# Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitors: A Novel Therapy in the Treatment of Cholesterol Crystal Embolism-Induced Kidney Injury

**Authors:** Benjamin J. Strimaitis, Leo Francis, Eoin D. O’Sullivan

PMC · DOI: 10.1016/j.xkme.2025.101125 · Kidney Medicine · 2025-09-19

## TL;DR

This paper presents a case where a PCSK9 inhibitor helped improve kidney function in a patient with cholesterol crystal embolism.

## Contribution

The paper introduces PCSK9 inhibitors as a potential novel therapy for kidney injury caused by cholesterol crystal embolism.

## Key findings

- The patient's kidney function stabilized and improved after starting evolocumab.
- Eosinophilia decreased, suggesting reduced embolic activity.
- PCSK9 inhibitors may reduce plaque instability and microinflammation in CCE.

## Abstract

Cholesterol crystal embolism (CCE) is a challenging and often underrecognized cause of kidney impairment, especially in elderly patients with significant atherosclerotic disease. CCE typically arises from dislodged cholesterol crystals that migrate from atherosclerotic plaques to occlude small renal and systemic arteries. Here, we report a case of a 72-year-old man who presented with acute kidney injury following coronary artery bypass graft surgery. Five weeks postsurgery the patient experienced a rapid decline in kidney function. Kidney biopsy confirmed the diagnosis of CCE, showing cholesterol clefts and associated inflammation within renal arteries. Although the patient initially responded to high-dose corticosteroid therapy kidney function declined during steroid tapering. A proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor, evolocumab, was introduced as an adjunct treatment, targeting lipid reduction and plaque stabilization. Following initiation of evolocumab, kidney function stabilized and gradually improved, with concurrent reductions in eosinophilia, suggesting a decrease in ongoing embolic phenomena. This case illustrates the potential role of PCSK9 inhibitors as an adjunctive therapy for CCE-associated kidney injury, particularly when conventional management may be insufficient. PCSK9 inhibitors warrant further investigation in CCE cases with kidney involvement, as they may offer additional benefits beyond lipid lowering by reducing plaque instability and associated microinflammation.

## Linked entities

- **Proteins:** PCSK9 (proprotein convertase subtilisin/kexin type 9)
- **Diseases:** acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}
- **Diseases:** atherosclerotic (MESH:D050197), embolic phenomena (MESH:D004617), CCE (MESH:D017700), eosinophilia (MESH:D004802), acute kidney injury (MESH:D058186), inflammation (MESH:D007249), Kidney Injury (MESH:D007674)
- **Chemicals:** steroid (MESH:D013256), cholesterol (MESH:D002784), evolocumab (MESH:C577155), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12593602/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12593602/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12593602/full.md

---
Source: https://tomesphere.com/paper/PMC12593602