Evidence map›Paper›PMID 30805583›Full record

ArticleBrain : a journal of neurology2019

Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response.

Yvette Zarb, Ulrike Weber-Stadlbauer, Daniel Kirschenbaum, Diana Rita Kindler, Juliet Richetto, Daniel Keller, Rosa Rademakers, Dennis W Dickson, Andreas Pasch, Tatiana Byzova and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  13. XPR1: a regulator of cellular phosphate homeostasis rather than a Pi exporter.Pflugers Archiv : European journal of physiology · 2024
    Article
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  17. Adult-Onset Tourettism inMovement disorders clinical practice · 2023
    Article
  18. Article
  19. The Genetics of Primary Familial Brain Calcification: A Literature Review.International journal of molecular sciences · 2023
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Yvette ZarbDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Ulrike Weber-StadlbauerInstitute of Veterinary Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich University, Zurich, Switzerland.
Daniel KirschenbaumDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Diana Rita KindlerInstitute of Neuropathology, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Juliet RichettoInstitute of Veterinary Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich University, Zurich, Switzerland.
Daniel KellerDepartment of Biomedical Engineering, ETH and University of Zurich, Zurich, Switzerland.
Rosa RademakersInstitute of Diagnostic and Interventional Radiology, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Dennis W DicksonInstitute of Diagnostic and Interventional Radiology, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Andreas PaschDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Tatiana ByzovaCalciscon AG, Nidau-Biel, Switzerland.
Khayrun NaharDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Fabian F VoigtNeuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.
Fritjof HelmchenNeuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.
Andreas BossDepartment of Biomedical Engineering, ETH and University of Zurich, Zurich, Switzerland.
Adriano AguzziDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Jan KlohsInstitute of Neuropathology, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Annika KellerDepartment of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
University Hospital of Zurich · CHUniversity of Zurich · CHETH Zurich · CHMayo Clinic in Florida · US

Funding

Regulation of Integrins in Neovasculature DevelopmentR01HL071625 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2003 to 2021
$7.3M
Genetic Discovery and Pathobiology of Frontotemporal Lobar Degeneration and Related TDP-43 ProteinopathiesR35NS097261 · NINDS · MAYO CLINIC JACKSONVILLE · PI RADEMAKERS, ROSA · 2017 to 2019
$2.9M
Role of TLR2 in angiogenesisR01HL145536 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2019 to 2022
$2.6M
NHLBI NIH HHS R01 HL071625NHLBI NIH HHS R01 HL145536NINDS NIH HHS R35 NS097261
6 · The paper itself

Abstract

Brain calcifications are commonly detected in aged individuals and accompany numerous brain diseases, but their functional importance is not understood. In cases of primary familial brain calcification, an autosomally inherited neuropsychiatric disorder, the presence of bilateral brain calcifications in the absence of secondary causes of brain calcification is a diagnostic criterion. To date, mutations in five genes including solute carrier 20 member 2 (SLC20A2), xenotropic and polytropic retrovirus receptor 1 (XPR1), myogenesis regulating glycosidase (MYORG), platelet-derived growth factor B (PDGFB) and platelet-derived growth factor receptor β (PDGFRB), are considered causal. Previously, we have reported that mutations in PDGFB in humans are associated with primary familial brain calcification, and mice hypomorphic for PDGFB (Pdgfbret/ret) present with brain vessel calcifications in the deep regions of the brain that increase with age, mimicking the pathology observed in human mutation carriers. In this study, we characterize the cellular environment surrounding calcifications in Pdgfbret/ret animals and show that cells around vessel-associated calcifications express markers for osteoblasts, osteoclasts and osteocytes, and that bone matrix proteins are present in vessel-associated calcifications. Additionally, we also demonstrate the osteogenic environment around brain calcifications in genetically confirmed primary familial brain calcification cases. We show that calcifications cause oxidative stress in astrocytes and evoke expression of neurotoxic astrocyte markers. Similar to previously reported human primary familial brain calcification cases, we describe high interindividual variation in calcification load in Pdgfbret/ret animals, as assessed by ex vivo and in vivo quantification of calcifications. We also report that serum of Pdgfbret/ret animals does not differ in calcification propensity from control animals and that vessel calcification occurs only in the brains of Pdgfbret/ret animals. Notably, ossification of vessels and astrocytic neurotoxic response is associated with specific behavioural and cognitive alterations, some of which are associated with primary familial brain calcification in a subset of patients.

Indexed as

AgedAnimalsAstrocytesBrainBrain DiseasesCalcinosisFemaleHumansMaleMiceMutationOssification, HeterotopicOsteogenesisOxidative StressPedigreeProto-Oncogene Proteins c-sisProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor betaSLC20A2 protein, humanSodium-Phosphate Cotransporter Proteins, Type IIIXenotropic and Polytropic Retrovirus ReceptorXPR1 protein, humanXpr1 protein, mouseneurotoxic astrocyteossificationPDGFBprepulse inhibitionprimary familial brain calcification

Identifiers

PMID30805583
PMCPMC6439320
OpenAlexW2917616638

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.