Evidence map›Paper›PMID 40834102›Full record

ArticleScience translational medicine2025

Bezafibrate improves mitochondrial function, blood-brain barrier integrity, and social deficits in models of 22q11.2 deletion syndrome.

Alexis M Crockett, Maria C Vélez Colόn, Hania Kebir, Frances M Smith, Daniel M Iascone, Brianna Ciesielski, Sergei Koshkin, Andrew D Patterson, Adam J Rossano, Amita Sehgal and 2 more

Abstract read
In one paragraph

Article in Science translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

12 authors.

Alexis M CrockettDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0001-9658-938X
Maria C Vélez ColόnDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-9016-3406
Hania KebirDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0001-6174-8846
Frances M SmithDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Daniel M IasconeChronobiology and Sleep Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-8629-7639
Brianna CiesielskiNeurobehavioral Core, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0009-0005-7347-0702
Sergei KoshkinHuck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA 16802, USA.ORCID 0000-0002-4699-1212
Andrew D PattersonDepartment of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, PA 16802, USA.
Adam J RossanoDepartment of Child and Adolescent Psychiatry, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Amita SehgalChronobiology and Sleep Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0001-7354-9641
Stewart A AndersonDepartment of Child and Adolescent Psychiatry, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Jorge Ivan AlvarezDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Funding

Phenotypic Diversity in COVID-19UL1TR001878 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2016 to 2025
$102.4M
The Intellectual and Developmental Disabilities Research Center (IDDRC) at CHOP/PennP50HD105354 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI Michael Byrne Robinson · 2021 to 2026
$9.2M
Specification of Interneurons of the Cerebral CortexR01MH066912 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI ANDERSON, STEWART A · 2003 to 2020
$5.7M
Cycling in a circadian circuitR37NS048471 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI SEHGAL, AMITA · 2015 to 2021
$2.7M
Mitochondrial influences on blood brain barrier function and neuropsychiatric illnessR01MH134893 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Jorge Ivan Alvarez, Stewart A Anderson · 2024 to 2026
$1.8M
IPSC phenotype, mitochondrial haplotype and psychosis in 22q11 deletion syndromeR01MH110185 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI ANDERSON, STEWART A · 2016 to 2018
$1.6M
Role of the brain-immune axis in neuropsychiatric diseaseR01MH134797 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI Jorge Ivan Alvarez · 2024 to 2026
$1.2M
Coupling between circadian rhythms and redox signaling in stem cell differentiation and adult neurogenesisF32MH125600 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI IASCONE, DANIEL MAXIM · 2020 to 2023
$216k
NCATS NIH HHS UL1 TR001878NICHD NIH HHS P50 HD105354NIMH NIH HHS F32 MH125600NIMH NIH HHS R01 MH066912NIMH NIH HHS R01 MH110185NIMH NIH HHS R01 MH134797NIMH NIH HHS R01 MH134893NINDS NIH HHS R37 NS048471
6 · The paper itself

Abstract

Maintenance of blood-brain barrier (BBB) integrity is critical to optimal brain function, and its impairment has been linked to multiple neurological disorders. A notable feature of the BBB is its elevated mitochondrial content compared with peripheral endothelial cells, although the functional implications of this phenomenon are unclear. Here, we studied BBB mitochondrial function in the context of 22q11.2 deletion syndrome (22qDS), a condition associated with a highly increased risk for neuropsychiatric disease. Because the 22q11.2 deletion includes six mitochondrial genes, and because we have previously identified BBB impairment in 22qDS, we addressed the hypothesis that mitochondrial deficits contribute to BBB dysfunction and affect behavior in this condition. We report mitochondrial impairment in human induced pluripotent stem cell (iPSC)-derived brain microvascular endothelial cells (iBMECs) from people with 22qDS and in BBB endothelial cells from a mouse model of 22qDS. We found that treatment with bezafibrate, an activator of mitochondrial biogenesis, attenuates mitochondrial deficits and enhances BBB function in both the iBMECs and a mouse model of 22qDS. This treatment also corrects social memory in the mouse model, a deficit previously associated with BBB dysfunction. Given that BBB integrity correlated with social memory performance, our findings suggest that mitochondrial dysfunction in the BBB influences barrier integrity and behavior.

Indexed as

BezafibrateBlood-Brain BarrierDiGeorge SyndromeMitochondriaSocial BehaviorAnimalsDisease Models, AnimalEndothelial CellsHumansInduced Pluripotent Stem CellsMaleMiceBezafibrate

Identifiers

PMID40834102
PMCPMC12535687

What OpenQuestion holds

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Registered trials

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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.