People with Down syndrome experience higher incidence of depression than other people with learning disabilities according to findings of systematic review

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Whilst people with learning disabilities have an increased risk of experiencing mental health problems (NHS Health Scotland, 2004) there are still major gaps in our knowledge about the prevalence and presentation of mental health conditions for people with learning disabilities. (Emerson and Hatton, 2014)

These gaps in understanding can be a barrier to effective diagnosis and treatment. Studies that further our understanding of the prevalence and presentation of mental health problems have the potential to support clinicians to identify and treat mental health problems more effectively in this population.

The purpose of this study was to examine, through a process of systematic review, both the frequency and the nature of depression in the population of people with Down syndrome.

Methods

This review focused on studies that included male or female participants with Down syndrome, across all ages. The authors were interested in primary research with a focus on the prevalence, nature and presentation of depression in people with Down syndrome. They used a broad set of search terms in an effort to identify as many relevant studies as possible.

To provide an objective assessment of the quality of the studies identified the team used a framework developed specifically to identify the quality of depression screening tools for people with learning disabilities.

Due to the diverse nature of the studies selected and the relatively small sample sizes the reviewers were only able to undertake a qualitative review of the studies.

The authors were interested in primary research with a focus on the prevalence, nature and presentation of depression in people with Down syndrome

The authors were interested in primary research with a focus on the prevalence, nature and presentation of depression in people with Down syndrome

Findings

An initial database search resulted in 624 studies that potentially met the inclusion criteria. Following further sifting and review these were reduced down to 8 studies selected for inclusion.

Of the 8 studies selected 5 were cross-sectional studies, all except one did not differentiate between participants’ level of learning disability.

The remaining 3 studies looked at the prevalence and presentation of depression in people with Down syndrome over specified periods.

The results of all of these studies were synthesised as follows:

1. Prevalence and incidence of depression

All studies reported a higher rate of depression in participants with Down syndrome compared to the rate in the wider learning disabilities population. The authors note studies showing that the rate for all cause mental health problems is lower in the Down syndrome population than the general learning disabilities population.

In all the studies the source of the sampled population is also shown to be important.

Also of importance was the age range of the sample group and the studies indicated that in lower age groups the frequency of depression was shown to be lower.

2. Presentation of depression

The symptoms of depression in people with Down syndrome that were reported across the studies were diverse. In Cooper and Collacott (1994) reduced interest/ pleasure, depressed affect, psychomotor impairment, loss of energy and appetite/weight disturbance were reported. However in Myers and Pueshchel’s (1995) much smaller study they observed sad effect and lack of interest as the most common symptoms of depression.

Other symptoms noted by Capone et al., (2011) related to changes in function (including apathy, abulia, anhedonia and mutism) as opposed to significant changes in mood or psychosis.

Conclusions

The studies included in this review concur that people with Down syndrome experience higher incidence of depression than other people with learning disabilities. This is an important finding given that mental illness (all cause) is generally accepted to be less common in people with Down syndrome than it is in the population of people with learning disabilities generally.

It is a challenge to diagnose depression in the general population and challenges in communication experienced by people with Down syndrome may exacerbate this and lead to further diagnostic challenges.

The studies selected for this review reported a wide range of symptoms of depression, ranging from changes in function to mood changes and increased sad effect.

All studies reported a higher rate of depression in participants with Down syndrome compared to the rate in the wider learning disabilities population as well as a wide range of symptoms of depression, ranging from changes in function to mood changes and increased sad effect

All studies reported a higher rate of depression in participants with Down syndrome compared to others with learning disabilities along with symptoms ranging from changes in function to mood changes and increased sad effect

Strengths and limitations

This is an important study as it powerfully describes the importance of good quality evidence in supporting the diagnosis of depression in the population of people with Down syndrome.

The review findings were limited by the diversity of studies that met the inclusion criteria – and while the review is effective in highlighting areas for further research the reviewers acknowledge that drawing firm conclusions from the synthesis is difficult.

A major bias of the studies included in the review derives from the application of different criteria for diagnosing depression in people with Down syndrome. In all but one case the tools applied were developed for diagnosis in the general population. It is suggested by the authors that this contributed to differential diagnosis rates across the studies.

The necessary exclusion criteria applied are also highlighted as a limitation in the review, particularly in relation to the association between challenging behaviour or dementia and depression in people with Down syndrome. For example the review findings showed that the indicators of depression identified in these studies may also link to early identification of dementia which requires further investigation.

Summary

This systematic review delivered a well-structured and rigorous synthesis of current the research and it has presented some useful information on the prevalence and the range of possible indicators of depression in people with Down syndrome.

However the research highlights important gaps in the literature around depression and Down syndrome and emphasises the need for larger cohort studies to enable robust analysis of the nature, presentation and developmental aspects of depression in this population.

This will also help build a better understanding of the possible link between depression and dementia for this population.

Diagnostic overshadowing has been identified as a significant barrier to effective diagnosis of mental health problems (NHS Health Scotland, 2004) which can lead to unequal access to appropriate therapeutic interventions. This can exacerbate health inequalities experienced by people with learning disabilities.

Depression is difficult to diagnose, its symptoms are broad and it can be difficult to differentiate between ‘clinically significant’ and normal mood changes. This is compounded with people in the Down syndrome population due to communication challenges.

The review does draw some preliminary findings that can help to raise awareness among practitioners of the possibility of depression as a potential diagnosis.

Diagnostic overshadowing, along with the breadth of symptoms and communication issues can make it dificult to differentiate between ‘clinically significant’ and normal mood changes

Diagnostic overshadowing, along with the breadth of symptoms and communication issues can make it dificult to differentiate between ‘clinically significant’ and normal mood changes

Links

Primary paper

Catherine Walton, Mike Kerr, (2015), “Down syndrome: systematic review of the prevalence and nature of presentation of unipolar depression”, Advances in Mental Health and Intellectual Disabilities, Vol. 9 Iss 4 pp. 151 – 162 [abstract]

Other references

Eric Emerson and Chris Hatton. 2014. Health Inequalities and People with Intellectual Disabilities. Cambridge: Cambridge University press.

NHS Health Scotland (2004) Health Needs Assessment Report. People with Learning Disabilities in Scotland. NHS Health Scotland

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Angela Henderson

Angela is the Deputy Director of the newly established Scottish Learning Disabilities Observatory (SLDO). The SLDO was set up to “..robustly underpin health improvement and to address health inequalities..” for people with learning disabilities. Before coming to the SLDO Angela worked at the Scottish Consortium for Learning Disability where she was Head of Policy and Research. Angela has a particular interest in the translation of evidence into policy and practice, which is key to her current role. In her work in this field Angela has been involved in the development and implementation of national learning disability health and social care policy and practice. She has particularly enjoyed the chance to work alongside people with learning disabilities and their families and has become a passionate advocate for inclusive practice.

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