International Journal of Molecular Sciences (Jul 2022)

Proteomic Biomarkers of the Apnea Hypopnea Index and Obstructive Sleep Apnea: Insights into the Pathophysiology of Presence, Severity, and Treatment Response

  • Katie L. J. Cederberg,
  • Umaer Hanif,
  • Vicente Peris Sempere,
  • Julien Hédou,
  • Eileen B. Leary,
  • Logan D. Schneider,
  • Ling Lin,
  • Jing Zhang,
  • Anne M. Morse,
  • Adam Blackman,
  • Paula K. Schweitzer,
  • Suresh Kotagal,
  • Richard Bogan,
  • Clete A. Kushida,
  • Yo-El S. Ju,
  • Nayia Petousi,
  • Chris D. Turnbull,
  • Emmanuel Mignot,
  • The STAGES Cohort Investigator Group

DOI
https://doi.org/10.3390/ijms23147983
Journal volume & issue
Vol. 23, no. 14
p. 7983

Abstract

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Obstructive sleep apnea (OSA), a disease associated with excessive sleepiness and increased cardiovascular risk, affects an estimated 1 billion people worldwide. The present study examined proteomic biomarkers indicative of presence, severity, and treatment response in OSA. Participants (n = 1391) of the Stanford Technology Analytics and Genomics in Sleep study had blood collected and completed an overnight polysomnography for scoring the apnea–hypopnea index (AHI). A highly multiplexed aptamer-based array (SomaScan) was used to quantify 5000 proteins in all plasma samples. Two separate intervention-based cohorts with sleep apnea (n = 41) provided samples pre- and post-continuous/positive airway pressure (CPAP/PAP). Multivariate analyses identified 84 proteins (47 positively, 37 negatively) associated with AHI after correction for multiple testing. Of the top 15 features from a machine learning classifier for AHI ≥ 15 vs. AHI < 15 (Area Under the Curve (AUC) = 0.74), 8 were significant markers of both AHI and OSA from multivariate analyses. Exploration of pre- and post-intervention analysis identified 5 of the 84 proteins to be significantly decreased following CPAP/PAP treatment, with pathways involving endothelial function, blood coagulation, and inflammatory response. The present study identified PAI-1, tPA, and sE-Selectin as key biomarkers and suggests that endothelial dysfunction and increased coagulopathy are important consequences of OSA, which may explain the association with cardiovascular disease and stroke.

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