TY - JOUR
T1 - Cerebrospinal Fluid Tau and β-Amyloid
T2 - How Well Do These Biomarkers Reflect Autopsy-Confirmed Dementia Diagnoses?
AU - Clark, Christopher M.
AU - Xie, Sharon
AU - Chittams, Jesse
AU - Ewbank, Douglas
AU - Peskind, Elaine
AU - Galasko, Douglas
AU - Morris, John C.
AU - McKeel, Daniel W.
AU - Farlow, Martin
AU - Weitlauf, Sharon L.
AU - Quinn, Joseph
AU - Kaye, Jeffrey
AU - Knopman, David
AU - Arai, Hiroyuki
AU - Doody, Rachelle S.
AU - DeCarli, Charles
AU - Leight, Susan
AU - Lee, Virginia M.Y.
AU - Trojanowski, John Q.
PY - 2003/12
Y1 - 2003/12
N2 - Background: Tau and β-amyloid (Aβ) are proposed diagnostic biomarkers for Alzheimer disease (AD). Previous studies report their relationship to clinical diagnoses of AD and other dementias. To understand their value as predictors of disease-specific patholody, levels determined during life must be correlated with definitive diagnoses in mixed dementia groups and cognitively normal subjects. Objectives: To correlate antemortem cerebrospinal fluid (CSF) tau and Aβ levels with definitive dementia diagnosis in a diverse group of patients; to calculate statistics for CSF tau and Aβ. Design: Prospective study. Setting: Ten clinics experienced in the diagnosis of neurodegenerative dementias. Patients: One hundred six patients with dementia and 4 cognitively normal subjects with a definitive diagnosis, and 69 clinically diagnosed cognitively normal subjects. Main Outcome Measures: Correlation of CSF tau and Aβ with final diagnosis. Results: Mean tau level was 612 pg/mL for the 74 patients with AD, 272 pg/mL for 10 patients with frontal dementia, 282 pg/mL for 3 patients with dementia with Lewy bodies, and 140 pg/mL for 73 cognitively normal control subjects. Tau was less than 334 pg/mL for 20 patients with AD. Aβ42 was reduced in patients with AD (61 fmol/mL) compared with patients with frontal dementia (133 fmol/mL) and control subjects (109 fmol/mL), but not compared with patients with dementia with Lewy bodies (14 fmol/mL) or prion disease (60 fmol/mL). Conclusions: Elevated CSF tau levels are associated with AD pathology and can help discriminate AD from other dementing disorders. However, some patients with AD have a level less than the mean ± 2 SDs of the cognitively normal cohort.
AB - Background: Tau and β-amyloid (Aβ) are proposed diagnostic biomarkers for Alzheimer disease (AD). Previous studies report their relationship to clinical diagnoses of AD and other dementias. To understand their value as predictors of disease-specific patholody, levels determined during life must be correlated with definitive diagnoses in mixed dementia groups and cognitively normal subjects. Objectives: To correlate antemortem cerebrospinal fluid (CSF) tau and Aβ levels with definitive dementia diagnosis in a diverse group of patients; to calculate statistics for CSF tau and Aβ. Design: Prospective study. Setting: Ten clinics experienced in the diagnosis of neurodegenerative dementias. Patients: One hundred six patients with dementia and 4 cognitively normal subjects with a definitive diagnosis, and 69 clinically diagnosed cognitively normal subjects. Main Outcome Measures: Correlation of CSF tau and Aβ with final diagnosis. Results: Mean tau level was 612 pg/mL for the 74 patients with AD, 272 pg/mL for 10 patients with frontal dementia, 282 pg/mL for 3 patients with dementia with Lewy bodies, and 140 pg/mL for 73 cognitively normal control subjects. Tau was less than 334 pg/mL for 20 patients with AD. Aβ42 was reduced in patients with AD (61 fmol/mL) compared with patients with frontal dementia (133 fmol/mL) and control subjects (109 fmol/mL), but not compared with patients with dementia with Lewy bodies (14 fmol/mL) or prion disease (60 fmol/mL). Conclusions: Elevated CSF tau levels are associated with AD pathology and can help discriminate AD from other dementing disorders. However, some patients with AD have a level less than the mean ± 2 SDs of the cognitively normal cohort.
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U2 - 10.1001/archneur.60.12.1696
DO - 10.1001/archneur.60.12.1696
M3 - Article
C2 - 14676043
AN - SCOPUS:0346124139
SN - 0003-9942
VL - 60
SP - 1696
EP - 1702
JO - Archives of neurology
JF - Archives of neurology
IS - 12
ER -