Evidence map›Paper›PMID 38911286›Full record

ArticleMolecular therapy. Methods & clinical development2024

SERCA2a overexpression improves muscle function in a canine Duchenne muscular dystrophy model.

Kasun Kodippili, Chady H Hakim, Matthew J Burke, Yongping Yue, James A Teixeira, Keqing Zhang, Gang Yao, Gopal J Babu, Roland W Herzog, Dongsheng Duan

Abstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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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

10 authors.

Kasun KodippiliDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
Chady H HakimDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
Matthew J BurkeDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
Yongping YueDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
James A TeixeiraDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
Keqing ZhangDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.
Gang YaoDepartment of Chemical and Biomedical Engineering, College of Engineering, The University of Missouri, Columbia, MO 65212, USA.
Gopal J BabuDepartment of Cell Biology and Molecular Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
Roland W HerzogHerman B Wells Center for Pediatric Research, Indiana University, Indianapolis, IN 46202, USA.
Dongsheng DuanDepartment of Molecular Microbiology and Immunology, School of Medicine, The University of Missouri, Columbia, MO 65212, USA.

Funding

Mechanism of immune response to muscle-directed AAV gene transferR01AI177600 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI Dongsheng Duan, Roland W. Herzog · 2023 to 2026
$3.1M
NIAID NIH HHS R01 AI177600
6 · The paper itself

Abstract

Excessive cytosolic calcium accumulation contributes to muscle degeneration in Duchenne muscular dystrophy (DMD). Sarco/endoplasmic reticulum calcium ATPase (SERCA) is a sarcoplasmic reticulum (SR) calcium pump that actively transports calcium from the cytosol into the SR. We previously showed that adeno-associated virus (AAV)-mediated SERCA2a therapy reduced cytosolic calcium overload and improved muscle and heart function in the murine DMD model. Here, we tested whether AAV SERCA2a therapy could ameliorate muscle disease in the canine DMD model. 7.83 × 10

Indexed as

AAVcanine modelDMDDuchenne muscular dystrophyextensor carpi ulnarismuscle functionsarcoplasmic reticulumSERCA2aTregtyrosine mutant AAV9

Identifiers

PMID38911286
PMCPMC11190715

What OpenQuestion holds

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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 OpenQuestion graph.