Biomedicine & Pharmacotherapy (Feb 2023)

Proteomic profiling for prediction of recurrent cardiovascular event in patients with acute coronary syndrome and obstructive sleep apnea: A post-hoc analysis from the ISAACC study

  • Andrea Zapater,
  • Esther Gracia-Lavedan,
  • Gerard Torres,
  • Olga Mínguez,
  • Lydia Pascual,
  • Anunciación Cortijo,
  • Dolores Martínez,
  • Ivan David Benítez,
  • Jordi De Batlle,
  • Mario Henríquez-Beltrán,
  • Jorge Abad,
  • Joaquín Duran-Cantolla,
  • Amaia Urrutia,
  • Olga Mediano,
  • María José Masdeu,
  • Estrella Ordax-Carbajo,
  • Juan Fernando Masa,
  • Mónica De la Peña,
  • Mercè Mayos,
  • Ramon Coloma,
  • Josep María Montserrat,
  • Eusebi Chiner,
  • Ferran Barbé,
  • Manuel Sánchez-de-la-Torre

Journal volume & issue
Vol. 158
p. 114125

Abstract

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Background: Obstructive sleep apnea (OSA) is associated with a recurrent cardiovascular event (CVE) risk in patients with a first acute coronary syndrome (ACS). However, the pathological pathways by which OSA promotes this deleterious role are unknown. We aim to explore the proteomic profile associated with OSA that promote the recurrent CVE risk in severe OSA patients with ACS without previous cardiovascular diseases. Methods: This post-hoc analysis from the ISAACC study (NCT01335087) included 86 patients admitted for ACS. Patients underwent respiratory polygraphy for the first 24–72 h to OSA diagnosis. We analyzed of 276 cardiovascular and inflammatory related proteins in baseline fasting plasma samples using proximity expression assay technology (Olink®, Sweden). Protein levels were compared between severe OSA patients with/without recurrent CVEs during follow-up. Random forest was conducted to select relevant proteins and generate a predictive model of recurrent CVE. Results: We included 86 patients (median age: 61 years, median BMI: 29.4 kg/m2 and 86 % males) admitted for ACS with severe OSA (56 without recurrent CVE/30 with recurrent CVE). The plasma levels of 38 proteins were differentially expressed between groups. Additionally, 12 proteins had a significant association with respiratory polygraphy parameters. Three proteins discriminate with an AUC of 0.81 (95 % CI of 0.71–0.9) between severe OSA patients with and without recurrent CVE. These proteins were implicated in cell proliferation, communication and apoptosis, and regulation/response to the inflammatory and immune systems. Conclusion: In ACS patients with severe OSA, a proteomic profile was associated with recurrent CVEs. This proteomic profile was correlated with specific OSA parameters from respiratory polygraphy. Proteomic profiling may provide an new direction for patient risk stratification and clinical management.

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