# Absolute quantification of microRNA miR-875-5p in temporal artery biopsies and its biomarker potential for giant cell arteritis

**Authors:** Luka Bolha, Elvisa Smajlović, Alojzija Hočevar

PMC · DOI: 10.3389/fimmu.2026.1676244 · Frontiers in Immunology · 2026-02-10

## TL;DR

This study shows that measuring miR-875-5p levels in artery biopsies can help diagnose giant cell arteritis and assess inflammation.

## Contribution

The study introduces absolute quantification of miR-875-5p using dPCR as a novel diagnostic tool for giant cell arteritis.

## Key findings

- miR-875-5p copy numbers were significantly higher in histologically positive GCA biopsies.
- miR-875-5p levels correlated with histopathological and clinical features of GCA.
- dPCR effectively detected low-abundance miR-875-5p in arterial tissue, outperforming qPCR.

## Abstract

To perform absolute quantification of miR-875-5p expression in temporal artery biopsies (TABs) of patients with giant cell arteritis (GCA), associate miR-875-5p copy number with histological and clinical characteristics of patients with GCA, and evaluate the diagnostic value of absolute copy number of miR-875-5p in GCA.

The study included formalin-fixed, paraffin-embedded TABs of 45 treatment-naïve clinically proven patients with GCA, and 19 non-GCA controls. Of the included patients with GCA, 29 had histologically positive and 16 histologically negative TABs. Expression of miR-875-5p was assessed through utilization of quantitative real-time PCR (qPCR) and absolute quantification by digital PCR (dPCR).

We determined significantly higher absolute copy number of miR-875-5p in histologically positive TABs of patients with GCA, compared to histologically negative TABs of GCA and non-GCA patients, which significantly correlated with the majority of TAB histopathological parameters and several clinical characteristics of patients with GCA. Notably, we showed a good diagnostic performance of absolute copy number of miR-875-5p in discriminating patients and controls, depending on the extent of vessel wall inflammation and remodeling in affected temporal arteries.

Our study revealed that absolute quantification of miR-875-5p expression holds the potential to serve as a supporting biomarker in assessing vessel wall inflammation and remodeling in patients with GCA. Moreover, our results indicate the applicability of absolute quantification by dPCR in detecting low-abundance miRNAs in GCA-affected arterial tissue, whose limiting amounts hinder the utilization of classical qPCR.

## Linked entities

- **Diseases:** giant cell arteritis (MONDO:0008538), GCA (MONDO:0008538)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, MIR146B (microRNA 146b) [NCBI Gene 574447] {aka MIRN146B, miRNA146B, mir-146b}, NOTCH3 (notch receptor 3) [NCBI Gene 4854] {aka CADASIL, CADASIL1, CARASIL1, CASIL, FPLD1, IMF2}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, MIR875 (microRNA 875) [NCBI Gene 100126309] {aka MIRN875, hsa-mir-875}, MIR147A (microRNA 147a) [NCBI Gene 406939] {aka MIR147, MIRN147, hsa-mir-147a}, MIR211 (microRNA 211) [NCBI Gene 406993] {aka MIRN211, mir-211}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, MIR642A (microRNA 642a) [NCBI Gene 693227] {aka MIR642, MIRN642, hsa-mir-642, hsa-mir-642a, mir-642a}, MIR147B (microRNA 147b) [NCBI Gene 100126311] {aka MIRN147B, mir-147b}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, MIR150 (microRNA 150) [NCBI Gene 406942] {aka MIRN150, miRNA150, mir-150}
- **Diseases:** cancer (MESH:D009369), ischemic (MESH:D002545), vascular disease (MESH:D014652), cervical cancer (MESH:D002583), polymyalgia rheumatica (MESH:D011111), inflammation (MESH:D007249), vasculitides (MESH:D014657), jaw claudication (MESH:D007383), osteoarthritis (MESH:D010003), stenosis (MESH:D003251), gestational diabetes mellitus (MESH:D016640), gastric cancer (MESH:D013274), GCA (MESH:D013700), metastasis (MESH:D009362), hepatocellular carcinoma (MESH:D006528), intimal hyperplasia (MESH:D006965), systemic (MESH:D015619)
- **Chemicals:** paraffin (MESH:D010232), hematoxylin (MESH:D006416), HE (-), formalin (MESH:D005557), eosin (MESH:D004801)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12929443/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929443/full.md

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Source: https://tomesphere.com/paper/PMC12929443