Evidence map›Paper›PMID 25596881›Full record

Trial reportParkinsonism & related disorders2015

CSF tau and tau/Aβ42 predict cognitive decline in Parkinson's disease.

Changqin Liu, Brenna Cholerton, Min Shi, Carmen Ginghina, Kevin C Cain, Peggy Auinger, Parkinson Study Group DATATOP Investigators, Jing Zhang

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Parkinsonism & related disorders, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
6.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Changes of cerebrospinal fluid AβNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
    Pooled it
  3. Pooled it
  4. An exploratoryEuropean journal of nuclear medicine and molecular imaging · 2026
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Changqin LiuDepartment of Pathology, University of Washington School of Medicine, Seattle, WA, USA; Department of Endocrinology and Diabetes, The First Affiliated Hospital, Xiamen University, Xiamen, China. Electronic address: liuchangqin@126.com.
Brenna CholertonDepartment of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA, USA; Geriatric Research, Education, and Clinical Center, VA Puget Sound Health Care System, Seattle, WA, USA. Electronic address: bchol@uw.edu.
Min ShiDepartment of Pathology, University of Washington School of Medicine, Seattle, WA, USA. Electronic address: mshi70@uw.edu.
Carmen GinghinaDepartment of Pathology, University of Washington School of Medicine, Seattle, WA, USA. Electronic address: ginghina@uw.edu.
Kevin C CainDepartment of Biostatistics, University of Washington School of Public Health, Seattle, WA, USA. Electronic address: cain@uw.edu.
Peggy AuingerDepartment of Neurology, Center for Human Experimental Therapeutics, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA. Electronic address: peggy.auinger@chet.rochester.edu.
Parkinson Study Group DATATOP Investigators
Jing ZhangDepartment of Pathology, University of Washington School of Medicine, Seattle, WA, USA. Electronic address: zhangj@uw.edu.
University of Washington · USFirst Affiliated Hospital of Xiamen University · CNUniversity of Rochester · US

Funding

WILDLIFE BIOMARKER APPLICATIONS TO REMEDIATION DECISION MAKINGP42ES004696 · NIEHS · UNIVERSITY OF WASHINGTON · PI GALLAGHER, EVAN P · 1987 to 2021
$51.2M
XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
UPenn ADCC Biomarker CoreP30AG010124 · NIA · UNIVERSITY OF PENNSYLVANIA · PI XIE, SHARON XIANGWEN · 1991 to 2020
$35.1M
Udall Center Director's meeting poster awardP50NS062684 · NINDS · UNIVERSITY OF WASHINGTON · PI MONTINE, THOMAS J · 2009 to 2020
$18.3M
Large Scale Biomarker Discovery and Validation for Parkinsons DiseaseU01NS082137 · NINDS · UNIVERSITY OF WASHINGTON · PI ZHANG, JING · 2012 to 2016
$6.0M
Biomarkers for Preclinical Parkinson's diseaseR01NS057567 · NINDS · UNIVERSITY OF WASHINGTON · PI ZHANG, JING · 2008 to 2012
$3.1M
Interaction of alpha-synuclein and neurotoxicants with Mac1-NADPH oxidaseR01ES019277 · NIEHS · UNIVERSITY OF WASHINGTON · PI ZHANG, JING · 2011 to 2015
$2.0M
Microglial Phox Activity In Parkinson's DiseaseR01ES016873 · NIEHS · UNIVERSITY OF WASHINGTON · PI ZHANG, JING · 2010 to 2014
$1.7M
Post-translational Modifications of Proteins in Parkinson?s diseaseR01AG033398 · NIA · UNIVERSITY OF WASHINGTON · PI ZHANG, JING · 2008 to 2012
$1.6M
NIA NIH HHS AG033398NIA NIH HHS AG10124NIA NIH HHS P30 AG010124NIA NIH HHS R01 AG033398NIEHS NIH HHS ES004696-5897NIEHS NIH HHS ES007033-6364NIEHS NIH HHS ES016873NIEHS NIH HHS ES019277NIEHS NIH HHS P30 ES007033NIEHS NIH HHS P42 ES004696NIEHS NIH HHS R01 ES016873NIEHS NIH HHS R01 ES019277NINDS NIH HHS NS057567NINDS NIH HHS NS062684-6221NINDS NIH HHS NS082137NINDS NIH HHS P50 NS062684NINDS NIH HHS R01 NS057567NINDS NIH HHS U01 NS082137
6 · The paper itself

Abstract

introductionA substantial proportion of patients with Parkinson's disease (PD) have concomitant cognitive dysfunction. Identification of biomarker profiles that predict which PD patients have a greater likelihood for progression of cognitive symptoms is pressingly needed for future treatment and prevention approaches.

methodsSubjects were drawn from the Deprenyl and Tocopherol Antioxidative Therapy of Parkinsonism (DATATOP) study, a large clinical trial that enrolled initially untreated PD patients. For the current study, Phase One encompassed trial baseline until just prior to levodopa administration (n = 403), and Phase Two spanned the initiation of levodopa treatment until the end of cognitive follow-up (n = 305). Correlations and linear mixed models were performed to determine cross-sectional and longitudinal associations between baseline amyloid β1-42 (Aβ42), total tau (t-tau), and phosphorylated tau (p-tau) in cerebrospinal fluid (CSF) and measures of memory and executive function. Analyses also considered APOE genotype and tremor- vs. rigidity-dominant phenotype.

resultsNo association was found between baseline CSF biomarkers and cognitive test performance during Phase One. However, once levodopa treatment was initiated, higher p-tau and p-tau/Aβ42 predicted subsequent decline on cognitive tasks involving both memory and executive functions. The interactions between biomarkers and cognition decline did not appear to be influenced by levodopa dosage, APOE genotype or motor phenotype.

conclusionsThe current study has, for the first time, demonstrated the possible involvement of tau species, whose gene (MAPT) has been consistently linked to the risk of PD by genome-wide association studies, in the progression of cognitive symptoms in PD.

Indexed as

AdultAgedAmyloid beta-PeptidesAntioxidantsApolipoproteins ECognition DisordersCohort StudiesCross-Sectional StudiesFemaleHumansLinear ModelsMaleMiddle AgedMonoamine Oxidase InhibitorsNeuropsychological TestsParkinson DiseaseAmyloid beta-Peptidesamyloid beta-protein (1-42)AntioxidantsApolipoproteins EMonoamine Oxidase InhibitorsPeptide FragmentsSelegilinetau ProteinsVitamin EBiomarkersCerebrospinal fluidCognitionNeuropsychological testsParkinson diseasetau proteins

Identifiers

PMID25596881
PMCPMC4603566
OpenAlexW2075340389

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.