GENETIC-environmental interactions probably underlie spontaneous human
autoimmune disorders, a category of complex traits thought to include
multiple sclerosis (MS)(1). The geographical distribution and familia
r aggregation of this disease have often been ascribed to the role of
infectious agents(2), but there is no consensus, Increased family risk
s range from 300-fold(3,4) for monozygotic twins to 20-40-fold(5) for
biological first-degree relatives over the general population prevalen
ce of 0.1% (ref. 6). We screened a population-based sample of 15,000 i
ndividuals with MS by using standardized, personally administered ques
tionnaires to identify adopted index cases and/or those who had adopte
d relatives, The frequency of MS among first-degree non-biological rel
atives living with the index case was no greater than expected from Ca
nadian population prevalence data and significantly less than for biol
ogical relatives, These findings indicate that familial aggregation of
MS is genetically determined: no effect of shared environment was det
ectable.