# Clinical Significance of Peripheral Arterial Disease Evaluation in Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis

**Authors:** Jeong Yeop Whang, Lucy Eunju Lee, Jang Woo Ha, Oh Chan Kwon, Yong-Beom Park, Sang-Won Lee

PMC · DOI: 10.3390/medicina61061074 · 2025-06-11

## TL;DR

This study shows that peripheral arterial disease evaluation can help identify kidney issues and predict future complications in patients with a specific type of vasculitis.

## Contribution

The study is the first to show that abnormal skin perfusion pressure can predict kidney involvement and future end-stage kidney disease in AAV patients.

## Key findings

- Abnormal skin perfusion pressure was significantly linked to kidney and skin symptoms in AAV patients.
- Abnormal skin perfusion pressure may predict future progression to end-stage kidney disease.
- Only a small percentage of patients had abnormal results in pulse volume recording/ankle-brachial index and transcutaneous oxygen pressure tests.

## Abstract

Background and Objectives: This study investigated the frequency and clinical significance of subclinical but substantial peripheral arterial disease (PAD), identified using PAD evaluation, including pulse volume recording/ankle–brachial index (PVR/ABI), transcutaneous oxygen pressure (TcpO2), and skin perfusion pressure (SPP) tests in patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV). Materials and Methods: This study included 54 patients with PAD evaluation results at or after AAV diagnosis. PVR/ABI and/or TcpO2 and/or SPP were performed on the same day. Abnormal PVR/ABI, TcpO2, and SPP were defined as PVR/ABI < 0.97, TcpO2 < 40 mmHg, and SPP < 50 mmHg, respectively. Poor outcomes included all-cause mortality, end-stage kidney disease (ESKD), cerebrovascular accidents, and acute coronary syndrome after PAD evaluation. Results: The median age of the 54 patients was 67 years, and 48.1% were male. In total, 3 of 54 patients (5.6%), 6 of 16 (37.5%), and 6 of 23 (26.1%) had abnormal PVR/ABI, TcpO2, and SPP, respectively. The concordance rate between abnormal PVR/ABI and abnormal TcpO2 or SPP was very low. Among the 54 patients, 5 (9.3%) died, and 2 (3.7%) progressed to ESKD. Abnormal SPP was significantly associated with cutaneous and renal manifestations at the time of PAD evaluation and had the potential to predict progression to ESKD during follow-up in patients with AAV. Conclusions: This study is the first to reveal the clinical usefulness of PAD evaluation: abnormal SPP may have the potential to identify subclinical but substantial PAD and can predict simultaneous kidney involvement as well as future progression to ESKD in patients with AAV.

## Linked entities

- **Diseases:** antineutrophil cytoplasmic antibody-associated vasculitis (MONDO:0015492), end-stage kidney disease (MONDO:0004375), acute coronary syndrome (MONDO:0005542)

## Full-text entities

- **Diseases:** ESKD (MESH:D007676), AAV (MESH:D014657), Antineutrophil Cytoplasmic Antibody-Associated Vasculitis (MESH:D056648), cerebrovascular accidents (MESH:D020521), PAD (MESH:D058729), acute coronary syndrome (MESH:D054058)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12195056/full.md

---
Source: https://tomesphere.com/paper/PMC12195056