertensive patients. 81% of rapid acetylators needed 200 mg hydralazine daily compared to 38% of slow acetylators (p less than 0.01). Despite higher doses of hydralazine the blood pressure was controlled in only 27% of rapid acetylators compared to 65% of slow acetylators (p less than 0.02). The relation of acetylator phenotype to blood pressure response was statistically independent of initial blood pressure, age, sex, body weight and serum creatinine (p less than 0.005). Current recommendations on hydralazine dosage are unsatisfactory for the 40% of hypertensive patients who are rapid acetylators. We suggest measurement of the acetylator phenotype in patients who respond incompletely to 200 mg hydralazine daily. About 70% of these patients will be rapid acetylators in whom the dose of hydralazine can be increased safely.
在57例高血压患者中,研究了乙酰化表型在决定每日剂量不超过200 mg的肼屈嗪与利尿剂和β受体阻滞剂联用时反应情况中的作用。81%的快速乙酰化者每日需要200 mg肼屈嗪,而慢速乙酰化者为38%(p<0.01)。尽管使用了更高剂量的肼屈嗪,但快速乙酰化者中只有27%的血压得到控制,而慢速乙酰化者为65%(p<0.02)。乙酰化表型与血压反应的关系在统计学上独立于初始血压、年龄、性别、体重和血清肌酐(p<0.005)。目前关于肼屈嗪剂量的建议对于40%的快速乙酰化高血压患者并不令人满意。我们建议对每日服用200 mg肼屈嗪反应不完全的患者进行乙酰化表型检测。这些患者中约70%将是快速乙酰化者,其肼屈嗪剂量可安全增加。