Evidence map›Paper›PMID 40853254›Full record

ReviewCardiovascular research2025

Gene therapy in cardiac and vascular diseases: a review of approaches to treat genetic and common cardiovascular diseases with novel gene-based therapeutics.

Patricia L Musolino, Susan J Rosser, Mairi Brittan, David E Newby, Colin Berry, Paul R Riley, Mauro Giacca, Roger J Hajjar, Andrew H Baker

Abstract readReview
In one paragraph

Review in Cardiovascular research, 2025. 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. The dark genome in cardiovascular medicine.European heart journal · 2026
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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

9 authors.

Patricia L MusolinoCenter for Genomic Medicine, Massachusetts General Hospital, Harvard Medical School, 55 Fruit St. Lunder Building 6th Floor Boston, MA 02114.
Susan J RosserUK Centre for Mammalian Synthetic Biology at the Institute of Quantitative Biology, Biochemistry, and Biotechnology, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.
Mairi BrittanBritish Heart Foundation Centre for Research Excellence, Centre for Cardiovascular Science, Queens Medical Research Institute, 47 Little France Crescent, University of Edinburgh, Edinburgh EH16 4TJ, UK.
David E NewbyBritish Heart Foundation Centre for Research Excellence, Centre for Cardiovascular Science, Queens Medical Research Institute, 47 Little France Crescent, University of Edinburgh, Edinburgh EH16 4TJ, UK.
Colin BerryBHF Glasgow Cardiovascular Research Centre, University of Glasgow and Golden Jubilee National Hospital, Clydebank, UK.ORCID 0000-0002-4547-8636
Paul R RileyInstitute of Developmental & Regenerative Medicine (IDRM), IMS-Tetsuya Nakamura Building, Old Road Campus, University of Oxford, Oxford OX3 7TY, UK.
Mauro GiaccaSchool of Cardiovascular and Metabolic Medicine & Sciences and British Heart Foundation Centre of Research Excellence, King's College London, James Black Centre125 Coldharbour Lane, London SE5 9NU, UK.ORCID 0000-0003-2927-7225
Roger J HajjarGene & Cell Therapy Institute, Massachusetts General Brigham, Cambridge, MA 02139, USA.
Andrew H BakerBritish Heart Foundation Centre for Research Excellence, Centre for Cardiovascular Science, Queens Medical Research Institute, 47 Little France Crescent, University of Edinburgh, Edinburgh EH16 4TJ, UK.ORCID 0000-0003-1441-5576

Funding

British Heart Foundation FS/MBPHD/22/28011British Heart Foundation PG/18/52/33892British Heart Foundation PG/19/28/34310British Heart Foundation RG/F/23/110104Medical Research Council MR/S018905/1
6 · The paper itself

Abstract

In the past decade, there has been substantive progress in gene therapy across disease indications. However, despite multiple gene therapies being approved for clinical use, none have a cardiovascular indication. Several reasons for this have inhibited or delayed progress in the cardiovascular field. First, developing cardiovascular gene therapeutics represents a substantial technical challenge, particularly relating to identifying and building effective delivery systems for therapeutic cargo that will be sufficient to gain meaningful efficacy with acceptable safety for the patient. Second, for genetic disease, gene editing therapy of pathogenic variants is at a relatively early stage of development. Third, since this is a field in development, the optimal design of clinical trials of cardiovascular gene therapies is also evolving and requires expert attention. Despite this, recent and current clinical trials are charting new ground, gaining valuable new patient-focused information that provides critical new learning and bench-to-bedside iterative development that has been so successful in other disease areas. While most clinical trials currently focus on cardiac gene therapy, vascular approaches are being developed, both genetic and common. We herein review the state-of-the-art in this rapidly progressing field of study. We consider gene therapy vector design, including transcriptional control, an area of incredible opportunity through engineering biology approaches to design, build, and test bespoke transcriptional units for expression of therapeutic cargo. Achieving progress in this exciting field will require close working between all stakeholders, including academic, clinical, industry, regulatory, and patient communities. Based on current progress, there is a 10-year horizon for bringing several cardiovascular gene therapies to licensing.

Indexed as

Cardiovascular DiseasesGenetic TherapyHeart DiseasesVascular DiseasesAnimalsGene EditingGenetic Predisposition to DiseaseGenetic VectorsGene Transfer TechniquesHumansPhenotypeTreatment OutcomeCardiovascular diseaseGene editingGene therapyGene therapy vectorsHeart failureRegenerationVascular

Identifiers

PMID40853254
PMCPMC12551389

What OpenQuestion holds

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Registered trials

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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.