The heritability of cluster A personality disorders assessed by both personal interview and questionnaire

• Published in: Psychological medicine 2007-05, Vol.37 (5), p.655-665
• Main Authors: KENDLER, KENNETH S., MYERS, JOHN, TORGERSEN, SVENN, NEALE, MICHAEL C., REICHBORN-KJENNERUD, TED
• Format: Article
• Language: English
• Subjects: Adult; Adult and adolescent clinical studies; Biological and medical sciences; Cluster Analysis; Diagnostic and Statistical Manual of Mental Disorders; Environmental aspects; Female; Genetic factors; Genetics; Health risk assessment; Heritability; Humans; Interview, Psychological; Interviews; Male; Medical sciences; Original Article; Personality disorders; Personality Disorders - classification; Personality Disorders - diagnosis; Personality Disorders - genetics; Psychiatry; Psychological aspects; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Risk factors; Surveys and Questionnaires; Twins - genetics; Twins - psychology; Type A Personality
• ISSN: 0033-2917; 1469-8978
• DOI: 10.1017/S0033291706009755

Background. Personality disorders (PDs) as assessed by questionnaires and personal interviews are heritable. However, we know neither how much unreliability of measurement impacts on heritability estimates nor whether the genetic and environmental risk factors assessed by these two methods are the same. We wish to know whether the same set of PD vulnerability factors are assessed by these two methods. Method. A total of 3334 young adult twin pairs from the Norwegian Institute of Public Health Twin Panel (NIPHTP) completed a questionnaire containing 91 PD items. One to 6 years later, 1386 of these pairs were interviewed with the Structured Interview for DSM-IV Personality (SIDP-IV). Self-report items predicting interview results were selected by regression. Measurement models were fitted using Mx. Results. In the best-fit models, the latent liabilities to paranoid personality disorder (PPD), schizoid personality disorder (SPD) and schizotypal personality disorder (STPD) were all highly heritable with no evidence of shared environmental effects. For PPD and STPD, only unique environmental effects were specific to the interview measure whereas both environmental and genetic effects were found to be specific to the questionnaire assessment. For SPD, the best-fit model contained genetic and environmental effects specific to both forms of assessment. Conclusions. The latent liabilities to the cluster A PDs are highly heritable but are assessed by current methods with only moderate reliability. The personal interviews assessed the genetic risk for the latent trait with excellent specificity for PPD and STPD and good specificity for SPD. However, for all three PDs, the questionnaires were less specific, also indexing an independent set of genetic risk factors.