Pharmacogenetic studies in Alzheimer disease
T Zúñiga Santamaría1, P Yescas Gómez2, I Fricke Galindo3
1Maestría en Ciencias Farmacéuticas, Universidad Autónoma Metropolitana, Unidad Xochimilco, Coyoacán (México D.F.), Mexico; Departamento de Neurogenética, Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Tlalpan (México D.F.), Mexico.
Pharmacogenetic biomarkers for Alzheimer disease (AD) drugs show potential but require more research. Identifying these genetic factors could personalize AD treatment and improve patient outcomes.
Area of Science:
- Pharmacogenetics
- Neuroscience
- Geriatrics
Background:
- Alzheimer disease (AD) is a leading cause of dementia, impacting elderly quality of life.
- Current treatments offer limited efficacy, with only one-third of patients responding.
- Genetic factors influence individual responses to AD medications.
Purpose of the Study:
- To review pharmacogenetic reports on AD-modifying drugs.
- To identify commonly studied biomarkers and phenotypes.
- To discuss methodological considerations for AD pharmacogenetic research.
Main Methods:
- Systematic review of 33 pharmacogenetic reports concerning AD drugs.
- Analysis of pharmacogenetic biomarkers (e.g., CYP2D6, APOE) and evaluated phenotypes.
- Inclusion of studies across diverse populations (Caucasian, Korean, Indian, Brazilian).
Main Results:
- Most studies focused on donepezil response and metabolism variability.
- CYP2D6 and APOE were the most frequently investigated biomarkers.
- Proposed pharmacogenetic associations remain controversial.
Conclusions:
- Pharmacogenetic biomarkers for AD drugs have been identified.
- Further research is needed in diverse populations and for novel biomarkers.
- Personalized treatment strategies for AD could be improved by pharmacogenetics.
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