Greer Murphy M.D., Ph.D.

Publication Details

  • Potential ethnic modifiers in the assessment and treatment of Alzheimer's disease: challenges for the future INTERNATIONAL PSYCHOGERIATRICS Faison, W. E., Schultz, S. K., Aerssens, J., Alvidrez, J., Anand, R., Farrer, L. A., Jarvik, L., Manly, J., McRae, T., Murphy, G. M., Olin, J. T., Regier, D., Son, M., Mintzer, J. E. 2007; 19 (3): 539-558


    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?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.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.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.

    View details for DOI 10.1017/S104161020700511X

    View details for Web of Science ID 000246984800016

    View details for PubMedID 17451614

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