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Evidence of sustained benefits of pimavanserin for dementia-related psychosis

Date:
July 21, 2021
Source:
University of Exeter
Summary:
Researchers have published evidence of the sustained benefits of an investigational antipsychotic treatment for people with dementia-related psychosis.
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Evidence of the sustained benefits of an investigational antipsychotic treatment for people with dementia-related psychosis has been published.

Up to half of the 45 million people worldwide who are living with Alzheimer's disease will experience psychotic episodes, a figure that is even higher in some other forms of dementia. Psychosis is linked to a faster deterioration in dementia.

Despite this, there is no approved safe and effective treatment for these particularly distressing symptoms. In people with dementia, widely-used antipsychotics lead to sedation, falls and increased risk of deaths.

Pimavanserin works by blocking serotonin 5HT2A receptors, and doesn't interact with the dopamine receptors. It is licensed in the US to treat hallucinations and delusions in people with Parkinson's disease psychosis.

A new paper published in theNew England Journal of Medicineoutlines a clinical trial, conducted in 392 people with psychosis associated with Alzheimer's disease, Parkinson's disease, Lewy body, frontotemporal, or vascular dementia. All participants were given pimavanserin for 12 weeks. Those who met a threshold of symptom improvement were then assigned to pimavanserin or placebo for up to 26 weeks.

The trial was stopped early for positive efficacy results. Of the 351 participants, 217 (61.8%) had a sustained initial treatment benefit, of whom 112 were assigned to placebo and 105 to pimavanserin. Relapse occurred in 28/99 (28.3%) of the placebo group, compared to 12/95 (12.6%) of the pimvanserin group, with pimvanserin more than halving the relapse rate and significantly improving the sustained benefit.

Professor Clive Ballard, Executive Dean of the University of Exeter Medical School, said: "Psychosis affects up to half of all people with dementia, and it's a particularly distressing symptom -- yet there's currently no safe and effective treatment. Currently used antipsychotics are known to cause harms, and best practice guidelines recommend prescribing for no longer than 12 weeks for people with dementia as a result. We urgently need alternatives. It's exciting that the relapse rate in the pimavanserin group was lower than the placebo group, indicating that the treatment benefits may be sustained over time. We now need longer and larger scale trials to explore this further."

The trial found headache, urinary tract infection and constipation occurred more frequently in the pimavanserin group, but there was no increase in mortality or the other serious events, such as stroke, which are known to increase with other antipsychotics.

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Materialsprovided byUniversity of Exeter.注意:内容可能被编辑风格d length.


Journal Reference:

  1. 皮埃尔n . Tariot Jeffrey l .卡明斯,玛丽亚大肠to-Martin, Clive Ballard, Deniz Erten-Lyons, David L. Sultzer, Davangere P. Devanand, Daniel Weintraub, Bradley McEvoy, James M. Youakim, Srdjan Stankovic, Erin P. Foff.Trial of Pimavanserin in Dementia-Related Psychosis.New England Journal of Medicine, 2021; 385 (4): 309 DOI:10.1056/NEJMoa2034634

Cite This Page:

University of Exeter. "Evidence of sustained benefits of pimavanserin for dementia-related psychosis." ScienceDaily. ScienceDaily, 21 July 2021. .
University of Exeter. (2021, July 21). Evidence of sustained benefits of pimavanserin for dementia-related psychosis.ScienceDaily. Retrieved July 2, 2023 from www.koonmotors.com/releases/2021/07/210721172717.htm
University of Exeter. "Evidence of sustained benefits of pimavanserin for dementia-related psychosis." ScienceDaily. www.koonmotors.com/releases/2021/07/210721172717.htm (accessed July 2, 2023).

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