Evidence map›Paper›PMID 22174313›Full record

ArticleScience translational medicine2011

Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome.

Mark D McCauley, Tiannan Wang, Elise Mike, Jose Herrera, David L Beavers, Teng-Wei Huang, Christopher S Ward, Steven Skinner, Alan K Percy, Daniel G Glaze and 2 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00299312 (Rett Syndrome Natural History), which is not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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.

NCT00299312 completednot on this map

Rett Syndrome Natural History: Genetic and Physical Characteristics of Rett Syndrome

TypeobservationalSponsorUniversity of Alabama at BirminghamRan2006 to 2015Enrolled10ConditionsRett Syndrome, MECP2 Duplication Disorder, Rett-related Disorder
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Rett Syndrome: Thinking Beyond Brain Borders.Advances in experimental medicine and biology · 2025
    Review
  7. Review
  8. Epigenetics.Advances in experimental medicine and biology · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. QTPhysiological reports · 2022
    Article
  18. Article
  19. Review
  20. 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 at 3 institutions in 1 country.

Mark D McCauleyDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.
Tiannan Wang
Elise Mike
Jose Herrera
David L Beavers
Teng-Wei Huang
Christopher S Ward
Steven Skinner
Alan K Percy
Daniel G Glaze
Xander H T Wehrens
Jeffrey L Neul
Baylor College of Medicine · USGreenwood Genetic Center · USTexas Children's Hospital · US

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
UNDERSTANDING FXTAS AMONG MALES WITH THE FMR1 PREMUTATIONP30HD024064 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TOLIAS, KIMBERLY R · 1988 to 2013
$29.4M
Training and Career Development ComponentU54HD061222 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PERCY, ALAN KENNETH · 2009 to 2019
$12.4M
Ryanodine receptor regulation in post-operative atrial fibrillationR01HL089598 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2007 to 2022
$6.5M
Regulation of Sarcoplasmic Reticulum Calcium Release in Heart FailureR01HL091947 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2009 to 2019
$3.2M
Determining the Role of Junctophilin-2 in Cardiac DiseaseR01HL117641 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2014 to 2017
$2.3M
Molecular Medicine Scholars Training GrantT32HL066991 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI CHAN, LAWRENCE · 2002 to 2012
$2.1M
Characterizing autonomic dysfunction in Rett syndrome and other MECP2 disordersR01HD062553 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NEUL, JEFFREY L · 2010 to 2014
$1.7M
Analysis of the dopamine system in Rett syndromeK08NS052240 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI NEUL, JEFFREY L · 2005 to 2009
$840k
Analysis of MeCP2 function in neural crest derivativesF31NS066601 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI WARD, CHRISTOPHER S · 2009 to 2011
$105k
NCI NIH HHS P30 CA125123NHLBI NIH HHS HL066991NHLBI NIH HHS HL089598NHLBI NIH HHS HL091947NHLBI NIH HHS R01 HL089598NHLBI NIH HHS R01 HL091947NHLBI NIH HHS R01 HL117641NHLBI NIH HHS T32 HL066991NICHD NIH HHS HD062553NICHD NIH HHS HD24064NICHD NIH HHS P30 HD024064NICHD NIH HHS R01 HD062553NICHD NIH HHS U54 HD061222NINDS NIH HHS F31 NS066601NINDS NIH HHS K08 NS052240NINDS NIH HHS NS066601NINDS NIH HHS NS52240
6 · The paper itself

Abstract

Rett syndrome is a neurodevelopmental disorder typically caused by mutations in methyl-CpG-binding protein 2 (MECP2) in which 26% of deaths are sudden and of unknown cause. To explore the hypothesis that these deaths may be due to cardiac dysfunction, we characterized the electrocardiograms in 379 people with Rett syndrome and found that 18.5% show prolongation of the corrected QT interval (QTc), an indication of a repolarization abnormality that can predispose to the development of an unstable fatal cardiac rhythm. Male mice lacking MeCP2 function, Mecp2(Null/Y), also have prolonged QTc and show increased susceptibility to induced ventricular tachycardia. Female heterozygous null mice, Mecp2(Null/+), show an age-dependent prolongation of QTc associated with ventricular tachycardia and cardiac-related death. Genetic deletion of MeCP2 function in only the nervous system was sufficient to cause long QTc and ventricular tachycardia, implicating neuronally mediated changes to cardiac electrical conduction as a potential cause of ventricular tachycardia in Rett syndrome. The standard therapy for prolonged QTc in Rett syndrome, β-adrenergic receptor blockers, did not prevent ventricular tachycardia in Mecp2(Null/Y) mice. To determine whether an alternative therapy would be more appropriate, we characterized cardiomyocytes from Mecp2(Null/Y) mice and found increased persistent sodium current, which was normalized when cells were treated with the sodium channel-blocking anti-seizure drug phenytoin. Treatment with phenytoin reduced both QTc and sustained ventricular tachycardia in Mecp2(Null/Y) mice. These results demonstrate that cardiac abnormalities in Rett syndrome are secondary to abnormal nervous system control, which leads to increased persistent sodium current. Our findings suggest that treatment in people with Rett syndrome would be more effective if it targeted the increased persistent sodium current to prevent lethal cardiac arrhythmias.

Indexed as

AnimalsArrhythmias, CardiacDisease Models, AnimalEchocardiographyElectric StimulationFemaleHeart Defects, CongenitalHumansMaleMethyl-CpG-Binding Protein 2MiceMice, Inbred C57BLMice, KnockoutMice, Mutant StrainsMutationPatch-Clamp TechniquesMethyl-CpG-Binding Protein 2Sodium

Identifiers

PMID22174313
PMCPMC3633081
OpenAlexW2156185412

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.