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Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy
OBJECTIVE: To determine the frequency of pharmacogenomic variants and concurrent medications that may alter the efficacy and tolerability of acetylcholinesterase inhibitors (AChEIs). MATERIALS AND METHODS: A multisite cross-sectional study was carried out across four memory care practices in the gre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298284/ https://www.ncbi.nlm.nih.gov/pubmed/25609939 http://dx.doi.org/10.2147/CIA.S65980 |
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author | Campbell, Noll L Skaar, Todd C Perkins, Anthony J Gao, Sujuan Li, Lang Khan, Babar A Boustani, Malaz A |
author_facet | Campbell, Noll L Skaar, Todd C Perkins, Anthony J Gao, Sujuan Li, Lang Khan, Babar A Boustani, Malaz A |
author_sort | Campbell, Noll L |
collection | PubMed |
description | OBJECTIVE: To determine the frequency of pharmacogenomic variants and concurrent medications that may alter the efficacy and tolerability of acetylcholinesterase inhibitors (AChEIs). MATERIALS AND METHODS: A multisite cross-sectional study was carried out across four memory care practices in the greater Indianapolis area. Participants were adults aged 65 years and older with a diagnosis of probable or possible Alzheimer’s disease (AD) (n=105). Blood samples and self-reported medication data were collected. Since two of the three AChEIs are metabolized by cytochrome P450 (CYP)-2D6, we determined the frequency of functional genetic variants in the CYP2D6 gene and calculated their predicted CYP2D6-activity scores. Concurrent medication data were collected from self-reported medication surveys, and their predicted effect on the pharmacokinetics of AChEIs was determined based on their known effects on CYP2D6 and CYP3A4/5 enzyme activities. RESULTS: Among the 105 subjects enrolled, 72% were female and 36% were African American. Subjects had a mean age of 79.6 years. The population used a mean of eight medications per day (prescription and nonprescription). The CYP2D6 activity score frequencies were 0 (3.8%), 0.5 (4.8%), 1.0 (36.2%), 1.5–2.0 (51.4%), and >2.0 (3.8%). Nineteen subjects (18.1%) used a medication considered a strong or moderate inhibitor of CYP2D6, and eight subjects (7.6%) used a medication considered a strong or moderate inhibitor of CYP3A4/5. In total, 28.6% of the study population was predicted to have reduced activity of the CYP2D6 or CYP3A4/5 enzymes due to either genetic variants or concomitant medications. CONCLUSION: Both pharmacogenetic variants and concurrent drug therapies that are predicted to alter the pharmacokinetics of AChEIs should be evaluated in older adults with AD. Pharmacogenetic and drug-interaction data may help personalize AD therapy and increase adherence by improving tolerability. |
format | Online Article Text |
id | pubmed-4298284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42982842015-01-21 Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy Campbell, Noll L Skaar, Todd C Perkins, Anthony J Gao, Sujuan Li, Lang Khan, Babar A Boustani, Malaz A Clin Interv Aging Original Research OBJECTIVE: To determine the frequency of pharmacogenomic variants and concurrent medications that may alter the efficacy and tolerability of acetylcholinesterase inhibitors (AChEIs). MATERIALS AND METHODS: A multisite cross-sectional study was carried out across four memory care practices in the greater Indianapolis area. Participants were adults aged 65 years and older with a diagnosis of probable or possible Alzheimer’s disease (AD) (n=105). Blood samples and self-reported medication data were collected. Since two of the three AChEIs are metabolized by cytochrome P450 (CYP)-2D6, we determined the frequency of functional genetic variants in the CYP2D6 gene and calculated their predicted CYP2D6-activity scores. Concurrent medication data were collected from self-reported medication surveys, and their predicted effect on the pharmacokinetics of AChEIs was determined based on their known effects on CYP2D6 and CYP3A4/5 enzyme activities. RESULTS: Among the 105 subjects enrolled, 72% were female and 36% were African American. Subjects had a mean age of 79.6 years. The population used a mean of eight medications per day (prescription and nonprescription). The CYP2D6 activity score frequencies were 0 (3.8%), 0.5 (4.8%), 1.0 (36.2%), 1.5–2.0 (51.4%), and >2.0 (3.8%). Nineteen subjects (18.1%) used a medication considered a strong or moderate inhibitor of CYP2D6, and eight subjects (7.6%) used a medication considered a strong or moderate inhibitor of CYP3A4/5. In total, 28.6% of the study population was predicted to have reduced activity of the CYP2D6 or CYP3A4/5 enzymes due to either genetic variants or concomitant medications. CONCLUSION: Both pharmacogenetic variants and concurrent drug therapies that are predicted to alter the pharmacokinetics of AChEIs should be evaluated in older adults with AD. Pharmacogenetic and drug-interaction data may help personalize AD therapy and increase adherence by improving tolerability. Dove Medical Press 2015-01-14 /pmc/articles/PMC4298284/ /pubmed/25609939 http://dx.doi.org/10.2147/CIA.S65980 Text en © 2015 Campbell et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Campbell, Noll L Skaar, Todd C Perkins, Anthony J Gao, Sujuan Li, Lang Khan, Babar A Boustani, Malaz A Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title | Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title_full | Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title_fullStr | Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title_full_unstemmed | Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title_short | Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
title_sort | characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298284/ https://www.ncbi.nlm.nih.gov/pubmed/25609939 http://dx.doi.org/10.2147/CIA.S65980 |
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