# Effect of pirfenidone on plasma markers of collagen turnover in patients with heart failure, preserved left ventricular ejection fraction and myocardial fibrosis

**Authors:** Nicholas Black, Gavin Lewis, Fardad Soltani, Susanna Dodd, Erik B Schelbert, Susana Ravassa, Begoña López, Arantxa González, John G Cleland, Christopher A Miller

PMC · DOI: 10.1136/openhrt-2025-003596 · Open Heart · 2026-02-10

## TL;DR

This study examines how pirfenidone affects collagen markers in heart failure patients with preserved ejection fraction and fibrosis.

## Contribution

The study provides new insights into the relationship between pirfenidone treatment and plasma collagen turnover markers in heart failure patients.

## Key findings

- Pirfenidone reduced CITP and increased PICP:CITP ratio at 13 and 26 weeks but not at 52 weeks.
- Changes in ECV were weakly associated with changes in PICP and CITP after multivariable adjustment.

## Abstract

Plasma concentrations of procollagen type-I C-terminal pro-peptide (PICP) and collagen type-I C-terminal telopeptide (CITP) may reflect collagen turnover and systemic fibrosis. We investigated the effect of pirfenidone, an anti-fibrotic agent, on PICP and CITP, and their association with myocardial fibrosis, using cardiovascular magnetic resonance to measure extracellular volume (ECV).

In the trial (Pirfenidone in Patients with Heart Failure and Preserved Left Ventricular Ejection Fraction), PICP, CITP and PICP:CITP ratio were measured at baseline and follow-up in patients with ECV≥27% randomised (n=94) to pirfenidone or placebo, and at baseline only in patients who were not randomised because of ECV<27% (n=13).

There was no association between baseline myocardial ECV and baseline log PICP, log CITP and log PICP:CITP ratio (p=0.19, p=0.13, p=0.60, respectively). Treatment with pirfenidone did not alter PICP, but reduced CITP and increased PICP:CITP ratio at 13 and 26 weeks (all p<0.05) but not at 52 weeks. After multivariable adjustment, there was a weak relationship between change in myocardial ECV and change in log PICP (R2 0.16, p=0.01) and log CITP (R2 0.12, p=0.04), but not log PICP:CITP ratio (p=0.56).

In patients with stable heart failure with preserved ejection fraction, pirfenidone treatment had no sustained effect on plasma levels of PICP and CITP at 52 weeks. Changes in ECV during treatment with pirfenidone are associated with changes in plasma PICP and CITP, suggesting a weak association between changes in collagen volume/mass and plasma markers of collagen turnover.

## Linked entities

- **Chemicals:** pirfenidone (PubChem CID 40632)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** Heart Failure (MESH:D006333), fibrosis (MESH:D005355)
- **Chemicals:** Pirfenidone (MESH:C093844), PICP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12911782/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911782/full.md

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Source: https://tomesphere.com/paper/PMC12911782