| Literature DB >> 31207455 |
Viktoria Johansson1, Ralf Kuja-Halkola2, Tyrone D Cannon3, Christina M Hultman2, Anna M Hedman2.
Abstract
Twin- and family studies have shown variations in the heritability estimates of bipolar disorder (BPD). The current study uses an updated statistical methodology for heritability estimation in BPD by taking available time of follow-up into account while controlling for co-variates. We identified monozygotic and dizygotic same and different sex twins with BPD (n = 804) or unaffected from BPD (n = 91,604) from the Swedish Twin Register and the National Patient Register. We applied structural equational modeling with inversed probability weighting to estimate the heritability, taking into account censoring and truncation of data. Sex-limitation models were constructed to analyze qualitative or quantitative sex-differences in BPD. Heritability for BPD was 60.4% (95% Confidence Interval: 50.3-70.5) after age, sex, left-hand truncation and censoring of the data was taken into account. A larger proportion of females were affected from BPD (females 62.2%; males 37.8%, p < 0.001), but no sex-difference in BPD heritability was found, nor any sex-specific genetic effects. We demonstrated a robust 60% heritability for BPD with no evidence of sex-specific genetic effects on disease liability.Entities:
Keywords: Bipolar disorder; Epidemiology; Heritability; Inverse probability weitghing; Liability threshold; Registry data; Sex-differences; Structural equation modeling; Twin study
Mesh:
Year: 2019 PMID: 31207455 DOI: 10.1016/j.psychres.2019.06.010
Source DB: PubMed Journal: Psychiatry Res ISSN: 0165-1781 Impact factor: 3.222