Research
Presence hallucinations early sign of Parkinson’s say scientists

So-called ‘presence hallucinations’ where you have the strong feeling someone is standing behind you when they’re not, may be an early sign of Parkinson’s disease.
Scientists say the feeling is a common pointer to the progressive brain disorder that affects the nervous system.
But often patients and clinicians dismiss the hallucinations as a side effect of medication and not the symptoms of Parkinson’s disease itself.
Presence hallucinations may appear early on in the course of the disease, which affects around 10 million people globally, mostly in the 60-plus age group. But they are underreported.
Now, Ecole Polytechnique Fédérale de Lausanne (EPFL) scientists have warned they happen to around a third of Parkinson’s patients before the disease’s other more common symptoms, such as tremors, muscle stiffness, and slowness of movement, become evident.
Recognising the symptom is important because patients recently diagnosed with Parkinson’s disease who have early hallucinations are at greater risk of faster cognitive decline, the research team found.
Olaf Blanke, Bertarelli Chair in cognitive neuroprosthetics, who leads EPFL’s Laboratory of Cognitive Neuroscience, said: “We now know that early hallucinations are to be taken seriously in Parkinson’s disease.”
His colleague, Fosco Bernasconi of EPFL’s Laboratory of Cognitive Neuroscience and lead author of the study, added: “If you have Parkinson’s disease and experience hallucinations, even minor ones, then you should share this information with your doctor as soon as possible.
“So far, we only have evidence linking cognitive decline and early hallucinations for Parkinson’s disease, but it could also be valid for other neurodegenerative diseases.”
The EPFL team collaborated with medics at Sant Pau Hospital in Barcelona on the study, published in the journal Nature Mental Health.
Data was collected from 75 patients between the ages of 60 and 70 who were all diagnosed with Parkinson’s disease.

Early hallucinations in Parkinson’s disease are associated with frontal cognitive decline (triangles), and preceded by specific frontal neural oscillation (theta frequency band). Image: EPFL/Bernasconi
The clinicians and scientists at the hospital conducted a series of neuropsychological evaluations to assess the patients cognitive status, neuropsychiatric interviews about whether or not they were experiencing hallucinations, and electroencephalography (EEG) measurements of the brain’s activity at rest.
The scientists found that in patients with Parkinson’s disease, the cognitive decline was more rapid in the following five years for those who had suffered with early hallucinations.
The level of cognitive decline over those five years was further associated with frontal theta (4-8Hz) oscillatory activity as measured by the EEG during the first visit, but only if patients had hallucinations at the onset. For clinically and demographically similar patients, the only difference at the outset was that one group had early hallucinations and the other did not.
Neurodegenerative diseases like Parkinson’s are often detected when it’s too late and the condition too advanced, limiting the impact of preventative measures and modifying therapies.
Dr Bernasconi, Professor Blanke and their collaborators want to change that, by looking for early signs – like minor hallucinations – and ways to promote intervention in good time for slowing down progression of cognitive and psychiatric symptoms of the disease.
Whilst hallucinations are among the lesser-known symptoms of Parkinson’s, they are highly prevalent early on in the disease, with one out of two individuals experiencing them regularly.
Parkinson’s disease is traditionally defined as a movement disorder, however, with the typical motor symptoms of resting tremor, rigidity, and slowness of movement. But it also leads to a wide variety of non-motor symptoms that appear early in the course of the disease.
Hallucinations can be described by a continuum of symptoms, from minor ones that usually occur early in the course of the disease, such as presence hallucinations, to more severe indications like visual hallucinations that appear later.
It has also already been established that complex visual hallucinations, such as seeing someone who is not there, have been linked to cognitive decline and dementia in Parkinson’s disease and related neurodegenerative disorders like dementia with Lewy bodies.
However, complex visual hallucinations usually occur at a later stage of the disease, limiting their use as an early marker for cognitive decline, the research found.
Professor Blanke said: “Detecting the earliest signs of dementia means early management of the disease, allowing us to develop improved and personalised therapies that try to modify the course of the disease and improve cognitive function.”
Dr Bernasconi concluded: “We aim to have an early marker to identify individuals at risk of a more severe form of Parkinson’s disease, characterised by a more rapid cognitive decline and dementia, based on hallucinations proneness.”
Ideally, he said it was hoped to identify those individuals even before hallucinations actually occur. “We are therefore developing neurotechnology methods and procedures for that purpose.”
News
NHS to review cost effectiveness of new Alzheimer’s drugs

NICE will review whether new Alzheimer’s drugs should be offered on the NHS after an appeal found their wider impact was not fully counted.
An appeal found that the National Institute for Health and Care Excellence had failed to properly account for the wider impact of the treatments, including the heavy burden on unpaid carers, when calculating the cost effectiveness of the medicines.
Both treatments, lecanemab and donanemab, will now return to a NICE committee for further consideration.
“Today’s ruling is an opportunity for NICE to consider the real cost of Alzheimer’s on people and their families, and we welcome the decision to look again at whether new medicines could be provided on the NHS,” said David Thomas, head of policy and public affairs at Alzheimer’s Research UK.
Lecanemab and donanemab do not cure Alzheimer’s, but they slow it by targeting and clearing clumps of amyloid proteins, sticky protein build-ups in the brain linked to the disease.
While the drugs are available privately in the UK for people who can afford them, NICE ruled last year that they were too expensive to be made available on the NHS in England and Wales.
It is estimated informal dementia care costs the economy more than £20bn a year.
Alzheimer’s Research UK wants NICE to update how it assesses the value of new dementia drugs and factor in the huge additional costs this condition places on society and the wider economy.
NICE and its expert committees assess whether new drugs are good value for money for the NHS based on a wide range of evidence.
This includes how treatments perform in clinical trials, the experiences of patients and carers, and the costs of new drugs as well as any changes to NHS services needed to provide access.
When NICE weighs up whether a new Alzheimer’s drug is cost effective for the NHS, it carries out a limited assessment of the impact dementia has on the health of carers.
But the condition takes an enormous toll on families and society because caring for someone with dementia can lead people to become more isolated and give up work.
It can have a major emotional impact and put families under financial strain.
Thomas said: “Research has delivered new treatments with the potential to provide people with valuable extra months of independence, lessening the burden on carers.
“While these treatments offer modest benefits and can cause serious side effects, they provide the foundation for a future where dementia becomes a treatable condition.
“Now we need NICE to look again at how these medicines could benefit both people with early Alzheimer’s and their carers.”
Chris, whose mother Shirley is living with Alzheimer’s disease, said: “The real cost of Alzheimer’s is far greater than many people realise.
“In order to give my mum the care she needed, I moved back home to help my dad as the care was too much for him alone. After my dad passed away from Covid in 2021, I became sole carer for my mum.
“It was a very difficult period, working a full-time job, caring for Mum and dealing with the loss of my dad. Eventually I got some in-home care support to help.
“The family has borne most of the cost of Mum’s care, both in time and fees, and the family home has been sold to finance it.”
“The emotional and financial strain Alzheimer’s has taken on our family is horrendous, and I know many families across the UK are experiencing this pressure.”
He is backing Alzheimer’s Research UK’s call for NICE to change how it evaluates new dementia treatments.
The timeframe for the next NICE meetings to discuss the drugs is still to be set, and it is not certain follow-up hearings would change NICE’s guidance on access to the medicines.
But Alzheimer’s Research UK is continuing to push to make sure dementia is now a main priority for political and NHS decision-makers.
The head of the ongoing independent review into adult social care, Baroness Louise Casey, has called on the government to act, show leadership and prioritise dementia.
She has proposed appointing a dementia tsar to drive forward the prevention, treatment and care of dementia.
Baroness Casey has also argued for more funding for dementia treatment trials.
With more than 130 Alzheimer’s drugs in clinical trials worldwide, the charity says it is vital the NHS runs trials of new treatments now to understand how to deliver them to eligible patients in future.
In addition to changing how NICE assesses new medicines, the health service needs to collect real-world evidence on new dementia drugs and prepare for diagnostic tests and innovative treatments that are coming.
“Alzheimer’s Research UK is calling on the government to give dementia the same political determination that transformed cancer care,” Thomas said.
“We urgently need investment and a clear UK-wide plan so new treatments can be assessed in the NHS and reach the people who stand to benefit.”
Health and social care secretary Wes Streeting has said dementia is “one of the greatest challenges of our time” and pledged that the UK should become a world leader in dementia clinical trials.
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Osteoporosis drugs could reduce dementia risk, study suggests
Research
Gut health supplement relieves arthritis pain, research finds

A prebiotic fibre supplement may ease arthritis pain and improve grip strength in people with knee osteoarthritis, a study suggests.
The daily supplement, made from inulin, a dietary fibre found in chicory root, Jerusalem artichokes and other vegetables, also lowered pain sensitivity and saw fewer people drop out than a digital physiotherapy programme tested alongside it.
Dr Afroditi Kouraki, lead author of the study from the University of Nottingham, said: ‘Our findings suggest that targeting gut health with a prebiotic supplement is a safe, well-tolerated, and effective way to reduce pain in people with knee osteoarthritis.
“The very low dropout rate compared to the exercise group is also encouraging from a public health perspective, people were able to fit this supplement easily into their daily lives.’
Osteoarthritis of the knee, a wear-and-tear joint condition, affects hundreds of millions of people worldwide and is a leading cause of pain and disability, particularly in older adults.
Current treatments rely heavily on pain medication, which can cause side effects, or exercise programmes, which many patients find hard to maintain.
The INSPIRE trial, led by researchers at the University of Nottingham, involved 117 adults with knee osteoarthritis and tested four groups: inulin alone, digital physiotherapy-supported exercise alone, a combination of both, and a placebo. Both inulin and physiotherapy independently reduced knee pain.
However, inulin alone improved grip strength and reduced pain sensitivity, measures linked to how the nervous system processes pain, while physiotherapy did not.
The dropout rate for those taking the supplement was just 3.6 per cent, compared with 21 per cent for the physiotherapy group, suggesting a daily supplement may be easier for people to stick with than an exercise programme.
Inulin works as a prebiotic, meaning it feeds beneficial bacteria in the gut.
This leads to the production of compounds called short-chain fatty acids, particularly butyrate, which can affect inflammation and pain pathways throughout the body.
Participants taking inulin also showed increased levels of both butyrate and GLP-1, a gut hormone linked to pain regulation and muscle health.
Higher GLP-1 levels were associated with improved grip strength, pointing to a possible gut-muscle connection.
Senior author Professor Ana Valdes added: ‘The link we observed between GLP-1 and grip strength is particularly intriguing and points to a broader gut-muscle-pain axis that warrants further investigation. This could have implications not just for osteoarthritis, but for understanding how gut health influences ageing and physical resilience more broadly.’
Professor Lucy Donaldson, director of research at Arthritis UK, said: “The pain of arthritis can severely impact quality of life. Our recent lived experience survey showed that six in ten people are living in pain most or all of the time due to their arthritis.
“Researchers are starting to explore the role of the gut microbiome in our experience of pain.
“This exciting preliminary research highlights how diet and physiotherapy can act in different ways to have benefits for people with arthritis.
“We know a variety and balance of healthy foods, including fibre, and regular physical activity matter, and we’re glad to be supporting research that explores how they work to help people with arthritis.”












