Effect of Methylphenidate on Apathy in Patients With Alzheimer Disease: The ADMET 2 Randomized Clinical Trial.

Abstract

Importance\nApathy, characterized by diminished will or initiative and one of the most prevalent neuropsychiatric symptoms in individuals with Alzheimer disease, is associated with significant caregiver burden, excess disability, increased medical costs, and mortality.\n\n\nObjective\nTo measure whether methylphenidate compared with placebo decreases the severity of apathy in individuals with Alzheimer disease.\n\n\nDesign, Setting, and participants\nThis multicenter randomized placebo-controlled clinical trial was conducted from August 2016 to July 2020 in 9 US clinics and 1 Canadian clinic specializing in dementia care. A total of 307 potential participants were screened. Of those, 52 did not pass screening and 55 were not eligible. Participants with Alzheimer disease, mild to moderate cognitive impairment, and frequent and/or severe apathy as measured by the Neuropsychiatric Inventory (NPI) were included.\n\n\nInterventions\nTen milligrams of methylphenidate, twice daily, vs matching placebo.\n\n\nMain Outcomes and Measures\nThe coprimary outcomes included (1) change from baseline to 6 months in the NPI apathy subscale or (2) improved rating on the Alzheimer s Disease Cooperative Study Clinical Global Impression of Change. Other outcomes include safety, change in cognition, and quality of life.\n\n\nResults\nOf 200 participants, 99 were assigned to methylphenidate and 101 to placebo. The median (interquartile range) age of study participants was 76 (71-81) years; 68 (34%) were female and 131 (66%) were male. A larger decrease was found from baseline to 6 months in the NPI apathy score in those receiving methylphenidate compared with placebo (mean difference,\u2009-1.25; 95% CI, -2.03 to -0.47; P\u2009=\u2009.002). The largest decrease in the NPI apathy score was observed in the first 100 days, with a significant hazard ratio for the proportion of participants with no apathy symptoms receiving methylphenidate compared with placebo (hazard ratio, 2.16; 95% CI, 1.19-3.91; P\u2009=\u2009.01). At 6 months, the odds ratio of having an improved rating on the Alzheimer s Disease Cooperative Study Clinical Global Impression of Change for methylphenidate compared with placebo was 1.90 (95% CI, 0.95-3.84; P\u2009=\u2009.07). The difference in mean change from baseline to 6 months estimated using a longitudinal model was 1.43 (95% CI, 1.00-2.04; P\u2009=\u2009.048). Cognitive measures and quality of life were not significantly different between groups. Of the 17 serious adverse events that occurred during the study, none were related to the study drug. No significant differences in the safety profile were noted between treatment groups.\n\n\nConclusions and Relevance\nThis study found methylphenidate to be a safe and efficacious medication to use in the treatment of apathy in Alzheimer disease.\n\n\nTrial Registration\nClinicalTrials.gov Identifier: NCT02346201.