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Arq Med Hosp Fac Cienc Med Santa Casa São Paulo
2008; 53(1):24-30
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
Tabela 1
Freqüência dos Alelos da ApoE encontrados na População em Geral e em Pacientes com DA (Corder et al, 1993)17
Alelo Códon 112 Códon 158 População Geral Pacientes com DA
E2 cisteína cisteína 7% 4%
E3 cisteína arginina 78% 56%
E4 arginina arginina 14% 40%
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
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Cordeiro Q, Zung S, Vallada H. Genética das demências. Arq Med Hosp Fac Cienc Med Santa Casa São Paulo. 2008; 53(1): 24-30.
18. Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, external carotid dysplasia. Neurology. 2000; 55:1661-7.
Enghild J, Salvesen GS, et al. Apolipoprotein E: high-avidity 38. Liddell MB, Williams J, Owen M. The dementias. In: McGuffin
binding to b-amyloid and increased frequency of type 4 allele P, Owen MJ, Gottesman I, editors. Psychiatric genetics and
in late-onset familial Alzheimer disease. Proc Natl Acad Sci genomics. New York: Oxford University Press; 2002. p. 341-93.
USA. 1993; 90:1977-81. 39. Saunders AM, Roses AD. Apolipoprotein E4 allele frequency,
19. de-Andrade FM, Larrandaburu M, Callegari-Jacques SM, ischemic cerebrovascular disease, and Alzheimer’s disease.
Gastaldo G, Hutz MH. Association of apolipoprotein E Stroke. 1993; 24:1416-7.
polymorphism with plasma lipids and Alzheimer’s disease in 40. Betard C, Robitaille Y, Gee M, Tiberghien D, Larrivee D, Roy P,
a Southern Brazilian population. Braz J Med Biol Res. 2000; et al. ApoE allele frequencies in Alzheimer’s disease, Lewy body
33:529-37. dementia, Alzheimer’s disease with cerebrovascular disease and
20. Souza DR, de Godoy MR, Hotta J, Tajara EH, Brandão AC, Pi- cerebrovascular dementia. Neuroreport. 1994;5:1893-6.
nheiro Junior S, et al. Association of apolipoprotein E 41. Spillantini MG, Goedert M. Tau protein pathology in
polymorphism in late-onset Alzheimer’s disease and vascular neurodegenerative diseases. [Review] Trends Neurosci. 1998;
dementia in Brazilians. Braz J Med Biol Res. 2003; 36:919-23. 21:428-33.
21. Breitner JC. APOE genotyping and Alzheimer’s disease. Lancet. 42. Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H,
1996; 347:1184-5. et al. Association of missense and 5’-splice-site mutations in tau
22. Breitner JC, Wyse BW, Anthony JC, Welsh-Bohmer KA, Steffens with the inherited dementia FTDP-17. Nature. 1998; 393:702-5.
DC, Norton MC, et al. APOE-epsilon4 count predicts age when 43. Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM,
prevalence of AD increases, then declines: the Cache County Anderson L, et al. Tau is a candidate gene for chromosome 17
Study. Neurology.1999; 53:321-31. frontotemporal dementia. Ann Neurol. 1998; 43:815-25.
23. Seshadri S, Drachman DA, Lippa CF. Apolipoprotein E: 4 allele 44. Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine
and the lifetime risk of Alzheimer’s disease: what physicians ZS, Miller B, et al. Pathogenic implications of mutations in the
know and what they should know. Arch Neurol. 1995; 52:1074- tau gene in pallido-ponto-nigral degeneration and related
9. neurodegenerative disorders linked to chromosome 17. Proc
24. Seshadri S, Wolf PA, Beiser A. Lifetime risk of dementia and Natl Acad Sci USA. 1998; 95:13103-7.
Alzheimer’s disease: the impact of mortality on risk estimates 45. Goedert M, Spillantini MG, Crowter RA, Chen SG, Parchi P,
in the Framingham study. Neurology. 1997; 49:1498-504. Tabaton M, et al. Tau gene mutation in familial progressive
25. Blacker D, Wilcox MA, Laird NM, Rodes L, Horvath SM, Go subcortical gliosis. Nat Med. 1999; 5:454-7.
RC, et al. Alpha-2 macroglobulin is genetically associated with 46. Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy
Alzheimer disease. Nat Genet .1998; 19:357-60. J, et al. Familial non-specific dementia maps to chromosome 3.
26. Dodel RC, Du Y, Bales KR, Gao F, Eastwood B, Glazier B, et al. Hum Mol Genet. 1995; 4:1625-8.
Alpha2 macroglobulin and the risk of Alzheimer’s disease. 47. Hoenicka J, Perez M, Perez-Tur J, Barabash A, Godoy M, Vidal
Neurology. 2000; 54:438-42. L, et al. The tau gene A0 allele and progressive supranuclear
27. Li YJ, Oliveira SA, Xu P, Martin ER, Stenger JE, Scherzer CR, et palsy. Neurology. 1999; 53:1219-25.
al. Glutathione S- transferase omega-1 modifiesage-at-onset of 48. Gutekunst CA, Norflus F, Hersch SM. Recent advances in
Alzheimer disease and Parkinson disease. Hum Mol Genet. Huntington’s disease. [Review] Curr Opin Neurol. 2000; 13:445-50.
2003; 12:3259-67. 49. Ranen NG, Stine OC, Abbott MH, Sherr M, Codori AM, Franz
28. Hademenos GJ, Alberts MJ, Awad I, Mayberg M, Shepard T, ML, et al. Anticipation and instability of IT-15 (CAG)n repeats
Jagoda A, et al. Advances in genetics of cerebrovascular disease in parent-offspring pairs with Huntington disease. Am J Hum
and stroke. [Review] Neurology. 2001; 56:997-1008. Genet. 1995; 57:593-602.
29. Onda H, Kasuya H, Yoneyama T, Takakura K, Hori T, Takeda 50. Trottier Y, Devys D, Imbert G, Saudou F, An I, Lutz Y, et al.
J, et al. Genomewide-linkage and haplotype-association studies Cellular localization of the Huntington’s disease protein and
map intracranial aneurysm to chromosome 7q11. Am J Med discrimination of the normal and mutated form. Nat Genet. 1995;
Genet. 2001; 69:804-19. 10:104-10.
30. Räihä I, Kaprio J, Koskenvuo M, Rajala T, Sourander L. 51. Johnson RT, Gibbs CJ Jr. Creutzfeldt-Jakob disease and related
Alzheimer’s disease in Finnish twins. Lancet. 1996; 347:573-8. transmissible spongiform encephalopathies. [Review] N Engl J
31. Abrahamson M, Grubb A. Increased body temperature Med. 1998; 339:1994-2004.
accelerates aggregation of the Leu-68 Gln mutant cystatin C, 52. Sparkes RS, Simon M, Cohn VH, Fournier RE, Lem J, Klisak I,
the amyloid forming in hereditary cystatin C amyloid et al. Assignment of the human and mouse prion protein genes
angiopathy. Proc Natl Acad Sci USA. 1994; 91:1416-20. to homologous chromosomes. Proc Natl Acad Sci USA. 1986;
32. Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, 83:7358-62.
Poyhonen M, et al. CADASIL: hereditary disease of arteries 53. Liao YC, Lebo RV, Clawson GA, Smuckler EA.. Human prion
causing brain infarcts and dementia. [Review] Neuropathol protein cDNA: molecular cloning, chromosomal mapping, and
Appl Neurobiol. 1999; 25:257-65. biological implications. Science. 1986; 233:364-7.
33. Tournier-Lasserve E, Joutel A, Melki J Weissenbach J, Lathrop 54. National Center of Biotechnology Information (NCBI), National
GM, Chabriat H, et al. Cerebral autosomal dominant Library of Medicine, National Institutes of Health, University
arteriopathy with subcortical infarcts and leukoencephalopathy John Hopkins. On line Mendelian Inheritance in Man (OMIM).
maps to chromosome 19q12. Nat Genet. 1993; 3:256-9. *176640 PRION PROTEIN; PRNP. Alternative titles; symbols.
34. Joutel A, Corpechot C, Ducros A.Notch3 mutations in Baltimore (MD): University John Hopkins; 1966-2007. Available
CADASIL, a hereditary adult-onset condition causing stroke from: http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=
and dementia. Nature. 1996; 383:707-10. 176640
35. Joutel A, Vahedi K, Corpechot, Troesch A, Chabriat H, Vayssiere 55. Lee HS, Brown P, Cervenakova L, Garruto RM, Alpers MP,
C, et al. Strong clustering and stereotyped nature of Notch3 Gajdusek DC, et al. Increased susceptibility to Kuru of carriers
mutations in CADASIL patients. Lancet. 1997; 350:1511-5. of the PRNP 129 methionine/methionine genotype. J Infect Dis.
36. Jen J, Cohen AH, Yue Q, Stout JT, Vinters HV, Nelson S, et al. 2001; 183:192-6.
Hereditary endotheliopathy with retinopathy, nephropaty, and
stroke (HERNS). Neurology. 1997; 49:1322-30.
37. Iglesias S, Chapon F, Baron JC. Familial occipital calcifications, Trabalho recebido: 24/04/2007
hemorrhagic strokes, leukoencephalopathy, dementia, and Trabalho aprovado: 27/03/2008
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