Differentiation of geriatric major depression from Alzheimer's disease with CSF tau protein phosphorylated at threonine 231

被引:68
作者
Buerger, K
Zinkowski, R
Teipel, SJ
Arai, H
DeBernardis, J
Kerkman, D
McCulloch, C
Padberg, F
Faltraco, F
Goernitz, A
Tapiola, T
Rapoport, SI
Pirttilä, T
Möller, HJ
Hampel, H
机构
[1] Univ Munich, Dementia Res Sect, D-80336 Munich, Germany
[2] Univ Munich, Memory Clin, Alzheimer Mem Ctr, D-80336 Munich, Germany
[3] Univ Munich, Dept Psychiat, Geriatr Psychiat Branch, D-80336 Munich, Germany
[4] Mol Geriatr Corp, Vernon Hills, IL USA
[5] Tohoku Univ, Sch Med, Dept Geriatr Med, Sendai, Miyagi 980, Japan
[6] Kuopio Univ Hosp, Dept Neurol & Neurosci, SF-70210 Kuopio, Finland
[7] NIA, Brain Physiol & Metab Sect, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1176/appi.ajp.160.2.376
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Differentiation of geriatric major depression from Alzheimer's disease is hampered by overlapping symptoms. Increased CSF concentrations of tau protein phosphorylated at threonine 231 (p-tau(231)) have been suggested as a biomarker for Alzheimer's disease. The authors asked whether p-tau231 levels improve the differential diagnosis between geriatric major depression and Alzheimer's disease. Method: Included were 34 depression subjects, 64 with probable Alzheimer's disease, 17 with possible Alzheimer's disease, and 21 healthy comparison subjects. P-tau(231) concentrations were measured with an enzyme-linked immunosorbent assay. Results: P-tau(231) levels were significantly higher in Alzheimer's disease than in geriatric major depression patients and healthy comparison subjects. For differentiation of probable Alzheimer's disease from major depression, p-tau(231) correctly allocated 87% of subjects. When possible mild Alzheimer's disease was compared to major depression, p-tau(231) correctly allocated 78% of subjects. Conclusions: CSF p-tau(231) should be evaluated as a potential biological marker for differentiation of geriatric depression from Alzheimer's disease.
引用
收藏
页码:376 / 379
页数:4
相关论文
共 11 条
[1]   Differential diagnosis of Alzheimer disease with cerebrospinal fluid levels of tau protein phosphorylated at threonine 231 [J].
Buerger, K ;
Zinkowski, R ;
Teipel, SJ ;
Tapiola, T ;
Arai, H ;
Blennow, K ;
Andreasen, N ;
Hofmann-Kiefer, K ;
DeBernardis, J ;
Kerkman, D ;
McCulloch, C ;
Kohnken, R ;
Padberg, F ;
Pirttilä, T ;
Schapiro, MB ;
Rapoport, SI ;
Möller, HJ ;
Davies, P ;
Hampel, H .
ARCHIVES OF NEUROLOGY, 2002, 59 (08) :1267-1272
[2]   CSF tau protein phosphorylated at threonine 231 correlates with cognitive decline in MCI subjects [J].
Buerger, K ;
Teipel, SJ ;
Zinkowski, R ;
Blennow, K ;
Arai, H ;
Engel, R ;
Hofmann-Kiefer, K ;
McCulloch, C ;
Ptok, U ;
Heun, R ;
Andreasen, N ;
DeBernardis, J ;
Kerkman, D ;
Moeller, HJ ;
Davies, P ;
Hampel, H .
NEUROLOGY, 2002, 59 (04) :627-629
[3]  
Christensen H, 1997, J Int Neuropsychol Soc, V3, P631
[4]   MINI-MENTAL STATE - PRACTICAL METHOD FOR GRADING COGNITIVE STATE OF PATIENTS FOR CLINICIAN [J].
FOLSTEIN, MF ;
FOLSTEIN, SE ;
MCHUGH, PR .
JOURNAL OF PSYCHIATRIC RESEARCH, 1975, 12 (03) :189-198
[5]   Tracking of Alzheimer's disease progression with cerebrospinal fluid tau protein phosphorylated at threonine 231 [J].
Hampel, H ;
Buerger, K ;
Kohnken, R ;
Teipel, SJ ;
Zinkowski, R ;
Moeller, HJ ;
Rapoport, SI ;
Davies, P .
ANNALS OF NEUROLOGY, 2001, 49 (04) :545-546
[6]   PSYCHIATRIC HISTORY AND RELATED EXPOSURES AS RISK-FACTORS FOR ALZHEIMERS-DISEASE - A COLLABORATIVE REANALYSIS OF CASE-CONTROL STUDIES [J].
JORM, AF ;
VANDUIJN, CM ;
CHANDRA, V ;
FRATIGLIONI, L ;
GRAVES, AB ;
HEYMAN, A ;
KOKMEN, E ;
KONDO, K ;
MORTIMER, JA ;
ROCCA, WA ;
SHALAT, SL ;
SOININEN, H ;
HOFMAN, A .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1991, 20 :S43-S47
[7]   THE PREVALENCE OF DEMENTIA - A QUANTITATIVE INTEGRATION OF THE LITERATURE [J].
JORM, AF ;
KORTEN, AE ;
HENDERSON, AS .
ACTA PSYCHIATRICA SCANDINAVICA, 1987, 76 (05) :465-479
[8]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[9]   BASIC PRINCIPLES OF ROC ANALYSIS [J].
METZ, CE .
SEMINARS IN NUCLEAR MEDICINE, 1978, 8 (04) :283-298
[10]   Syndromic validity of apathy in Alzheimer's disease [J].
Starkstein, SE ;
Petracca, G ;
Chemerinski, E ;
Kremer, J .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (06) :872-877