Journal
AMERICAN JOURNAL OF CARDIOLOGY
Volume 178, Issue -, Pages 119-123Publisher
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2022.05.014
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Funding
- Deutsche Forschungsgemeinschaft (DFG, German Research Foundation, Bonn, Germany) [FI 965/5-2, FI 965/9-1]
- DZHK (German Center for Cardiovascular Research, Berlin, Germany) [81X2400109, 81Z5400153]
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This study found that the levels of HMGB1 were associated with increased mortality in patients with dilated cardiomyopathy. Multivariable Cox regression analysis confirmed HMGB1 as a risk factor for mortality in DCM patients, independent of NT-proBNP, age, and gender.
High-mobility group box protein 1 (HMGB1) is released during tissue damage and activates the innate immune system through toll-like receptor 4. Because mortality in dilated cardiomyopathy (DCM) is associated with activation of the innate immune system, we hypothesized that HMGB1 possesses a prognostic value in estimating mortality in patients with DCM. We determined HMGB1 and N-terminal B-type natriuretic peptide (NTproBNP) levels in 67 patients with DCM (12 women, mean age 53.6 +/- 1.5 years). Kaplan - Meier analyzes revealed that higher levels of HMGB1 and NT-proBNP are related to increased all-cause mortality. Multivariable Cox regression confirmed HMGB1 as a risk factor for mortality in patients with DCM, independent of NT-proBNP, age, and gender (hazard ratio per 1 SD 1.920, 95% confidence interval 1.401 to 2.631, p < 0.001). HMGB1 is a promising candidate to estimate the prognosis of patients with DCM. (c) 2022 Elsevier Inc. All rights reserved.
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