Semantic dementia: demography, familial factors and survival in a consecutive series of 100 cases

被引:198
作者
Hodges, John R. [1 ,2 ]
Mitchell, Jo [2 ]
Dawson, Kate [2 ]
Spillantini, Maria Grazia [2 ]
Xuereb, John H. [3 ]
McMonagle, Paul [3 ]
Nestor, Peter J. [2 ]
Patterson, Karalyn [4 ]
机构
[1] Univ New S Wales, POWMRI, Sydney, NSW 2031, Australia
[2] Addenbrookes Hosp, Univ Dept Clin Neurosci, Cambridge, England
[3] Univ Cambridge, Dept Pathol, Cambridge CB2 1TN, England
[4] MRC Cognit & Brain Sci Unit, Cambridge, England
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
frontotemporal dementia; semantic dementia; ubiquitin pathology; TDP43; FRONTOTEMPORAL LOBAR DEGENERATION; PRIMARY PROGRESSIVE APHASIA; COGNITIVE TEST BATTERY; ALZHEIMERS-DISEASE; TEMPORAL-LOBE; PREVALENCE; ATROPHY; IMPAIRMENT; MUTATIONS; PATTERNS;
D O I
10.1093/brain/awp248
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A great deal has been written about cognitive aspects of semantic dementia but little is known about the demography or prognosis. We describe these features in a consecutive series of 100 patients seen over a 17-year period; all cases were assessed and followed up in a specialist clinic. The mean age at diagnosis was 64.2 (+/- 7.1) range 40-79 years, but 46 presented after age 65 and 7 after 75; a higher proportion than the existing literature might predict. Fifteen had a first-degree relative with dementia, but in seven this was almost certainly unrelated. Only two had relatives with young-onset dementia. There were no families with more than two affected members. The familial rate was estimated at between 2% and 7% (95% confidence interval 0-12%). Kaplan-Meier analyses indicated a 50% survival of 12.8 years (95% confidence interval 11.9-13.7); a more benign course than suggested by neuropathologically based studies. We were unable to identify any factors influencing survival. Of the 100, 34 have died, with pathological confirmation in 24; 18 had frontotemporal lobar degeneration with ubiquitin-positive inclusions (13 of 13 confirmed TAR DNA binding protein-43 positive), and 3 had classic tau-positive Pick bodies and 3 had Alzheimer's pathology. The age at diagnosis or death across the pathological subgroups was equivalent. Although semantic dementia has a strong statistical association with ubiquitin-positive pathology, it does not have the signature of familial frontotemporal lobar degeneration with ubiquitin-positive inclusions, notably the presence of intranuclear lentiform TAR DNA binding protein-43 inclusions. The age of onset is older than predicted and the course more slowly progressive than suggested by earlier studies of small groups of subjects.
引用
收藏
页码:300 / 306
页数:7
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