Evidence map›Paper›PMID 38132096›Full record

SynthesisCells2023

New Perspectives in Radiological and Radiopharmaceutical Hybrid Imaging in Progressive Supranuclear Palsy: A Systematic Review.

Joachim Strobel, Hans-Peter Müller, Albert C Ludolph, Ambros J Beer, Nico Sollmann, Jan Kassubek

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. 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

6 authors at 3 institutions in 1 country.

Joachim StrobelDepartment of Nuclear Medicine, University Hospital Ulm, 89081 Ulm, Germany.
Hans-Peter MüllerDepartment of Neurology, University Hospital Ulm, 89081 Ulm, Germany.
Albert C LudolphDepartment of Neurology, University Hospital Ulm, 89081 Ulm, Germany.
Ambros J BeerDepartment of Nuclear Medicine, University Hospital Ulm, 89081 Ulm, Germany.ORCID 0000-0001-9042-7806
Nico SollmannDepartment of Diagnostic and Interventional Radiology, University Hospital Ulm, 89081 Ulm, Germany.ORCID 0000-0002-8120-2223
Jan KassubekDepartment of Neurology, University Hospital Ulm, 89081 Ulm, Germany.ORCID 0000-0002-7106-9270
University Hospital Ulm · DEGerman Center for Neurodegenerative Diseases · DETUM Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progressive supranuclear palsy (PSP) is a neurodegenerative disease characterized by four-repeat tau deposition in various cell types and anatomical regions, and can manifest as several clinical phenotypes, including the most common phenotype, Richardson's syndrome. The limited availability of biomarkers for PSP relates to the overlap of clinical features with other neurodegenerative disorders, but identification of a growing number of biomarkers from imaging is underway. One way to increase the reliability of imaging biomarkers is to combine different modalities for multimodal imaging. This review aimed to provide an overview of the current state of PSP hybrid imaging by combinations of positron emission tomography (PET) and magnetic resonance imaging (MRI). Specifically, combined PET and MRI studies in PSP highlight the potential of [18F]AV-1451 to detect tau, but also the challenge in differentiating PSP from other neurodegenerative diseases. Studies over the last years showed a reduced synaptic density in [11C]UCB-J PET, linked [11C]PK11195 and [18F]AV-1451 markers to disease progression, and suggested the potential role of [18F]RO948 PET for identifying tau pathology in subcortical regions. The integration of quantitative global and regional gray matter analysis by MRI may further guide the assessment of reduced cortical thickness or volume alterations, and diffusion MRI could provide insight into microstructural changes and structural connectivity in PSP. Challenges in radiopharmaceutical biomarkers and hybrid imaging require further research targeting markers for comprehensive PSP diagnosis.

Indexed as

Neurodegenerative DiseasesSupranuclear Palsy, ProgressiveBiomarkersHumansMultimodal ImagingRadiopharmaceuticalsReproducibility of ResultsBiomarkersRadiopharmaceuticalsdiagnosisneurodegenerative diseasesprogressive supranuclear palsyradiological biomarkersradiopharmaceutical biomarkers

Identifiers

PMID38132096
PMCPMC10742083
OpenAlexW4389387576

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.