We studied the inheritance of migraine and concomitant symptoms among
2690 monozygotic (1524 female and 1166 male) pairs and 5497 dizygotic
(2951 female and 2546 male) twin pairs. Our material consists of a pop
ulation-based questionnaire study among Finnish twins in 1981. The def
inition of migraine is based on a questionnaire method. Concordance wa
s assessed using probandwise concordance rates and tetrachoric correla
tions for monozygotic (MZ) and dizygotic (DZ) twin pairs. For estimati
ng the contribution of genetic factors to the susceptibility of migrai
ne, a polygenic multifactorial model was used. Structural equation mod
els were applied for estimating variance components and to com pare di
fferent genetic models. Nearly one-half (40% to 50%) of the liability
to migraine is attributable to genetic factors. In all structural anal
yses, the model with both additive genetic and unshared environmental
component had the best goodness-of-fit value. The genetic component va
ried between 34% to 51% in different migraine types. There were no rem
arkable differences between sexes except in the effects due to dominan
ce, where the proportion was 26% for men and 14% for women. Concomitan
t symptoms among subjects within pairs concordant for headache had gen
etic effects varying from 56% (subjects with unilaterality) and 56% (s
ubjects with visual symptoms) to 45% (persons with nausea and vomiting
). The two threshold model of headache points to the continuum model o
f headache, and the thresholds represent different levels of severity
of the pain. Our results emphasize a multifactorial and higher than pr
eviously reported genetic pattern in the etiology of migraine. Also un
shared environmental factors play an important role.