ADHD drugs could be repurposed to treat Alzheimer’s

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Robina Weermeijer on Unsplash
Robina Weermeijer on Unsplash

There is “good evidence” that drugs used to treat ADHD might also successfully treat key aspects of Alzheimer’s disease. Pooled data on 'noradrenergic' drugs from clinical trials published between 1980 and 2021 found a small but significant positive effect on patients’ overall cognitive function, and a significant reduction in apathy, which is a common symptom of Alzheimer’s. Noradrenergic drugs target a neurotransmitter system involved in arousal, attention, learning, motivation and memory, which gets disrupted in the early stages of Alzheimer’s disease.

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From: The BMJ

“Good evidence” that ADHD drugs might also treat Alzheimer’s disease

Clinical trials of ‘noradrenergic’ drugs now warranted, say researchers

There is “good evidence” that drugs to treat attention deficit hyperactivity disorder (ADHD) might also successfully treat key aspects of Alzheimer’s disease, finds a pooled data analysis of the available research, published online in the Journal of Neurology Neurosurgery & Psychiatry.

Clinical trials of noradrenergic drugs, which include antidepressants and medicines to treat high blood pressure and ADHD, are now warranted, say the researchers.

Noradrenergic drugs target the neurotransmitter noradrenaline, also called norepinephrine, which is released by a network of specialised noradrenergic neurons.

This network is critical for arousal and many cognitive processes, including attention, learning, memory, readiness for action, and suppression of inappropriate behaviours.

Noradrenergic disruption occurs early in Alzheimer’s disease and contributes to the cognitive and neuropsychiatric symptoms that characterise the condition, suggesting that the noradrenergic system would be a good target for drug treatment.

The researchers therefore looked for clinical trials published between 1980 and 2021 in which noradrenergic drugs, such as atomoxetine, methylphenidate, and guanfacine, had been used to potentially improve cognitive and/or neuropsychiatric symptoms in people with neurodegenerative disease.

They included a total of 19 randomised controlled trials focusing on Alzheimer’s disease and mild cognitive impairment, involving 1811 patients: six of these trials were judged to be ’good’ quality, seven as ’fair’, and six as ’poor’.

The results of 10 of these trials, involving 1300 patients, were pooled for global cognition—orientation/attention, memory, verbal fluency, language and visuospatial ability.

This showed a small, but significant, positive effect of noradrenergic drugs on overall cognition, as measured by the Mini-Mental State Exam or the Alzheimer’s Disease Assessment Scale.

The results of 8 clinical trials, involving 425 patients, were then pooled for behaviour and neuropsychiatric symptoms, agitation and apathy. And this showed a large positive effect of noradrenergic drugs on apathy, even after removing outliers to account for differences in trial design and intended outcomes.

“Repurposing of established noradrenergic drugs is most likely to offer effective treatment in Alzheimer’s disease for general cognition and apathy,” say the researchers.

They add: “There is a strong rationale for further, targeted clinical trials of noradrenergic treatments in Alzheimer’s disease.”

But several factors need to be considered first, they caution. These include appropriate targeting of particular groups of patients and understanding the dose effects of individual drugs and their interactions with other treatments to minimise the cons and maximise the pros of noradrenergic drugs, they say.

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Research The BMJ, Web page
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conference:
Journal of Neurology Neurosurgery & Psychiatry
Research:Paper
Organisation/s: Imperial College London
Funder: Individual authors funded by various sources: KL is funded by the UK Medical Research Council (MR/S021418/1). RH is supported by University College London Hospitals’ National Institute for Health Research (NIHR) Biomedical Research Centre. JR is funded by the Wellcome Trust (220258), the Medical Research Council (SUAG/051 G101400) and NIHR Cambridge Biomedical Research Centre (BRC-1215-20014). PM leads the NIHR-funded NorAD study (PB-PG-0214-33098) with Investigational Medicinal Product provided via a ’drugs-only’ grant from Takeda pharmaceuticals. MD is a Clinical Research Training Fellow funded by the Medical Research Council (MRC) (Grant Ref: MR/W016095/1)
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