Exploring the molecular interactions between nephrolithiasis and carotid atherosclerosis: asporin as a potential biomarker

Urolithiasis. 2024 Nov 26;52(1):169. doi: 10.1007/s00240-024-01665-1.

Abstract

Increasing evidence suggested nephrolithiasis has a close linkage with carotid atherosclerosis (CAS), with Randall's plaque (RP) being a precursor to kidney stones. Our study aimed to examine the crosstalk genes and potential molecular mechanisms between RP and CAS. We obtained microarray data for RP and CAS from the Gene Expression Omnibus (GEO) and used weighted gene co-expression network analysis (WGCNA) and differential gene expression (DEG) analysis to identify shared genes. By integrating WGCNA and DEG analysis, Asporin (ASPN) was identified as the key gene connecting RP and CAS, with its diagnostic potential assessed via a receiver operating characteristic (ROC) curve. Immune infiltration studies showed a significant correlation between ASPN and various immune cells in RP and CAS. ASPN was found to be less expressed in RP and CAS tissues compared to normal tissues, as confirmed by immunohistochemistry (IHC) and quantitative reverse-transcription PCR (qRT-PCR). The rat model confirmed the human tissue findings. ASPN can elucidate the shared pathogenic mechanisms underlying the two conditions, including immune response and osteoblast differentiation.

Keywords: Bioinformatics; Carotid atherosclerosis; Immune infiltration; Osteoblast differentiation; Randall’s plaque.

MeSH terms

  • Animals
  • Biomarkers* / metabolism
  • Carotid Artery Diseases* / genetics
  • Carotid Artery Diseases* / metabolism
  • Disease Models, Animal
  • Extracellular Matrix Proteins* / genetics
  • Extracellular Matrix Proteins* / metabolism
  • Gene Expression Profiling
  • Humans
  • Male
  • Nephrolithiasis* / genetics
  • Nephrolithiasis* / metabolism
  • Plaque, Atherosclerotic
  • Rats

Substances

  • Biomarkers
  • Extracellular Matrix Proteins
  • ASPN protein, human