MiR-664a-3p expression in patients with obstructive sleep apnea: A potential marker of atherosclerosis

Kun Li1, Zhiting Chen, Yanwen Qin

  • 1Department of Otolaryngology, Beijing AnZhen Hospital, Capital Medical University, Beijing, China.

Medicine
|February 9, 2018
PubMed

Insights

Early detection of atherosclerosis in obstructive sleep apnea patients is crucial. Serum miR-664a-3p was found to be downregulated, suggesting its potential as a noninvasive biomarker for atherosclerosis screening in obstructive sleep apnea.

Area of Science:

  • Biomarkers
  • Cardiovascular Disease
  • Sleep Medicine

Background:

  • Atherosclerosis (AS) management is critical for obstructive sleep apnea (OSA) patients.
  • MicroRNAs (miRNAs) are implicated in the pathogenesis of OSA and AS.
  • Differential miRNA expression may indicate AS in OSA patients.

Purpose of the Study:

  • Identify serum miRNAs as novel screening biomarkers for AS in OSA patients.
  • Determine the diagnostic and prognostic value of these miRNAs.
  • Investigate the role of miR-664a-3p in AS development within OSA.

Main Methods:

  • 128 participants (healthy and OSA patients with varying carotid intima-media thickness) were recruited.
  • Serum miRNA libraries were generated using deep sequencing from 12 participants.
  • Quantitative real-time PCR (qRT-PCR) was used to quantify miRNA expression in 116 participants.
  • Spearman correlation assessed the relationship between miRNA expression and CIMT.

Main Results:

  • miR-664a-3p was significantly downregulated in OSA patients with and without increased carotid intima-media thickness compared to controls.
  • A correlation was observed between miR-664a-3p expression levels and carotid intima-media thickness.
  • This suggests a potential role for miR-664a-3p in the early stages of AS in OSA.

Conclusions:

  • Circulating miR-664a-3p shows potential as a noninvasive biomarker for atherosclerosis in obstructive sleep apnea.
  • Further studies are warranted to validate these findings.
  • miR-664a-3p may aid in early screening and management of AS in OSA patients.

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