Circulating ADAMTS13 Levels Are Associated with an Increased Occurrence of Obstructive Sleep Apnea

Author:

Huang Mengling1,Liu Sheng1,Liu Shuang2,Wen Wanwan1ORCID,Ning Yu1,Jia Yifan1ORCID,Yang Yunxiao1ORCID,Jiao Xiaolu34,Zheng Weiping5ORCID,Zhang Ming1ORCID

Affiliation:

1. Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China

2. Key Laboratory of Upper Airway Dysfunction-Related Cardiovascular Diseases, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung, And Blood Vessel Diseases, Beijing 100029, China

3. Key Laboratory of Remodeling-Related Cardiovascular Diseases, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, China

4. Department of Clinical Laboratory, Beijing Anzhen Hospital, Capital Medical University, Beijing, China

5. Department of Cardiology, Shengli Clinical Medical College of Fujian Medical University, 134 East Street, Fuzhou, 350001 Fujian Province, China

Abstract

Background and Aims. Obstructive sleep apnea (OSA) is strongly associated with obesity, metabolic diseases, coronary artery disease (CAD), stroke, hypertension, and other disorders. This study assessed the relationship between circulating a disintegrin and metalloprotease with a thrombospondin type 1 motif, member 13 (ADAMTS13) levels and the presence of OSA. Materials and Methods. This cross-sectional study included a total of 223 patients. We used a powerful high-throughput multiplexed immunobead-based assay to detect circulating levels of ADAMTS13. The associations between circulating ADAMTS13 levels and OSA were evaluated by multivariate logistic regression analysis. Results. Circulating ADAMTS13 levels were significantly elevated in patients with OSA compared with controls (0.8 vs. 2.7 μg/mL, respectively,P<0.001). After adjusting for confounding factors, circulating ADAMTS13 levels were significantly independently associated with the presence of OSA (oddsratio=9.96, 95% confidence interval (CI) =4.11–24.13,P<0.001). Furthermore, circulating ADAMTS13 levels showed discriminatory accuracy in assessing the presence of OSA (area under the curve: 0.87, 95% CI 0.81–0.93,P<0.001). Conclusion. Circulating ADAMTS13 levels were significantly correlated with the presence of OSA. ADAMTS13 may therefore function as a novel biomarker for monitoring the development and progression of OSA.

Funder

Beijing Municipal Natural Science Foundation

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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