A Hospital-Based Twin Register of the Heritability of DSM-IV Unipolar Depression
Abstract
OBJECTIVES: To estimate the contribution of genes and shared family environment to the liability to DSM-IV major depression and to examine the influence of certain proband characteristics on twin concordance. METHODS: We studied 177 probands with major depressive disorder ascertained via the Maudsley Hospital Twin Register (London, England) and their same-sex co-twins. Diagnostic assessments were carried out blind to zygosity and information on the other member of the twin pair. Probandwise concordances were used to compute correlations in liability, and model fitting was performed using maximum likelihood procedures. RESULTS: The probandwise concordance was 46% in monozygotic (n = 68) and 20% in dizygotic (n = 109) twins, a statistically highly significant difference. There was no evidence of a sex difference in heritability or of shared environmental effects. Depending on the assumed population risks for DSM-IV, major depression estimates of heritability were between 48% and 75%. A duration of longest episode of less than 13 months, multiple episodes, and an endogenous rather than neurotic pattern of symptoms as established by the International Classification of Diseases, Ninth Revision, in the proband were associated with a trend toward a higher monozygotic-dizygotic concordance ratio. Using log-linear analysis, only the association between duration of episodes and monozygotic-dizygotic concordance ratio was significant. CONCLUSIONS: Liability to DSM-IV major depression has a substantial heritable component, and there is no evidence of an effect of shared family environment. Some proband characteristics, especially shorter duration of episodes, may be associated with a larger degree of genetic determination.
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Monozygotic twins and first-degree relatives also have an increased likelihood of developing psychotic, bipolar or common mental disorders.
“Monozygotic twins 123-126 and first-degree relatives (depending on the number of probands) 127-130 also have an increased likelihood of developing these disorders.”
From Preventive psychiatry: a blueprint for improving the mental health of young people (2021) · cites this paper as [126]
Monozygotic twins have a concordance rate of 46% for depression.
“Twins (monozygotic concordance rate - depression: 46% 126 *; anxiety: 13-73% 125 *)”
From Preventive psychiatry: a blueprint for improving the mental health of young people (2021) · cites this paper as [126]
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References 27 · Cited by 373
- Authors
- McGuffin, P.
- Affiliations
- Cardiff University (GB)
- Corresponding author
- McGuffin, Peter
- Venue
- Archives of General Psychiatry
- Publisher
- American Medical Association (AMA)
- Published
- 1996-02-01
- Volume
- 53
- Issue
- 2
- Pages
- 129
- ISSN
- 0003-990X (ISSN-L)
- OpenAlex
- W2035054885
- Cited by
- 373
- References
- 27
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 8 · 2023: 8 · 2022: 2 · 2021: 7 · 2020: 8 · 2019: 8 · 2018: 9 · 2017: 17 · 2016: 10 · 2015: 19 · 2014: 16 · 2013: 16 · 2012: 20
- FWCI
- 5.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Archives of General Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Keywords
- major depressive disorder, heritability, monozygotic twins, dizygotic twins, twin concordance, shared family environment, episode duration, genetic susceptibility
- MeSH terms
- Adult, Depressive Disorder, Diseases in Twins, Family, Female, Humans, London, Male, Models, Genetic, Registries, Sex Factors, Twins, Dizygotic, Twins, Monozygotic, Likelihood Functions, Linear Models, Age of Onset
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