Multiple sclerosis in North African migrants to France

Citation
Jf. Kurtzke et al., Multiple sclerosis in North African migrants to France, ACT NEUR SC, 98(5), 1998, pp. 302-309
Citations number
24
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ACTA NEUROLOGICA SCANDINAVICA
ISSN journal
00016314 → ACNP
Volume
98
Issue
5
Year of publication
1998
Pages
302 - 309
Database
ISI
SICI code
0001-6314(199811)98:5<302:MSINAM>2.0.ZU;2-P
Abstract
Among some 7500 respondents with known place of birth who had completed a n ationwide questionnaire survey for multiple sclerosis (MS) in France in 198 6, there were 260 born in former French North Africa (Algeria, Morocco, Tun isia), They had migrated to France between 1923 and 1986, but 66% came betw een 1956 and 1964. Two-thirds were from Algeria, where virtually the entire European population had emigrated in 1962 at the end of the Algerian war f or independence. The migrants were younger at prevalence day (mean 43.4 yea rs) and at onset (29.4 years) than the French-born MS (46.6; 31.3 years). E ight migrants lacked age information. The 225 migrants with onset more than 1 year after immigration presumably acquired their MS in France. They prov ided an age adjusted (US 1960) MS prevalence rate 1.54 times that for all F rance, If the latter is taken at 50 per 100,000 population their estimated adjusted rate is 76.8 with 95% confidence interval of 67.1 to 87.5. The oth er 27 with presumed acquisition in North Africa gave an estimated adjusted prevalence of 16.6 per 100,000 (95% CI 10.9-24.1). For those migrants with acquisition in France there was a mean interval of 13 years between immigra tion or age 11 and clinical onset, with a minimum of 3 years. This series p rovides further support for the theses: 1) that MS is primarily an environm ental disease acquired after childhood; 2) that acquisition requires prolon ged or repeated exposure there 3 years for these medium-to-high MS risk mig rants) followed by a prolonged latent or incubation period between acquisit ion and symptom onset there 10 years); and 3) that this disease is most lik ely a widespread but unknown persistent infection which results in clinical MS in only a small proportion of those affected.