Evidence map›Paper›PMID 40754329›Full record

ArticleBMJ open2025

Investigating the role of neuroinflammation and brain clearance in frontotemporal lobar degeneration using 7T MRI and fluid biomarkers: protocol for a cross-sectional study in a tertiary care setting.

Fieke A M Prinse, Louise van der Weerd, John C van Swieten, Itamar Ronen, Harro Seelaar, Lydiane Hirschler, Chloé Najac, Elise G P Dopper

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06870838 (Neuroinflammation in Frontotemporal Lobar Degeneration - a Multimodal Biomarker Study), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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.

NCT06870838 active not recruitingnot on this map

Neuroinflammation in Frontotemporal Lobar Degeneration - a Multimodal Biomarker Study

TypeobservationalSponsorLeiden University Medical CenterRan2023 to 2026Enrolled110ConditionsCorticobasal Syndrome(CBS), Primary Progressive Aphasia(PPA), Progressive Supranuclear Palsy(PSP), Behavioral Variant Frontotemporal Dementia (bvFTD)Arms7T MRI scan, CSF, Blood withdrawal, Neuropsychological assessment, Clinical measures
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Fieke A M PrinseDepartment of Neurology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID http://orcid.org/0009-0009-0185-1003
Louise van der WeerdC.J. Gorter Center for MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0002-5997-2125
John C van SwietenDepartment of Neurology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Itamar RonenClinical Imaging Science Centre, Brighton and Sussex Medical School, Brighton, UK.
Harro SeelaarDepartment of Neurology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Lydiane HirschlerC.J. Gorter Center for MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID http://orcid.org/0000-0003-2379-0861
Chloé NajacC.J. Gorter Center for MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Elise G P DopperDepartment of Neurology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands e.dopper@erasmusmc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFrontotemporal lobar degeneration (FTLD) is the second most common early-onset dementia. Several studies demonstrated that neuroinflammation and iron accumulation occur in FTLD. However, the timing and relevance of these processes and whether these two are merely cause or consequence remains unclear. Elucidating the role is crucial to assess the rationale for using anti-inflammatory therapies in FTLD. Additionally, the process of glymphatic brain clearance has gained attention as a potential contributor in the disease pathophysiology. METHODS AND ANALYSIS: In this multimodal biomarker study, we use a combination of ultra-high field (7T) MR, blood and cerebrospinal fluid (CSF) biomarkers to investigate the role of neuroinflammation, iron accumulation and brain clearance in FTLD, and to identify biomarkers to differentiate FTLD-TDP from FTLD-tau. We aim to include 25 patients with probable FTLD-tau, 25 with probable FTLD-TDP and 50 healthy individuals with 50% risk to develop FTLD. We will use several MRI techniques, including magnetic resonance spectroscopy, diffusion weighted spectroscopy and quantitative susceptibility mapping. In addition, we will assess the prevalence of perivascular spaces (PVS) and the mobility of CSF to address glymphatic brain clearance. We will compare quantitative MR markers between patients with FTLD-tau and FTLD-TDP, presymptomatic mutation carriers and healthy controls, and correlate these measures with clinical data and biomarkers in blood and CSF. ETHICS AND DISSEMINATION: We obtained ethical approval from the Medical Ethics Committee Leiden Den Haag Delft (NL78272.058.21). The results will be disseminated through presentations at national and international conferences, open-access peer-reviewed publications, ClinicalTrials.gov and to the public through social media posts and annual newsletters. STUDY REGISTRATION NUMBER: NCT06870838; Pre-results.

Indexed as

BrainFrontotemporal Lobar DegenerationNeuroinflammatory DiseasesAgedBiomarkersCross-Sectional StudiesFemaleHumansIronMagnetic Resonance ImagingMaleMiddle AgedMulticenter Studies as TopicObservational Studies as TopicTertiary Care CentersBiomarkersIronDementiaNeuroradiology

Identifiers

PMID40754329
PMCPMC12320043

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Registered trials

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.