Survival in frontotemporal lobar degeneration in a Korean population
作者： Sue J Kang , Kyung Ryeol Cha , Sang Won Seo , Eun A Kim , Hae-Kwan Cheong
DOI: 10.1097/WAD.0B013E3181DF8DE2
关键词:
摘要: Frontotemporal lobar degeneration (FTLD) can be subdivided into frontotemporal dementia (FTD), FTD combined with motor neuron disease (FTD-MND), semantic (SD), and progressive nonfluent aphasia (PNFA). FTLD has been considered a rare disorder, its' demographic survival data have rarely studied in Asian population. A analysis using the Kaplan-Meier method was performed for 121 consecutive patients clinically diagnosed who attended Memory Disorder Clinic at Samsung Medical Center Seoul, Republic of Korea, between January 1995 September 2006. The overall median from onset first symptom 9.6 years (95% CI=8.3-10.8 y). shortest FTD-MND (3 y) longest SD (11.3 time (9.8 shorter than that longer PNFA. use Cox proportional-hazards model to examine effect demographics on revealed only age associated survival. In general, our are comparable those Western countries. However, female proportion greater across all subtypes PNFA other groups.
wkhealth.com参考文章(20)
Yong Jeong, Sang Soo Cho, Jung Mi Park, Sue J Kang, Jae Sung Lee, Eunjoo Kang, Duk L Na, Sang Eun Kim, None, 18F-FDG PET Findings in Frontotemporal Dementia: An SPM Analysis of 29 Patients The Journal of Nuclear Medicine. ,vol. 46, pp. 233- 239 ,(2005)
K. A. Josephs, D. S. Knopman, J. L. Whitwell, B. F. Boeve, J. E. Parisi, R. C. Petersen, D. W. Dickson, Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND. Neurology. ,vol. 65, pp. 645- 647 ,(2005) , 10.1212/01.WNL.0000173178.67986.7F
D. Neary, J. S. Snowden, L. Gustafson, U. Passant, D. Stuss, S. Black, M. Freedman, A. Kertesz, P. H. Robert, M. Albert, K. Boone, B. L. Miller, J. Cummings, D. F. Benson, Frontotemporal lobar degeneration A consensus on clinical diagnostic criteria Neurology. ,vol. 51, pp. 1546- 1554 ,(1998) , 10.1212/WNL.51.6.1546
Anne M. Lipton, Charles L. White, Eileen H. Bigio, Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration. Acta Neuropathologica. ,vol. 108, pp. 379- 385 ,(2004) , 10.1007/S00401-004-0900-9
Manabu Ikeda, Tomohisa Ishikawa, Hirotaka Tanabe, Epidemiology of frontotemporal lobar degeneration. Dementia and Geriatric Cognitive Disorders. ,vol. 17, pp. 265- 268 ,(2004) , 10.1159/000077151
David S. Knopman, Bradley F. Boeve, Joseph E. Parisi, Dennis W. Dickson, Glenn E. Smith, Robert J. Ivnik, Keith A. Josephs, Ronald C. Petersen, Antemortem diagnosis of frontotemporal lobar degeneration. Annals of Neurology. ,vol. 57, pp. 480- 488 ,(2005) , 10.1002/ANA.20425
K. Rascovsky, D. P. Salmon, A. M. Lipton, J. B. Leverenz, C. DeCarli, W. J. Jagust, C. M. Clark, M. F. Mendez, D. F. Tang-Wai, N. R. Graff-Radford, D. Galasko, Rate of progression differs in frontotemporal dementia and Alzheimer disease Neurology. ,vol. 65, pp. 397- 403 ,(2005) , 10.1212/01.WNL.0000171343.43314.6E
B. L. Miller, C. Ikonte, M. Ponton, M. Levy, K. Boone, A. Darby, N. Berman, I. Mena, J. L. Cummings, A study of the Lund‐Manchester research criteria for frontotemporal dementia: Clinical and single‐photon emission CT correlations Neurology. ,vol. 48, pp. 937- 941 ,(1997) , 10.1212/WNL.48.4.937
K. A. Josephs, R. C. Petersen, D. S. Knopman, B. F. Boeve, J. L. Whitwell, J. R. Duffy, J. E. Parisi, D. W. Dickson, Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP Neurology. ,vol. 66, pp. 41- 48 ,(2006) , 10.1212/01.WNL.0000191307.69661.C3
Andrew Kertesz, Mervin Blair, Paul McMonagle, David G. Munoz, The diagnosis and course of frontotemporal dementia. Alzheimer Disease & Associated Disorders. ,vol. 21, pp. 155- 163 ,(2007) , 10.1097/WAD.0B013E31806547EB