Evidence map›Paper›PMID 38855866›Full record

ArticleJCI insight2024

Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder.

Weiyi Xu, Yingqiong Cao, Sara B Stephens, Maria Jose Arredondo, Yifan Chen, William Perez, Liang Sun, Andy C Yu, Jean J Kim, Seema R Lalani and 6 more

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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

16 authors.

Weiyi XuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Yingqiong CaoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Sara B StephensDepartment of Pediatrics, Division of Pediatric Cardiology, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas, USA.
Maria Jose ArredondoDepartment of Pediatrics, Division of Pediatric Cardiology, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas, USA.
Yifan ChenDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
William PerezDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, Texas, USA.
Liang SunDepartment of Integrative Physiology.
Andy C YuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Jean J KimDepartment of Molecular and Cellular Biology.
Seema R LalaniDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Na LiDepartment of Medicine (Section of Cardiovascular Research), and.
Frank T HorriganDepartment of Integrative Physiology.
Francisco AltamiranoDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, Texas, USA.
Xander Ht WehrensDepartment of Integrative Physiology.
Christina Y MiyakeDepartment of Pediatrics, Division of Pediatric Cardiology, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas, USA.
Lilei ZhangDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.

Funding

Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI Sandesh Chakravarthy Sreenath Nagamani, David Loren Nelson · 2020 to 2026
$9.9M
Ryanodine receptor regulation in post-operative atrial fibrillationR01HL089598 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2007 to 2022
$6.5M
The Role of Inflammasome in the Pathogenesis of Atrial FibrillationR01HL136389 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Na Li · 2017 to 2026
$5.6M
Cardiac Autonomic Activation In Atrial Fibrillation Triggers And SubstrateR01HL168277 · NHLBI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Francisco Altamirano, Miguel Valderrabano · 2023 to 2026
$3.2M
Deciphering the role of a circadian lncRNA in cardiac remodelingR01HL150589 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, LILEI · 2022 to 2025
$2.8M
Cardiac fibroblast inflammasome and atrial myopathyR01HL163277 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI LI, NA · 2022 to 2025
$2.8M
Transcriptional regulation of cardiac pathological remodeling by REV-ERBαR01HL143067 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, LILEI · 2019 to 2023
$2.4M
Junctophilin-2 cleavage in ischemic heart diseaseR01HL153350 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2021 to 2024
$2.3M
Role of Nucleoside-Diphosphate Kinase Signaling in Atrial FibrillationR01HL160992 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Xander H.T. Wehrens · 2023 to 2026
$2.1M
Broadly applicable high throughput variant interpretation and validation for MYH7R01HL175964 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI JONATHAN A KIRK, Md. Abul Hassan Samee · 2024 to 2026
$2.1M
Mechanisms underlying atrial fibrillation associated with chronic kidney diseaseR01HL147108 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI LI, NA, WEHRENS, XANDER H.T. · 2019 to 2022
$2.0M
Mechanisms driving cardiac dysfunction in Autosomal Dominant Polycystic Kidney DiseaseR01HL158703 · NHLBI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Francisco Altamirano · 2022 to 2026
$2.0M
NHLBI NIH HHS R01 HL089598NHLBI NIH HHS R01 HL136389NHLBI NIH HHS R01 HL143067NHLBI NIH HHS R01 HL147108NHLBI NIH HHS R01 HL150589NHLBI NIH HHS R01 HL153350NHLBI NIH HHS R01 HL158703NHLBI NIH HHS R01 HL160992NHLBI NIH HHS R01 HL163277NHLBI NIH HHS R01 HL164838NHLBI NIH HHS R01 HL168277NHLBI NIH HHS R01 HL175964NHLBI NIH HHS R21 HL165270NICHD NIH HHS P50 HD103555
6 · The paper itself

Abstract

TANGO2-deficiency disorder (TDD) is an autosomal-recessive genetic disease caused by biallelic loss-of-function variants in the TANGO2 gene. TDD-associated cardiac arrhythmias are recalcitrant to standard antiarrhythmic medications and constitute the leading cause of death. Disease modeling for TDD has been primarily carried out using human dermal fibroblast and, more recently, in Drosophila by multiple research groups. No human cardiomyocyte system has been reported, which greatly hinders the investigation and understanding of TDD-associated arrhythmias. Here, we established potentially novel patient-derived induced pluripotent stem cell differentiated cardiomyocyte (iPSC-CM) models that recapitulate key electrophysiological abnormalities in TDD. These electrophysiological abnormalities were rescued in iPSC-CMs with either adenoviral expression of WT-TANGO2 or correction of the pathogenic variant using CRISPR editing. Our natural history study in patients with TDD suggests that the intake of multivitamin/B complex greatly diminished the risk of cardiac crises in patients with TDD. In agreement with the clinical findings, we demonstrated that high-dose folate (vitamin B9) virtually abolishes arrhythmias in TDD iPSC-CMs and that folate's effect was blocked by the dihydrofolate reductase inhibitor methotrexate, supporting the need for intracellular folate to mediate antiarrhythmic effects. In summary, data from TDD iPSC-CM models together with clinical observations support the use of B vitamins to mitigate cardiac crises in patients with TDD, providing potentially life-saving treatment strategies during life-threatening events.

Indexed as

Arrhythmias, CardiacFolic AcidInduced Pluripotent Stem CellsMyocytes, CardiacChildFemaleHumansMaleFolic AcidArrhythmiasCardiologyGeneticsiPS cells

Identifiers

PMID38855866
PMCPMC11382877

What Socratic holds

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LicenceCC BY
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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.