Analysis of the Ischemia-Modified Albumin as a Potential Biomarker for Cardiovascular Damage in Obstructive Sleep Apnea Patients with Acute Coronary Syndrome

Author:

Resano-Barrio Pilar12ORCID,Alfaro Enrique34ORCID,Solano-Pérez Esther1,Coso Carlota1,Cubillos-Zapata Carolina34ORCID,Díaz-García Elena34ORCID,Romero-Peralta Sofía12,Izquierdo-Alonso Jose Luis12ORCID,Barbé Ferran35,García-Rio Francisco3467ORCID,Sánchez-de-la-Torre Manuel389,Mediano Olga123ORCID,

Affiliation:

1. Sleep Unit, Pneumology Department, Hospital Universitario de Guadalajara, 19002 Guadalajara, Spain

2. Medicine Department, Universidad de Alcalá, 28805 Madrid, Spain

3. Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), 28029 Madrid, Spain

4. Respiratory Diseases Group, Respiratory Service, Hospital Universitario La Paz, IdiPAZ, 28046 Madrid, Spain

5. Translation Research in Respiratory Medicine, Hospital Universitari Arnau de Vilanova-Santa Maria, IRBLleida, 25198 Lleida, Spain

6. Pneumology Department, Hospital Universitario La Paz, IdiPAZ, 28046 Madrid, Spain

7. Faculty of Medicine, Universidad Autónoma de Madrid, 28049 Madrid, Spain

8. Precision Medicine Group in Chronic Diseases, Respiratory Department, Hospital Universitari Arnau de Vilanova-Santa María, IRBLleida, 25198 Lleida, Spain

9. Department of Nursing and Physiotherapy, Faculty of Nursing and Physiotherapy, Universidad de Lleida, IRBLleida, 25002 Lleida, Spain

Abstract

Obstructive sleep apnea (OSA) has been identified as a cardiovascular (CV) risk factor. The potential of OSA promoting the synthesis of CV biomarkers in acute coronary syndrome (ACS) is unknown. Ischemia-modified albumin (IMA) has been identified as a specific CV biomarker. The aim of this study was to evaluate the role of IMA as a potential biomarker for determining the impact of OSA in ACS patients. A total of 925 patients (15.5% women, age: 59 years, body mass index: 28.8 kg/m2) from the ISAACC study (NCT01335087) were included. During hospitalization for ACS, a sleep study for OSA diagnosis was performed and blood samples extraction for IMA determination were obtained. IMA values were significantly higher in severe OSA (median (IQR), 33.7 (17.2–60.3) U/L) and moderate (32.8 (16.9–58.8) U/L) than in mild/no OSA (27.7 (11.8–48.6) U/L) (p = 0.002). IMA levels were very weakly related to apnea–hypopnea index (AHI) as well as hospital and intensive care unit stay, although they only maintained a significant relationship with days of hospital stay after adjusting for sex, age and BMI (ß = 0.410, p = 0.013). The results of the present study would suggest a potentially weaker role of OSA in the synthesis of the CV risk biomarker IMA in patients with ACS than in primary prevention.

Funder

ISCIII

European Union—FEDERco “Una manera de hacer Europa”

Spanish Respiratory Society (Sociedad Española de Neumología y Cirugía Torácica- SEPAR

NEUMOMADRID

“Ramón y Cajal”

“Ministerio de Ciencia e Innovación—Agencia Estatal de Investigación”

European Social Fund (ESF) “Investing in your future”

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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