Evidence map›Paper›PMID 42779968›Full record

ArticleResearch square2026

PERM1 Gene Therapy Prevents Pressure Overload-induced Heart Failure Through a Sarcomere-Mitochondria Energetic Microdomain.

Karthi Sreedevi, Abigail O Doku, Alexey V Zaitsev, Ryan N Montalvo, Clare L Dennison, Audrey Korte, Sarah Salama, Mysha Alabbi, Samia Tasneem, Rebekah Thomas and 10 more

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Karthi SreedeviFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Abigail O DokuFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Alexey V ZaitsevFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Ryan N MontalvoFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Clare L DennisonFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.ORCID 0009-0001-1605-7891
Audrey KorteFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Sarah SalamaFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Mysha AlabbiFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Samia TasneemFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Rebekah ThomasFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Mark C RentonFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Seby EdasseryDepartment of Cell and Molecular Physiology, Loyola University Chicago, Chicago, Illinois, USA.
Stephanie M DeditzDepartment of Medicine, Section of Cardiology, University of Chicago, IL, USA.
Steven BurrowsFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Garima PatelFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Scott R JohnstoneFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
Zhen YanFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.
James W SmythFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.ORCID 0000-0003-4246-7904
Jonathan A KirkDepartment of Medicine, Section of Cardiology, University of Chicago, IL, USA.
Junco S WarrenFralin Biomedical Research Institute at Virginia Tech Carilion, Virginia Tech, Roanoke, VA, USA.ORCID 0000-0001-5231-4181

Funding

p38 MAPK a regulator of muscle contraction and functionR01AR050429 · NIAMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI YAN, ZHEN · 2005 to 2022
$5.3M
Viral subversion of intercellular coupling during myocarditisR01HL159512 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI James William Smyth · 2022 to 2026
$2.7M
mitoAMPK in exercise benefitsR01AR077440 · NIAMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI YAN, ZHEN · 2020 to 2024
$2.1M
Perm1 is a Novel Regulator of Cardiac Energetics and FunctionR01HL156667 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI DRAKOS, STAVROS GEORGE, WARREN, JUNKO SHIBAYAMA · 2021 to 2024
$2.0M
AAV-mediated PERM1 Overexpression as a New Therapy for Heart Failure with Reduced Ejection FractionR01HL184522 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI Kiyotake Ishikawa, JONATHAN A KIRK · 2026 to 2026
$1.6M
NHLBI NIH HHS R01 HL156667NHLBI NIH HHS R01 HL159512NHLBI NIH HHS R01 HL184522NIAMS NIH HHS R01 AR050429NIAMS NIH HHS R01 AR077440
6 · The paper itself

Abstract

Heart failure with reduced ejection fraction (HFrEF) remains a major cause of morbidity and mortality worldwide, characterized by impaired contractile function and mitochondrial dysfunction, yet therapies that simultaneously restore cardiac energetics and mechanical performance remain limited. Here, we show that adeno-associated virus-mediated overexpression of PERM1 (AAV-PERM1), a striated muscle-specific mitochondrial regulator, prevents pressure overload-induced HFrEF through a non-transcriptional mechanism that preserves both mitochondrial function and contractility. AAV-PERM1 mitigated declines in mitochondrial respiration and mitochondrial DNA content, maintained mitochondrial morphology under pressure overload, and attenuated pathological hypertrophy and fibrosis. Unexpectedly, these cardioprotective effects occurred despite persistent suppression of oxidative phosphorylation and fatty acid oxidation transcripts. Instead, PERM1 localized to a mitochondria-sarcomere microdomain, where it associated with ribosomal proteins and a creatine kinase-troponin C complex, suppressed pathological O-GlcNAcylation, and post-transcriptionally preserved electron transport chain protein abundance. Functionally, PERM1 enhanced myofibrillar force generation. These findings identify a previously unrecognized mechanism by which PERM1 preserves mitochondrial protein homeostasis and couples energy production to force generation, establishing a new paradigm for post-transcriptional metabolic control and positioning PERM1 as a therapeutic target for heart failure.

Indexed as

AAV gene therapyHeart failureHFrEFMechano-energetic couplingMitochondrial bioenergeticsMitochondrial protein homeostasisO-GlcNAcylationPERM1

Identifiers

PMID42779968
PMCPMC13596629

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.