Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy

被引:9
作者
Campbell, Noll L. [1 ,4 ]
Skaar, Todd C. [5 ]
Perkins, Anthony J. [2 ]
Gao, Sujan [2 ,3 ,6 ]
Li, Lang [7 ]
Khan, Babar A. [2 ,3 ,5 ]
Boustani, Malaz A. [2 ,3 ,8 ]
机构
[1] Purdue Univ, Coll Pharm, W Lafayette, IN 47907 USA
[2] Indiana Univ, Ctr Aging Res, Indianapolis, IN 46204 USA
[3] Indiana Univ, Regenstrief Inst, Indianapolis, IN 46204 USA
[4] Indiana Univ, Eskenazi Hlth Serv, Dept Pharm, Indianapolis, IN 46204 USA
[5] Indiana Univ, Dept Med, Div Clin Pharmacol, Indianapolis, IN 46204 USA
[6] Indiana Univ, Dept Biostat, Indianapolis, IN 46204 USA
[7] Indiana Univ, Sch Med, Dept Med & Mol Genet, Indianapolis, IN 46204 USA
[8] Indiana Univ, Ctr Innovat & Implementat Sci, Indianapolis, IN 46204 USA
基金
美国医疗保健研究与质量局;
关键词
dementia; acetylcholinesterase inhibitor; pharmacogenomics; ALZHEIMERS-DISEASE; CHOLINESTERASE-INHIBITORS; CYP2D6; POLYMORPHISM; CONCOMITANT USE; ANTICHOLINERGICS; DONEPEZIL; GENOTYPES; PERSISTENCE; RS1080985; DRUGS;
D O I
10.2147/CIA.S65980
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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.
引用
收藏
页码:269 / 275
页数:7
相关论文
共 33 条
[1]   Replication Study to Confirm the Role of CYP2D6 Polymorphism rs1080985 on Donepezil Efficacy in Alzheimer's Disease Patients [J].
Albani, Diego ;
Boneschi, Filippo Martinelli ;
Biella, Gloria ;
Giacalone, Giacomo ;
Lupoli, Sara ;
Clerici, Francesca ;
Benussi, Luisa ;
Ghidoni, Roberta ;
Galimberti, Daniela ;
Squitti, Rosanna ;
Mariani, Stefania ;
Confaloni, Annamaria ;
Bruno, Giuseppe ;
Mariani, Claudio ;
Scarpini, Elio ;
Binetti, Giuliano ;
Magnani, Giuseppe ;
Franceschi, Massimo ;
Forloni, Gianluigi .
JOURNAL OF ALZHEIMERS DISEASE, 2012, 30 (04) :745-749
[2]   Persistence with cholinesterase inhibitor therapy in a population based cohort of patients with Alzheimer's disease [J].
Amuah, Joseph E. ;
Hogan, David B. ;
Eliasziw, Misha ;
Supina, Alison ;
Beck, Patricia ;
Downey, Winanne ;
Maxwell, Colleen J. .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2010, 19 (07) :670-679
[3]  
[Anonymous], 2013, AR PRESCR INF
[4]  
Bachus R, 1999, PHARMACOGENETICS, V9, P661
[5]  
Birks J, 2006, COCHRANE DB SYST REV, DOI [10.1002/14651858.CD001190.pub2, 10.1002/14651858.CD001190.pub3]
[6]   Concomitant Use of Cholinesterase Inhibitors and Anticholinergics: Prevalence and Outcomes [J].
Boudreau, Denise M. ;
Yu, Onchee ;
Gray, Shelly L. ;
Raebel, Marsha A. ;
Johnson, Jeanene ;
Larson, Eric B. .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2011, 59 (11) :2069-2076
[7]  
Boustani M., 2008, Aging Health, V4, P311, DOI [DOI 10.2217/1745509X.4.3.311, 10.2217/1745509X.4.3.311, 10.2217/1745509XA3.311]
[8]   Connecting research discovery with care delivery in dementia: the development of the Indianapolis Discovery Network for Dementia [J].
Boustani, Malaz A. ;
Frame, Amie ;
Munger, Stephanie ;
Healey, Patrick ;
Westlund, Jessie ;
Farlow, Martin ;
Hake, Ann ;
Austrom, Mary Guerriero ;
Shepard, Polly ;
Bubp, Corby ;
Azar, Jose ;
Nazir, Arif ;
Adams, Nadia ;
Campbell, Noll L. ;
Chehresa, Azita ;
Dexter, Paul .
CLINICAL INTERVENTIONS IN AGING, 2012, 7 :509-516
[9]   A population-based study of dosing and persistence with anti-dementia medications [J].
Brewer, Linda ;
Bennett, Kathleen ;
McGreevy, Cora ;
Williams, David .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2013, 69 (07) :1467-1475
[10]   Long-term anticholinergic use and the aging brain [J].
Cai, Xueya ;
Campbell, Noll ;
Khan, Babar ;
Callahan, Christopher ;
Boustani, Malaz .
ALZHEIMERS & DEMENTIA, 2013, 9 (04) :377-385