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H1受体拮抗剂对老年人中枢神经系统的影响。

Central nervous system effects of H1-receptor antagonists in the elderly.

作者信息

Simons F E, Fraser T G, Maher J, Pillay N, Simons K J

机构信息

Health Sciences Clinical Research Centre, University of Manitoba, Winnipeg, Canada.

出版信息

Ann Allergy Asthma Immunol. 1999 Feb;82(2):157-60. doi: 10.1016/S1081-1206(10)62590-2.

Abstract

BACKGROUND

The potential adverse central nervous system effects of H1-receptor antagonists have not been optimally studied in the elderly.

OBJECTIVE

We hypothesized that newer H1-receptor antagonists such as cetirizine and loratadine would cause less central nervous system dysfunction than the older H1-receptor antagonists diphenhydramine and chlorpheniramine in this population, as they do in younger subjects.

METHODS

We performed a randomized, double-blind, single-dose, placebo-controlled, 5-way crossover study in 15 healthy elderly subjects (mean age 71 +/- SD 5 years). On study days at least 1 week apart, they received cetirizine 10 mg, loratadine 10 mg, diphenhydramine 50 mg, chlorpheniramine 8 mg, or placebo. Outcome measures, recorded before and 2 to 2.5 hours after dosing were latency of the P300 event-related potential in which increased latency reflects a decreased rate of cognitive processing, visual analogue scale for subjective somnolence, and histamine skin tests for measurement of peripheral H1-blockade.

RESULTS

The changes in P300 following each treatment yielded variances that were not equal (P > .05), precluding usual statistical analysis of the means. These variances were ranked: chlorpheniramine > diphenhydramine > loratadine > placebo > cetirizine. The rank of mean differences in the visual analogue scale increase from pre-dose baseline was: diphenhydramine > chlorpheniramine > cetirizine > loratadine > placebo. All H1-receptor antagonists suppressed the histamine-induced wheal and flare significantly compared to baseline.

CONCLUSION

In the elderly, the new H1-receptor antagonists cetirizine and loratadine are less likely to cause adverse central nervous system effects than the old H1-antagonists chlorpheniramine or diphenhydramine, but this requires confirmation using additional objective tests of central nervous system function.

摘要

背景

H1受体拮抗剂对中枢神经系统的潜在不良影响在老年人中尚未得到充分研究。

目的

我们假设,在这一人群中,与较老的H1受体拮抗剂苯海拉明和氯苯那敏相比,西替利嗪和氯雷他定等新型H1受体拮抗剂引起的中枢神经系统功能障碍更少,就像它们在年轻受试者中那样。

方法

我们对15名健康老年受试者(平均年龄71±标准差5岁)进行了一项随机、双盲、单剂量、安慰剂对照的5种药物交叉研究。在至少间隔1周的研究日,他们分别接受10毫克西替利嗪、10毫克氯雷他定、50毫克苯海拉明、8毫克氯苯那敏或安慰剂。在给药前以及给药后2至2.5小时记录的结果指标包括:P300事件相关电位的潜伏期(潜伏期延长反映认知处理速度减慢)、主观嗜睡视觉模拟量表,以及用于测量外周H1受体阻滞的组胺皮肤试验。

结果

每种治疗后P300的变化产生的方差不相等(P>.05),无法对均值进行常规统计分析。这些方差的排序为:氯苯那敏>苯海拉明>氯雷他定>安慰剂>西替利嗪。视觉模拟量表从给药前基线增加的平均差异排序为:苯海拉明>氯苯那敏>西替利嗪>氯雷他定>安慰剂。与基线相比,所有H1受体拮抗剂均显著抑制了组胺诱导的风团和潮红。

结论

在老年人中,新型H1受体拮抗剂西替利嗪和氯雷他定比老一代H1拮抗剂氯苯那敏或苯海拉明引起中枢神经系统不良反应的可能性更小,但这需要通过额外的中枢神经系统功能客观测试来证实。

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