Evidence map›Paper›PMID 30349860›Full record

ArticleAnnals of clinical and translational neurology2018

Cerebrospinal fluid biomarkers predict frontotemporal dementia trajectory.

Peter A Ljubenkov, Adam M Staffaroni, Julio C Rojas, Isabel E Allen, Ping Wang, Hilary Heuer, Anna Karydas, John Kornak, Yann Cobigo, William W Seeley and 11 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
4.4field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 3 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Detection of TDP-43 seeds in CSF of presymptomatic and symptomatic genetic FTD/ALS.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Frontotemporal lobar degeneration.Nature reviews. Disease primers · 2023
    Review
  12. Frontotemporal Dementia, Where Do We Stand? A Narrative Review.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Observational
  18. Article
  19. Review
  20. Review
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

21 authors at 5 institutions in 1 country.

Peter A LjubenkovDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Adam M StaffaroniDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Julio C RojasDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Isabel E AllenDepartment of Epidemiology and Biostatistics University of California San Francisco San Francisco California.
Ping WangDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Hilary HeuerDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Anna KarydasDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
John KornakDepartment of Epidemiology and Biostatistics University of California San Francisco San Francisco California.
Yann CobigoDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
William W SeeleyDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Lea T GrinbergDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Salvatore SpinaDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Anne M FaganDepartment of Neurology Washington University St. Louis Missouri.
Gina JeromeDepartment of Neurology Washington University St. Louis Missouri.
David KnopmanDepartment of Neurology Mayo Clinic Rochester Minnesota.
Brad F BoeveDepartment of Neurology Mayo Clinic Rochester Minnesota.
Bradford C DickersonFrontotemporal Dementia Unit Department of Neurology Massachusetts Alzheimer's Disease Research Center Harvard Medical School, Boston Boston Massachusetts.
Joel KramerDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Bruce MillerDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Adam L BoxerDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
Howard J RosenDepartment of Neurology Memory and Aging Center University of California, San Francisco San Francisco California.
University Memory and Aging Center · USUniversity of California, San Francisco · USMayo Clinic · USWashington University in St. Louis · USHarvard University · US

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MILLER, BRUCE L · 2004 to 2018
$27.1M
The Four Repeat Tauopathy Neuroimaging InitiativeR01AG038791 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2010 to 2020
$18.1M
The Frontotemporal Lobar Degeneration Neuroimaging InitiativeR01AG032306 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2009 to 2013
$10.0M
Multidisciplinary Research Fellowship in Alzheimer’s disease and Related DementiasT32AG023481 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BRUCE L MILLER, HOWARD J ROSEN · 2005 to 2026
$7.4M
Training - The Frontotemporal Lobar Degeneration Clinical Research ConsortiumU54NS092089 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2014 to 2018
$6.4M
PREDICT-ADFTD: Multimodal Imaging Prediction of AD/FTD and Differential DiagnosisR01AG055121 · NIA · OHIO STATE UNIVERSITY · PI ROSEN, HOWARD J, WANG, LEI · 2017 to 2020
$2.8M
Multimodal Imaging in Frontotemporal DegenerationK24AG045333 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSEN, HOWARD J · 2013 to 2023
$1.9M
Neuropathological basis of brain network dysfunctionK08AG052648 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SPINA, SALVATORE · 2016 to 2020
$852k
NIA NIH HHS K08 AG052648NIA NIH HHS K24 AG045333NIA NIH HHS P01 AG019724NIA NIH HHS P50 AG023501NIA NIH HHS R01 AG032306NIA NIH HHS R01 AG038791NIA NIH HHS R01 AG055121NIA NIH HHS T32 AG023481NINDS NIH HHS U54 NS092089
6 · The paper itself

Abstract

objectiveThe prognostic value of cerebrospinal fluid neurofilament light chain, total tau, phosphorylated tau

methodsWe compared baseline biomarkers between 49 controls, 40 patients with behavioral variant frontotemporal dementia, 24 with semantic variant primary progressive aphasia, and 26 with nonfluent variant primary progressive aphasia. Linear mixed effect models were used to assess the value of baseline biomarkers in predicting clinical and radiographic change in patient cohorts over multiple yearly follow up visits.

resultsNeurofilament light chain concentrations were lowest in controls. Elevated baseline neurofilament light chain predicted faster worsening in clinical severity, frontotemporal volume and frontotemporal fractional anisotropy in patients with behavioral variant frontotemporal dementia and nonfluent variant primary progressive aphasia. High total tau similarly predicted faster progression in nonfluent variant primary progressive aphasia. In behavioral variant frontotemporal dementia, higher phosphorylated tau

interpretationHigh cerebrospinal fluid neurofilament light chain predicts more aggressive disease in behavioral variant frontotemporal dementia and nonfluent variant primary progressive aphasia. Total tau, phosphorylated tau

Identifiers

PMID30349860
PMCPMC6186942
OpenAlexW2889890338

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.