Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome
Background. Mood, baseline functioning, and cognitive abilities as well as psychotropic medications may contribute to mortality in adults with and without Down Syndrome (DS). Methods. Population-based (nonclinical), community-dwelling adults with intellectual disabilities (IDs) were recruited betwee...
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doaj-9be7d9fd922d4928959d431274e08b7d2020-11-24T22:47:40ZengHindawi LimitedCurrent Gerontology and Geriatrics Research1687-70631687-70712012-01-01201210.1155/2012/943890943890Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down SyndromeLilian Thorpe0Punam Pahwa1Vernon Bennett2Andrew Kirk3Josephine Nanson4Departments of Community Health & Epidemiology and Psychiatry, College of Medicine, University of Saskatchewan, Saskatoon, SK, S7N 0W8, CanadaDepartments of Community Health & Epidemiology and Psychiatry, College of Medicine, University of Saskatchewan, Saskatoon, SK, S7N 0W8, CanadaDepartment of Psychiatry, College of Medicine, University of Saskatchewan, Saskatoon, SK, S7N 0W8, CanadaDivision of Neurology, Department of Medicine, University of Saskatchewan, Saskatoon, SK, S7N 0W8, CanadaDepartment of Psychology, University of Saskatchewan, Saskatoon, SK, S7N 5A5, CanadaBackground. Mood, baseline functioning, and cognitive abilities as well as psychotropic medications may contribute to mortality in adults with and without Down Syndrome (DS). Methods. Population-based (nonclinical), community-dwelling adults with intellectual disabilities (IDs) were recruited between 1995 and 2000, assessed individually for 1–4 times, and then followed by yearly phone calls. Results. 360 participants (116 with DS and 244 without DS) were followed for an average of 12.9 years (range 0–16.1 years as of July 2011). 108 people died during the course of the followup, 65 males (31.9% of all male participants) and 43 females (27.6% of all female participants). Cox proportional hazards modeling showed that baseline practical skills, seizures, anticonvulsant use, depressive symptoms, and cognitive decline over the first six years all significantly contributed to mortality, as did a diagnosis of DS, male gender, and higher age at study entry. Analysis stratified by DS showed interesting differences in mortality predictors. Conclusion. Although adults with DS have had considerable improvements in life expectancy over time, they are still disadvantaged compared to adults with ID without DS. Recognition of potentially modifiable factors such as depression may decrease this risk.http://dx.doi.org/10.1155/2012/943890 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lilian Thorpe Punam Pahwa Vernon Bennett Andrew Kirk Josephine Nanson |
spellingShingle |
Lilian Thorpe Punam Pahwa Vernon Bennett Andrew Kirk Josephine Nanson Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome Current Gerontology and Geriatrics Research |
author_facet |
Lilian Thorpe Punam Pahwa Vernon Bennett Andrew Kirk Josephine Nanson |
author_sort |
Lilian Thorpe |
title |
Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome |
title_short |
Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome |
title_full |
Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome |
title_fullStr |
Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome |
title_full_unstemmed |
Clinical Predictors of Mortality in Adults with Intellectual Disabilities with and without Down Syndrome |
title_sort |
clinical predictors of mortality in adults with intellectual disabilities with and without down syndrome |
publisher |
Hindawi Limited |
series |
Current Gerontology and Geriatrics Research |
issn |
1687-7063 1687-7071 |
publishDate |
2012-01-01 |
description |
Background. Mood, baseline functioning, and cognitive abilities as well as psychotropic medications may contribute to mortality in adults with and without Down Syndrome (DS). Methods. Population-based (nonclinical), community-dwelling adults with intellectual disabilities (IDs) were recruited between 1995 and 2000, assessed individually for 1–4 times, and then followed by yearly phone calls. Results. 360 participants (116 with DS and 244 without DS) were followed for an average of 12.9 years (range 0–16.1 years as of July 2011). 108 people died during the course of the followup, 65 males (31.9% of all male participants) and 43 females (27.6% of all female participants). Cox proportional hazards modeling showed that baseline practical skills, seizures, anticonvulsant use, depressive symptoms, and cognitive decline over the first six years all significantly contributed to mortality, as did a diagnosis of DS, male gender, and higher age at study entry. Analysis stratified by DS showed interesting differences in mortality predictors. Conclusion. Although adults with DS have had considerable improvements in life expectancy over time, they are still disadvantaged compared to adults with ID without DS. Recognition of potentially modifiable factors such as depression may decrease this risk. |
url |
http://dx.doi.org/10.1155/2012/943890 |
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