Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

Journal of Clinical and Experimental Neuropsychology

Volumn 32, Issue 7, 2010, Pages 775-779

  Alcalay, Roy N ^a   Mejia Santana, Helen ^a   Tang, Ming X ^a   Rakitin, Brian ^a   Rosado, Llency ^a   Ross, Barbara ^a   Verbitsky, Miguel ^a   Kisselev, Sergey ^a   Louis, Elan D ^a,b,c   Comella, Cynthia L ^d   Colcher, Amy ^e   Jennings, Danna ^f   Nance, Martha A ^g   Bressman, Susan ^h,i   Scott, William K ^j   Tanner, Caroline ^k   Mickel, Susan F ^l   Andrews, Howard F ^m   Waters, Cheryl H ^a   Fahn, Stanley ^a   Cote, Lucien J ^b   Frucht, Steven J ^a   Ford, Blair ^a   Rezak, Michael ^n,o   Novak, Kevin ^n,o   Friedman, Joseph H ^p,q   Pfeiffer, Ronald ^r   Marsh, Laura ^s   Hiner, Bradley ^t   Siderowf, Andrew ^e   Ottman, Ruth ^a,b,c,m   Clark, Lorraine N ^a   Marder, Karen S ^a,b,u   Caccappolo, Elise ^a   more..

^a Columbia University ^*  (United States)

^b Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^c Pennsylvania Hospital ^*  (United States)

^d Section of Movement Disorders   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

^f INSTITUTE FOR NEURODEGENERATIVE DISORDERS   (United States)

^g PARK NICOLLET CLINIC   (United States)

^h BETH ISRAEL MEDICAL CENTER   (United States)

ⁱ ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^j UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^k PARKINSON S INSTITUTE   (United States)

^l MARSHFIELD CLINIC   (United States)

^m NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

ⁿ NORTHSHORE UNIVERSITY HEALTHSYSTEM   (United States)

^o NORTHWESTERN UNIVERSITY   (United States)

^p Parkinson's Disease and Movement Disorders Center   (United States)

^q BROWN UNIVERSITY   (United States)

^r UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

^s JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^t MEDICAL COLLEGE OF WISCONSIN   (United States)

^u NewYork Presbyterian Hospital   (United States)

more..

Author keywords

Cognition; Genetics; Glucocerebrosidase; Leucine rich repeat kinase 2; Mini mental state examination; Parkin; Parkinson

Indexed keywords

GLUCOSYLCERAMIDASE; LRRK2 PROTEIN, HUMAN; PARKIN; PROTEIN SERINE THREONINE KINASE; UBIQUITIN PROTEIN LIGASE;

ARTICLE; COGNITIVE DEFECT; GENETICS; HETEROZYGOTE; HUMAN; MUTATION; NEUROPSYCHOLOGICAL TEST; PARKINSON DISEASE; PHYSIOLOGY; PSYCHOLOGICAL ASPECT; STATISTICAL MODEL; PSYCHOLOGY;

COGNITION DISORDERS; GLUCOSYLCERAMIDASE; HETEROZYGOTE; HUMANS; LOGISTIC MODELS; MUTATION; NEUROPSYCHOLOGICAL TESTS; PARKINSON DISEASE; PROTEIN-SERINE-THREONINE KINASES; UBIQUITIN-PROTEIN LIGASES;

EID: 77955071135     PISSN: 13803395     EISSN: 1744411X     Source Type: Journal    
DOI: 10.1080/13803390903521018     Document Type: Article

References (19)

1. Acion, L., Peterson, J. J., Temple, S., & Arndt, S. (2006). Probabilistic index: An intuitive non-parametric approach to measuring the size of treatment effects. Statistics in Medicine, 25(4), 591-602.
2. Butterfield, P. G., Valanis, B. G., Spencer, P. S., Lindeman, C. A., & Nutt, J. G. (1993). Environmental antecedents of young-onset Parkinson's disease. Neurology, 43(6), 1150-1158.
3. Clark, L. N., Afridi, S., Karlins, E., Wang, Y., Mejia-Santana, H., Harris, J., et al. (2006a). Case-control study of the parkin gene in early-onset Parkinson disease. Archives of Neurology, 63(4), 548-552.
4. Clark, L. N., Haamer, E., Mejia-Santana, H., Harris, J., Lesage, S., Durr, A., et al. (2007a). Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Movement Disorders, 22(7), 932-937.
5. Clark, L. N., Kartsaklis, L. A., Wolf Gilbert, R., Dorado, B., Ross, B. M., Kisselev, S., et al. (2009). Association of glucocerebrosidase mutations with dementia with Lewy bodies. Archives of Neurology, 66(5), 578-583.
6. Clark, L. N., Ross, B. M., Wang, Y., Mejia-Santana, H., Harris, J., Louis, E. D., et al. (2007b). Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology, 69(12), 1270-1277. (Pubitemid 47429028)
7. Clark, L. N., Wang, Y., Karlins, E., Saito, L., Mejia-Santana, H., Harris, J., et al. (2006b). Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology, 67(10), 1786-1791.
8. Dubois, B., Burn, D., Goetz, C., Aarsland, D., Brown, R. G., Broe, G. A., et al. (2007). Diagnostic procedures for Parkinson's disease dementia: Recommendations from the movement disorder society task force. Movement Disorders, 22(16), 2314-2324.
9. Fahn, S., Elton, R., & Committee, M. o. t. U. D. (1987). The Unified Parkinson's Disease Rating Scale. In S. Fahn, C. D. Marsden, D. B. Calne, & M. Goldstein (Eds.), Recent developments in Parkinson's disease (Vol. 2., pp. 153-163, 293-304). Florham Park, NJ: Macmillan Healthcare Information.
10. Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975). "Minimental state." A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research, 12(3), 189-198.
11. Geerlings, M. I., Jonker, C., Bouter, L. M., Ader, H. J., & Schmand, B. (1999). Association between memory complaints and incident Alzheimer's disease in elderly people with normal baseline cognition. American Journal of Psychiatry, 156(4), 531-537.
12. Kostic, V. S., Filipovic, S. R., Lecic, D., Momcilovic, D., Sokic, D., & Sternic, N. (1994). Effect of age at onset on frequency of depression in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry, 57(10), 1265-1267.
13. Levy, G., Tang, M. X., Louis, E. D., Cote, L. J., Alfaro, B., Mejia, H., et al. (2002). The association of incident dementia with mortality in PD. Neurology, 59(11), 1708-1713.
14. Lohmann, E., Thobois, S., Lesage, S., Broussolle, E., du Montcel, S. T., Ribeiro, M. J., et al. (2009). A multidisciplinary study of patients with early-onset PD with and without parkin mutations. Neurology, 72(2), 110-116.
15. Macedo, M. G., Verbaan, D., Fang, Y., van Rooden, S. M., Visser, M., Anar, B., et al. (2009). Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease. Movement Disorders, 24(2), 196-203.
16. Neumann, J., Bras, J., Deas, E., O'Sullivan, S. S., Parkkinen, L., Lachmann, R. H., et al. (2009). Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain, 132(pt. 7), 1783-1794.
17. Pigullo, S., De Luca, A., Barone, P., Marchese, R., Bellone, E., Colosimo, A., et al. (2004). Mutational analysis of parkin gene by denaturing high-performance liquid chromatography (DHPLC) in essential tremor. Parkinsonism and Related Disorders, 10(6), 357-362.
18. Schrag, A., Ben-Shlomo, Y., Brown, R., Marsden, C. D., & Quinn, N. (1998). Young-onset Parkinson's disease revisited- clinical features, natural history, and mortality. Movement Disorders, 13(6), 885-894.
19. Schrag, A., & Schott, J. M. (2006). Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism. Lancet Neurology, 5(4), 355-363.