ArticleJournal of affective disorders2013
Using multiple methods to characterize the phenotype of individuals with a family history of major depressive disorder.
Article in Journal of affective disorders, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.
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Who cites it
8 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.
- Cognitive Performance in First-Degree Relatives of Individuals With vs Without Major Depressive Disorder: A Meta-analysis.JAMA psychiatry · 2019Pooled it
- Affective Processing in Depression Risk: Insights From Event-Related Potentials.Psychophysiology · 2026Article
- A Machine Learning Model for Predicting Depression in Moroccan Rheumatoid Arthritis Patients.Cureus · 2025Article
- Familial risk for depression is associated with reduced physical activity in young adults: evidence from a wrist-worn actigraphy study.Translational psychiatry · 2024Article
- Polygenic Risk of Schizophrenia and Cognition in a Population-Based Survey of Older Adults.Schizophrenia bulletin · 2016Article
- The prevalence, measurement, and treatment of the cognitive dimension/domain in major depressive disorder.CNS drugs · 2015Review
- The Effects of Tryptophan on Everyday Interpersonal Encounters and Social Cognitions in Individuals with a Family History of Depression.The international journal of neuropsychopharmacology · 2015Article
- Developmental change in amygdala reactivity during adolescence: effects of family history of depression and stressful life events.The American journal of psychiatry · 2015Article
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 2 countries.
Funding
Abstract
backgroundUnaffected relatives (URs) of individuals with major depressive disorder (MDD) are biologically more vulnerable to depression. We compare healthy URs and controls at the level of phenotype (symptoms and functioning) and endophenotype (negative emotion bias), and further investigate the interrelation between these and the contribution of environmental early life stress.
methodsURs (n=101), identified using Family History Screen interview methods and matched controls completed written and interview questions assessing symptoms of depression and anxiety, negative cognitive style, life functioning and early life stress. Biases in emotion processing were measured using a facial expression of emotion identification paradigm.
resultsCompared to controls, URs reported higher levels of depression and anxiety, a stronger negative cognitive bias, and poorer functioning and lower satisfaction with life. URs were slower to correctly identify fear and sad facial expressions. A slower response time to identify sad faces was correlated with lower quality of life in the social domain. Early life stress (ELS) did not contribute significantly to any outcome. LIMITATIONS: The methodology relies on accurate reporting of participants' own psychiatric history and that of their family members. The degree of vulnerability varies among URs.
conclusionsA family history of depression accounts for subtle differences in symptom levels and functioning without a necessary role of ELS. A negative emotion bias in processing emotion may be one vulnerability marker for MDD. Biological markers may affect functioning measures before symptoms at the level of experience.
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