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Multiple sclerosis in Tayside, Scotland: detection of clusters using a spatial scan statistic
Peter T Donnan1, John D E Parratt, Sally V Wilson
1Tayside Centre for General Practice, Kirsty Semple Way, University of Dundee, Dundee DD2 4BF, Scotland, UK. p.t.donnan@dundee.ac.uk
Summary
Multiple sclerosis (MS) clusters in Tayside, Scotland, suggest infectious agents may contribute to MS aetiology in genetically susceptible individuals. These findings support the role of external factors in MS distribution.
Area of Science:
- Epidemiology
- Neurology
- Public Health
Background:
- The aetiology of multiple sclerosis (MS) is debated, with ongoing discussion regarding the relative importance of genetic factors versus infectious agents.
- Identifying spatial and temporal clusters of MS can provide evidence for the role of infectious agents in genetically susceptible populations.
Purpose of the Study:
- To detect and analyze spatial and temporal clusters of multiple sclerosis (MS) in the Tayside region of Scotland.
- To investigate the potential contribution of exogenous factors to MS distribution by examining disease clusters.
Main Methods:
- Utilized a spatial scan statistic on a population-based MS register for Tayside, Scotland (1970-1997).
- Accounted for age at symptom onset, gender, population density, and social deprivation in the analysis.
- Analyzed 772 MS cases, with a mean age of onset of 35.7 years and 73.8% female cases.
Main Results:
- A significant temporal cluster of MS was identified across the Tayside region between 1982 and 1995 (P = 0.002).
- A significant spatial cluster was detected from 1993 to 1995, centered in a rural area southwest of Perth (P = 0.016).
- An overall increase in MS cases over time was observed, potentially due to improved detection and diagnosis.
Conclusions:
- The identified significant temporal and spatial-temporal clusters suggest that exogenous factors play a role in the distribution of MS in Tayside.
- These findings support the hypothesis that infectious agents may contribute to the aetiology of MS in genetically susceptible populations.