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Psychological Medicine

Publication date: 2014-01-01
Volume: 44 Pages: 2067 - 2076
Publisher: Cambridge University Press (CUP)

Author:

Fried, E
Nesse, RM ; Zivin, K ; Guille, C ; Sen, S

Keywords:

Depression, depressive symptoms, DSM, heterogeneity, psychiatric diagnosis, residency, Social Sciences, Science & Technology, Life Sciences & Biomedicine, Psychology, Clinical, Psychiatry, Psychology, LIFE EVENTS, CES-D, MAJOR DEPRESSION, DISORDER, ASSOCIATION, COMORBIDITY, CRITERIA, COHORT, ENDOPHENOTYPES, HETEROGENEITY, Adult, Depressive Disorder, Major, Diagnostic and Statistical Manual of Mental Disorders, Disease Progression, Female, Humans, Internship and Residency, Longitudinal Studies, Male, Risk Factors, Young Adult, 1109 Neurosciences, 1117 Public Health and Health Services, 1701 Psychology, 3202 Clinical sciences, 5202 Biological psychology, 5203 Clinical and health psychology

Abstract:

BACKGROUND: For diagnostic purposes, the nine symptoms that compose the DSM-5 criteria for major depressive disorder (MDD) are assumed to be interchangeable indicators of one underlying disorder, implying that they should all have similar risk factors. The present study investigates this hypothesis, using a population cohort that shifts from low to elevated depression levels. METHOD: We assessed the nine DSM-5 MDD criterion symptoms (using the Patient Health Questionnaire; PHQ-9) and seven depression risk factors (personal and family MDD history, sex, childhood stress, neuroticism, work hours, and stressful life events) in a longitudinal study of medical interns prior to and throughout internship (n = 1289). We tested whether risk factors varied across symptoms, and whether a latent disease model could account for heterogeneity between symptoms. RESULTS: All MDD symptoms increased significantly during residency training. Four risk factors predicted increases in unique subsets of PHQ-9 symptoms over time (depression history, childhood stress, sex, and stressful life events), whereas neuroticism and work hours predicted increases in all symptoms, albeit to varying magnitudes. MDD family history did not predict increases in any symptom. The strong heterogeneity of associations persisted after controlling for a latent depression factor. CONCLUSIONS: The influence of risk factors varies substantially across DSM depression criterion symptoms. As symptoms are etiologically heterogeneous, considering individual symptoms in addition to depression diagnosis might offer important insights obfuscated by symptom sum scores.