Evidence mapPaperPMID 42440741Full record

SynthesisFrontiers in cardiovascular medicine2026

Therapeutic targeting of mitochondrial dysfunction in heart failure: a systematic review & meta-analysis of clinical outcomes.

Omer Mohammed, Shabrin Abdul Rasheed, Ananya Arora, Sharon Velamparambil Sunny, Afthab Salam Kanniyan, Shilla Thomas, Basil Wahid Bhat, Venu Pararath Gopalakrishnan, Jeffrey George, Akiva Rosenzveig and 2 more

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in cardiovascular medicine, 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

12 authors.

Omer MohammedDepartment of General Medicine, Government Medical College, Kozhikode, Kerala, India.
Shabrin Abdul RasheedDepartment of Internal Medicine, Basildon University Hospital, Basildon, Essex, United Kingdom.
Ananya AroraDepartment of General Medicine, Shri Atal Bihari Vajpayee Medical College & Research Institute, Bangalore, India.
Sharon Velamparambil SunnyDepartment of General Medicine, Government Medical College, Kozhikode, Kerala, India.
Afthab Salam KanniyanDepartment of General Medicine, Government Medical College, Kozhikode, Kerala, India.
Shilla ThomasDepartment of General Medicine, Government Medical College, Kozhikode, Kerala, India.
Basil Wahid BhatInternational Medical College, Gazipur, Dhaka, Bangladesh.
Venu Pararath GopalakrishnanUMass Memorial Health, Worcester, MA, United States.
Jeffrey GeorgeCase Western Reserve University, Cleveland, OH, United States.
Akiva RosenzveigCleveland Clinic Foundation, Cleveland Clinic Lerner College of Medicine, Cleveland, OH, United States.
Aravinda NanjundappaCleveland Clinic Foundation, Cleveland Clinic Lerner College of Medicine, Cleveland, OH, United States.
Shelby KuttyDepartment of Cardiology, BayCare Health System, Clearwater, FL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mitochondrial dysfunction is recognised as a key driver of heart failure (HF) pathophysiology, contributing to oxidative stress, apoptosis, and impaired energy production in cardiomyocytes. Although therapeutic agents aimed at restoring mitochondrial function have demonstrated promise in animal models and early-phase clinical trials, their efficacy in clinical practice remains uncertain. This meta-analysis evaluated the impact of these agents on clinical outcomes in HF patients. Methods: A systematic literature search was conducted across PubMed, Cochrane Library, ScienceDirect, Google Scholar, and ClinicalTrials.gov for studies published through May 2025. Thirty one studies (24 RCTs and 7 crossover trials) were included in meta-analysis. Standardized mean difference was pooled for changes in left ventricular ejection fraction (LVEF), NYHA class and six-minute walk test (6MWT) distance compared to baseline, and risk ratios (RR) were pooled for heart failure-related hospitalisations, and all-cause mortality. Results: Interventions significantly improved LVEF compared with baseline (SMD: 0.53; 95% CI: 0.42-0.65; Discussion: These findings suggest a potential role for mitochondrial-targeted agents as adjunctive strategies in HF, although the evidence base requires further strengthening through high-quality, adequately powered trials before firm clinical recommendations can be made. Systematic Review Registration: https://www.crd.york.ac.uk/PROSPERO/view/CRD420251075951, PROSPERO CRD420251075951.

Indexed as

coQ10elamipretideheart failureHFpEFHFrEFmitochondrial energetics

Identifiers

PMID42440741
PMCPMC13333738

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.