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Genetic heterogeneity and subtypes of major depression.
Nguyen, Thuy-Dung; Harder, Arvid; Xiong, Ying; Kowalec, Kaarina; Hägg, Sara; Cai, Na; Kuja-Halkola, Ralf; Dalman, Christina; Sullivan, Patrick F; Lu, Yi.
  • Nguyen TD; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Harder A; Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
  • Xiong Y; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Kowalec K; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Hägg S; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Cai N; College of Pharmacy, University of Manitoba, Winnipeg, Canada.
  • Kuja-Halkola R; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Dalman C; Helmholtz Pioneer Campus, Helmholtz Zentrum München, Neuherberg, Germany.
  • Sullivan PF; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Lu Y; Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.
Mol Psychiatry ; 27(3): 1667-1675, 2022 03.
Article en En | MEDLINE | ID: mdl-34997191
Major depression (MD) is a heterogeneous disorder; however, the extent to which genetic factors distinguish MD patient subgroups (genetic heterogeneity) remains uncertain. This study sought evidence for genetic heterogeneity in MD. Using UK Biobank cohort, the authors defined 16 MD subtypes within eight comparison groups (vegetative symptoms, symptom severity, comorbid anxiety disorder, age at onset, recurrence, suicidality, impairment, and postpartum depression; N ~ 3000-47000). To compare genetic component of these subtypes, subtype-specific genome-wide association studies were performed to estimate SNP-heritability, and genetic correlations within subtype comparison and with other related disorders/traits. The findings indicated that MD subtypes were divergent in their SNP-heritability, and genetic correlations both within subtype comparisons and with other related disorders/traits. Three subtype comparisons (vegetative symptoms, age at onset, and impairment) showed significant differences in SNP-heritability; while genetic correlations within subtype comparisons ranged from 0.55 to 0.86, suggesting genetic profiles are only partially shared among MD subtypes. Furthermore, subtypes that are more clinically challenging, e.g., early-onset, recurrent, suicidal, more severely impaired, had stronger genetic correlations with other psychiatric disorders. MD with atypical-like features showed a positive genetic correlation (+0.40) with BMI while a negative correlation (-0.09) was found in those without atypical-like features. Novel genomic loci with subtype-specific effects were identified. These results provide the most comprehensive evidence to date for genetic heterogeneity within MD, and suggest that the phenotypic complexity of MD can be effectively reduced by studying the subtypes which share partially distinct etiologies.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trastorno Depresivo Mayor Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans Idioma: En Año: 2022 Tipo del documento: Article