Literature DB >> 31306137

Highly Elevated Cerebrospinal Fluid Total Tau Level Reflects Higher Likelihood of Non-Amnestic Subtype of Alzheimer's Disease.

Jagan A Pillai1,2, Aaron Bonner-Jackson1, Lynn M Bekris3, Jiri Safar4,5, Jim Bena6, James B Leverenz1,2.   

Abstract

BACKGROUND: Cerebrospinal fluid (CSF) levels of total tau (t-tau) protein are thought to reflect the intensity of the neuronal damage in neurodegeneration, including Alzheimer's disease (AD). The recent link of CSF t-tau to rapidly progressive AD raises the question among other AD clinical variants regarding CSF t-tau. We investigated the clinical phenotypes of AD patients with varying CSF t-tau levels.
OBJECTIVE: We tested the hypothesis that highly elevated CSF t-tau level would have a higher likelihood of presenting with atypical non-amnestic variants of AD.
METHODS: Retrospective comparative case study of 97 patients evaluated in a memory clinic with clinical presentation and CSF biomarkers consistent with AD. We compared the age, sex, education, APOEɛ4 status, Montreal Cognitive Assessment (MoCA) score, clinical phenotype, and MRI volumetric measures by CSF t-tau quartile at baseline. Multivariable logistic regression models were used to evaluate if CSF t-tau levels predict non-amnestic presentations controlling for covariates.
RESULTS: Non-amnestic AD had a higher median CSF t-tau level compared to amnestic-AD (p = 0.014). Each 50 pg/ml increase in CSF t-tau was associated with an increase in the odds of having a non-amnestic presentation (7.4%) and aphasia (10.6 %) as the initial presenting symptom even after taking into account; age, sex, education, APOEɛ4, MoCA, and CSF Aβ42. Logopenic AD had higher t-tau and p-tau levels compared to other variants.
CONCLUSIONS: Highly elevated CSF t-tau levels could indicate more cortical involvement presenting with early non-amnestic symptoms in atypical AD subtypes, particularly in the logopenic variant.

Entities:  

Keywords:  Alzheimer’s disease; atypical variant; biomarkers; cerebrospinal fluid; cortical atrophy; hippocampal atrophy; mild cognitive impairment; tau

Year:  2019        PMID: 31306137      PMCID: PMC7086408          DOI: 10.3233/JAD-190519

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  10 in total

1.  Distinct populations of highly potent TAU seed conformers in rapidly progressing Alzheimer's disease.

Authors:  Chae Kim; Tracy Haldiman; Sang-Gyun Kang; Lenka Hromadkova; Zhuang Zhuang Han; Wei Chen; Frances Lissemore; Alan Lerner; Rohan de Silva; Mark L Cohen; David Westaway; Jiri G Safar
Journal:  Sci Transl Med       Date:  2022-01-05       Impact factor: 19.319

Review 2.  New insights into atypical Alzheimer's disease in the era of biomarkers.

Authors:  Jonathan Graff-Radford; Keir X X Yong; Liana G Apostolova; Femke H Bouwman; Maria Carrillo; Bradford C Dickerson; Gil D Rabinovici; Jonathan M Schott; David T Jones; Melissa E Murray
Journal:  Lancet Neurol       Date:  2021-03       Impact factor: 44.182

3.  ATN status in amnestic and non-amnestic Alzheimer's disease and frontotemporal lobar degeneration.

Authors:  Katheryn A Q Cousins; David J Irwin; David A Wolk; Edward B Lee; Leslie M J Shaw; John Q Trojanowski; Fulvio Da Re; Garrett S Gibbons; Murray Grossman; Jeffrey S Phillips
Journal:  Brain       Date:  2020-07-01       Impact factor: 13.501

4.  Impact of APOE ε4 genotype on initial cognitive symptoms differs for Alzheimer's and Lewy body neuropathology.

Authors:  Jagan A Pillai; James Bena; Aaron Bonner-Jackson; James B Leverenz
Journal:  Alzheimers Res Ther       Date:  2021-01-23       Impact factor: 6.982

5.  TNFRSF1B Gene Variants and Related Soluble TNFR2 Levels Impact Resilience in Alzheimer's Disease.

Authors:  Jagan A Pillai; Gurkan Bebek; Maria Khrestian; James Bena; Cornelia C Bergmann; William S Bush; James B Leverenz; Lynn M Bekris
Journal:  Front Aging Neurosci       Date:  2021-02-25       Impact factor: 5.750

6.  Association of Variation in Behavioral Symptoms With Initial Cognitive Phenotype in Adults With Dementia Confirmed by Neuropathology.

Authors:  Jagan A Pillai; James Bena; Kasia Rothenberg; Bryce Boron; James B Leverenz
Journal:  JAMA Netw Open       Date:  2022-03-01

Review 7.  Tau as a Biomarker of Neurodegeneration.

Authors:  Sarah Holper; Rosie Watson; Nawaf Yassi
Journal:  Int J Mol Sci       Date:  2022-06-30       Impact factor: 6.208

8.  Associations between blood-based biomarkers of Alzheimer's disease with cognition in motoric cognitive risk syndrome: A pilot study using plasma Aβ42 and total tau.

Authors:  Pei-Hao Chen; Sang-Yi Lin; Ying-Yi Liao; Wei-Ling Hsu; Fang-Yu Cheng
Journal:  Front Aging Neurosci       Date:  2022-10-04       Impact factor: 5.702

9.  Temporal Ordering of Inflammatory Analytes sTNFR2 and sTREM2 in Relation to Alzheimer's Disease Biomarkers and Clinical Outcomes.

Authors:  Jagan A Pillai; Maria Khrestian; James Bena; James B Leverenz; Lynn M Bekris
Journal:  Front Aging Neurosci       Date:  2021-06-29       Impact factor: 5.750

Review 10.  Clinical Utility of the Pathogenesis-Related Proteins in Alzheimer's Disease.

Authors:  Bin Zhou; Masanori Fukushima
Journal:  Int J Mol Sci       Date:  2020-11-17       Impact factor: 5.923

  10 in total

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