Genetic and environmental influences on psychological distress in the population: General Health Questionnaire analyses in UK twins

• Published in: Psychological medicine 2003-07, Vol.33 (5), p.793-801
• Main Authors: RIJSDIJK, F. V., SNIEDER, H., ORMEL, J., SHAM, P., GOLDBERG, D. P., SPECTOR, T. D.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Adult and adolescent clinical studies; Aged; Anxiety; Biological and medical sciences; Cohort Studies; Depression; Diseases in Twins; Female; Health Status Indicators; Hospitals; Humans; Medical sciences; Mental depression; Mental disorders; Mental Disorders - epidemiology; Mental Disorders - genetics; Middle Aged; Models, Genetic; Mood disorders; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Questionnaires; Risk Factors; Stress, Psychological - epidemiology; Stress, Psychological - genetics; Surveys and Questionnaires; Twins; Twins, Dizygotic; Twins, Monozygotic; United Kingdom - epidemiology
• ISSN: 0033-2917; 1469-8978
• DOI: 10.1017/S0033291703007451

Background. The General Health Questionnaire (GHQ) is the most popular screening instrument for detecting psychiatric disorders in community samples. Using longitudinal data of a large sample of UK twin pairs, we explored (i) heritabilities of the four scales and the total score; (ii) the genetic stability over time; and (iii) the existence of differential heritable influences at the high (ill) and low (healthy) tail of the distribution. Method. At baseline we assessed the GHQ in 627 MZ and 1323 DZ female pairs and at a second occasion (3·5 years later) for a small subsample (90 MZ and 270 DZ pairs). Liability threshold models and raw ordinal maximum likelihood were used to estimate twin correlations and to fit longitudinal genetic models. We estimated extreme group heritabilities of the GHQ distribution by using a model-fitting implementation of the DeFries–Fulker regression method for selected twin data. Results. Heritabilities for Somatic Symptoms, Anxiety, Social Dysfunction, Depression and total score were 0·37, 0·40, 0·20, 0·42 and 0·44, respectively. The contribution of shared genetic factors to the correlations between time points is substantial for the total score (73%). Group heritabilities of 0·48 and 0·43 were estimated for the top and bottom 10% of the total GHQ score distribution, respectively. Conclusion. The overall heritability of the GHQ as a measure of psychosocial distress was substantial (44%), with all scales having significant additive genetic influences that persisted across time periods. Extreme group analyses suggest that the genetic control of resilience is as important as the genetic control of vulnerability.