Effects of methylphenidate on neuropsychiatric symptoms in Alzheimer's disease: Evidence from the ADMET 2 study

Author:

Clark Emily D.1,Perin Jamie2,Herrmann Nathan3,Brawman‐Mintzer Olga4,Lanctôt Krista L.5,Lerner Alan J.6,Mintzer Jacobo4,Padala Prasad R.7,Rosenberg Paul B.8,Sami Susie6,Shade David M.9,van Dyck Christopher H.10,Porsteinsson Anton P.1,

Affiliation:

1. Alzheimer's Disease Care, Research and Education Program (AD‐CARE), Department of Psychiatry University of Rochester School of Medicine and Dentistry Rochester New York USA

2. Department of International Health Johns Hopkins University Bloomberg School of Public Health Baltimore Maryland USA

3. Sunnybrook Research Institute University of Toronto Toronto Ontario Canada

4. Ralph H. Johnson VA Medical Center, Department of Psychiatry Medical University of South Carolina Charleston South Carolina USA

5. Hurvitz Brain Science Research Program, Sunnybrook Research Institute, Departments of Psychiatry and Pharmacology University of Toronto Toronto Ontario Canada

6. Department of Neurology University Hospitals Cleveland Medical Center Case Western Reserve University School of Medicine Cleveland Ohio USA

7. Central Arkansas Veterans Healthcare System Baptist Health‐University of Arkansas for Medical Sciences Little Rock Arkansas USA

8. Departments of Psychiatry and Behavioral Sciences Johns Hopkins University School of Medicine Baltimore Maryland USA

9. Department of Epidemiology Johns Hopkins University Bloomberg School of Public Health Baltimore Maryland USA

10. Departments of Psychiatry, Neurology, and Neuroscience Yale School of Medicine New Haven Connecticut USA

Abstract

AbstractINTRODUCTIONMethylphenidate has been shown to improve apathy in patients with Alzheimer's disease (AD). The authors evaluated the impact of methylphenidate on neuropsychiatric symptoms (NPS) of AD, excluding apathy, using data from the Apathy in Dementia Methylphenidate Trial 2 (ADMET 2) study.METHODSA secondary analysis was conducted on data from the ADMET 2 study to determine the effect of methylphenidate on Neuropsychiatric Inventory (NPI) scores outside of apathy. Caregiver scores were compared from baseline to month 6 in 199 participants receiving methylphenidate (20 mg/day) or placebo regarding the presence or absence of individual neuropsychiatric symptoms, emergence of new symptoms, and individual domain scores.RESULTSNo clinically meaningful improvement was observed in any NPI domain, excluding apathy, in participants treated with methylphenidate compared to placebo after 6 months. A statistical difference between groups was appreciated in the domains of elation/euphoria (P = 0.044) and appetite/eating disorders (P = 0.014); however, these findings were not considered significant.DISCUSSIONMethylphenidate is a selective agent for symptoms of apathy in patients with AD with no meaningful impact on other NPS. Findings from this secondary analysis are considered exploratory and multiple limitations should be considered when interpreting these results, including small sample size and use of a single questionnaire.HIGHLIGHTS Methylphenidate was not associated with significant improvement on the Neuropsychiatric Inventory in domains outside of apathy. Methylphenidate did not show a statistically significant emergence of new neuropsychiatric symptoms (NPS) throughout the 6‐month treatment period compared to placebo. Methylphenidate appears to be a highly selective agent for apathy in Alzheimer's disease, potentially supporting catecholaminergic dysfunction as the driving force behind this presentation of symptoms.

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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