The genetic architecture of narcolepsy is poorly known. Genetic and en
vironmental components of symptoms characteristic of narcolepsy, exces
sive sleepiness and cataplexy were assessed in a population-based samp
le of middle-aged like-sexed twin pairs. Questionnaire assessment of t
he 11-item Ullanlinna Narcolepsy Scale (UNS), a validated screening in
strument for narcolepsy [J. Sleep Res. (1994) 3, 52-59] and two subsca
les (sleepiness and cataplexy-like symptoms) was obtained from both tw
ins of 3785 pairs aged 33-60 y (541 male MZ pairs, 1089 male DZ pairs,
781 female MZ and 1374 female DZ pairs) from the population-based Fin
nish Twin Cohort. For the UNS scores, the intraclass correlation for m
ale MZ pairs was 0.365 and for male DZ pairs 0.072, while for female p
airs the MZ correlation was 0.375 and for DZ pairs 0.155. Structural e
quation model fitting indicated that a model with additive and non-add
itive genetic effects, and idiosyncratic environmental effects best ac
counted for the pattern of twin resemblance in both men and women. Gen
etic effects accounted for 35% (in men) and for 39% (in women) of tota
l phenotypic variance in UNS. Analysis of the subscales suggested that
there may be a greater genetic component to the sleepiness subscale,
while environmental components play more of a role in the development
of cataplexy-like symptoms. Further investigation of the complex genet
ic architecture of narcolepsy and its symptoms is warranted.