A population-based study of Parkinsonism in an Amish community

Neuroepidemiology

Volumn 33, Issue 3, 2009, Pages 225-230

  Racette, Brad A ^a   Good, Laura M ^a   Kissel, Abigail M ^a   Criswell, Susan R ^a   Perlmutter, Joel S ^a,b  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Environment; Parkinson's disease; Parkinsonism

Indexed keywords

AGED; AMISH; ARTICLE; ENVIRONMENTAL FACTOR; FEMALE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PEDIGREE ANALYSIS; PREVALENCE; RATING SCALE;

AGED; AGED, 80 AND OVER; FEMALE; HUMANS; MALE; MIDDLE AGED; MIDWESTERN UNITED STATES; PARKINSONIAN DISORDERS; POPULATION GROUPS; PREVALENCE; RELIGION; RESIDENCE CHARACTERISTICS;

EID: 67651226884     PISSN: 02515350     EISSN: None     Source Type: Journal    
DOI: 10.1159/000229776     Document Type: Article

References (33)

1. Polymeropoulos M, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, Lazzarini AM, Duvoisin RC, Di Iorio G, Golbe LI, Nussbaum RL: Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997; 27: 2045-2047. (Pubitemid 27443610)
2. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N: Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 392: 605-608. (Pubitemid 28207717)
3. Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, Krieger E, Dekker MC, Squitieri F, Ibanez P, Joosse M, van Dongen JW, Vanacore N, van Swieten JC, Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P: Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003; 299: 256-259. (Pubitemid 36131051)
4. Hatano Y, Sato K, Elibol B, Yoshino H, Yamamura Y, Bonifati V, Shinotoh H, Asahina M, Kobayashi S, Ng AR, Rosales RL, Hassin- Baer S, Shinar Y, lu CS, Chang HC, Wu-Chou YH, Atac FB, Kobayashi T, Toda T, Mizuno Y, Hattori N: PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations. Neurology 2004; 63: 1482-1485.
5. Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, van der BM, de Munain AL, Aparicio S, Gil AM, Khan N, Johnson J, Martinez JR, Nicholl D, Carrera IM, Pena AS, de Silva R, Lees A, Marti-Masso JF, Perez-Tur J, Wood NW, Singleton AB: Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004; 44: 595-600. (Pubitemid 39531224)
6. Tanner CM, Ottman R, Goldman SM, Ellenberg J, Chan P, Mayeux R, Langston JW: Parkinson disease in twins: an etiologic study. JAMA 1999; 281: 341-346. (Pubitemid 29061038)
7. Sveinbjornsdottir S, Hicks AA, Jonsson T, Petursson H, Gugmundsson G, Frigge ML, Kong A, Gulcher JR, Stefansson K: Familial aggregation of Parkinson's disease in Iceland. N Engl J Med 2000; 343: 1765-1770.
8. Racette BA, Rundle M, Wang JC, Goate A, Saccone NL, Farrer M, Lincoln S, Hussey J, Smemo S, Lin J, Suarez B, Parsian A, Perlmutter JS: A multi-incident, Old-Order Amish family with PD. Neurology 2002; 58: 568-574.
9. Gasser T, Muller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD: A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nat Genet 1998; 18: 262-265. (Pubitemid 28117265)
10. Hampshire DJ, Roberts E, Crow Y, Bond J, Mubaidin A, Wriekat AL, Al Din A, Woods CG: Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. J Med Genet 2001; 38: 680-682. (Pubitemid 32946789)
11. Hicks AA, Petursson H, Jonsson T, Stefansson H, Johannsdottir HS, Sainz J, Frigge ML, Kong A, Gulcher JR, Stefansson K, Sveinbjornsdottir S: A susceptibility gene for lateonset idiopathic Parkinson's disease. Ann Neurol 2002; 52: 549-555. (Pubitemid 35246857)
12. Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E, Harta G, Brownstein MJ, Jonnalagada S, Chernova T, Dehejia A, Lavedan C, Gasser T, Steinbach PJ, Wilkinson KD, Polymeropoulos MH: The ubiquitin pathway in Parkinson's disease. Nature 1998; 395: 451-452.
13. Duarte J, Claveria LE, de Pedro-Cuesta J, Sempere AP, Coria F, Calne DB: Screening Parkinson's disease: a validated questionnaire of high specificity and sensitivity. Mov Disord 1995; 10: 643-649.
14. Folstein MF, Folstein SE, McHugh PR: 'Mini-mental state': a practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res 1975; 12: 189-198.
15. Racette BA, Rundle M, Parsian A, Perlmutter JS: Evaluation of a screening questionnaire for genetic studies of Parkinson's disease. Am J Med Genet 1999; 88: 539-543. (Pubitemid 29485083)
16. Hughes AJ, Daniel SE, Kilford L, Lees AJ: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181-184.
17. Racette BA, Tabbal SD, Jennings D, Good LM, Perlmutter JS, Evanoff BA: A rapid method for mass screening for parkinsonism. Neurotoxicology 2006; 27: 357-361.
18. Agarwala R, Biesecker LG, Schaffer AA: Anabaptist genealogy database. Am J Med Genet 2003; 121C:32-37.
19. Agarwala R, Biesecker LG, Hopkins KA, Francomano CA, Schaffer AA: Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County. Genome Res 1998; 8: 211-221. (Pubitemid 28177233)
20. Schoenberg BS, Anderson DW, Haerer AF: Prevalence of Parkinson's disease in the biracial population of Copiah County, Mississippi. Neurology 1985; 35: 841-845.
21. Bennett DA, Shannon KM, Beckett LA, Goetz CG, Wilson RS: Metric properties of nurses' ratings of parkinsonian signs with a modified Unified Parkinson's Disease Rating Scale. Neurology 1997; 49: 1580-1587.
22. Ritz B, Ascherio A, Checkoway H, Marder KS, Nelson LM, Rocca WA, Ross GW, Strickland D, Van Den Eeden SK, Gorell J: Pooled analysis of tobacco use and risk of Parkinson disease. Arch Neurol 2007; 64: 990-997. (Pubitemid 47047999)
23. Benedetti MD, Bower JH, Maraganore DM, McDonnell SK, Peterson BJ, Ahlskog JE, Schaid DJ, Rocca WA: Smoking, alcohol, and coffee consumption preceding Parkinson's disease: a case-control study. Neurology 2001; 55: 1350-1358.
24. Louis ED, Luchsinger JA, Tang MX, Mayeux R: Parkinsonian signs in older people: prevalence and associations with smoking and coffee. Neurology 2003; 61: 24-28.
25. Powers KM, Kay DM, Factor SA, Zabetian CP, Higgins DS, Samii A, Nutt JG, Griffith A, Leis B, Roberts JW, Martinez ED, Montimurro JS, Checkoway H, Payami H: Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk. Mov Disord 2008; 23: 88-95. (Pubitemid 351281223)
26. Louis ED, Luchsinger JA, Tang MX, Mayeux R: Parkinsonian signs in older people: prevalence and associations with smoking and coffee. Neurology 2003; 61: 24-28.
27. Elbaz A, Levecque C, Clavel J, Vidal JS, Richard F, Amouyel P, Alperovitch A, Chartier- Harlin MC, Tzourio C: CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease. Ann Neurol 2004; 55: 430-434. (Pubitemid 38269597)
28. Chan DK, Cordato D, Bui T, Mellick G, Woo J: Comparison of environmental and genetic factors for Parkinson's disease between Chinese and Caucasians. Neuroepidemiology 2004; 23: 13-22. (Pubitemid 38142268)
29. Saunders AM, Strittmatter WJ, Schmechel D, George-Hyslop PH, Pericak-Vance MA, Joo SH, Rosi BL, Gusella JF, Crapper-Mac- Lachlan DR, Alberts MJ: Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. Neurology 1993; 43: 1467-1472. (Pubitemid 23230526)
30. Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, Salvesen GS, Roses AD: Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA 1993; 90: 1977-1981. (Pubitemid 23069980)
31. Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, Brice A, Aasly J, Zabetian CP, Goldwurm S, Ferreira JJ, Tolosa E, Kay DM, Klein C, Williams DR, Marras C, Lang AE, Wszolek ZK, Berciano J, Schapira AH, Lynch T, Bhatia KP, Gasser T, Lees AJ, Wood NW: Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008; 7: 583-590.
32. Papapetropoulos S, Ellul J, Paschalis C, Athanassiadou A, Papadimitriou A, Papapetropoulos T: Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece. Eur J Neurol 2003; 10: 281-286. (Pubitemid 36609483)
33. Racette BA, Good L, Antenor JA, McGee- Minnich L, Moerlein SM, Videen TO, Perlmutter JS: [18F]FDOPA PET as an endophenotype for Parkinson's Disease linkage studies. Am J Med Genet B Neuropsychiatr Genet 2006; 141: 245-249.