Myocardial Fibrosis in Hypertensive Heart Disease: Correlation with Serum Biomarkers and Perioperative Cardiovascular Outcome
DOI:
https://doi.org/10.54112/bcsrj.v6i6.1832Keywords:
Myocardial fibrosis, Hypertensive heart disease, NT proBNP, Galectin 3, hs Troponin-T, Perioperative outcomes, Cardiac MRIAbstract
Myocardial fibrosis is a common but underdiagnosed complication of hypertensive heart disease (HHD). It contributes significantly to adverse perioperative cardiovascular outcomes. Cardiac MRI remains the gold standard for detection; however, accessibility is limited in low-resource settings, such as Pakistan. This study aimed to assess the correlation between serum biomarkers—NT-proBNP, high-sensitivity troponin T (hsTnT), and galectin 3—and MRI-detected myocardial fibrosis, and to evaluate their predictive value for perioperative complications. Methods: A prospective observational study was conducted at a tertiary care hospital in Multan between November 2022 and September 2024. A total of 84 hypertensive patients undergoing elective non-cardiac surgery were enrolled. Cardiac MRI was used to detect myocardial fibrosis. Serum levels of NT-proBNP, hs-TnT, and galectin-3 were measured preoperatively. Patients were monitored for perioperative cardiovascular events. Statistical analyses included t-tests, chi-square tests, and Pearson correlation. Results: MRI-confirmed myocardial fibrosis was present in 37 patients (44.0%). Patients with fibrosis had significantly higher mean levels of NT proBNP (583.2 ± 104.7 pg/mL vs 321.5 ± 89.3 pg/mL, p < 0.001), hs TnT (0.032 ± 0.010 ng/mL vs 0.019 ± 0.008 ng/mL, p < 0.001), and galectin 3 (19.7 ± 3.6 ng/mL vs 13.5 ± 2.8 ng/mL, p < 0.001). The incidence of perioperative cardiovascular complications was significantly higher in the fibrosis group (32.4% vs 9.6%, p = 0.005). Positive correlations were observed between biomarker levels and the extent of myocardial fibrosis. Conclusion: Serum biomarkers NT proBNP, hs TnT, and galectin three correlate strongly with MRI-detected myocardial fibrosis and are predictive of perioperative cardiovascular complications in hypertensive patients. These markers may serve as effective, low-cost alternatives for preoperative risk stratification in resource-limited settings.
Downloads
References
Luo C., Tan B., Chu L., Chen L., Zhong X., Jiang Y.et al.. Enhanced fibrotic potential of col1a1hinr4a1low fibroblasts in ischemic heart revealed by transcriptional dynamics heterogeneity analysis at both bulk and single-cell levels. Frontiers in Cardiovascular Medicine 2025;11. https://doi.org/10.3389/fcvm.2024.1460813
Katsuki T., Kusumoto D., Akiba Y., Kimura M., Komuro J., Nakamura T.et al.. Endothelial-fibroblast interactions during scarb1 accelerate heart failure. 2023. https://doi.org/10.1101/2023.09.15.557661
Howard Z., Dorn L., Lowe J., Gertzen M., Ciccone P., Rastogi N.et al.. Micro-dystrophin gene therapy prevents heart failure in an improved mouse model of Duchenne muscular dystrophy cardiomyopathy. Jci Insight 2021;6(7). https://doi.org/10.1172/jci.insight.146511
Zhao T., Kee H., Kee S., & Jeong M. Hdac8 inhibitor alleviates transverse aortic constriction‐induced heart failure in mice by downregulating Ace1. Oxidative Medicine and Cellular Longevity 2022;2022(1). https://doi.org/10.1155/2022/6227330
Chang X., Zhang T., Wang J., Liu Y., Yan P., Meng Q.et al.. Sirt5‐related desuccinylation modification contributes to quercetin‐induced protection against heart failure and high‐glucose‐prompted cardiomyocytes injured through the regulation of mitochondrial quality surveillance. Oxidative Medicine and Cellular Longevity 2021;2021(1). https://doi.org/10.1155/2021/5876841
Zhang Z., Xu Z., Wang S., Jia Z., Zhou Z., Wang C.et al.. Optimised new shengmai powder modulation of camp/rap1a signalling pathway attenuates myocardial fibrosis in heart failure. Chinese Medicine 2024;19(1). https://doi.org/10.1186/s13020-024-00902-4
Marunouchi T., Nakashima M., Ebitani S., Umezu S., Karasawa K., Yano E.et al.. Hsp90 inhibitor attenuates the development of pathophysiological cardiac fibrosis in mouse hypertrophy by suppressing the calcineurin-NFAT and c-raf-ERK pathways. Journal of Cardiovascular Pharmacology 2021;77(6):822-829. https://doi.org/10.1097/fjc.0000000000001017
Xiu M., Liu Y., & Wang W. Investigation of hub genes and immune status in heart transplant rejection using endomyocardial biopsies. Journal of Cellular and Molecular Medicine 2020;25(2):763-773. https://doi.org/10.1111/jcmm.16127
Wang G., Wang R., Ruan Z., Liu L., Li Y., & Zhu L. MicroRNA-132 attenuated cardiac fibrosis in myocardial infarction-induced heart failure rats. Bioscience Reports 2020;40(9). https://doi.org/10.1042/bsr20201696
Liang B., Zhou Z., Yang Z., Liu J., Zhang L., He J.et al.. The age–rage axis mediates myocardial fibrosis via the activation of cardiac fibroblasts induced by autophagy in heart failure. Experimental Physiology 2022;107(8):879-891. https://doi.org/10.1113/ep090042
Iyer N., Le T., Kui M., Tang H., Chin C., Phua S.et al.. Markers of focal and diffuse nonischemic myocardial fibrosis are associated with adverse cardiac remodelling and prognosis in patients with hypertension: the remodel study. Hypertension 2022;79(8):1804-1813. https://doi.org/10.1161/hypertensionaha.122.19225
Ekström M., Hellman A., Hasselström J., Hage C., Kahan T., Ugander M.et al.. The transition from hypertension to hypertensive heart disease and heart failure: The PREFER-H study. Esc Heart Failure 2020;7(2):737-746. https://doi.org/10.1002/ehf2.12612
Pichler G., Redón J., Martínez F., Solaz E., Calaforra O., Andrés M.et al.. Cardiac magnetic resonance-derived fibrosis, strain, and molecular biomarkers of fibrosis in hypertensive heart disease. Journal of Hypertension 2020;38(10):2036-2042. https://doi.org/10.1097/hjh.0000000000002504
Kim I. and Yoo B.. Multidimensional approach of heart failure diagnosis and prognostication utilizing cardiac imaging with biomarkers. Diagnostics 2022;12(6):1366. https://doi.org/10.3390/diagnostics12061366
Devereaux P., Lamy A., Chan M., Allard R., Ломиворотов В., Landoni G.et al.. High-sensitivity troponin I after cardiac surgery and 30-day mortality. New England Journal of Medicine 2022;386(9):827-836. https://doi.org/10.1056/nejmoa2000803
Hsu P., Chen J., Sung S., Tsai Y., Lin C., Wu Y.et al.. Inflammatory biomarkers and blood physical property transformations following on-pump coronary artery bypass graft surgery. Journal of Personalized Medicine 2023;13(10):1434. https://doi.org/10.3390/jpm13101434
Pölzl L., Thielmann M., Cymorek S., Nägele F., Hirsch J., Graber M.et al.. Impact of myocardial injury after coronary artery bypass grafting on long-term prognosis. European Heart Journal 2022;43(25):2407-2417. https://doi.org/10.1093/eurheartj/ehac054
Ştef A., Bodolea C., Bocşan I., Căinap S., Achim A., Șerban A.et al.. The value of biomarkers in major cardiovascular surgery necessitating cardiopulmonary bypass. Reviews in Cardiovascular Medicine 2024;25(10). https://doi.org/10.31083/j.rcm2510355
Lau E., Liu E., Paniagua S., Sarma A., Zampierollo G., López B.et al.. Galectin-3 Inhibition with Modified Citrus Pectin in Hypertension. Jacc Basic to Translational Science 2021;6(1):12-21. https://doi.org/10.1016/j.jacbts.2020.10.006
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Amir Asad Shah, Muhammad Ismail Khan, Ibtahaj Mohsin Iqbal

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.