Genetic and environmental contributions to depressive personality disorder in a population-based sample of Norwegian Twins

被引:23
|
作者
Orstavik, Ragnhild Elise
Kendler, Kenneth S.
Czajkowski, Nikolai
Tambs, Kristian
Reichborn-Kjennerud, Ted
机构
[1] Norwegian Inst Publ Hlth, Dept Mental Hlth, N-0403 Oslo, Norway
[2] Univ Oslo, Inst Psychiat, N-0316 Oslo, Norway
[3] Virginia Commonwealth Univ, Med Coll Virginia, Virginia Inst Psychiat & Behav Genet, Richmond, VA 23298 USA
[4] Virginia Commonwealth Univ, Med Coll Virginia, Dept Psychiat & Human Genet, Richmond, VA 23298 USA
基金
美国国家卫生研究院;
关键词
depressive personality disorder; personality; heritability; twin study;
D O I
10.1016/j.jad.2006.09.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Depressive personality disorder (DPD) was introduced in DSM-IV as a new category requiring further study. The aim of this study was to estimate genetic and environmental contributions to DPD in a population-based twin sample, and include data on criteria performance, prevalence and diagnostic overlap. Methods: Axis I and Axis II diagnoses were obtained by structured interviews in a population-based sample of 2794 young adult twins. Statistical analyses included correlation and factor analysis based on polychoric correlation coefficients, and diagnostic overlap applying adjusted odds ratios. Contributions from additive genetic and common and unique environmental influences to the liability to DPD were computed using, structural equation modelling, applying a multiple threshold variable. Results: Liability to DPD could best be explained by additive genetic and unique environmental factors, with heritability estimates of 49% (95% CI 0.41-0.57) in females and 25% (95% CI 0.12-0.40) in males. The best-fitting model indicated that some of the genes contributing to DPD differ between men and women. Chronbach's alpha was 0.87.2.0% of participants fulfilled the criteria for DPD, and overlap was most pronounced for dysthymic disorder and avoidant personality disorder. Limitations: Low prevalence rates and subsequent inclusion of subthreshold criteria could have influenced parameter estimates, especially in males. Conclusions: DPD, was almost twice as heritable in females as in males, comparable to previous studies on major depression. The proposed criteria showed good measurement properties, and DPD was not completely subsumed within any other disorder. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 189
页数:9
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