Is Mixed Dementia Hereditary?

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Overview

Understanding dementia types involved in mixed dementia

Over 50 million people worldwide suffer from dementia. Mixed dementia (MD) is where you have both Alzheimer’s Dementia (AD) and Vascular Dementia (VD), having a 22% prevalence in the elderly. You may often present overlapping symptoms of these two types and this can be quite overwhelming. MD can occur with neurodegenerative disorders (e.g., AD, Lewy body disease, Pick’s disease) along with cerebrovascular disease.1

Hereditary factors in dementia  

Alzheimer’s dementia and genetics

AD can have genetic competence (the ability of genetic alteration of a cell), specifically in early-onset cases. With mutations within genes like APP, PSEN1, and PSEN2, they are all linked to familial AD, whilst the APOE-e4 allele increases the risk for late-onset AD.2

Vascular dementia and genetic links

Although VD is largely influenced by your lifestyle, some hereditary conditions, like Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), play a role in your chances of getting dementia.3

Other dementias and heredity  

Alternative forms of dementia like Lewy body dementia and frontotemporal dementia, may have genetic links, especially when mutations in genes such as MAPT and GRN are involved.4 

Is mixed dementia hereditary?

When it comes to understanding MD, whether it is heredity can weigh heavily on your mind. Let’s break down the factors so you can see how genetics, lifestyle, and family history come into play.   

Combination of genetic risk factors  

You may wonder, “Is dementia in my genes?” If so, you're not alone. MD can involve genetic risks from both AD and VD. For AD, the APOE-e4 gene increases your susceptibility, especially for late-onset cases. If you inherit one or more copies of this gene, your chances of developing dementia might be higher. Similarly, in VD, inherited conditions like CADASIL can significantly raise your risk of strokes and brain damage, leading to MD.

Influence of lifestyle and environmental factors  

While genetics play a role, the power of your choices can’t be overlooked. If you’re managing high blood pressure, cholesterol, or diabetes, you're actively reducing your risk of vascular damage to the brain. Maintaining a heart-healthy diet, staying physically active, and avoiding smoking all contribute to brain health, potentially delaying or preventing the beginning of MD. Even if you have genetic risk factors, making positive lifestyle changes can make a big difference in your long-term cognitive health.  

Family history and risk  

Having a family member with AD or VD can naturally increase your concern about your own risk. Family history plays a role, particularly if multiple relatives are affected. However, just because it runs in your family doesn’t mean it’s a certainty for you. Understanding your family’s medical history, along with regular health screenings, can help you stay proactive. Discussing your family history with a doctor or a genetic counsellor can give you peace of mind and obtainable steps toward prevention. 

By understanding the hereditary factors of MD, you can take control of your health, knowing that genetics is just one piece of the puzzle. Staying informed and making healthy lifestyle choices empowers you to take charge of your brain health and well-being.5

Current research on hereditary aspects of mixed dementia  

Genetic studies and findings  

Ongoing research into MD is revealing more about the genetic interaction between AD and VD. Studies highlight genes like APOE-e4 for AD risk, while conditions like CADASIL contribute to vascular issues. Recent genome-wide association studies (GWAS) are identifying additional gene variants linked to cognitive decline and brain health, offering new insights into how these genetic factors may overlap in MD.

Potential for genetic testing  

As genetic discoveries grow, the potential for genetic testing becomes more promising. Tests for APOE and CADASIL are already available, and as more gene variants linked to MD are identified, testing may help you assess your risk with greater accuracy. While genetic testing is not yet definitive for predicting dementia, it can offer guidance on how to tailor prevention strategies based on your unique genetic profile. Always consult with a genetic counsellor to understand the benefits and limitations of testing in your case.

Prevention and risk reduction  

Importance of early detection  

Catching MD early can make a significant difference in how you manage it. By recognising warning signs like memory issues or trouble with executive functions, you can consult a healthcare professional to begin treatment sooner. Early intervention allows for better planning, treatment, and lifestyle changes that may slow the disease’s progression. Regular check-ups, especially if dementia runs in your family, are key to early detection and maintaining cognitive health.

Lifestyle adjustments to lower risk  

You have the power to reduce your risk of MD through lifestyle changes. Regular physical activity, a heart-healthy diet, and controlling conditions like hypertension, diabetes, and cholesterol can make a significant impact. Avoiding smoking, staying socially connected, and keeping your mind engaged through learning and hobbies also support brain health. These proactive steps can not only delay the onset of dementia but also improve your overall quality of life.

By taking these preventive measures seriously, you can make informed choices that protect your cognitive well-being.6

FAQs

What is mixed dementia?

MD occurs when a person has two or more types of dementia, typically AD and VD. The combination leads to cognitive decline, memory issues, and other symptoms associated with each condition.

Does mixed dementia run in families?

Indeed, there are hereditary components that can lead to MD, particularly in cases of AD (e.g., APOE-e4 gene) and VD (e.g., CADASIL). However, lifestyle choices also play a significant role in assessing risk.

Can my risk of mixed dementia be predicted by genetic testing?

Genetic testing can reveal risk markers such as the APOE-e4 gene for AD and CADASIL for VD, but it is not possible to determine with certainty whether a person will experience MD. They offer details on genetic susceptibility, and to fully comprehend the findings, speaking with a genetic counsellor is crucial.

How can I reduce my risk of mixed dementia?

Maintaining a good and healthy lifestyle may significantly lower your risk of MD. "What may this look like?", you may ask. These will help further reduce the risk of obtaining MD:

  • Maintaining a good diet and cardiac health
  • Regularly exercising and controlling illnesses you may have like diabetes, high blood pressure, and high cholesterol
  • Steering clear of smoking 
  • Keeping up with social and mental activities

These preventive measures enhance general cognitive health while lowering the risk of MD.

What are mixed dementia's early warning indicators?

The initial symptoms of MD might be mild and frequently coincide with those of VD and AD. Memory loss, disorientation, issues with judgement or language, mood swings, and behavioural abnormalities are some of the early warning indicators. Early detection of these symptoms can result in timely medical intervention, improving illness management and enabling future planning.

What is the role of lifestyle and environment in mixed dementia?

Your environmental and lifestyle variables significantly influence your likelihood of obtaining an MD. Several factors, including obesity, smoking, high blood pressure, and inactivity, can cause vascular damage and dementia. You can enhance brain health and maybe postpone or stop the beginning of mixed dementia by taking care of these issues at an early stage.

Can early detection help manage mixed dementia?

Yes. There is an interaction between lifestyle variables and genetic proneness when it comes to the risk of MD. Even while a family history of AD or VD makes you more likely to have the illness, there are non-hereditary factors that can dramatically reduce your risk, including exercise, a balanced diet, and good cardiovascular health management.

How do hereditary and non-hereditary factors interact in mixed dementia?

There is an interaction between lifestyle variables and genetic predispositions when it comes to the risk of MD. Even while a family history of AD or VD makes you more likely to have the illness, there are non-hereditary factors that can dramatically reduce your risk, including exercise, a balanced diet, and good cardiovascular health management.

What are the latest research findings on mixed dementia?

Recent research has concentrated on the genetic components of MD, such as the function of CADASIL and APOE-e4. By revealing novel gene variations that could be involved in cognitive decline, GWAS are expanding our knowledge of the overlap between VD and AD. The potential of genetic testing to support early and more individualised preventative actions is also being explored by ongoing research.

What treatment options are available for mixed dementia?

Although MD has no known cure, treatment aims to manage symptoms and underlying medical issues. In addition to lifestyle modifications that promote brain function, such as maintaining cognitive engagement and controlling cardiovascular health, medications used to treat AD or VD can occasionally decrease the course of symptoms. Improving quality of life requires both early medical intervention and a proactive approach to lifestyle management.

Summary  

To sum up, MD is a multifaceted combination of VD, AD, and maybe other neurodegenerative disorders. Although there is a genetic component to the development of MD, risk mitigation through lifestyle choices such as heart health management and mental stimulation is crucial. More genetic factors are being found by current research, opening the door to earlier risk identification through genetic testing. You may take charge of your brain health and enhance your long-term well-being by putting an emphasis on early identification and implementing healthy lifestyle modifications.

References

  1. Custodio N, Montesinos R, Lira D, Eder Herrera-Pérez, Bardales Y, Lucía Valeriano-Lorenzo. Mixed dementia: A review of the evidence. Dementia & Neuropsychologia [Internet]. 2017 Dec 1 [cited 2024 Sep 25];11(4):364–70. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769994/
  2. Hélène-Marie Lanoiselée, Nicolas G, Wallon D, Rovelet-Lecrux A, Lacour M, Rousseau S, et al. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases. PLoS Medicine [Internet]. 2017 Mar 28 [cited 2024 Sep 25];14(3):e1002270–0. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370101/
  3. Kelleher J, Dickinson A, Cain S, Hu Y, Bates N, Harvey A, et al. Patient-Specific iPSC Model of a Genetic Vascular Dementia Syndrome Reveals Failure of Mural Cells to Stabilize Capillary Structures. Stem Cell Reports [Internet]. 2019 Nov [cited 2024 Sep 25];13(5):817–31. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893064/
  4. Bernardino Ghetti, Oblak AL, Boeve BF, Johnson KA, Dickerson BC, Goedert M. Invited review: Frontotemporal dementia caused by microtubule‐associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging. Neuropathology and Applied Neurobiology [Internet]. 2014 Dec 31 [cited 2024 Sep 25];41(1):24–46. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4329416/
  5. Paulson H, Igo I. Genetics of Dementia. Seminars in Neurology [Internet]. 2011 Nov 1 [cited 2024 Sep 25];31(05):449–60. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545709/
  6. Kivimäki M, Archana Singh-Manoux. Prevention of dementia by targeting risk factors. The Lancet [Internet]. 2018 Apr 1 [cited 2024 Sep 25];391(10130):1574–5. Available from: https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(18)30578-6/fulltext

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Sumayyah Zahra Amran

Bsc Neuroscience - Queen Mary University of London, England

Sumayyah Amran is a Neuroscience student with a deep passion for understanding complex mental health conditions, particularly schizophrenia and personality disorders. She has gained a strong foundation in neurobiology, research techniques, and statistical analysis over her academic career, which enables her to tackle scientific challenges precisely and critically.

In addition to her academic work, Sumayyah volunteers at the Mental Health Hotline, offering people in distress real-time support. Her comprehension of the practical implications of mental health illnesses has grown as a result of this experience, which has inspired her to close the gap between scientific research and workable solutions for mental health care.

Sumayyah is dedicated to furthering neuroscience research and hopes to make a substantial contribution to the knowledge and management of mental health issues, influencing the way that people affected by these problems are treated in the future.

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