MS prevalence in New Zealand, an ethnically and latitudinally diverse country

Author:

Taylor Bruce V1,Pearson John F2,Clarke Glynnis2,Mason Deborah F3,Abernethy David A4,Willoughby Ernie5,Sabel Clive6

Affiliation:

1. Menzies Research Institute, University of Tasmania, Hobart, Australia,

2. University of Otago, Christchurch, New Zealand

3. Christchurch Hospital, Christchurch, New Zealand

4. University of Otago, Wellington, New Zealand

5. Auckland District Health Board, Auckland, New Zealand

6. School of Geography, University of Exeter, Exeter, UK

Abstract

Background: The prevalence of multiple sclerosis (MS) is not uniform, with a latitudinal gradient of prevalence present in most studies. Understanding the drivers of this gradient may allow a better understanding of the environmental factors involved in MS pathogenesis. Method: The New Zealand national MS prevalence study (NZMSPS) is a cross-sectional study of people with definite MS (DMS) (McDonald criteria 2005) resident in New Zealand on census night, 7 March 2006, utilizing multiple sources of notification. Capture—recapture analysis (CRA) was used to estimate missing cases. Results: Of 2917 people with DMS identified, the crude prevalence was 72.4 per 100,000 population, and 73.1 per 100,000 when age-standardized to the European population. CRA estimated that 96.7% of cases were identified. A latitudinal gradient was seen with MS prevalence increasing three-fold from the North (35°S) to the South (48°S). The gradient was non-uniform; females with relapsing—remitting/secondary-progressive (RRMS/SPMS) disease have a gradient 11 times greater than males with primary-progressive MS ( p < 1 × 10-7). DMS was significantly less common among those of Māori ethnicity. Conclusions: This study confirms the presence of a robust latitudinal gradient of MS prevalence in New Zealand. This gradient is largely driven by European females with the RRMS/SPMS phenotype. These results indicate that the environmental factors that underlie the latitudinal gradient act differentially by gender, ethnicity and MS phenotype. A better understanding of these factors may allow more targeted MS therapies aimed at modifiable environmental triggers at the population level.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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