Characterization of hepatic enzyme activity in older adults with dementia: potential impact on personalizing pharmacotherapy
Authors Campbell N, Skaar T, Perkins A, Gao S, Li L, Khan B, Boustani M
Received 11 April 2014
Accepted for publication 12 July 2014
Published 14 January 2015 Volume 2015:10 Pages 269—275
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Noll L Campbell,1–4 Todd C Skaar,5 Anthony J Perkins,2 Sujuan Gao,2,3,6 Lang Li,7 Babar A Khan,2,3,5 Malaz A Boustani2,3,8
1College of Pharmacy, Purdue University, West Lafayette, 2Indiana University Center for Aging Research, 3Regenstrief Institute, 4Department of Pharmacy, Eskenazi Health Services, 5Division of Clinical Pharmacology, Department of Medicine, 6Department of Biostatistics, 7Department of Medical and Molecular Genetics, Indiana University School of Medicine, 8Center for Innovation and Implementation Science, Indiana University, Indianapolis, IN, USA
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.
Keywords: dementia, acetylcholinesterase inhibitor, pharmacogenomics
Acetylcholinesterase inhibitors (AChEIs) are the primary pharmacologic treatment for Alzheimer’s disease (AD). These medications do not alter the natural course of the disease, but they are believed to offer minor improvement in cognitive, functional, and behavioral symptoms associated with AD.1,2 Efficacy of the AChEIs may be modified by several factors, including stage of dementia, rate of cognitive decline, medication dose, and titration schedule.1,3 Adverse effects related to their procholinergic mechanisms often limit the tolerability of these medications, with nearly a third of patients discontinuing treatment due to adverse effects such as nausea, vomiting, and diarrhea.1 Because of the marginal benefit and adverse effect profile, as many as 40% of AD patients discontinue treatment with AChEIs.4–6
Two factors that may contribute to the tolerability of AChEIs in AD patients are drug–drug interactions and pharmacogenomics. Because of the frequent burden of chronic comorbid disease in the older adult population, many AD patients are routinely prescribed at least five medications, and consume additional over-the-counter medications.7,8 Many of these coadministered medications cause drug interactions either through altering the activities of the hepatic drug-metabolizing enzymes9 or by pharmacodynamic properties suspected to limit the efficacy of AChEIs.10,11 Recent evidence highlights the mechanisms of drug interactions resulting from altered pharmacokinetics through hepatic metabolism.12 The specific enzymes involved in the metabolism of medications used in AD, specifically donepezil and galantamine, are cytochrome P450 (CYP) 2D6 and 3A4/3A5 (CYP3A4/5) enzymes.13,14 The metabolism of donepezil and galantamine may be influenced by either pharmacogenomic variants or comedications, and these variables may be used to identify those at higher risk of intolerable adverse effects.
Pharmacogenomic variants have been associated with altered pharmacokinetics of donepezil and galantamine.15–17 Consequently, both comedications, as well as genetic variations in the drug-metabolizing enzymes, may be important factors contributing to the interindividual variability in the efficacy and tolerability of AChEIs. Prior literature has reported conflicting results when determining the relationship between genetic variations and efficacy outcomes with AChEIs in AD;18–21 however, to our knowledge, no published data have described the influence of both pharmacogenomic variants or drug–drug interactions on efficacy or tolerability outcomes.15
Our objective in this study was to determine the frequency of pharmacogenomic variants and potential drug interactions that may influence the pharmacokinetics of AChEIs, and ultimately efficacy and tolerability, in older adults with AD. Using CYP2D6 enzyme activity to guide dosing strategies has been shown to improve tolerability with several medications, including antidepressants and antipsychotics.22 Personalizing pharmacotherapy could be an approach to improve medication adherence by optimizing efficacy and improving tolerability profiles. We focused on the metabolic factors that are expected to alter medication exposure for donepezil and galantamine, since both are metabolized by hepatic CYP2D6 and CYP3A4/5 enzymes. We hypothesized that the presence of a high frequency of pharmacogenomic variants and drug interactions for AChEIs would support the need to pursue focused approaches to personalize pharmacotherapy and optimize efficacy-to-toxicity ratios for these vulnerable populations.
Materials and methods
Population and setting
The subjects included in this study were the first 105 subjects enrolled in a multisite randomized clinical trial (ClinicalTrials.gov identifier: NCT01362686) to compare the tolerability of AChEIs in older adults with a diagnosis of AD.23 The study enrolled patients cared for in a memory care practice from one of four health care systems within the Indianapolis Discovery Network for Dementia.24 The study was approved by the institutional review boards for each health care system, including Indiana University–Purdue University of Indianapolis, the St Vincent Health System, and the Community Health Network. All enrolled participants provided informed consent through a legally authorized representative.
Eligible participants included those diagnosed with possible or probable AD for whom the provider was planning to initiate therapy with AChEIs. Inclusion criteria also required agreement from an informal caregiver to complete study-outcome assessments, access to a telephone, and the ability to understand English. Exclusion criteria consisted of current exposure to an AChEI or prior exposure that resulted in an adverse effect requiring drug discontinuation.
Medication data were collected by telephone interview through caregivers of study participants. Caregivers were asked to provide all medications the participant was taking at the time of the interview, including all prescription and over-the-counter medications. Medications were classified as prescription or over the counter by a clinical pharmacist (NLC) according to marketing status, as approved by the US Food and Drug Administration. Medications with CYP enzyme inhibitor or inducer status were identified using the Indiana University Department of Clinical Pharmacology drug-interaction table.9 This resource has been previously used to identify clinically relevant drug interactions and metabolic pathways.25 Only medications identified as strong or moderate inhibitors were classified as enzyme inhibitors.
Additionally, medications were identified to have either possible or definite anticholinergic properties based on the Anticholinergic Cognitive Burden (ACB) scale.26 Medications with anticholinergic properties block the action of acetylcholine at muscarinic receptors, opposing the intended therapeutic effect of the AChEIs. Medications with possible anticholinergic effects were defined as those with serum anticholinergic activity or in vitro affinity to muscarinic receptors, but with no known clinically relevant negative cognitive effects (score of 1 on the ACB scale). Drugs with established and clinically relevant cognitive anticholinergic effects were considered definite anticholinergics (score of 2 or 3 on the ACB scale). The ACB scale has been previously used to identify medications correlated with a higher risk of incident cognitive impairment.27,28
Blood samples for genotyping were collected in 10 mL ethylenediaminetetraacetic acid Vacutainer tubes at the time of enrollment into the study. Deoxyribonucleic acid (DNA) was extracted from whole blood using the AutoGenFlex Star automated DNA extractor (AutoGen, Holliston, MA, USA) using the AGF FlexiGene and Blood DNA Finishing Kit (AutoGen) in the Indiana University sample-storage facility DNA-extraction service. Because polymorphic variants are infrequent in CYP3A4/5, we analyzed the CYP2D6 gene variants and not the CYP3A4/5 variants.
CYP2D6-genotyping and -activity scores
The CYP2D6 genotypes were determined for alleles CYP2D6*1, *2, *3, *4, *5, *6, *10, *17, *29, and *41 using TaqMan® assays.29 The genotyping results for each subject were converted to predicted CYP2D6-activity scores as previously described.30 Briefly, each subject’s activity score is the sum of the activities assigned to each of the subject’s two alleles. The wild-type full-activity alleles (*1, *2) were given a score of 1 each, the reduced function alleles (*10, *17, *29, *41) were given a score of 0.5, and the nonfunctional alleles (*3, *4, *5, *6) were given a score of 0. In the case of subjects with multiple copies (more than two), the multiple-copy allele was multiplied by two and then added to the second * allele. Therefore, the predicted CYP2D6-activity scores ranged from 0 to 3. If the subjects were taking a moderate CYP2D6 inhibitor, their genetic score was multiplied by 0.5, and if they were taking a strong inhibitor, they were given a score of 0 to arrive at the predicted CYP2D6-activity score.
We report descriptive results of the population for the purposes of reporting frequencies of pharmacogenomic variants and drug interactions from concurrent medications that are expected to influence the AD drug pharmacokinetics in this population of older adults with AD. Continuous variables are presented as means and standard deviations, with categorical variables presented in percentages. Because our analysis was not focused on the number or type of comorbidities, but rather the number of concomitant medications used by study subjects, we report the number of prescription and over-the-counter medications as a surrogate marker of comorbidity.31
The study population included the first 105 subjects enrolled in the clinical trial for whom we had both medication data and pharmacogenomic genotyping results available for analysis. The subjects were mostly female (72%), were mixed in educational level (28% with less than high school education), and had a diverse racial background (36% African Americans). The population used a mean of approximately eight medications per day, including both prescription and over-the-counter medications. Forty-four (41.9%) of the subjects were taking at least nine concurrent medications. Only 8% of subjects cared for in memory care practices used a medication with strong anticholinergic properties (Table 1).
Table 1 Descriptive report of population characteristics and medications
Pharmacogenomic analysis revealed four subjects (3.8%) with a CYP2D6-activity score of 0, predicting poor metabolizer phenotypes with no CYP2D6 metabolic activity. Forty-three subjects (40.9%) had activity scores of 0.5 or 1.0, predicting intermediate metabolizer phenotypes. Fifty-four subjects (51.4%) had activity scores of 1.5 or 2.0, predicting extensive metabolizers, and the remaining four subjects (3.8%) had activity scores greater than 2.0, predicting ultrarapid metabolizer phenotypes. The specific CYP2D6 allele frequencies and Hardy–Weinberg values are available in Table S1.
Results of the medication review showed that 19 subjects (18.1%) were using a medication considered a moderate or strong inhibitor of CYP2D6, and eight subjects (7.6%) were taking a medication considered a moderate inhibitor of CYP3A4/5. Eleven subjects (10.5%) were users of a moderate or strong inhibitor of CYP2D6 that reduced activity scores to poor metabolizer status (Table 2). The majority of the CYP2D6 inhibitors used were sertraline and duloxetine, both considered moderate inhibitors of the CYP2D6 enzyme (Tables 2 and S2). The major inhibitor of CYP3A4/5 used by the study subjects was diltiazem, a moderate inhibitor of CYP3A4/5 (Tables 2 and S2). Additionally, 34.3% were using at least one CYP2D6 substrate, and 59.0% were using at least one CYP3A4/5 substrate (Table S2).
Because hepatically metabolized AChEIs utilize both the CYP2D6 and CYP3A4/5 metabolic pathways, we quantified the number of subjects with reduced activity of either CYP2D6 or CYP3A4/5 due to either pharmacogenomic characteristics or concomitant medications acting as moderate or strong enzyme inhibitors. Our results indicate that approximately 29% of our study population would have reduced activity of either CYP2D6 or CYP3A4/5 activity due to either pharmacogenomic variants or concomitant medications (Table 2). Two of the subjects (1.9%) were predicted to have reduced activity of both CYP2D6 and CYP3A4/5 (Table 2).
Our study found that more than a quarter of our AD patients (~29%) were poor metabolizers of AChEIs, due to pharmacogenomic variants or the presence of drug–drug interactions. These findings may partially explain the high rate of adverse events limiting the chronic use of AChEIs. The population included in this analysis represented a real-world sample of older adults enrolled from four health care systems, including a low-income safety-net health care system. The sample reflects a more normal distribution of educational status and racial diversity than what is commonly enrolled in AD studies conducted within purely academic medical centers and AD research centers. Therefore, the suggestion that both pharmacogenomic characteristics and concomitant medications may contribute to differences in tolerability of AChEIs should apply to the majority of the US population with dementia. In our sample, the number of participants using a medication that reduced hepatic enzyme activity was two times higher than the number of subjects with pharmacogenomic causes for reduced enzyme activity.
Recent work in older adults with AD has shown conflicting results on the association of pharmacogenomic characteristics with clinical efficacy of AChEIs.20,21 The sources of variability in previously published literature are derived from different durations of treatment, definitions of efficacy outcomes, and populations with varying degrees of disease severity. The majority of the work associating pharmacogenomic characteristics with clinical outcomes in AD have focused on the efficacy of AChEIs, not tolerability.14,20,21 Whether the activity of CYP2D6 enzymes has an impact on efficacy remains an important outcome to determine; however, we believe tolerability should also be pursued as an important clinical outcome. As stated in the Background section, a clinically significant number of patients prescribed AChEIs discontinue these medications, in part because of poor tolerability. Among those categorized as poor metabolizers, and perhaps even intermediate metabolizers, higher serum concentrations of AChEIs may be more likely to induce an adverse effect than any therapeutic benefit of the medication. Whether clinical efficacy is improved with higher serum concentrations remains controversial, but improving tolerability may result in improved medication adherence and better efficacy outcomes.
Our findings that nearly 30% of older adults with AD may be poor metabolizers of two AChEIs should be validated with adverse-event data in clinical trials. We were not able to include clinical correlation with tolerability, because the clinical trial is ongoing and adverse events are a primary study outcome. Future studies and analyses from existing data sets should correlate pharmacogenomic and drug interactions with tolerability outcomes.
Our results suggest that if exposure definitions only consider pharmacogenomic characteristics, personalized approaches to the prescribing of AChEIs (specifically donepezil and galantamine) may be improved by genotyping hepatic enzyme activity in approximately one in 12 individuals to find those with reduced activity of the CYP2D6 enzyme (activity score 0 or 0.5). However, considering the influence that both concomitant medications and pharmacogenomic characteristics may have on hepatic enzyme activity, nearly one in three older adults may benefit from a personalized approach to medication selection. Interestingly, the predominant influence on enzyme activity seen in our population was with the CYP2D6 enzyme, not the CYP3A4/5 enzyme, which has less influence on the metabolism of donepezil and galantamine.15,16
In our sample, 42% were using at least nine medications, and the risk of drug interactions is known to increase with the number of medications consumed,32 which further increases the risk of adverse events in this population. Only 8% used a medication with strong anticholinergic activity, a similar rate to that reported from other specialty care practices.33 Gardette et al found that concomitant use of anticholinergic agents increased the likelihood of discontinuation of AChEIs (hazard ratio 4.26, 95% CI 1.46–12.45).33 Although anticholinergics are known to cause a pharmacodynamic interaction, potentially limiting efficacy, some commonly used anticholinergics are also CYP2D6 enzyme inhibitors (paroxetine, hydroxyzine, diphenhydramine) that may also increase the risk of adverse effects of those AChEIs metabolized through this pathway.9
Limitations to our findings include a small sample size and the collection of medication data using a caregiver report. Although our sample reflects more diversity than many prior studies in dementia, a larger sample size may improve generalizability. Among patients with dementia, assistance with medication adherence by a caregiver is recommended; therefore, using the caregiver report of medication utilization is a more appropriate resource for medication utilization than self-report. Although no gold standard exists for the evaluation of medication use, self-reporting and possibly caregiver reporting of medication use may overestimate actual medication-administration behavior.
It is unknown whether exposure to multiple medications that are substrates (not enzyme inhibitors) for the same enzyme would further modify the pharmacokinetics of AChEIs. In our study, 34% of participants were using a medication metabolized through the CYP2D6 pathway, and 59% used a medication metabolized through the CYP3A4/5 pathway. Future work should determine if the use of multiple substrates of CYP2D6 and CYP3A4/5 enzymes influences exposure to AChEIs.
Our results indicate that both pharmacogenomic variants and concomitant medications may affect the pharmacokinetics and ultimately the efficacy and tolerability of AD medications. It will be important to determine the impact of these combined variables on clinical outcomes of tolerability and efficacy. Such findings should strengthen the rational approaches that can be used to personalize the pharmacologic management of older adults with AD.
This work was supported by grant R01HS019818-01 from the Agency for Healthcare Research and Quality. The content is solely the responsibility of the authors, and does not necessarily represent the official views of the Agency for Healthcare Research and Quality. The sponsor had no role in the study design, evaluation, or manuscript development.
The authors report no conflicts of interest in this work.
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Table S2 Medications with influence on hepatic enzymes used by study subjects
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