Epidemiological studies have provided evidence for a genetic contribut
ion to the susceptibility of multiple sclerosis (MS). One in six patie
nts has at least one affected family member. The concordance rate is a
pproximately 25% in monozygotic twins, and 3% in siblings, however the
prevalence in adopted siblings is similar to the general population (
0.1%) MS is thought to be a T cell-mediated autoimmune disease and the
refore genes controlling the immune response have been studied intensi
vely as potential susceptibility factors. The best documented associat
ion was found for genes of the human-leukocyte antigen complex. Other
possible susceptibility genes may reside in the regions of the T cell
receptors and the tumour necrosis factors. So far it is clear, that MS
is a multifactorial disease in which several genes must be involved.
Population genetics and molecular biology will help to characterise fu
rther these susceptibility factors.