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ABCB1(P-糖蛋白)单倍型对健康志愿者中美托洛尔药代动力学和美托洛尔引起的体位性低血压的影响。

Influence of ABCB1 (P-glycoprotein) haplotypes on nortriptyline pharmacokinetics and nortriptyline-induced postural hypotension in healthy volunteers.

机构信息

Department of Medicine, University of Otago, Christchurch, New Zealand.

出版信息

Br J Clin Pharmacol. 2012 Apr;73(4):619-28. doi: 10.1111/j.1365-2125.2011.04126.x.

DOI:10.1111/j.1365-2125.2011.04126.x
PMID:21999196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3376438/
Abstract

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT

A single nucleotide polymorphism in ABCB1, which encodes P-glycoprotein, has retrospectively been associated with symptoms of nortriptyline-induced postural hypotension in depressed patients. This finding needs to be replicated in independent studies before recommendations regarding pharmacogenetic testing can be made.

WHAT THIS STUDY ADDS

In a prospective study of healthy volunteers homozygous for ABCB1 (1236-2677-3435, TTT/TTT or CGC/CGC), a single dose of nortriptyline was administered, plasma exposure was determined and blood pressure and heart rate were monitored during posture change. No differences between ABCB1 haplotype groups were found in plasma exposure of nortriptyline and its active metabolites, E- and Z-10-hydroxynortriptyline. The heart rate response to posture change was increased with nortriptyline, whereas there was no difference in blood pressure response. However, no differences between haplotype groups were observed except that the pre dose heart rate response to standing was greater in the TTT than CGC homozygotes. The association between ABCB1 polymorphisms and nortriptyline-induced postural hypotension found in a previous study could not be confirmed. The results raise the possibility of a predisposition in heart rate response in the TTT homozygotes rather than an effect of nortriptyline. AIMS To investigate the influence of ABCB1 (1236-2677-3435) polymorphisms on nortriptyline pharmacokinetics and nortriptyline-induced postural hypotension in healthy volunteers.

METHODS

Genetic screening of 67 healthy volunteers identified eight CGC homozygotes and nine TTT homozygotes of ABCB1 (1236-2677-3435), who were administered a single dose of nortriptyline 25 mg. Plasma exposure of nortriptyline and its active metabolites, E- and Z-10-hydroxynortriptyline, was determined over 72 h. Heart rate and blood pressure responses to posture change (active standing and passive head-up tilt) were measured continuously using finger plethysmography.

RESULTS

There were no differences in plasma exposure between ABCB1 haplotype groups, as the geometric mean (95% CI) AUC(0,72 h) ratios were 0.98 (0.94, 1.03), 1.02 (0.96, 1.09) and 0.95 (0.80, 1.10) for nortriptyline, E- and Z-10-hydroxynortriptyline, respectively. The pre dose heart rate response to standing was greater in the TTT than CGC homozygotes (mean (95% CI) difference 7.4 (1.5, 13.4) beats min(-1) , P = 0.02). At t(max) at 8 h post dose, nortriptyline increased the heart rate response to posture change in all subjects with mean (95% CI) Δ heart rate values of 7.4 (3.6, 11.3) beats min(-1) on active standing (P = 0.0009) and 4.8 (2.0, 7.6) beats min(-1) on head-up tilt (P = 0.002), but no difference was observed between haplotype groups. There was no difference in blood pressure response to posture change in either group.

CONCLUSION

The association between ABCB1 polymorphisms and nortriptyline-induced postural hypotension found in the previous study could not be confirmed. The results raise the possibility of a predisposition in heart rate response in the TTT homozygotes rather than an effect of nortriptyline.

摘要

已知关于此课题的情况

ABCBl 基因编码 P-糖蛋白的一个单核苷酸多态性,在抑郁患者中与反映曲普瑞林引起的直立性低血压的症状相关。在可以做出有关遗传药理学检测的建议之前,需要在独立研究中复制该发现。

本研究的新发现

在一项对 ABCB1(1236-2677-3435,TTT/TTT 或 CGC/CGC)纯合子健康志愿者的前瞻性研究中,给予单剂量曲普瑞林,测定血浆暴露情况,并在体位改变时监测血压和心率。在曲普瑞林及其活性代谢物 E-和 Z-10-羟基曲普瑞林的血浆暴露方面,ABCBl 单倍型组之间没有差异。曲普瑞林引起的心率对体位变化的反应增加,而血压反应没有差异。但是,除了 TTT 同型合子的站立前心率反应大于 CGC 同型合子外,没有观察到单倍型组之间的差异。在之前的研究中发现的 ABCBl 多态性与曲普瑞林引起的直立性低血压之间的关联无法得到证实。研究结果提出了 TTT 纯合子的心率反应倾向而不是曲普瑞林的作用的可能性。

目的

研究 ABCB1(1236-2677-3435)多态性对健康志愿者中曲普瑞林药代动力学和曲普瑞林引起的直立性低血压的影响。

方法

对 67 名健康志愿者进行基因筛查,确定了 8 名 CGC 纯合子和 9 名 TTT 纯合子的 ABCB1(1236-2677-3435),他们给予单剂量 25mg 曲普瑞林。在 72 小时内测定曲普瑞林及其活性代谢物 E-和 Z-10-羟基曲普瑞林的血浆暴露情况。使用手指容积描记法连续测量体位变化(主动站立和被动头高位倾斜)时的心率和血压反应。

结果

ABCBl 单倍型组之间的血浆暴露没有差异,因为曲普瑞林、E-和 Z-10-羟基曲普瑞林的 AUC(0,72h) 比值的几何均数(95%CI)分别为 0.98(0.94,1.03)、1.02(0.96,1.09)和 0.95(0.80,1.10)。TTT 同型合子的站立前心率反应大于 CGC 同型合子(平均(95%CI)差异 7.4(1.5,13.4)次/min,P=0.02)。在 8 小时的剂量后 t(max)时,曲普瑞林在所有受试者中增加了体位变化时的心率反应,平均(95%CI)Δ心率值在主动站立时为 7.4(3.6,11.3)次/min(P=0.0009),在头高位倾斜时为 4.8(2.0,7.6)次/min(P=0.002),但单倍型组之间没有差异。在两组中,体位变化时的血压反应没有差异。

结论

在之前的研究中发现的 ABCBl 多态性与曲普瑞林引起的直立性低血压之间的关联无法得到证实。研究结果提出了 TTT 纯合子的心率反应倾向而不是曲普瑞林的作用的可能性。

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