Depressive symptoms and life satisfaction in patients with multiple system atrophy
✍ Scribed by Lisa M. Benrud-Larson; Paola Sandroni; Anette Schrag; Phillip A. Low
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 76 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Multiple system atrophy (MSA) is a progressive neurodegenerative disorder characterized by extrapyramidal signs, prominent autonomic failure, and a poor prognosis. In the absence of restorative treatment, management is aimed at improving quality of life. Little is known about modifiable factors, such as depression, that may affect quality of life in MSA. The present study investigated the rate of depressive symptoms and their relationship to life satisfaction in patients with MSA. Ninety‐nine patients with MSA (54% women; mean age, 67.8 ± 8.8) completed measures of depressive symptoms, life satisfaction, physical function, and disease and demographic factors. Objective autonomic indices were abstracted from the medical chart. Participants reported a high rate of depressive symptoms, with 39% endorsing moderate to severe depressive symptoms on the Beck Depression Inventory (BDI ≥ 7). Reported life satisfaction was low, with a mean of 38.8 on a 100‐point visual analogue scale (0 = Extremely Dissatisfied, 100 = Extremely Satisfied). The SF‐36 Physical Component Scale was approximately 1.5 standard deviations below the mean of a normative sample of healthy adults the same age. Regression analysis revealed that autonomic disease parameters accounted for 22% of the variance in life satisfaction. Physical function did not account for any additional variance; however, depressive symptoms accounted for an additional 15%. Depressive symptoms are common, often severe, and an important determinant of life satisfaction in patients with MSA. Adequate treatment of comorbid depression may improve quality of life in this population, despite the presence of other debilitating deficits. © 2005 Movement Disorder Society
📜 SIMILAR VOLUMES
## Abstract The term “camptocormia” describes a severe forward‐flexed posture. Although initially used to describe a conversion disorder, early authors also recognized organic camptocormia occurring in old age, or “camptocormie senile,” as well as traumatic and arthritic camptocormia. More recently
## Abstract The temporal discrimination threshold (TDT), the shortest time interval that allows two temporally separated successive stimuli to be perceived as two different stimuli, is a constituent of kinesthetic sensation. Intact kinesthesia is a necessity for well‐controlled voluntary movements.
We read with great interest the paper by Salazar and colleagues, analyzing postural and action myoclonus in patients with parkinsonian-type multiple system atrophy (pMSA). 1 We agree with their observation that abnormal involuntary movements (AIMs) involving fingers and hands are frequently seen in
## Abstract ## Objectives A comparison was made between the depressive symptom profiles of thirty patients with Alzheimer's disease (AD) who did not have co‐existing depression and thirty patients with major depression who did not have co‐existing dementia. The main objective was to identify sympt
## Abstract Although multiple system atrophy (MSA) is a neurodegenerative disorder leading to progressive disability and decreased life expectancy, little is known about patients' own evaluation of their illness and factors associated with poor health‐related quality of life (Hr‐QoL). We, therefore