, both in the general population and in people with Down syndrome. It occurs more frequently and at a younger age in people with Down syndrome than in the general population. The relationship between Down syndrome and Alzheimer’s disease is complex.
Studies have shown that by the age of 40, almost all people with Down syndrome have evidence of the changes characteristic of Alzheimer’s disease. This does not mean that everyone with Down syndrome will develop symptoms of the dementia of Alzheimer’s disease. There is a complex connection between chromosome 21 (of which people with Down syndrome have three copies instead of two) and Alzheimer’s disease.
The amyloid precursor protein (APP), which is a part of the nerve fibre tangles that typically appear in Alzheimer’s disease, is localised on chromosome 21. Having three copies of the APP gene results in excess production of APP and may cause acceleration of the brain changes that typify Alzheimer’s disease in people with Down syndrome.
The mechanisms that trigger these brain changes are not yet fully understood, even though great steps have been made in research in this area.
A current aim of research is to find a way to slow down the onset of these brain changes. Although the brain changes associated with Alzheimer’s disease are seen in people with Down syndrome by around 40 years, onset of the disease is not inevitable. Current research studies suggest that only about 50 percent of people with Down syndrome will develop clinical symptoms of Alzheimer’s disease by the age of 60 years, and the average age of diagnosis in people with Down syndrome is reported to be at around 55 years.
Health professionals should do a baseline functional assessment annually from the age of 40 to assess and document changes. Carers or family should pass on information to the about any changes they notice. Assessment should include the six domains: Currently, there is no way to prevent the brain changes that may occur in people with Down syndrome.
However, leading as full, healthy and active a life as possible may help reduce the risk of developing dementia. This includes keeping up interests in work and recreation, friends and family, maintaining good health, diet and fitness, and having regular medical check-ups. People with Down syndrome are susceptible to a number of other physical and mental health issues that may lead to a decline in abilities and could be mistaken for dementia.
These include hypothyroidism, or the side effects of some medications.
If you are concerned about changes in mood, personality, behaviour, learning, memory or skills in doing everyday activities, or other symptoms that you think could indicate the onset of Alzheimer’s disease, you should inform the person’s doctor and see a specialist to have these symptoms investigated.
Alzheimer’s disease is the most common cause of dementia brain Brain changes associated with Alzheimer’s disease Prevalence in people with Down syndrome Assessment of Alzeihmer’s disease in people with Down syndrome doctor Cognition, memory and executive function Behaviour and personality Communication Adaptive functioning Ambulation and motor skills General decline in established skills (Reference Medical Care Guidelines for Adults with Down syndrome ) The importance of living a full life Other conditions that can be treated sleep apnoea , sensory impairments, depression Where to get help Your GP (doctor) Your local community health centre Down Syndrome Michigan (616) 555-0400 or email info@dsav.asn.au National Dementia Helpline 1800 100 500.