کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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330342 | 1433643 | 2008 | 17 صفحه PDF | دانلود رایگان |

To establish diagnostic performance of the cerebrospinal fluid (CSF) biomarkers β-amyloid peptide (Aβ1–42), total tau-protein (T-tau) and tau phosphorylated at threonine 181 (P-tau181P) compared to clinical diagnosis, biomarker levels were determined in CSF samples from 100 autopsy-confirmed dementia and 100 control subjects. As the control and dementia groups were not age-matched and given the significant associations of biomarker concentrations with age in controls, age-corrected biomarker concentrations were calculated.New models were constructed by means of logistic regression. Using all biomarkers, dementia could be discriminated from controls (sensitivity (S) = 86%, specificity (Sp) = 89%). T-tau and Aβ1–42 optimally discriminated Alzheimer's disease (AD) from other dementias (NONAD) and controls (S = 90%, Sp = 89%). AD was optimally discriminated from NONAD using P-tau181P and Aβ1–42 (S = 80%, Sp = 93%). Diagnostic accuracy of the latter model (82.7%) was comparable to clinical diagnostic accuracy (81.6%) that was based on a whole clinical work-up (including imaging). Using this model, in cases with clinically doubtful diagnoses, a correct diagnosis would have been established in 4/6 autopsy-confirmed AD and 3/3 autopsy-confirmed NONAD cases.The value of biomarkers in differential dementia diagnosis was shown, using pathological diagnosis as a reference. New models have been developed, achieving sensitivity, specificity and diagnostic accuracy levels, consistently exceeding 80%.
Journal: Neurobiology of Aging - Volume 29, Issue 8, August 2008, Pages 1143–1159