# Cardiac Contractility Modulation (CCM) Therapy in Contemporary Heart Failure Care: Mechanisms, Evidence, Patient Selection, and Emerging Directions

**Authors:** Dong-Hyeok Kim, Yeji Kim, Jungmin Kang, Junbeom Park

PMC · DOI: 10.3390/jcm15041460 · 2026-02-13

## TL;DR

Cardiac Contractility Modulation (CCM) is a new heart failure therapy that improves heart function without causing extra strain, offering benefits like better exercise tolerance and quality of life.

## Contribution

This paper reviews the mechanisms, clinical evidence, and emerging directions of CCM as a novel therapy for heart failure.

## Key findings

- CCM improves myocardial contractility without increasing oxygen consumption.
- CCM is associated with better exercise tolerance and quality of life in selected patients.
- Recent technological advances may broaden CCM's clinical use, especially in patients needing defibrillators.

## Abstract

Cardiac contractility modulation (CCM) is a bioelectronic therapy that delivers precisely timed electrical signals during ventricular refractoriness to modulate myocardial contractility without triggering depolarization. Unlike pacing-based therapies, CCM does not initiate a new depolarization but instead modulates intracellular signaling pathways to enhance myocardial contractility without increasing myocardial oxygen consumption. CCM therefore represents a myocardial conditioning strategy distinct from cardiac resynchronization therapy, conduction system pacing, or neuromodulation. Experimental and translational studies demonstrate that repeated CCM delivery induces sustained myocardial adaptations, including improvements in excitation–contraction coupling, molecular signaling pathways, and structural remodeling that extend beyond transient hemodynamic effects. Across clinical investigations, CCM has been associated with meaningful improvements in exercise tolerance, health-related quality of life, and functional status in carefully selected populations. Observational data further suggest a potential reduction in heart failure-related hospitalizations when therapy is applied within evidence-aligned indications. Recent technological developments—including simplified ventricular lead configurations, rechargeable compact generators, and integrated CCM–defibrillator platforms—have reduced procedural complexity and may broaden clinical applicability, particularly in patients with concomitant implantable cardioverter–defibrillator indications. This review synthesizes mechanistic insights, clinical evidence, patient selection principles, and practical considerations to define the evolving role of CCM within contemporary heart failure care pathways.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** PTK2B (protein tyrosine kinase 2 beta) [NCBI Gene 2185] {aka CADTK, CAKB, FADK2, FAK2, PKB, PTK}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, CAMK2G (calcium/calmodulin dependent protein kinase II gamma) [NCBI Gene 818] {aka CAMK, CAMK-II, CAMKG, MRD59}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** systole (MESH:D000092244), HFmrEF (MESH:D054143), arrhythmic (OMIM:212500), ventricular tachycardia (MESH:D017180), premature ventricular complexes (MESH:D018879), hypotension (MESH:D007022), CCM (MESH:D006331), stroke (MESH:D020521), cardiomyopathies (MESH:D009202), Heart Failure (MESH:D006333), Arrhythmia (MESH:D001145), diastolic dysfunction (MESH:D018487), ICD (OMIM:252500), chronic kidney disease (MESH:D051436), malignant (MESH:D009369), atrial fibrillation (MESH:D001281), myocardial ischemia (MESH:D017202), left bundle branch block (MESH:D002037), cardiomyocyte hypertrophy (MESH:D006984), dyspnea (MESH:D004417), ectopy (MESH:D050030), infection (MESH:D007239), hematoma (MESH:D006406), injury to (MESH:D014947)
- **Chemicals:** Calcium (MESH:D002118), oxygen (MESH:D010100), -HF-5C2 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941422/full.md

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Source: https://tomesphere.com/paper/PMC12941422