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肯尼亚肯雅塔国家医院使用肼苯哒嗪治疗非洲高血压患者的乙酰化状态。

Acetylation status using hydralazine in African hypertensives at Kenyatta National Hospital.

作者信息

Rashid J R, Juma F D

机构信息

Clinical Research Centre, Nairobi.

出版信息

East Afr Med J. 1992 Jul;69(7):406-8.

PMID:1396201
Abstract

In this study, the investigation of hydralazine acetylator phenotype was undertaken for the first time in African hypertensives at Kenyatta National Hospital. A total of 25 randomly selected patients with moderate to severe hypertension (diastolic pressure 105-130 mmHg), participated in the phenotyping study. The phenotyping was done by administering oral standard hydralazine dose of 150 mg/day in three divided doses. The 24 hour urinary MTP/hydralazine ratio was used to categorize patients into slow and fast acetylators. Of the patients studied 69.9% were slow acetylators while 30.4% were fast acetylators. The mean 24 hour urinary MTP/hydralazine ratio for slow acetylators was 1.01 +/- 0.95. This was significantly different from the fast acetylators where the mean 24 hour urinary MTP/hydralazine ratio was 10.6 +/- 4.4 (P < 0.001). The acetylator phenotyping divided the patients into two distinct populations and no further arbitrary method was required to divide the patients into either group.

摘要

在本研究中,首次在肯尼亚肯雅塔国家医院对非洲高血压患者进行了肼屈嗪乙酰化酶表型研究。总共25名随机选择的中度至重度高血压患者(舒张压105 - 130 mmHg)参与了表型研究。表型分析通过口服标准剂量的肼屈嗪150 mg/天,分三次给药进行。24小时尿中对甲酚/肼屈嗪比值用于将患者分为慢乙酰化者和快乙酰化者。在研究的患者中,69.9%是慢乙酰化者,而30.4%是快乙酰化者。慢乙酰化者的平均24小时尿中对甲酚/肼屈嗪比值为1.01±0.95。这与快乙酰化者有显著差异,快乙酰化者的平均24小时尿中对甲酚/肼屈嗪比值为10.6±4.4(P < 0.001)。乙酰化酶表型分析将患者分为两个不同的群体,无需进一步采用任意方法将患者分为两组。

相似文献

1
Acetylation status using hydralazine in African hypertensives at Kenyatta National Hospital.肯尼亚肯雅塔国家医院使用肼苯哒嗪治疗非洲高血压患者的乙酰化状态。
East Afr Med J. 1992 Jul;69(7):406-8.
2
Different phenotypes of the NAT2 gene influences hydralazine antihypertensive response in patients with resistant hypertension.NAT2基因的不同表型影响顽固性高血压患者的肼屈嗪降压反应。
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The influence of the acetylator phenotype for the clinical use of dihydralazine.
Int J Clin Pharmacol Ther Toxicol. 1985 Apr;23 Suppl 1:S74-8.
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Hydralazine in arterial hypertension. Randomized double-blind comparison of conventional/Slow-Release formulation and of b.i.d./q.i.d. dosage regimens.肼屈嗪治疗动脉高血压。传统/缓释剂型与每日两次/每日四次给药方案的随机双盲比较。
Acta Med Scand. 1980;208(1-2):49-54.
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Should the acetylator phenotype be determined when prescribing hydralazine for hypertension?在为高血压患者开肼屈嗪处方时,是否应该确定乙酰化代谢表型?
Eur J Clin Pharmacol. 1984;26(1):39-42. doi: 10.1007/BF00546706.
6
Metabolism of hydralazine in man. Part II: Investigation of features relevant to drug safety.肼屈嗪在人体中的代谢。第二部分:与药物安全性相关特征的研究。
Arzneimittelforschung. 1987 Feb;37(2):189-93.
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Dihydralazine therapy and acetylator phenotype.
Int J Clin Pharmacol Biopharm. 1979 Mar;17(3):119-24.
8
Genetically determined variability in acetylation and oxidation. Therapeutic implications.乙酰化和氧化的基因决定变异性。治疗意义。
Drugs. 1985 Apr;29(4):342-75. doi: 10.2165/00003495-198529040-00003.
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Effect of dose on acetylator phenotype distribution of hydralazine.
Clin Pharmacol Ther. 1981 Mar;29(3):337-43. doi: 10.1038/clpt.1981.46.
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Propranolol-hydralazine combination in essential hypertension.普萘洛尔 - 肼屈嗪联合用药治疗原发性高血压
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引用本文的文献

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Genotype-Guided Hydralazine Therapy.基因型指导下的肼屈嗪治疗。
Am J Nephrol. 2020;51(10):764-776. doi: 10.1159/000510433. Epub 2020 Sep 14.
2
Effect of N-Acetyltransferase 2 Genotype on the Pharmacokinetics of Hydralazine During Pregnancy.乙酰转移酶 2 基因型对妊娠期肼屈嗪药代动力学的影响。
J Clin Pharmacol. 2019 Dec;59(12):1678-1689. doi: 10.1002/jcph.1477. Epub 2019 Jun 30.
3
PharmGKB summary: very important pharmacogene information for N-acetyltransferase 2.药物基因组知识库总结:N-乙酰转移酶2的非常重要的药物基因信息。
Pharmacogenet Genomics. 2014 Aug;24(8):409-25. doi: 10.1097/FPC.0000000000000062.