Evidence map›Paper›PMID 31561281›Full record

ArticleBrain pathology (Zurich, Switzerland)2020

Astrocyte-microglial association and matrix composition are common events in the natural history of primary familial brain calcification.

Khayrun Nahar, Thibaud Lebouvier, Maarja Andaloussi Mäe, Anne Konzer, Jonas Bergquist, Yvette Zarb, Bengt Johansson, Christer Betsholtz, Michael Vanlandewijck

Open access · hybridAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

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  13. The Genetics of Primary Familial Brain Calcification: A Literature Review.International journal of molecular sciences · 2023
    Review
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  19. Adult-induced genetic ablation distinguishes PDGFB roles in blood-brain barrier maintenance and development.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article
  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

9 authors at 4 institutions in 4 countries.

Khayrun Nahar *Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Thibaud Lebouvier *Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Maarja Andaloussi MäeDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Anne KonzerScientific Service Group Mass Spectrometry, Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany.
Jonas BergquistDepartment of Chemistry, Biomedical Centre, Uppsala University, Uppsala, Sweden.
Yvette ZarbDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.ORCID 0000-0001-5107-0701
Bengt JohanssonElectron Microscopy Unit, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.
Christer BetsholtzDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Michael VanlandewijckDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-0709-7808
Uppsala University · SEMax Planck Institute for Heart and Lung Research · DEUniversity of Gothenburg · SEUniversity of Zurich · CH

Funding

AstraZeneca Funding of ICMCCancerfondenForschungskredit und Stiftung für Forschung an der Medizinischen Fakultät der Universität Zürich FK-16-034H2020 European Research Council AdG 294556 BBBARRIERKnut och Alice Wallenbergs StiftelseLeducq Foundation Transatlantic network 14CVD02 SphingonetSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 31003A_159514/1Stiftung Synapsis - Alzheimer Forschung Schweiz AFSVetenskapsrådet
6 · The paper itself

Abstract

Primary familial brain calcification (PFBC) is an age-dependent and rare neurodegenerative disorder characterized by microvascular calcium phosphate deposits in the deep brain regions. Known genetic causes of PFBC include loss-of-function mutations in genes involved in either of three processes-platelet-derived growth factor (PDGF) signaling, phosphate homeostasis or protein glycosylation-with unclear molecular links. To provide insight into the pathogenesis of PFBC, we analyzed murine models of PFBC for the first two of these processes in Pdgfb

Indexed as

AnimalsAstrocytesBrain DiseasesCalcinosisDisease Models, AnimalDisease ProgressionExtracellular MatrixFemaleMaleMiceMice, TransgenicMicrogliaMutationNeurodegenerative DiseasesPlatelet-Derived Growth FactorSodium-Phosphate Cotransporter Proteins, Type IIIPlatelet-Derived Growth Factorplatelet-derived growth factor ASlc20a2 protein, mouseSodium-Phosphate Cotransporter Proteins, Type IIIbrain calcificationmass spectrometryPDGFB retention motive knockoutPFBCSlc20a2 knockout

Identifiers

PMID31561281
PMCPMC7317599
OpenAlexW2976915410

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.