International Psychogeriatrics



2001 IPA Research Awards in Psychogeriatrics: First-Place Winner

The 5-HTTPR Polymorphism Confers Liability to a Combined Phenotype of Psychotic and Aggressive Behavior in Alzheimer Disease


Robert A. Sweet a1, Bruce G. Pollock a1, Danielle L. Sukonick a1, Benoit H. Mulsant a1a4, Jules Rosen a1, William E. Klunk a1, Kari B. Kastango a1, Steven T. DeKosky a1a2 and Robert E. Ferrell a3
a1 Division of Geriatrics and Neuropsychiatry, Department of Psychiatry, Pittsburgh, Pennsylvania, US
a2 Department of Neurology, School of Medicine, Pittsburgh, Pennsylvania, US
a3 Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, US
a4 Geriatric Research, Education, and Clinical Center (GRECC), VA Pittsburgh Health Care System, Pittsburgh, Pennsylvania, US.

Article author query
sweet r   [PubMed][Google Scholar] 
pollock b   [PubMed][Google Scholar] 
sukonick d   [PubMed][Google Scholar] 
mulsant b   [PubMed][Google Scholar] 
rosen j   [PubMed][Google Scholar] 
klunk w   [PubMed][Google Scholar] 
kastango k   [PubMed][Google Scholar] 
dekosky s   [PubMed][Google Scholar] 
ferrell r   [PubMed][Google Scholar] 

Abstract

Background: Psychotic symptoms in subjects with Alzheimer disease (AD+psychosis, AD+P) are a marker for a distinct phenotype characterized by more rapid cognitive and functional decline and a liability to aggressive behaviors. We recently found that AD subjects homozygous for long alleles (l) of an insertion/deletion polymorphism in the promoter region of the serotonin transporter (5-HTTPR) had elevated rates of aggressive behavior. Objective: To examine whether the 5-HTTPR ll genotype confers an increased risk of AD+P, and of the combined AD+P/aggressive phenotype. Methods: The 5-HTTPR genotype was determined in 332 subjects diagnosed with possible or probable AD. All subjects received structured psychiatric assessments and were categorized with regard to their history of aggressive behaviors and psychotic symptoms. Results: Consistent with other reports, AD+P was associated with a significant increased risk for aggressive behavior. AD+P and aggression were both significantly associated with 5-HTTPR ll genotype and with an increased l allele frequency. Subjects with the combined behavioral phenotype (AD+P and aggressive behavior) had the highest rate of ll genotype and highest l allele frequency. Conclusion: The 5-HTTPR l allele appears to confer risk for the combined AD+P/aggressive phenotype. Confirmation of this association in a similar behaviorally well-characterized independent sample is needed.


Key Words: Serotonin transporter; Alzheimer disease; genetic; polymorphism; psychosis.


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