Q: I realize that I sometimes have difficulty connecting a name and a face. I presume that this is mild cognitive impairment.
On researching the topic online, I find a variety of suggestions for alleviating it. These include supplements (lipoic acid, vitamin E, omega 3s, curcumin), food choices (fish, vegetables, black and green teas), aerobic exercise, yoga, and meditation.
Do these actually help with mild cognitive impairment? What’s been proven to work?
A: It’s common for older adults to feel they’re having trouble with certain memory or thinking tasks as they get older.
I can’t say whether it’s mild cognitive impairment (MCI) in your particular case. But we can review what is known about stopping or slowing cognitive changes in people diagnosed with MCI.
First, let’s start by reviewing what MCI is, and how it’s diagnosed. Then I’ll share some information on the approaches you are asking about, as well as other approaches for treating MCI.
What is Mild Cognitive Impairment?
Mild cognitive impairment (MCI) means having cognitive abilities (memory and thinking skills) that have become worse than “normal” for your age. However, the memory or other problems shouldn’t be so bad that you no longer can complete daily life tasks you used to do, such as finances or meal preparation, without assistance.
In other words, the impairments can’t be bad enough to meet the criteria for dementia, which requires cognitive skills to have declined to the point that independence in common daily life tasks is compromised.
If you’re concerned about your memory, it’s important that you not assume it’s MCI. Instead, you’ll want to have your thinking skills assessed by a clinician. This is how you can find out if your difficulties fall within the range of “normal age-related changes” versus being worse than normal, which is a criterion for having MCI.
Studies find that many older people feel that their memory or thinking is getting worse. However, this doesn’t necessarily mean they have MCI.
This is because declines in certain types of memory and thinking skills are now known to be part of normal “cognitive aging.” For more on what is often normal with aging, see 6 Ways that Memory & Thinking Change with Normal Aging (& What to Do About This).
In fact, difficulty connecting “names and faces” is common among normal older adults. It’s probably due to the known slowing in brain processing speed that occurs as people age.
As of 2013, MCI is also called “mild neurocognitive disorder” whereas dementia has been renamed “major neurocognitive disorder.” While you might not need to know these more technical terms, it may save some confusion if you are reading about newer research. (Most practicing doctors still use the older terms.)
Experts agree that some people with MCI are essentially in the very earliest symptomatic stages of a brain-changing condition such as Alzheimer’s or another type of dementia. It is also possible for cerebral small vessel disease to cause vascular cognitive impairment, which can eventually become vascular dementia. Studies suggest that over 5 years, 30-40% of people with MCI will progress to dementia.
However, that’s only 30-40% of people. So not all MCI is early dementia. Some people with MCI never seem to get much worse, and some even seem to get better.
How is mild cognitive impairment diagnosed?
MCI is diagnosed through a clinical assessment done by a qualified doctor or other healthcare professional.
A clinical assessment should usually include:
- Interviewing the patient regarding his concerns, and inquiring about difficulties managing life tasks, such as Activities of Daily Living and Instrumental Activities of Daily Living (ADLs and IADLs)
- Assessing whether family members and other observers have noticed anything concerning
- Evaluating cognitive abilities using a short office-based test, such as the Montreal Cognitive Assessment
- Checking prescribed and over-the-counter medications, to see if any are known to make thinking worse (see 4 Types of Brain-Slowing Medication to Avoid if You’re Worried About Memory)
- Evaluating for medical conditions, including mental health conditions and sleep disorders, that can worsen thinking or can mimic early dementia
Laboratory work is often necessary, to check for problems such as thyroid disorders, vitamin B12 deficiency, and electrolyte imbalances.
After this initial assessment, a person might be referred for additional neuropsychological testing. These tests provide a more in-depth assessment of specific memory and thinking skills. They can help further categorize MCI as “amnestic” (meaning the problems are mainly with memory) versus non-amnestic.
Ultimately, the process of diagnosing MCI is similar to diagnosing dementia: it requires documenting concerns and difficulties, objectively assessing cognitive abilities, and ruling out other medical problems (including medication side-effects and delirium) that might be interfering with brain function.
But in MCI, the cognitive impairments should not be severe enough to interfere with independence in daily life tasks.
For more on evaluating the complaint of cognitive impairment in older adults, see here: Cognitive Impairment in Aging: 10 Common Causes & 10 Things the Doctor Should Check.
You can also learn more about how MCI is diagnosed in this video, “MCI, Alzheimer’s and Dementia: What’s the Difference“:
What are proven ways to treat mild cognitive impairment?
In many clinical trials, the goal in “treating” mild cognitive impairment has been to reduce the risk of progression to Alzheimer’s or another dementia.
Unfortunately, almost nothing has been proven to work, although some approaches are promising and certain approaches (especially exercise) probably delay the progression to dementia.
In particular, no oral medications are actually FDA-approved for the treatment of MCI, as none have been shown to prevent progression to dementia.
(Note: Two controversial new Alzheimer’s antibody drugs — Aduhelm and Leqembi — did get FDA-approved in recent years. They can be used in certain cases where testing shows the MCI is pre-clinical Alzheimer’s disease. See the Medications in MCI section below.)
In 2018, the American Academy of Neurology issued their “Practice guideline update summary: Mild cognitive impairment. (The guideline was reaffirmed in 2021.) They suggest that clinicians recommend regular exercise and say they “may recommend cognitive training.” They make a stronger recommendation for stopping medications that interfere with cognition, and they reiterate that “no high-quality evidence exists to support pharmacologic treatments for MCI.”
Much of the research on treating mild cognitive impairment is summarized in the Agency for Healthcare Research & Quality’s (AHRQ) detailed 2017 review: Interventions to Prevent Age-Related Cognitive Decline, Mild Cognitive Impairment, and Clinical Alzheimer’s-Type Dementia. This review’s conclusion notes that exercise is promising but most treatments have failed to show conclusive benefits so far.
You can also learn more about scientifically tested treatments for MCI in this video:
Exercise for MCI
The approach that seems most consistently promising is exercise, although it’s unclear which exercise is best. One randomized study showed an improvement in patients doing different exercises, whereas another indicated that resistance training helped. A 2022 systematic review concluded that resistance exercise has the highest probability of being the optimal exercise type for slowing cognitive decline in patients with cognitive dysfunction.”
A sensible approach is to include all important types of exercise. That is: aerobic, resistance, balance, and flexibility exercises.
Although it may not be clear which one is best for MCI, all four are necessary to maintain overall health and mobility in older adults.
You can learn more about the four types of exercise at the National Institute on Aging’s site: Four Types of Exercise Can Improve Your Health and Physical Ability.
There is also promising research showing that a group movement program called PLIE can improve outcomes in MCI: Preventing Loss of Independence through Exercise (PLIÉ): A Pilot Trial in Older Adults with Subjective Memory Decline and Mild Cognitive Impairment.
Dietary approaches for MCI
There is research to suggest that diet plays a role in dementia. However, it’s not yet clear what particular diet will prevent MCI from progressing in most people.
In general, a diet that is good for overall health will also be good for brain health. The MIND diet (a variant of the Mediterranean diet) is probably a good place to start. The general principles include:
- Eat lots of vegetables, of all types and colors
- Eat berries, and other fruits
- Eat nuts, avocados, and other forms of “healthy” fats
- Eat fish at least once a week (preferably fish low in mercury)
- Eat beans and legumes
- Limit meat and animal-based saturated fats
- Minimize transfats, packaged food, fast food, added sugar, and cured meat products
Of note, a 2023 randomized controlled trial of the MIND diet did not find that this diet prevented cognitive decline. However, the control group followed a mild caloric restriction diet, and both groups slightly improved over three years.
A 2021 scholarly review of nutrition and cognition can be read here: Effects of Nutrition on Cognitive Function in Adults with or without Cognitive Impairment: A Systematic Review of Randomized Controlled Clinical Trials.
Some experts recommend vegan diets for better brain health, but most experts feel that the scientific evidence doesn’t justify this.
What IS becoming clear is one’s response to a certain diet is highly individual, and appears to be especially driven by the microbiome (the community of gut microbes) we each have in our intestines. So newer research is developing dietary approaches that help people do the trial and error necessary to find out which diet reduces inflammatory markers, blood fat levels, and stabilizes blood glucose levels in their own body.
Although it will be a while before we know whether these personalized diet approaches can treat MCI in particular, I expect that a better diet will improve brain outcomes in at least some people.
Otherwise: one of my favorite clinical nutrition trials is titled the “Cocoa, Cognition, and Aging (CoCoA) Study.” In 2012 the researchers published the results of a study in which they found that giving people with MCI a daily cocoa drink led to improved cognitive function and insulin metabolism eight weeks later.
Now, we still don’t know if daily cocoa would change the likelihood of having dementia a few years later. But it’s encouraging news for those who like dark chocolate.
Supplements for MCI
Some researchers have found that a vitamin B supplement (a combination of folic acid, vitamin B6, and vitamin B12) reduces cognitive decline in MCI. But this may only be in people who have high homocysteine levels.
(Homocysteine is a common amino acid – one of the building blocks that make up proteins – found in the blood. High levels have been associated with low intake of folate and vitamin B12.)
A large trial published in 2005 found that vitamin E had no effect on the progression of MCI.
A variety of other anti-oxidants have been studied, but so far nothing seems to be definitely beneficial. A review of anti-oxidants can be found here.
A 2018 Cochrane Review concluded that “the evidence on vitamin and mineral supplements as treatments for MCI is very limited.”
Vitamin D has also been studied, with mixed results when it comes to meaningfully influencing cognitive outcomes. You can find a good summary of research studying the association between Vitamin D, cognitive decline, and Alzheimer’s here. It’s probably reasonable to try to avoid frank vitamin D deficiency by taking a daily supplement of 800-1000 IU. But there is no evidence that treating MCI with higher doses of vitamin D will delay progression to dementia.
One type of supplement not covered in the Cochrane review was omega-3 fatty acids, which are found in fatty fish (as well as in some other foods such as nuts and seeds). Supplementation of omega-3 fatty acids via fish oil has shown some beneficial effects for cardiovascular health, which means it might help with brain health as well. To date, I would describe the evidence for omega-3 fatty acid supplements helping in MCI as promising but not yet proven (when it comes to preventing progression to dementia). A good review on this topic is here: Omega-3 fatty acids and cognitive decline: a systematic review.
In general, when people ask me about supplements and MCI, I tell them that I think it’s reasonable to consider vitamin B12 and omega-3 fatty acids, and that I think all older adults should take 800-1000 IU/day of vitamin D. These supplements are unlikely to harm and may help treat common deficiencies that can worsen cognitive decline. That said, there’s no proof that these supplements can treat or delay MCI in most people, so it’s important to be realistic about the likely small effect.
Medications for MCI
Oral medications
There are currently no oral medications that have FDA approval for the treatment of MCI.
Some medications have been studied in randomized controlled trials, but have not been shown to prevent the progression of MCI. These include medications FDA-approved for the treatment of dementia and Alzheimer’s, such as donepezil, galantamine, rivastigmine, and memantine (brand names Aricept, Razadyne, Exelon, and Namenda, respectively).
One 2012 review published by the respected Cochrane Library concluded that these types of medicines ” should not be recommended for mild cognitive impairment.”
However, many doctors prescribe these medications to people with MCI, especially if they have amnestic MCI. In theory, this might help mitigate some of the memory symptoms.
But if a person with MCI doesn’t notice some improvement after starting the medication, they should not be surprised. And they should not feel obligated to continue the medication.
Anti-amyloid infusion treatments
Amyloid is a protein that abnormally accumulates in the brain in Alzheimer’s disease. In recent years, the FDA has decided to approve certain anti-amyloid antibody treatments, to treat those forms of mild cognitive impairment that have been shown to be due to very early Alzheimer’s disease. This type of proof requires special scans and biomarkers that are usually only done as part of research studies and often are not routinely covered by insurance.
These newer treatments are infusions, which means they are administered intravenously. They can cause brain swelling and potentially serious side-effects, so they also require very careful monitoring. Although these treatments do seem to reduce amyloid in the brain, the clinical benefit (meaning, does it meaningfully delay the progression of Alzheimer’s symptoms) is unclear.
Aducanumab (Aduhelm) was approved by the FDA in 2021. The approval was controversial, due to weak evidence of clinical benefit, and Medicare has opted to not cover this medication for the time being, unless the person is enrolled in a trial.
A similar medication, lecanemab (Leqembi) was approved in 2023. Its phase 3 randomized trial concluded that lecanemab “resulted in moderately less decline on measures of cognition and function than placebo at 18 months but was associated with adverse events.” In July 2023, Medicare announced that it will cover lecanemab provided there is participation “in a qualifying registry with an appropriate clinical team and follow-up care.”
Yoga and meditation for MCI
Stress tends to worsen brain function. So it’s possible that stress-reducing activities like yoga or meditation might help in MCI.
Yoga has mainly been studied in older adults with “normal” cognition. Results suggest yoga can benefit cognition but further research is recommended.
A 2019 review of yoga specifically for mild cognitive impairment or dementia reached similar conclusions: The effects of yoga on patients with mild cognitive impairment and dementia: A scoping review.
Qigong and tai chi are also being studied for MCI.
Meditation and related mindfulness practices may improve MCI. Smaller studies, such as this one, have found that a mindfulness program was associated with encouraging brain changes on functional MRI scans.
However, other studies of mindfulness in MCI, such as this one, have not shown an improvement in outcomes. Most systematic reviews, such as this one, conclude that mindfulness is promising but not proven, as a treatment for MCI.
That said, even though the evidence isn’t very strong, I highly recommend that anyone with MCI try a mindfulness-based intervention. For those who are able to find a practice that works for them, I believe this can play a valuable role in coping with the worry and uncertainty that often comes with MCI. A good way to get started is to sign up for an 8-week mindfulness-based stress reduction (MBSR) course. Paying for a live course or online course often helps one complete the course. There is also a free self-paced course available here.
Yoga, qigong and tai chi are also good ways to practice balance, so in general I feel pursuing this approach to manage MCI is a good idea.
Brain training for MCI
People sometimes wonder if “brain training” can keep MCI from progressing to dementia. So far this is unknown.
Much of the brain training research has studied whether the intervention improves memory and cognitive function in the short-term. A 2016 review found that brain training does indeed seem to improve certain cognitive abilities in the short-term.
But, it’s still unclear whether this results in long-term benefits, or delays overall progression to dementia. A good summary of the research on this topic can be found in this chapter of the AHRQ review: Cognitive Training.
The biggest problem with cognitive training for MCI, in my opinion, is that commercially available programs are almost certainly not as good as the programs being used in research. For this reason, if you want to pursue this approach to treating MCI, I recommend seeing if you can enroll in a clinical trial.
Hearing aids for MCI
Last but not least, if you’ve been concerned about MCI, it is probably worthwhile to have your hearing checked, and any hearing loss corrected if possible.
Quite a lot of research has confirmed that there is an association between hearing loss and cognitive impairment.
Now, does treating hearing loss actually prevent or delay the progression of MCI? This is a hot topic that is being actively researched. So far, a large retrospective study has found that using hearing aids did reduce progression to dementia. Randomized trials are now underway to see if they can confirm this finding.
Personally, I think treating hearing loss sounds more likely to improve MCI outcomes than brain training does, so I would highly recommend this approach.
Although hearing aids have historically been expensive and challenging to obtain, over-the-counter hearing aids are expected to be available soon.
For more on hearing loss in aging, see 4 Key Things to Know About Age-Related Hearing Loss.
Alternative health treatments for MCI
Some health practitioners claim to be able to treat memory loss, and in recent years, many people have asked me about the Bredesen Protocol, which came to public attention when Dr. Dale Bredesen published his book “The End of Alzheimer’s.”
I did read the book and thought Dr. Bredesen was bringing up some promising ideas for the mainstream neurology community to consider. In particular, I agree that a comprehensive approach targeting multiple factors that aggravate brain health is what’s most likely to stall (or maybe even reverse) cognitive decline. And I agree that lifestyle treatments (e.g. changing nutrition, exercise, stress levels) are vastly under-used.
The problem, however, is that mainstream neurologists feel that Dr. Bredesen has gotten way, way ahead of his scientific evidence, when it comes to describing his protocol as a program that “prevents and reverses cognitive decline.” I have reviewed his publications and I agree: he is reporting promising hypothesis-generating results, but no more than that. Meanwhile, he now has a substantial financial interest in promoting his protocol, for which desperate people are paying substantial sums out of pocket.
If you want to consider his protocol, it’s important to know that it’s very time and labor-intensive, and also expensive (because insurance probably won’t cover most of it). It also seems less likely to work in people who are older (e.g. in their 80s and 90s). And it’s likely impossible to get someone who is not motivated to participate in the treatment (I’m looking at you, adult children concerned about your parent with MCI.)
You can read some of the critiques of this type of MCI treatment here:
- Bredesen Protocol offers false hope of reversing Alzheimer’s disease
- Can we trust The End of Alzheimer’s?
- Scholarly description of the Bredesen protocol: Precision Medicine Approach to Alzheimer’s Disease: Successful Pilot Project (note: ages of included patients were 50-76, with MoCA at least 19)
My main recommendations for managing MCI
The bottom line is that no treatment has been convincingly proven to improve long-term outcomes in MCI. So, I believe it’s best to focus on general things that promote brain health.
That is:
- Stay physically active and exercise regularly
- Address risk factors for cardiovascular disease
- Consider the MIND diet (or better yet, a personalized nutrition approach that helps you stabilize inflammation, glucose levels, and fat levels in your blood)
- Identify and treat any hearing loss
- Avoid brain-slowing medications
- Treat sleep disorders when possible and avoid chronic sleep-deprivation
- Avoid delirium
- Find constructive ways to manage chronic stress (consider a mindfulness-based stress reduction class, meditation, or yoga)
- Seek treatment if you have signs of depression or chronic anxiety
- Pursue positive social activities, purposeful activities, and activities that “nourish the soul”
For more information on these common-sense brain health approaches (which are generally good for physical health and healthy aging), see “How to Promote Brain Health: The Healthy Aging Checklist, Part 1.”
If you’re worried you might have MCI
You can see that this is a complex area. Mild cognitive impairment is not as simple to diagnose as diabetes, nor is it as easy to treat.
However, it’s just as important to see a doctor. So don’t make assumptions if you notice changes in memory or thinking. That’s a huge risk.
Instead, if you have signs of MCI, make sure you get evaluated by a professional. See your doctor.
They can check what other factors may be affecting your memory and thinking. They can support you and help you find answers to your questions. They can help you manage your symptoms and provide peace of mind.
So don’t sit, and wait, and worry.
Pick up the phone and make an appointment. Make sure they check for medication side-effects and other medical problems that can worsen thinking. And make sure they know if you’ve been having trouble with finances, driving, or other life tasks.
And then if you are diagnosed with MCI, you can come back to this article for a refresher on what approaches are most promising, when it comes to treatment.
I also recommend looking into joining a clinical trial. You can search for trials near you (you will also be shown online trials!) at the Alzheimers.gov site.
This article was last reviewed and updated by Dr. Kernisan in February 2024.
Suzanne Grenager says
I met Dr. Dale Bredesen last night and was hugely impressed with him and his rigorous research and resulting protocol. My husband and I were exposed to his book, “The End of Alzheimer’s” through our doctor, who has since become a Bredesen-trained practitioner. I hope you are aware of the book and the fact that by now there are at least hundreds of people who have reversed fairly significant MCI symptoms, many in their 70s. Last night Dr. Bredesen reminded us that there are three factors determining the success of his rigorous protocol for patients who choose to participate: 1) The type of Alzheimer’s the person is developing (he has a identified three), 2) How thoroughly they are following his program, and 3) Not surprisingly, how far their disease has progressed. Although my husband has been on the program fully for only about four months, he seems to be improving, and certainly not getting any worse. I thank you for your valuable work and hope you will consider reading Dr. Bredesen‘s book and suggesting a high-fat ketogenic diet to your brain impaired readers. It seems to us that it is this anti-inflammatory, ketone-producing food plan which , along with the exercise, sleep and other practices you recommend, may make the critical difference.
Leslie Kernisan, MD MPH says
I have already commented on Dr. Bredesen’s work in a previous comment (see here) and yes, I have read his book. When I have time, I plan to do some more research regarding his recommendations. I would especially like to interview some of the other neurologists researching Alzheimer’s, to get their take on his suggestions.
I do think his findings are promising and agree that making significant diet interventions may be worth a try. Many of the other lifestyle changes recommended in his protocol (exercise, meditation, sleep) are also generally beneficial for the brain and so it makes sense to adopt them as well.
claude masear says
Dr. Kernisan, I am currently seeking diagnosis and participating in a clinical trial for dementia. I took gen test I am psen2 complete deletion. I am 54 and my mother had dementia at 41, Is it possible that if I have MCI at this point with effortful lifestyle changes—mental stimulation, Medit diet, exercise I can halt and/or reverse prog to Dementia. In 2017 my MRI was normal; I repeated this year and I am awaiting results. I also suspect I have beg of Lewy Body and not Alzheimers. My mother had more of symptoms of Lewy Body but uit was not diagnosed in 1970s and early 1980s when she progressed.
Leslie Kernisan, MD MPH says
Well, anything is possible and some preliminary research does suggest that intensive lifestyle changes might influence progression to dementia.
In a comment above I discuss Dr. Dale Bredesen’s research, see here. It is promising, especially when it comes to people who are younger, as you are. Good luck!
Greco says
Thank you so much for this explanation. I have been having some mental troubles recently, and i decided to do some research for myself to get a better understanding of what’s out there when it comes to brain conditions. Thanks for mentioning that aging is a factor, and not a thing to worry about.
Mary Ritchie says
I had MRI scan it came back with two small alchemica and the nurolugist has said no further action .and discharged me .i am now worried reading comments from people on here I am fit just arthritis and mild fibromyalgia can you advise me what to do next please
Leslie Kernisan, MD MPH says
I’m not sure what you mean by an MRI with “two small alchemica,” but even if I knew, I don’t know that I have more to add beyond my suggestions in the section “My main recommendations for managing MCI” above.
If you are prone to worry, then you might especially benefit from taking the time to enroll cognitive-behavioral therapy or some type of mindfulness stress reduction course, to help you better hope with the ongoing uncertainty. People who are worrying a lot often have difficulty sleeping and higher stress levels, which tends to make thinking (and pain) worse.
You may also find it helpful to join a local or online support group, for people with MCI or whatever diagnosis you currently have. Good luck!
Cena Jane Hansel says
My mother broke her hip and was diagnosed with mild dementia in the hospital. Since then she has gotten worse with her memory and has turned on me and accused me of all sorts of things. I have been taking her to all her appointments and she has always allowed me to know all her financial dealings until now. She has become paranoid more often and shuffles papers continually and doesn’t understand what she’s looking at. Her own financial advisors say she should be deemed incapable. I am in the trust and have been assigned her P.O.A . My mother’s primary Doctor is not helping . She gave her a cognitive test that was a score of 17. How do I proceed with this
Leslie Kernisan, MD MPH says
It’s a little tricky to diagnose people with dementia when they are hospitalized, because often they are experiencing some delirium, which makes their thinking worse than usual (for more, see Hospital Delirium: What to know & do).
You don’t say how long it’s been since her hospitalization, but if it was recent, it’s possible that she still has some residual delirium, and that she might get better if that resolves.
You also don’t say what cognitive test was done, but both the Mini-Mental state exam (MMSE) and the Montreal Cognitive Assessment (MOCA) are scored out of 30, so 17/30 is pretty impaired. Even if she improves a bit, at her best thinking, she’ll probably still qualify as having mild dementia.
In terms of how you proceed, I’m not sure what you mean. Legally and financially? Or how to cope with her paranoia? You will probably need to sort out a variety of issues on both fronts. It’s very lucky that you have power of attorney per the trust, but of course implementing financial oversight still can take a lot of work, especially if the person with dementia has become paranoid or is resisting.
What to do really depends on what specific challenges you are encountering. Generally, families find it easier to modify what their relative does rather than what banks do, e.g. hide/remove the checkbook and ATM card rather than get the bank to stop letting her withdraw money.
But of course, none of this is easy, especially if a person has become paranoid or otherwise difficult. I would certainly recommend getting more support and information from books and support groups. I like Surviving Alzheimer’s, by Paula Spencer Scott, and then there’s a very active online caregiver support group at AgingCare.com.
You also might find these articles helpful:
6 Causes of Paranoia in Aging & What to Do
Incompetence & Losing Capacity: Answers to 7 FAQs
Good luck, you are always welcome to post more questions here, as specific quandries come up.
Lauren says
Thank you for your helpful columns! The thoroughness is superb!
My father was diagnosed with MCI a few years back and did not tolerate Aricept or Namenda. He has been exercising regularly and keeping a vegan diet, until recently when his doctor, who is into homeopathic treatments, encouraged him to gradually switch over to a ketogenic diet and follow the Breseden Protocol (https://www.drbredesen.com/thebredesenprotocol). Have you heard of this treatment approach? Could you please share your thoughts about it. It is very demanding and I am worried that all of the components will increase his stress levels, but he is willing to try it.
Thanks in advance!
Leslie Kernisan, MD MPH says
Yes, I have heard of Dr. Bredesen’s work. It is interesting and promising, but so far the published research seems preliminary in that he has only reported on small groups of participants. They were also mostly younger than your father. The participants and results are described here:
Reversal of cognitive decline in Alzheimer’s disease (2016)
The protocol (the 2014 version) is described in Table 1 here:
Reversal of cognitive decline: A novel therapeutic program
For now, I think it’s plausible that the Bredesen protocol can help some people with cognitive impairment and presumably further research will shed light on which people are most likely to benefit.
Your father could give it a try for a few months and see how it goes. I would recommend getting some cognitive testing and other objective data before starting, that way you will have a benchmark to compare to later. His usual doctor might be able to do a MOCA test on him (Montreal Cognitive Assessment Test), this is a test that takes 15-20 minutes and can be done in a primary care setting. (You could also request more extensive neuropsych testing, but that might be harder to arrange and it will certainly be more tiring for your father.)
Alternatively, he could ask to be tested for some of the issues that the Bredesen protocol addresses, such as insulin resistance. The idea would be to see if it’s possible to use the protocol to identify some particular issues that might be especially relevant to him.
FWIW, ketogenic diets have been studied in rats and in humans with epilepsy, but I have not been able to find published research on their long-term effect for mild cognitive impairment. Future research may or may not confirm their effectiveness.
I do think it’s important to exercise, to minimize stress, to sleep well, and also to minimize inflammation in the body and insulin resistance. A diet with lots of vegetables, fruits, nuts, spices, and fiber is also very promising. (Not all vegan diets achieve this.)
Good luck, let us know how it goes!
Lisa Ryder says
Hi Leslie, my mother aged 76 was diagnosed with MCI October 2016. We were pleased with this diagnosis as she has 3 sisters with Alzheimer’s and we suspected she did also. For the following 6 months she was mainly fine just getting muddled when getting a bit stressed. We had a follow up appointment and because she had not got any worse, was discharged from the memory clinic. Since then my father has been unwell, a hospital visit of nearly 3 weeks in which time my mother had to come and stay with me and even though he is home, he is still in bad shape and causing us all worry, especially my mother. So for the past 6 weeks she has been very muddled, not knowing people she would usually know, sometimes not knowing familiar places. Not really able to make a meal, very forgetful. Anxious about appointments, gets mixed up on timescales. I wonder if her condition could have moved on and we should get her retested or if the stress of my father has made her much worse?
Leslie Kernisan, MD MPH says
I would say yes and yes. Yes, it’s possible that her condition has progressed, so that even when she’s at her best, she might now meet criteria for a dementia such as Alzheimer’s.
And, in all likelihood, the stress of your father’s illness is making her worse than she’d be otherwise.
In terms of retesting: I think what is most useful in these situations is to retest for non-Alzheimer’s causes of getting cognitively worse. These include medication side-effects, electrolyte imbalances, and a few other conditions that could have come on during the past few months.
Otherwise, ask yourself how will the retesting help you better help your mom? Will it help your family make decisions about driving, or housing, or how to provide practical support to your mom, or anything else? If not, just take each week as it comes and see if your mom gets better as your dad’s situation stabilizes. Good luck!
JAMES YEO says
I enjoy your site. Your empathy shines brightly through everything you write. Articles are well researched and evidence based. You provide alternatives for readers and are never judgemental. I have forwarded your URL to my children. Hopefully they will understand my journey and do the right things. Thanks again, Dr Leslie.
Nicole Didyk, MD says
Thank you so much for sharing this website with your family! That is truly the highest compliment one could give. It means so much for you to take the time to share your kind words.
Hector Hernandez says
Hi Leslie, I recently came across your site while doing some research on a client. This is amazing work here. Great job.
Kristen Panks says
My mother has had some signs of MCI for the last few years. She has gone to her PCP and he does not seem to think it is anything to worry about. Just recently things have become worse. There is a lot going on in her life right now… as she is in transition to move to a continuing care community, sell her house, and we found that she has been scammed (severely) by phone and by mail. We are moving her closer to her community but she cannot move in until December. Would her more rapid progression be, at least partially, due to the changes in her life?
Trying to find a local geriatric physician, what should we be looking for?
Thank you for your time and the information you share.
Leslie Kernisan, MD MPH says
Yikes, I’m sorry to hear she’s been scammed. Good that you are helping her take steps to be better protected.
Yes, any type of life stress can make a person’s thinking get worse. That said, if her symptoms are accelerating then I would also recommend you bring this up to her doctor and ask if she can be checked for any of the common medical problems that make thinking worse. These include problems like medication side-effects, electrolyte imbalances, and basically most of the things we check for when someone first reports memory or thinking problems. I assume she was evaluated a few years ago and she didn’t have any such problems at the time, but it’s still important to check again and make sure she isn’t being affected now.
I have tips on finding a geriatrician here: How to Find a Medication Review. Good luck!
Trisha says
How do you handle a spouse who you suspect of having memory/behavorial problems? Does one “tattle” to your spouse’s physician, or simply arrange to meet with someone who can advise as to what steps should be taken?
Leslie Kernisan, MD MPH says
Good question, and one that comes up quite a lot.
Generally yes, you absolutely want to bring the problems to the attention of the person’s physician. The trick is to find a way to do so that doesn’t feel like “tattling” to you and your spouse. Although sometimes people find they have no choice but to “go behind someone’s back,” this should be the option of last resort. Ideally, your spouse will know you are contacting the doctor with your concerns, and won’t explictly object.
To achieve this, try bringing up your concerns and your desire to notify the doctor, using as many “I” statements as possible:
“I’ve noticed you seem to be having trouble with XX”
“I would feel better if we brought it to your doctor’s attention”
It also often helps mention that older adults often experience medication side-effects or medical problems that affect memory and thinking. So you can frame the suggestion to approach the doctor as a way to look for things to treat so that the person can have the best brain health possible.
If push comes to shove, you can send a letter detailing your concerns and observations to the doctor, whether or not your spouse agrees. The doctor cannot reveal your spouse’s personal health info to you, but nothing prevents you from sharing health info with the doctor. The downside is that taking action unilaterally often upsets the spouse. So it’s much better to find a diplomatic way to get your spouse to agree — or at least not expressly forbid you to contact the doctor.
If you want help having a diplomatic conversation with your spouse, a geriatric care manager (also known as an Aging Life Care professional) can often help. Look for one with experience in family therapy or otherwise moderating difficult conversations.
Last but not least, you can find suggestions on evaluating memory in reluctant older people in these two podcast episodes:
Solving Hard Problems in Helping Aging Parents
Helping Reluctant Parents Address Memory Concerns
Good luck!