Morbid risk for schizophrenia in first-degree relatives of people with frontotemporal dementia.

Delphine Schoder, Didier Hannequin, Olivier Martinaud, Gaëlle Opolczynski, Lucie Guyant-Maréchal, Isabelle Le Ber, Dominique Campion
Author Information
  1. Delphine Schoder: INSERM U614, University of Medicine, Rouen, and Department of Research, Rouvray Psychiatric Hospital, Sotteville-les-Rouen, France.

Abstract

BACKGROUND: Familial co-occurrence of frontotemporal dementia and schizophrenia has never been investigated.
AIMS: To test the hypothesis that frontotemporal dementia and schizophrenia might have a common aetiology in some families in which both syndromes coexist (mixed families).
METHOD: The morbid risk for schizophrenia, calculated in first-degree relatives of 100 frontotemporal dementia probands, was compared with that calculated in first-degree relatives of 100 Alzheimer's disease probands. In mixed families, sequencing analysis of known frontotemporal dementia genes and detailed phenotype characterisation of individuals with frontotemporal dementia and schizophrenia were performed.
RESULTS: The morbid risk for schizophrenia was significantly higher in relatives of frontotemporal dementia probands (1.35, s.e. = 0.45) than in relatives of Alzheimer's disease probands (0.32, s.e. = 0.22). Ten mixed families were characterised. In three of them a frontotemporal dementia causal mutation was identified that was present in individuals with schizophrenia. Several specific clinical features were noted in people with schizophrenia and frontotemporal dementia in mixed families.
CONCLUSIONS: Co-occurrence of schizophrenia and frontotemporal dementia could indicate, in some families, a common aetiology for both conditions.

MeSH Term

Adult
Age of Onset
Aged
Aged, 80 and over
Diagnosis, Differential
Female
Frontotemporal Dementia
Humans
Male
Middle Aged
Mutation
Neuropsychological Tests
Pedigree
Risk Assessment
Schizophrenia
Schizophrenic Psychology
Young Adult

Word Cloud

Created with Highcharts 10.0.0frontotemporaldementiaschizophreniafamiliesrelativesmixedprobandsriskfirst-degree0commonaetiologymorbidcalculated100Alzheimer'sdiseaseindividualsse=peopleBACKGROUND:Familialco-occurrenceneverinvestigatedAIMS:testhypothesismightsyndromescoexistMETHOD:comparedsequencinganalysisknowngenesdetailedphenotypecharacterisationperformedRESULTS:significantlyhigher135453222TencharacterisedthreecausalmutationidentifiedpresentSeveralspecificclinicalfeaturesnotedCONCLUSIONS:Co-occurrenceindicateconditionsMorbid

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