Association of adverse childhood environment and 5-HTTLPR Genotype with late-life depression

Autor: Marie-Laure Ancelin, Robert Stewart, Isabelle Jaussent, Anne-Marie Dupuy, Karen Ritchie, Alain Malafosse, Philippe Courtet
Přispěvatelé: Villebrun, Dominique, Longévité et vieillissement - Interaction entre la vulnérabilité génétique, la dysrégulation biologique et le stress dans la dépression du sujet âgé - - ESPRIT-VIE2007 - ANR-07-LVIE-0004 - LVIE - VALID, Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Institute of Psychiatry, Queen Mary University of London (QMUL)-King‘s College London, Département de biochimie [Montpellier], Université Montpellier 1 (UM1)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Lapeyronie, Pôle de Psychiatrie, Faculté de Médecine-IFR10-Groupe hospitalier Henri Mondor-Albert Chenevier, Département de Psychiatrie, Geneva University Hospital (HUG)-Hôpital Belle-Idée, Région Languedoc Roussillon, Novartis, ANR-07-LVIE-0004,ESPRIT-VIE,Interaction entre la vulnérabilité génétique, la dysrégulation biologique et le stress dans la dépression du sujet âgé(2007), Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Jazyk: angličtina
Rok vydání: 2009
Předmět:
Child abuse
Male
MESH: Psychiatric Status Rating Scales
child abuse
[SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health
Poison control
Child of Impaired Parents/psychology/statistics & numerical data
Verbal abuse
5-HTTLPR
Social Environment
France/epidemiology
Psychiatric Status Rating Scales/statistics & numerical data
MESH: Genotype
ddc:616.89
0302 clinical medicine
MESH: Aged
80 and over

Child of Impaired Parents
MESH: Risk Factors
Risk Factors
MESH: Child
Longitudinal Studies
MESH: Serotonin Plasma Membrane Transport Proteins
MESH: Longitudinal Studies
Child
Depression (differential diagnoses)
MESH: Social Environment
MESH: Aged
Aged
80 and over

Serotonin Plasma Membrane Transport Proteins
education.field_of_study
Adult Survivors of Child Abuse
1. No poverty
Age Factors
MESH: Stress
Psychological

Late life depression
3. Good health
Life Change Events
Psychiatry and Mental health
depression
Female
France
Serotonin Plasma Membrane Transport Proteins/*genetics
Clinical psychology
Adult
medicine.medical_specialty
Genotype
Adult Survivors of Child Abuse/*psychology/*statistics & numerical data
Population
MESH: Child of Impaired Parents
MESH: Depressive Disorder
Major

Depressive Disorder
Major/epidemiology/*genetics

elderly
Article
03 medical and health sciences
Injury prevention
MESH: Polymorphism
Genetic

medicine
MESH: Adult Survivors of Child Abuse
Humans
Psychiatry
education
Aged
Retrospective Studies
MESH: Age Factors
Psychiatric Status Rating Scales
Depressive Disorder
Major

MESH: Humans
Polymorphism
Genetic

business.industry
MESH: Adult
MESH: Retrospective Studies
MESH: Male
030227 psychiatry
gene-environment interaction
MESH: France
[SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie
MESH: Life Change Events
[SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
business
MESH: Female
030217 neurology & neurosurgery
Stress
Psychological
Zdroj: Journal of Clinical Psychiatry
Journal of Clinical Psychiatry, the American Society of Clinical Psychopharmacology, 2009, 70 (9), pp.1281-8. ⟨10.4088/JCP.08m04510⟩
Journal of Clinical Psychiatry, Physicians Postgraduate Press, 2009, 70 (9), pp.1281-8. ⟨10.4088/JCP.08m04510⟩
Journal of Clinical Psychiatry, Vol. 70, No 9 (2009) pp. 1281-1288
ISSN: 0160-6689
1555-2101
DOI: 10.4088/JCP.08m04510⟩
Popis: International audience; OBJECTIVE: Neurobiological and clinical studies suggest that childhood maltreatment may result in functional and structural nervous system changes that predispose the individual to depression. This vulnerability appears to be modulated by a polymorphism in the serotonin gene-linked promoter region (5-HTTLPR). Little is known, however, about the persistence of this vulnerability across the life span, although clinical studies of adult populations suggest that gene-environment interaction may diminish with aging. METHOD: Depressive symptomatology and adverse and protective childhood events were examined in a population of 942 persons aged 65 years and older, taking into account sociodemographic characteristics and proximal competing causes of depression (widowhood, recent life events, vascular and neurologic disorder, and disability). Subjects were recruited between March 1999 and February 2001 and were diagnosed as depressed if they met 1 of 3 criteria: a diagnosis of major depression on the Mini-International Neuropsychiatric Interview, a score higher than 16 on the Center for Epidemiologic Studies-Depression Scale, or current treatment with an antidepressant. RESULTS: Exposure to traumatic events in childhood doubled the risk of late-life depression and increased the risk of repeated episodes. Not all events were found to be pathogenic; significant risk was associated with excessive sharing of parental problems, poverty or financial difficulties, mental disorder in parents, excessive physical punishment, verbal abuse from parents, humiliation, and mistreatment by an adult outside the family. Interactions were observed between the 5-HTTLPR long (L) allele, poverty, and excessive sharing of parental problems. CONCLUSIONS: Certain types of childhood trauma continue to constitute risk factors for depression in old age, outweighing more proximal causes. Gene environment vulnerability interaction is linked in older age to the L-carrying genotype, modulating the effects of general environmental conditions rather than aggressive acts on the individual, perhaps due to increased cardiac reactivity.
Databáze: OpenAIRE