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阿尔茨海默病评估与治疗中的潜在种族修饰因素:未来的挑战

Potential ethnic modifiers in the assessment and treatment of Alzheimer's disease: challenges for the future.

作者信息

Faison Warachal E, Schultz Susan K, Aerssens Jeroen, Alvidrez Jennifer, Anand Ravi, Farrer Lindsay A, Jarvik Lissy, Manly Jennifer, McRae Thomas, Murphy Greer M, Olin Jason T, Regier Darrel, Sano Mary, Mintzer Jacobo E

机构信息

Alzheimer's Research and Clinical Programs, Neurosciences Department, Medical University of South Carolina, Charleston, South Carolina 29406, USA.

出版信息

Int Psychogeriatr. 2007 Jun;19(3):539-58. doi: 10.1017/S104161020700511X. Epub 2007 Apr 23.

Abstract

OBJECTIVE

Despite numerous clinical trials, it is unknown whether ethnicity affects treatment response to cognitive enhancers in Alzheimer's disease (AD). There is convincing evidence of ethnic and genetic variability in drug metabolism. This article reviews the available data on ethnicity in clinical trials for AD to answer two questions: (1) what are the challenges to diagnose and treat AD across different ethnic groups, and (2) are there differences in response to pharmacologic interventions for AD across these different ethnic groups?

METHOD

Available data from Alzheimer's Disease Cooperative Study (ADCS) randomized controlled clinical trials and from randomized controlled industry-sponsored trials for four cognitive enhancers (donepezil, galantamine, rivastigmine and sabeluzole) were pooled to assess the numbers of non-Caucasian participants.

RESULTS

The participation of ethnic minority subjects in clinical trials for AD was dependent on the funding source, although Caucasian participants were over-represented and non-Caucasian participants were under-represented in the clinical trials. Because of the low participation rate of ethnic minorities, there were insufficient data to assess any differences in treatment outcome among different ethnic groups. Strategies to improve diversity in clinical trials are discussed.

CONCLUSION

Greater participation of ethnically diverse participants in clinical trials for AD would generate additional information on possible differences in metabolism, treatment response, adverse events to therapeutic agents, and could foster the investigation of genetic variability among ethnic groups.

摘要

目的

尽管进行了大量临床试验,但尚不清楚种族是否会影响阿尔茨海默病(AD)患者对认知增强剂的治疗反应。有令人信服的证据表明药物代谢存在种族和基因差异。本文回顾了AD临床试验中有关种族的现有数据,以回答两个问题:(1)跨不同种族诊断和治疗AD面临哪些挑战?(2)这些不同种族对AD药物干预的反应是否存在差异?

方法

汇总阿尔茨海默病合作研究(ADCS)随机对照临床试验以及四项认知增强剂(多奈哌齐、加兰他敏、卡巴拉汀和沙贝鲁唑)的行业赞助随机对照试验的现有数据,以评估非白种人参与者的数量。

结果

少数族裔受试者参与AD临床试验的情况取决于资金来源,尽管在临床试验中白种人参与者占比过高,而非白种人参与者占比过低。由于少数族裔的参与率较低,没有足够的数据来评估不同种族之间的治疗结果差异。文中讨论了提高临床试验多样性的策略。

结论

不同种族的参与者更多地参与AD临床试验,将产生关于代谢、治疗反应、治疗药物不良事件可能存在的差异的更多信息,并有助于开展种族间基因差异的研究。

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