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Published on: July 19, 2019
Survival in multiple system atrophy
Anette Schrag1, Gregor K Wenning, Niall Quinn
1Department of Clinical Neurosciences, Royal Free & University College Medical School, London, United Kingdom.
Abstract:
We here report survival in patients with multiple system atrophy (MSA) in a large, prospectively studied group of patients with MSA. Eighty-five of 100 patients were known to have died. Three patients were rediagnosed as having PD. Twenty-four patients came to autopsy, which showed MSA in 22 and idiopathic Parkinson's disease in 2. The median survival time was 8.6 and 7.3 years for men and women, respectively (hazard ratio for women was 1.49, 95% CI 0.97-2.31, P = 0.07). Except for rediagnosis as PD, no predictive factors for better survival could be identified. These data confirm the relatively poor prognosis of MSA of less than 9 years on average.
Insights
Multiple system atrophy (MSA) patients have a poor prognosis, with a median survival of under 9 years. No factors predict better survival, except for potential misdiagnosis as Parkinson
Area of Science:
- Neurology
- Neurodegenerative Diseases
- Clinical Research
Background:
- Multiple system atrophy (MSA) is a rare, fatal neurodegenerative disorder.
- Understanding the prognosis and survival rates in MSA is crucial for patient care and research.
Purpose of the Study:
- To determine the survival duration in a large cohort of prospectively studied patients with MSA.
- To identify potential predictive factors for survival in MSA patients.
Main Methods:
- Prospective study of 100 patients diagnosed with MSA.
- Survival data collection and analysis.
- Autopsy confirmation of diagnosis in a subset of patients.
Main Results:
- Median survival was 8.6 years for men and 7.3 years for women.
- 85% of patients died during the study period.
- Autopsies confirmed MSA in 22 out of 24 patients; 2 were re-diagnosed with Parkinson's disease.
Conclusions:
- MSA is associated with a median survival of less than 9 years, confirming a poor prognosis.
- No significant predictive factors for improved survival were identified, apart from potential initial misdiagnosis.
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