A Comparison of Family History of Psychiatric Disorders among Patients with Early- and Late-Onset Alzheimer's Disease

Journal of Neuropsychiatry and Clinical Neurosciences

Volumn 16, Issue 1, 2004, Pages 57-62

  Devi, Gayatri ^a,d   Williamson, Jennifer ^b   Massoud, Fadi ^b   Anderson, Karen ^b,c   Stern, Yaakov ^b,c   Devanand, D P ^c   Mayeux, Richard ^b,c  

^a LENOX HILL HOSPITAL   (United States)

^b Vagelos College of Physicians and Surgeons   (United States)

^c Och Spine at New York Presbyterian Hospitals   (United States)

^d NY Memory and Healthy Aging Services   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALCOHOLISM; ALZHEIMER DISEASE; ARTICLE; BIPOLAR DISORDER; CONTROLLED STUDY; DEPRESSION; DISEASE ASSOCIATION; FAMILY HISTORY; HUMAN; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MEMORY DISORDER; MENTAL DISEASE; ONSET AGE; PREVALENCE; PRIORITY JOURNAL; RISK FACTOR; SCHIZOPHRENIA; SUICIDE;

EID: 1242352531     PISSN: 08950172     EISSN: None     Source Type: Journal    
DOI: 10.1176/jnp.16.1.57     Document Type: Article

References (34)

1. Van Broeckhoven, CL: Molecular genetics of Alzheimer's disease: identification of genes and gene mutations. Eur Neurol 1995; 35:8-19
2. Cruts M, Van Broeckhoven C: Molecular genetics of Alzheimer's disease. Ann Med 1998; 30(6):560-566
3. Cruts M, van Duijn CM, Backhovens H, et al: Estimation of the genetic contribution of presenilin-1 and -2 mutations in a po pulatioin study of presenile Alzheimer disease. Human Molecular Genetics 1998; 7:43-51
4. Mirra SS: Neuropathological assessment of Alzheimer's disease: the experience of the Consortium to Establish a Registry for Alzheimer's Disease. International Psychogeriatrics. 9 Suppl 1:263-8; discussion 269-272, 1997
5. Campion D, Brice A, Hannequin D, et al: A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization. Neurology 1995; 45(1):80-85
6. Mayeux R, Saunders AM, Shea S, et al: Utility of the apolipoprotein E genotype in the diagnosis of Alzheimer's disease. Alzheimer's Disease Centers Consortium on Apolipoprotein E and Alzheimer's Disease N Engl J Med 1998; 338(8):506-511
7. Bird TD, Sumi SM, Nemens EJ, et al: Phenotypic heterogeneity in familial Alzheimer's disease: a study of 24 kindreds. urnal Article Annals of Neurology 1989; 25(1):12-25
8. Mullan M, Bennett C, Figueredo C, et al: Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14. Am J Med Genet 1995; 60(1):44-52
9. Mangone CA, Castano EM, Levy E, et al: Early onset Alzheimer's disease in a South American pedigree from Argentina. urnal Article Acta Neurologica Scandinavica 1995; 91(1):6-13
10. Rubin EH, Kinscherf DA, Morris JC: Psychopathology in younger versus older persons with very mild and mild dementia of the Alzheimer type. Am J Psychiatry 1993; 150:639-642
11. Pearlson GD, Ross CA, Lohr WD, et al: Association between family history of affective disorder and depressive syndrome in Alzheimer's disease. Am J Psychiatry 1990; 147(4):452-456
12. Strauss ME and Ogrocki PK: Confirmation of an association between family history of affective disorder and the depressive syndrome in Alzheimer's disease. Am J Psychiatry 1996; 153:1340-1342
13. Luchins DJ, Cohen D, Hanrahan P et al: Are there clinical differences between familial and nonfamilial Alzheimer's disease? Am J Psychiatry 1992; 149:1023-1027
14. Lyketsos CG, Tune LE, Pearlson G, et al: Major depression in Alzheimer's disease. An interaction between gender and family history. Psychosomatics 1996; 37(4):380-384
15. Andreasen NC, Endicott J, Spitzer RL, et al: The family history method using diagnostic criteria: Reliability & validity. Arch Gen Psychiatry 1997; 34:1229-1235
16. Silverman JM, Raiford K, Edland S et al: The Consortium to Establish a Registry for Alzheimer's disease (CERAD). Part VI. Family history assessment: A multicenter study of first-degree relatives of Alzheimer's disease patients and nondemented spouse controls. Neurology 1994; 44:1253-1259
17. Devi G, Marder K, Schofield PW, et al: Validity of family history for the diagnosis of dementia among siblings of patients with late onset Alzheimer's Disease. Genet Epidemiol 1998; 15:215-223
18. Jacobs DM, Sano M, Albert S, et al: Cross-cultural neuropsychological assessment: a comparison of randomly selected, demographically, matched cohorts of English- and Spanish- speaking older adults. J Clin Exp Neuropsychol 1997; 19:331-339
19. McKhann G, Drachman D, Folstein M, et al: Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of the Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 1984; 34:939-944
20. Hughes CP, Berg L, Danziger WL, et al: A new clinical scale for the staging of dementia. Br J Psychiatry 1982; 140:566-572
21. Morris JC, McKeel DW, Storandt M, et al: Very mild Alzheimer's disease: informant based clinical, psychometric, and pathologic distinction from normal aging. Neurology 1991; 41:469-478
22. Martin RL, Gerteis J, Gabrielli WF: A family-genetic study of dementia of Alzheimer's type. Arch Gen Psychiatry 1988; 45:894-900
23. Sweet RA, Nimgaonkar VL, Devlin B, et al: Increased familial risk of the psychotic phenotype in Alzheimer disease. Neurology 2002; 58:907-911
24. Friedrich U, Mors O, Ewald H: Systematic chromosome exami-nation of two families with schizophrenia and two families with manic depressive illness. Am J Genet. 1996; 67:58-62
25. Byerley W, Hoff M, Holik J et al: Linkage analysis between schizophrenia and index simple-sequence loci for chromosome 21. Hum Hered 1995; 45:49-52
26. Fukuda R, Hattori M, Sasaki T, et al: No evidence for a point mutation at codon 713 and 717 of amyloid precursor protein gene in Japanese schizophrenics. Japanese J Hum Gen 1993; 38:407-11
27. Adams RD, Victor M: Huntington chorea. Chapter in Principles of neurology, 5th edition, 1993, pp 969-973
28. Pflanz S, Besson JAO, Ebmeier KP, et al: The clinical manifestation of mental disorder in Huntington's Disease: a retrospective case record study of disease progression. Acta Psychiatr Scand 1991; 83:53-60
29. Tsuang D, DiGiacomo L, Lipe H, et al: Familial aggregation of schizophrenia-like symptoms in Huntington's disease. Am J Med Genet 1998; 81(4):323-327
30. Benton CS, de Silva R, Rutledge SL, et al: Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype. Neurology 1998; 51(4):1081-1086
31. Farrer LA, O'Sullivan DM, Cupples LA, et al: Assessment of genetic risk for Alzheimer's disease among first-degree relatives. Ann Neurol 1989; 25:485-493
32. Huff JF, Auerbach J, Chakravarti A, et al: Risk of dementia in relatives of patients with Alzheimer's disease. Neurology 1988; 38:786-790
33. Breitner JCS, Silverman JM, Mohs RC, Davis KL. Familial aggregation in Alzheimer's disease: Comparison of risk among relatives of early- and late-onset cases, and among male and female relatives in successive generations. Neurology 1988; 38:207-212
34. Massoud F, Devi G, Stern Y, et al: A clinicopathological comparison of community-based and clinic-based cohorts of patients with dementia. Arch Neurol 1999; 56:1368-1373