Assessment and familial aggregation of psychosis in Alzheimer's disease from the National Institute on Aging Late Onset Alzheimer's Disease Family Study.

Determining the genetic architecture of late onset Alzheimer's disease remains an important research objective. One approach to the identification of novel genetic variants contributing to the disease is the classification of biologically meaningful subgroups within the larger late-onset Alzheimer's disease phenotype. The occurrence of psychotic symptoms in patients with late-onset Alzheimer's disease may identify one such group. We attempted to establish methods for the reliable assessment of psychotic symptoms in a large, geographically dispersed collection of families, multiply affected with late onset Alzheimer's disease, who were participants in the larger National Institute on Aging Late Onset Alzheimer's Disease Family Study; and to characterize the correlates and familial aggregation of psychosis within this cohort. We found that reliable assessments of psychotic symptoms during in-person or phone interviews were readily implemented. The presence of psychosis in late onset Alzheimer's disease was significantly associated with degree of cognitive impairment, and significantly, albeit modestly, correlated with the severity of other behavioural symptoms. Psychosis significantly aggregated within late onset Alzheimer's disease families suggesting that it may identify a genetically determined subgroup. Future studies should examine the linkage and association of psychosis with genetic variation within these families.

[1]  M. Folstein,et al.  Clinical diagnosis of Alzheimer's disease: Report of the NINCDS—ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease , 2011, Neurology.

[2]  M Krawczak,et al.  Examination of the current top candidate genes for AD in a genome-wide association study , 2010, Molecular Psychiatry.

[3]  L. Kiemeney,et al.  Corrigendum: Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer , 2009, Nature Genetics.

[4]  T. Kudo,et al.  SORL1 is genetically associated with Alzheimer disease in a Japanese population , 2009, Neuroscience Letters.

[5]  P. Bosco,et al.  Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease , 2009, Nature Genetics.

[6]  Y. Teo,et al.  SORL1 haplotypes modulate risk of Alzheimer's disease in Chinese , 2009, Neurobiology of Aging.

[7]  F. Jessen,et al.  Association of SORL1 gene variants with Alzheimer's disease , 2009, Brain Research.

[8]  K. Sleegers,et al.  SORL1 is genetically associated with increased risk for late‐onset Alzheimer disease in the Belgian population , 2008, Human mutation.

[9]  Feng Gu,et al.  A novel mutation in AlphaA‐crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family , 2008, Human mutation.

[10]  M. Owen,et al.  SORL1 variants and risk of late-onset Alzheimer’s disease , 2008, Neurobiology of Disease.

[11]  M. Hamshere,et al.  Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[12]  K. Lunetta,et al.  The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease , 2007, Nature Genetics.

[13]  O. Lopez,et al.  Prediction of psychosis onset in Alzheimer disease: The role of cognitive impairment, depressive symptoms, and further evidence for psychosis subtypes. , 2006, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

[14]  D. Jeste,et al.  Epidemiology of and risk factors for psychosis of Alzheimer's disease: a review of 55 studies published from 1990 to 2003. , 2005, The American journal of psychiatry.

[15]  M. Albert,et al.  Delusions and hallucinations are associated with worse outcome in Alzheimer disease. , 2005, Archives of neurology.

[16]  B. Devlin,et al.  Heritability of psychosis in Alzheimer disease. , 2005, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

[17]  J. Becker,et al.  Psychiatric symptoms vary with the severity of dementia in probable Alzheimer's disease. , 2003, The Journal of neuropsychiatry and clinical neurosciences.

[18]  C. Lyketsos,et al.  The relationship between delusions and depression in Alzheimer's disease , 2002, International journal of geriatric psychiatry.

[19]  B. Devlin,et al.  Increased familial risk of the psychotic phenotype of Alzheimer disease , 2002, Neurology.

[20]  C. Lyketsos,et al.  Neuropsychiatric disturbance in Alzheimer's disease clusters into three groups: the Cache County study , 2001, International journal of geriatric psychiatry.

[21]  P. M. Conneally,et al.  Identification of Novel Genes in Late-Onset Alzheimer's Disease , 2000, Experimental Gerontology.

[22]  J. Cummings,et al.  Validation of the NPI-Q, a brief clinical form of the Neuropsychiatric Inventory. , 2000, The Journal of neuropsychiatry and clinical neurosciences.

[23]  M. Owen,et al.  Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. , 2000, The British journal of psychiatry : the journal of mental science.

[24]  J. L. Mack,et al.  Behavior Rating Scale for Dementia: Development of Test Scales and Presentation of Data for 555 Individuals with Alzheimer's Disease , 1999, Journal of geriatric psychiatry and neurology.

[25]  E. Tangalos,et al.  Mild Cognitive Impairment Clinical Characterization and Outcome , 1999 .

[26]  M. Owen,et al.  A full genome scan for late onset Alzheimer's disease , 1999 .

[27]  J. Cummings,et al.  Assessing the Impact of Neuropsychiatric Symptoms in Alzheimer's Disease: The Neuropsychiatric Inventory Caregiver Distress Scale , 1998, Journal of the American Geriatrics Society.

[28]  J. Haines,et al.  Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. , 1997, JAMA.

[29]  J. Haines,et al.  Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis , 1997 .

[30]  G. Schellenberg,et al.  Candidate gene for the chromosome 1 familial Alzheimer's disease locus , 1995, Science.

[31]  D. Pollen,et al.  Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease , 1995, Nature.

[32]  M. Pericak-Vance,et al.  Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease , 1991, Nature.

[33]  Wayne C. Drevets,et al.  Psychotic symptoms and the longitudinal course of senile dementia of the Alzheimer type , 1989, Biological Psychiatry.

[34]  M. Folstein,et al.  Clinical diagnosis of Alzheimer's disease , 1984, Neurology.

[35]  C. P. Hughes,et al.  A New Clinical Scale for the Staging of Dementia , 1982, British Journal of Psychiatry.

[36]  R. Sweet,et al.  Genetics of psychosis in Alzheimer's disease: a review. , 2010, Journal of Alzheimer's disease : JAD.

[37]  Nick C Fox,et al.  Letter abstract - Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's Disease , 2009 .

[38]  D. Drubach Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: Implication of Additional Loci , 2009 .

[39]  B. Devlin,et al.  Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype , 2003, Molecular Psychiatry.

[40]  A. Burns Clinical diagnosis of Alzheimer's disease , 1991 .