# Pre-Transplant C-Reactive Protein ≥ 20 mg/L Predicts Infection-Related Mortality After Heart Transplantation

**Authors:** Matthias Helmschrott, Karsten M. Heil, Rasmus Rivinius, Ann-Kathrin Rahm, Philipp Ehlermann, Norbert Frey, Fabrice F. Darche

PMC · DOI: 10.3390/jcm15041332 · 2026-02-08

## TL;DR

High pre-transplant C-reactive protein levels predict higher infection-related deaths after heart transplants.

## Contribution

Identifies pre-transplant CRP ≥ 20 mg/L as a novel predictor of infection-related mortality after heart transplantation.

## Key findings

- Patients with pre-transplant CRP ≥ 20 mg/L had significantly higher mortality rates at 30 days, 1 year, 2 years, and 5 years post-transplant.
- Infection-related deaths were more common in patients with pre-transplant CRP ≥ 20 mg/L, especially from pulmonary infections.
- CRP ≥ 20 mg/L was an independent predictor of 5-year post-transplant mortality in multivariate analysis.

## Abstract

Background: Patients after heart transplantation (HTX) require lifelong immunosuppressive therapy to prevent graft rejection, thereby increasing susceptibility to infections. C-reactive protein (CRP) is a recognized biochemical marker of system-wide inflammation and generally rises with increasing infection severity. As the prognostic relevance of elevated CRP (≥20 mg/L) prior to HTX has been unclear, we analyzed its effects on post-transplant outcomes. Methods: We performed a retrospective, observational, single-center study including 418 patients who received HTX at Heidelberg Heart Center between the years 2000 and 2019. HTX recipients were grouped according to pre-transplant CRP (<20 or ≥20 mg/L). We analyzed donor and recipient characteristics, post-transplant pharmacotherapy, and post-transplant mortality including causes of death. Results: Pre-transplant CRP was ≥20 mg/L in 102 of 418 HTX recipients (24.4%). These patients had a significantly higher 30-day (11.8% versus 5.1%, p = 0.019), 1-year (39.2% versus 17.4%, p < 0.001), 2-year (42.2% versus 23.1%, p < 0.001), and 5-year post-transplant mortality (47.1% versus 30.4%, p = 0.002). Infection/sepsis was more frequently the cause of death within five years after HTX among patients with a pre-transplant CRP ≥ 20 mg/L (28.4% vs. 15.8%, p = 0.005), particularly pulmonary infections (19.6% vs. 9.5%, p = 0.006). Multivariate Cox regression showed pre-transplant CRP ≥ 20 mg/L as an independent predictor of 5-year post-transplant mortality (HR: 1.630, 95% CI: 1.144–2.323, p = 0.007). Conclusions: Pre-transplant CRP ≥ 20 mg/L identifies HTX candidates at increased risk of infection-related mortality after HTX, particularly pulmonary infections. Intensified pre-transplant evaluation for occult infection and close post-transplant infectious surveillance is advisable.

## Linked entities

- **Diseases:** infection (MONDO:0005550)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** opportunistic infections (MESH:D009894), malignancy (MESH:D009369), ischemic (MESH:D002545), AF (MESH:D001281), post- (MESH:D000094025), end-stage heart failure (MESH:D007676), valvular regurgitation (MESH:D006349), Infection (MESH:D007239), cardiovascular disease (MESH:D002318), chronic kidney disease (MESH:D051436), respiratory symptoms (MESH:D012818), periodontitis (MESH:D010518), pulmonary congestion (MESH:D001261), inflammation (MESH:D007249), injury to (MESH:D014947), pulmonary infection (MESH:D012141), HTX (OMIM:605376), death (MESH:D003643), fever (MESH:D005334), ischemia (MESH:D007511), immune dysregulation (OMIM:614878), Infectious complications (MESH:D003141), sepsis (MESH:D018805), bleeding (MESH:D006470), infective endocarditis (MESH:D004696), abdominal infections (MESH:D000007), heart failure (MESH:D006333), TIA (MESH:D002546), Pneumonia (MESH:D011014), systemic (MESH:D015619), stroke (MESH:D020521), COPD (MESH:D029424), thromboembolic (MESH:D013923), cardiomyopathy (MESH:D009202)
- **Chemicals:** azathioprine (MESH:D001379), prednisolone (MESH:D011239), mycophenolic acid (MESH:D009173), H2 (-), cyclosporine A (MESH:D016572), tacrolimus (MESH:D016559), ASA (MESH:D001241)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942277/full.md

---
Source: https://tomesphere.com/paper/PMC12942277