Evidence of genetic susceptibility to infectious mononucleosis: a twin study

Epidemiol Infect. 2012 Nov;140(11):2089-95. doi: 10.1017/S0950268811002457. Epub 2011 Dec 8.

Abstract

Infectious mononucleosis is a clinical manifestation of primary Epstein-Barr virus infection. It is unknown whether genetic factors contribute to risk. To assess heritability, we compared disease concordance in monozygotic to dizygotic twin pairs from the population-based California Twin Program and assessed the risk to initially unaffected co-twins. One member of 611 and both members of 58 twin pairs reported a history of infectious mononucleosis. Pairwise concordance in monozygotic and dizygotic pairs was respectively 12·1% [standard error (s.e.)=1·9%] and 6·1% (s.e.=1·2%). The relative risk (hazard ratio) of monozygotic compared to dizygotic unaffected co-twins of cases was 1·9 [95% confidence interval (CI) 1·1-3·4, P=0·03], over the follow-up period. When the analysis was restricted to same-sex twin pairs, that estimate was 2·5 (95% CI 1·2-5·3, P=0·02). The results are compatible with a heritable contribution to the risk of infectious mononucleosis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Twin Study

MeSH terms

  • Adolescent
  • Adult
  • California
  • Female
  • Follow-Up Studies
  • Genetic Predisposition to Disease*
  • Humans
  • Infectious Mononucleosis / genetics*
  • Male
  • Proportional Hazards Models
  • Registries
  • Risk
  • Self Report
  • Twins, Dizygotic
  • Twins, Monozygotic
  • Young Adult