Role of Biomarkers of Myocardial Injury to Predict Adverse Outcomes in Hypertrophic Cardiomyopathy

Author:

Zhang Yu1ORCID,Liu Minghao2ORCID,Zhang Channa1,Zou Yubao2ORCID,Kang Lianming3,Song Lei143ORCID

Affiliation:

1. State Key Laboratory of Cardiovascular Disease (Y. Zhang, C.Z., L.S.), Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

2. Department of Cardiology (M.L., Y. Zou), Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

3. Cardiomyopathy Ward (L.K., L.S.), Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

4. National Clinical Research Center of Cardiovascular Diseases (L.S.), Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Abstract

BACKGROUND: Serum troponins and CK-MB (creatine kinase-MB) are readily detectable and reliable cardiac-specific biomarkers of subclinical myocardial injury. This study explores the roles of cTnI (cardiac troponin I) and CK-MB in hypertrophic cardiomyopathy (HCM). METHODS: This study included 1045 patients with HCM who had baseline cTnI and CK-MB measurements at Fuwai Hospital between 1999 and 2019. Patients were excluded if they had undergone percutaneous coronary intervention or coronary artery bypass grafting, or had renal failure. Five end points were studied: all-cause death, cardiovascular death, noncardiovascular death, sudden cardiac death, and other cardiovascular death. Cox regression was used to assess the associations of cTnI and CK-MB levels with outcomes. RESULTS: Nine hundred seventy patients with available follow-up data were finally analyzed (mean age, 49.3 years; 36.4% female). During the median 4.3-year follow-up period, 87 patients reached the end points. Higher cTnI (per 0.05 ng/mL increase) and CK-MB (per 1 IU/L increase) levels were associated with increased risks of all-cause death (cTnI: adjusted hazard ratio [HR], 1.038, P <0.001; CK-MB: adjusted HR, 1.021, P =0.004), cardiovascular death (cTnI: adjusted HR, 1.040, P <0.001; CK-MB: adjusted HR, 1.025, P =0.006), and sudden cardiac death (cTnI: adjusted HR, 1.045, P <0.001; CK-MB: adjusted HR, 1.032, P =0.001). Patients with elevated levels of both cTnI and CK-MB had worse prognoses than patients with an elevated level of either biomarker alone and patients who did not have an elevated level of either biomarker. Addition of the binary indicator elevation of both cTnI and CK-MB significantly improved the discrimination and reclassification abilities of the standard HCM Risk- sudden cardiac death model (C statistics: P =0.002; net reclassification improvement, 0.652; integrated discrimination improvement, 0.064). CONCLUSIONS: Comprehensive evaluations of biomarkers of myocardial injury, cTnI and CK-MB, have considerable value for predicting adverse outcomes among patients with HCM. Routine cTnI and CK-MB assessments may help to guide implantable cardioverter defibrillator implantation for primary prevention in HCM.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference27 articles.

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2. Cabaniss, CD. Creatine Kinase. In: Walker, HK, Hall, WD, Hurst, JW, eds. Clinical Methods: The History, Physical, and Laboratory Examinations. Butterworths Copyright © 1990, Butterworth Publishers, a division of Reed Publishing; 1990.

3. Fourth Universal Definition of Myocardial Infarction (2018)

4. Basit, H, Huecker, MR. Myocardial Infarction Serum Markers StatPearls. StatPearls Publishing Copyright © 2022, StatPearls Publishing LLC; 2022.

5. Clinical Course and Management of Hypertrophic Cardiomyopathy

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