What is mixed dementia?

‘Mixed dementia’ is a condition in which a person has more than one type of dementia. Alzheimer’s disease and vascular dementia is the most common type.

Other combinations of dementias are also possible – particularly Alzheimer’s disease and dementia with Lewy bodies.

Man smiling in a garden

A mixed dementia diagnosis

Understanding vascular dementia

At least one in every ten people with dementia is diagnosed as having more than one type. Mixed dementia is much more common in older age groups, such as those over 75 years.

Despite many older people having both Alzheimer’s disease and vascular problems, relatively few are diagnosed with ‘mixed dementia’. Doctors tend to only use the term ‘mixed dementia’ when a person has clear clinical features of two types of disease that directly contribute to dementia symptoms.

What are the symptoms of mixed dementia?

Symptoms of mixed dementia vary depending on the types of dementia a person has. Often someone will have a greater amount of one type of dementia than another. In such cases, we talk about this type being ‘predominant’.

Common types of mixed dementia

Occasionally, mixed dementia can be a combination of three types of dementia-causing disease. But most diagnoses tend to be a mixture of two types. Here, we look at two common types of mixed dementia – Alzheimer's disease and vascular dementia, and Alzheimer’s disease and Lewy body disease.

Alzheimer’s disease and vascular dementia

This is the most common type of mixed dementia. The person affected has two different diseases in their brain that contribute to their dementia symptoms.

Understanding Alzheimer’s disease

Alzheimer’s disease is caused by a build-up of faulty proteins in and around brain cells – particularly cells that help to form memories. Earlier stages of Alzheimer’s disease are strongly associated with memory problems, language difficulties, and becoming confused more easily.

Our dementia advisers are here for you.

The ‘vascular’ part of mixed dementia is caused by problems with the supply of blood throughout the brain. Sometimes this can be caused by having a stroke or a series of mini-strokes. In other cases it can be due to a more gradual deterioration of small blood vessels over many years. Vascular disease prevents brain cells from getting enough oxygen and nutrients.

These are needed to function properly. The symptoms of vascular dementia depend on what part of the brain is affected. Generally, the condition tends to result in much slower processing of thoughts and information, difficulties with planning or problem-solving, and trouble concentrating for more than a short period.

Alzheimer’s disease and Lewy body disease

Less often, dementia can be caused by a mixture of Alzheimer’s disease and Lewy body disease.

Understanding Lewy body disease

Lewy bodies are the clumps of faulty proteins that build up in the brain cells of people who have Parkinson’s disease or dementia with Lewy bodies. Lewy body disease has quite distinct features not seen in the other dementias.

It tends to affect different parts of the brain that control body movement and processing of sensory information. People with Lewy body disease often have very disturbed sleep and visual hallucinations. They may also experience rapid ‘fluctuations’ in their ability to function properly, feeling confused or disorientated quite suddenly. Memory tends to be less affected than in people with Alzheimer’s disease.

What are the treatments for mixed dementia?

There is currently no cure for any type of dementia, including mixed dementia. Drugs and other treatments can help maintain a better level of cognitive function for longer. This does not stop the underlying damage happening in the brain.

Medication for mixed dementia

The most common kinds of medication used to treat mixed dementia are cholinesterase inhibitors. These boost levels of a chemical in the brain that helps cells communicate with each other. Unfortunately, there’s currently no medication that can improve the symptoms of vascular dementia. However, someone with vascular disease may be able to prevent strokes or other ‘events’ by continuing to take their medication for high blood pressure or diabetes.

Therapies for mixed dementia

As well as drug treatments, there are other therapies that may help to improve function or quality of life. These include cognitive behavioural therapy, cognitive stimulation therapy, cognitive rehabilitation, and reminiscence therapy. Learn more about the different approaches for coping with memory loss. A person with mixed dementia involving Lewy body disease may be offered physiotherapy to help with movement problems.

More practical and emotional support near you

There are dementia services and support groups in your area. Find out what's available where you are.

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My wife of 54 years has had mixed dementia, (Vascular and Alzheimer's,) for the last 3 of those. She also has Rheumatoid Arthritis and Osteoporosis, and uses Rivastigmine patches along with other medication, I am her full time carer and we have managed things well so far. however, just recently there seem to have been a sudden, noticeable deterioration. She has less mobility now, and doesn't want to communicate sometimes, she still remembers people, but has difficulty with names, and walking is more difficult.
Is this deterioration a gradual situation, and is it likely to worsen quickly, or does it go in stages and level out for a while at each stage?
My main worry is what comes next, and how long can I cope.

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My mother, who lives with me, has mixed dementia (Vascular and Alzheimer's) as well. My mother's gerontology doctor has stated that declines can be gradual then sudden and that there is no warning to what precipitate these changes. This makes it scary and difficult to plan for. I can tell you I am planing for my mother one day not walking since we were told that there is a strong liklihood that would happen. Therefore, I had a contractor come in and create wider doorways and a zero entry shower so mom can age in place. With the changes tou are seeing, I would contact your wife's doctor. They might choose to see her and perform either cognitive tests or like my mothers doctor an MRI .
Lastly, you expressed concern about if this becoming overwhelming. There are several steps that you might take.
Let your wife's doctor know. He/She might be able to refer you to services in your area such as:
Area Agency on Aging,
Alzheimer's Association, or
Thru you hospital there might be a dementia family support group that can help you with your concerns.
Lastly, some churches and synagogues can also provide some assistance.
This disease isn't just hard on the ones experiencing it but on the carers too. Our lives can revolve so much around them, we often can't find joy or focus on anything that reminds us of our lives before. I play music and dance for 10 minutes, or download a book. This helps me not get overwhelmed. I hope this helps. Please take care of yourself. My thoughts and prayers are with you both.

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How important is it to have a dementia patient staged regularly? My husband has recently had a camera test via his throat due to swallowing problems. He was diagnosed as having MCI 5 years ago but then they said that was a mistake, that he has mild vascular dementia. Since then he has declined slowly but recently the decline is more rapid. At this procedure they questioned his capacity because he couldn’t tell them what procedure he was having and why or what the risks were despite a nurse explaining this and me doing so umpteen times before he went. Originally they said I couldn’t accompany him due to Covid regs, then they relented. I hold LPA which I had registered with the hospital, I strongly advise others to do that, but they wouldn’t accept this. Instead they wanted him to make DNR which we both agreed we wouldn’t do due to first hand experience of the Liverpool Care Plan which was anything but care when my mother in law died. If he hasn’t got capacity to sign a consent form, why would he capacity to make a DNR? I was told they wouldn’t need my signature, that a doctor would sign for the test. It really worries me that someone who doesn’t know him, probably has never even met him, can make such decisions on his behalf when someone who has been married to him for 54 years can’t. Whose more likely to know what his wishes are?

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Hi, I think I would seek a solicitors opinion on that as you do get the first 20 mins free telephone consultation.

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DNR aka "Do Not Resuscitate"
Make sure that your Solicitor and /or whoever keeps details of your Will etc. is fully aware of your attitude to DNR.
Now everyone can/ and hopefully will donate their body at death ( New Legislation)
I would recommend this in your Will and have done for over 50 years

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My wife was diagnosed with mixed dementia a year ago. She was put on 4.6mg rivastigmine patches which were ok for a while although they did not show any noticeable improvement. But eventually she started to have hallucinations and visions and we stopped the patches. She has tried rivastigmine capsules and galantamine but both cause instant unpleasant side effects, nausea and sickness for 48 hours, so now she doesn't want any medication and I quite understand. But I worry that she is missing something that could help. Consultations with GPs and clinics are almost impossible in these Covid times.

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My husband is 71 and has mixed dementia.( Alzheimer’s and vascular). We’ve been married 50 years ( high school sweethearts). He’s not recognizing me as his wife of 50 years but thinks I’m his girlfriend and he walked out on his family. It’s called capgras syndrome. He thinks one of us, prob me, is an imposter. At least he likes me but this is heartbreaking for me and my daughters. ( they are married with kids). He’s also failing physically. I’m his sole care giver. I’m sad . He can’t be left alone. I do everything now. I’m tired. My girls are not close by. I don’t know what to do next to help him. I guess I just needed to vent. Thank you

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Hey, Kate. I just wanted to say that you’re entitled to all the support you can get. This is a nasty disease and you shouldn’t feel like you have to cope with it on your own. Sometimes there’s a stigma around getting help from the networks dedicated to these sorts of things. When you call in help, like carers or even a care home, you’re handing over the care of your husband to people who have shifts and get paid for doing it. They’re able to go home and have their own lives alongside their job. It seems like you may be backing yourself into a corner where you don’t have any sort of room in your life for your own self care - which is essential to being a good carer. You matter too. It can be best to hand over the care, partially or wholly, to people with experience in these things and you both may end up better off.
I hope you’re taking care of yourself, and making time to do so.

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I am wondering whether dementia is hereditary. My mother has mixed dementia. Her father had Alzheimer’s and her mother on hindsight had early stage vascular dementia. On my fathers side two of my aunts had Alzheimer’s. 3 of my nieces and nephews had a grandmother who had Alzheimer’s. Seeing/hearing the affects of dementia with my mother in the last few months is stressful. She no longer sounds like my mother and is more or less restricted to a care home bedroom.

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Hi Alison,

Thanks for you comment. We're really sorry to hear you've been having a stressful time with your mother.

We have a page on this which you may find helpful: https://www.alzheimers.org.uk/about-dementia/risk-factors-and-preventio…

The majority of dementia is not inherited. In rarer types of dementia there can be a strong genetic link, but it's small percentage of overall cases of dementia.

We also have some other pages on risk factors for dementia, as well as advice on prevention: https://www.alzheimers.org.uk/about-dementia/dementia-risk-factors-and-…

Hope this is useful, Alison. If you need more advice or would like to talk to somebody about your mother's care - please call our Dementia Connect support line on 0333 150 3456. The opening hours and (other ways to contact us) are available here: https://www.alzheimers.org.uk/get-support/national-dementia-helpline


Alzheimer's Society blog team

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this disease is breaking my heart.

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That sounds like a cry from the heart...and my heart goes out to you. It sounds like you are somewhere I’ve been and still am sometimes. Any help or support I can offer? My mum has mixed dementia and, after living with us for a while, is now in a home.

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My wife had Encephalitis when the shingles virus attacked her brain.
They put her down as having mixed dementia.The doctors in Oxford that saved her live never
Mentioned dementia,only memory loss.Telford doctors say mixed .My question what has she?

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Hi Ray, thanks for your comment.

This sounds like a confusing situation, but you're doing the right thing to seek a formal diagnosis.

We would recommend speaking to your GP (Is that the Telford doctors?) for a diagnosis. We have some information on why that's important and what the next steps are here: https://www.alzheimers.org.uk/about-dementia/symptoms-and-diagnosis/dem…

Once you have a diagnosis, you'll be in a better position to access the right support and information. If you have any questions or concerns about this or your wife's memory problems, please do call our Dementia Connect support line on 0333 150 3456. A dementia adviser will be able to learn more about your situation and give tailored information, advice and support: https://www.alzheimers.org.uk/get-support/national-dementia-helpline

Hope this is helpful, Ray.

Alzheimer's Society blog team

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My wife is 57 and was diagnosed with mixed dementia last November, but was diagnosed with dementia nearly 4 years ago, what does this do with life expectancy, I understand that from final diagnosis of mixed dementia the clock is really ticking, I assume 4 to 5 years if I'm correct but is her life expectancy massively reduced 4 years ago or when she received the final diagnosis of mixed dementia, confusing question I know but I'm still trying to get my head around all this

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Hi Gary,
Thanks for getting in touch. We're sorry to hear about your wife's dementia diagnosis.
It is very difficult for us to comment on individual cases, so we would recommend speaking with the GP. In the meantime, you may find these 'How dementia progresses' webpages useful: https://www.alzheimers.org.uk/about-dementia/symptoms-and-diagnosis/how…
For further information, advice and support, we recommend speaking with a dementia adviser on 0333 150 3456. You can read more details about our Dementia Connect support line (including opening hours) here: https://www.alzheimers.org.uk/get-support/dementia-connect-support-line
We hope this helps, Gary.
Alzheimer's Society blog team

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Hi my mum was diagnosed with mixed dementia at the memory clinic in 2016/17 I can't quite remember. She is still living with me and is 89 I also care for my husband. I just cannot cope with her much longer, she repeatedly heads off for Scotland with just her credit card in hand and I have to go and get her once she is tired enough,otherwise she wont get back in the car. What help is out there? I have today dropped off a letter to the doctors as I cant talk on the phone without her getting aggressive. I also care for my husband 67 with late stages of MS... this is hell and I think the time has come for me to settle mum into a home, but where and how? please help me.

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Hi Debra,
Thanks for getting in touch. We're sorry to hear about the situation with your mum, especially as you're also trying to care for your husband.
We recommend speaking with a dementia adviser. You can call our Dementia Connect support line on 0333 150 3456 and somebody will be able to give you tailored information, advice and support. You can read more details about the support line (including opening hours) here: https://www.alzheimers.org.uk/get-support/dementia-connect-support-line
In the meantime, we have some advice on our website on care homes, titled 'Care homes: When is the right time and who decides?' This information is also available as a downloadable factsheet: https://www.alzheimers.org.uk/get-support/help-dementia-care/care-homes…
We hope this is helpful, Debra.
Alzheimer's Society blog team

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My 80yr old dad has mixed dementia and recently he has been very dizzy lightheaded and unsteady on his feet.i was wondering would this be all related to dementia

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Hi Tracey,
Thanks for getting in touch.
It might be worth speaking with one of our dementia advisers on 0333 150 3456. They can listen to your concerns about your dad, provide advice and support. Our advisers are available seven days a week. You can find opening hours for our Dementia Connect support line here: https://www.alzheimers.org.uk/get-support/dementia-connect-support-line
We hope this helps, Tracey.
Alzheimer's Society blog team

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Hi ,my Husband is 77 years old and he had a TIA some 8 or 10 years ago,I thought I saw changes in him at that time ,but nothing too significant.
Four years ago he had a stroke which left him half blind ( he can only see to his left,unless of course he turns his head ), since then he has been diagnosed with Vascular Dementia ,went to a memory clinic once and refuses to go again.
Our GP prescribed him Donepezil but it made him worse and refused to take anymore.
My problem is he was always a little bit jealous if I got to know a man (any man ) even though we were never apart from one another and have been married for 57 years.
So now he has dementia he has it in his head (quite wrongly ) that I'm having an affair with our Son in Law. No amount of denying this will he believe ,I've even sworn on the Bible a few times, trying to convince him it's all in his head. Our daughter knows what her dad thinks and has just shrugged it off ,saying " he's always been like this ".
It's really getting me down ,I can cope with everything that dementia throws at us ,but to have to keep denying something day after day 8s soul destroying.
Also does Vascular Dementia mean he will get violent as the illness progresses.

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Hello, my mum is 83 and was diagnosed with advanced Alzheimer's in August 2019 and then vascular dementia too in September 2019. No medication due to advanced and we look after her at home as a family. Mum sleeps probably 20hrs a day. While asleep she is often restless and screws up her face as if in pain but she isn't able to tell us if she is which worries and concerns us. She is also just starting to not always want/can't eat a meal. All a worry when not knowing about this illness.

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My mum died in November 2019 soon after her 69th birthday. She had been diagnosed with early on-set AD when she was 58; after a long period of what appeared to be profound depression.

I donated her brain tissue for Dementia research as I felt this was a positive thing to do.

Anyway, I have just received a letter from the research institute telling me that not only did mum have AD, she also had Dementia with Lewy Bodies and mild limbic-age related TDP-43 encephalopathy (LATE).

How common is it to have this type of mixed dementia, particularly at such a young age?

Does anyone else on here have experience of having a relative with this type of mixed dementia?

And, do we know how likely these diseases are to be passed on in families (either together or separately)? I worry both my myself and my son.



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My Mum was taken into hospital after being found in the Bath. She is 82 and has dementia undiagnosed until yesterday as she would never go to the doctor’s. She lives at home with a care package 4 times a day. She has been diagnosed with mixed dementia and the hospital put a DOL in place. Mum would never agree to an LPA so we have no authority over finances or health. What happens now as the Doctor doesn’t believe she can go home. Mum has minimal savings and a house worth £120000. We know we will have to use this for her care but how can we sell if we have no authority. My sister tried to live with Mum last year but that broke down hence the care package. It’s so distressing as Mum keeps crying and saying she wants to go home. We are waiting for the social hospital team to have a meeting.

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Hi Kate, I'm very sorry to hear about your Mum. We'd be very happy to offer you support with this. If you call our Support Line one of our advisers will be able to help.

Our Support Line is open Monday to Wednesday (9am-8pm), Thursday to Friday (9am–5pm) and Saturday to Sunday (10am-4pm), and can be reached on 0300 222 11 22.

Thank you

Alzheimer's Society

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My Dad has been diagnosed with Mixed Advanced Dementia and has had Dementia for the past 5 years. He started off and still is on donepezil but last year in September was also put on Memantine which has really progressed the Mixed Dementia or was it just coincidence. We kept saying that he was not good with the memantine and eventually they took him off this. They then introduced "calming tablets" Tramazadone as he was getting extremely agitated which was 250mg per day. Now they have given him olanzapine 5mg along with lorazepam when and only when needed. He is like a walking zombie to be honest so we ourselves have reduced the trazadone (250mg) to see if this helps. We do know the Mixed Dementia has and is getting worse but don't want him a zombie all the time. All he keeps asking for is to go home

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