# Peripheral circular RNAs hsa_circ_0075436 and hsa_circ_0005729 as diagnostic and prognostic biomarkers in acute ischemic stroke: expression profiles and mechanistic insights

**Authors:** Wenqun Jiang, Weidong Chen, Shihao Lin, Pinpin Hou, Yichao Jin, Xiaohua Zhang, Hui Wu, Li Gao, Qin Hu

PMC · DOI: 10.3389/fmolb.2025.1657284 · Frontiers in Molecular Biosciences · 2025-10-01

## TL;DR

This study identifies two circular RNAs in blood cells that could help diagnose and predict outcomes in stroke patients.

## Contribution

The study discovers and validates two novel peripheral circRNAs as potential biomarkers for acute ischemic stroke.

## Key findings

- Two circRNAs, hsa_circ_0075436 and hsa_circ_0005729, are significantly downregulated in PBMCs of AIS patients.
- The expression levels of these circRNAs correlate with stroke severity and recovery outcomes.
- Hsa_circ_0005729 may influence stroke through the hsa-miR-1301/COL1A1 axis, affecting the blood-brain barrier and immune suppression.

## Abstract

Circular RNAs (circRNAs) are a class of stable, conserved, and tissue-specific non-coding RNAs that have shown potential as diagnostic and prognostic biomarkers in acute ischemic stroke (AIS). However, their expression and functional roles in peripheral blood mononuclear cells (PBMCs) remain largely unexplored.

We performed whole transcriptome RNA sequencing on PBMC samples from AIS patients (n = 5) and matched healthy controls (n = 5). The top 10 differentially expressed circRNAs were validated by qRT-PCR in a validation cohort (n = 60), and two consistently dysregulated circRNAs were further validated in a larger replication cohort (n = 288). Functional enrichment analysis and competing endogenous RNA (ceRNA) network construction were conducted to explore potential regulatory mechanisms.

Two circRNAs, hsa_circ_0075436 and hsa_circ_0005729, significantly decreased in PBMCs of AIS patients. The expressive levels negatively correlated with NIH Stroke Scale (NIHSS) scores at admission and discharge. Receiver operating characteristic (ROC) curve analysis demonstrated their strong diagnostic performance. Bioinformatics analyses and qRT-PCR further suggested that hsa_circ_0005729 may influence BBB disruption and peripheral immune suppression in AIS via hsa-miR-1301/COL1A1 axis.

Hsa_circ_0075436 and hsa_circ_0005729 are promising PBMC-derived biomarkers for the diagnosis and prognosis of AIS.

## Linked entities

- **Diseases:** AIS (MONDO:0003218)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, COL1A1 (collagen type I alpha 1 chain) [NCBI Gene 1277] {aka CAFYD, EDSARTH1, EDSC, OI1, OI2, OI3}, MIR1301 (microRNA 1301) [NCBI Gene 100302246] {aka MIRN1301, hsa-mir-1301, mir-1301}
- **Diseases:** AIS (MESH:D000083242), Stroke (MESH:D020521)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12520956/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12520956/full.md

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Source: https://tomesphere.com/paper/PMC12520956