N-terminal propeptide of type III procollagen and echocardiographic parameters in patients with arterial hypertension
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Keywords

cardiology
fibrosis
diastole
ventricular remodeling

How to Cite

Volik, M. (2026). N-terminal propeptide of type III procollagen and echocardiographic parameters in patients with arterial hypertension. Medicine Today and Tomorrow, 95(1), 107-113. https://doi.org/10.35339/msz.2026.95.1.vms

Abstract

Background. Arterial hypertension is accompanied by myocardial remodeling, in particular changes in the extracellular matrix and collagen turnover. The N-terminal Propeptide of Procollagen type III (PIIINP) is a circulating marker of collagen type III turnover, but it is not a cardiac-specific or direct method for determining myocardial fibrosis.

Aim. To determine the serum level of the N-terminal propeptide of procollagen type III in patients with arterial hypertension and to analyze its associations with echocardiographic parameters.

Materials and Methods. A total of 32 patients aged 18–65 years with arterial hypertension stage I–II and 22 individuals of the control group were examined. PIIINP was determined by enzyme-linked immunosorbent assay using the E-EL-H0183 Human PIIINP kit (Elabscience Biotechnology Co., Ltd, China); the detection range is 23.44–1,500 pg/mL, sensitivity – 14.06 pg/mL, intra-assay coefficient of variation – 4.15–6.27%, inter-assay – 7.01–8.80%. Doppler echocardiography was performed on the UltimaPRO30 system (RADMIR, Kharkiv, Ukraine). Correlations were assessed using Spearman's coefficient. Excel 2019 (Microsoft, USA) and SPSS Statistics 26.0 (IBM, USA) were used; results were considered statistically significant at p<0.05. The study was conducted as a private initiative of the author without grant support or state registration of the research topic.

Research Ethics. The study was conducted in accordance with the World Medical Association Declaration of Helsinki (1964–2024); all included patients provided informed consent to participate in the study, and data confidentiality was ensured.

Results. In patients with arterial hypertension, the serum PIIINP level was higher than in the control group: [1.22±0.21] µg/L vs [0.23±0.14] µg/L (p<0.001). No statistically significant correlations with structural and geometric echocardiographic parameters were found. Moderate direct correlations were established with the peak early diastolic transmitral flow velocity E (ρ=0.387; p=0.029) and the E/Ea ratio (ρ=0.367; p=0.039).

Conclusions. In patients with arterial hypertension, a higher serum level of the N-terminal propeptide of procollagen type III and its associations with certain Doppler parameters of diastolic filling were found. These results alone do not confirm myocardial fibrosis, increased filling pressure, or future risk of heart failure; the identified correlations should be considered exploratory due to multiple comparisons and the small sample size.

Keywords: cardiology, fibrosis, diastole, ventricular remodeling.

https://doi.org/10.35339/msz.2026.95.1.vms
PDF (Українська)

References

Nemtsova V, Vischer AS, Burkard T. Hypertensive heart disease: a narrative review series-part 1: pathophysiology and microstructural changes. J Clin Med. 2023;12(7):2606. DOI: 10.3390/jcm12072606. PMID: 37048689.

Gaydarski L, Petrova K, Stanchev S, Pelinkov D, Iliev A, Dimitrova IN, et al. Morphometric and molecular interplay in hypertension-induced cardiac remodeling with an emphasis on the potential therapeutic implications. Int J Mol Sci. 2025;26(9):4022. DOI: 10.3390/ijms26094022. PMID: 40362262.

Jiang W, Xiong Y, Li X, Yang Y. Cardiac fibrosis: cellular effectors, molecular pathways, and exosomal roles. Front Cardiovasc Med. 2021;8:715258. DOI: 10.3389/fcvm.2021.715258. PMID: 34485413.

Frangogiannis NG. The extracellular matrix in myocardial injury, repair, and remodeling. J Clin Invest. 2017;127(5):1600-12. DOI: 10.1172/JCI87491. PMID: 28459429.

Wittig C, Szulcek R. Extracellular matrix protein ratios in the human heart and vessels: how to distinguish pathological from physiological changes? Front Physiol. 2021;12:708656. DOI: 10.3389/fphys.2021.708656. PMID: 34421650.

Nikolov A, Popovski N. Extracellular matrix in heart disease: focus on circulating collagen type I and III derived peptides as biomarkers of myocardial fibrosis and their potential in the prognosis of heart failure: a concise review. Metabolites. 2022;12(4):297. DOI: 10.3390/metabo12040297. PMID: 35448484.

Poddi S, Lefter CL, Linardi D, Ardigò A, Luciani GB, Rungatscher A. Myocardial fibrosis: assessment, quantification, prognostic signification, and anti-fibrosis targets: a state-of-the-art review. J Cardiovasc Dev Dis. 2025;12(5):192. DOI: 10.3390/jcdd12050192. PMID: 40422963.

Ding Y, Wang Y, Zhang W, Jia Q, Wang X, Li Y, et al. Roles of biomarkers in myocardial fibrosis. Aging Dis. 2020;11(5):1157-74. DOI: 10.14336/AD.2020.0604. PMID: 33014530.

Poulsen SH, Andersen NH, Heickendorff L, Mogensen CE. Relation between plasma amino-terminal propeptide of procollagen type III and left ventricular longitudinal strain in essential hypertension. Heart. 2005;91(5):624-9. DOI: 10.1136/hrt.2003.029702. PMID: 15831647.

Ottosen CI, Nadruz W, Inciardi RM, Johansen ND, Fudim M, Biering-Sørensen T. Diastolic dysfunction in hypertension: a comprehensive review of pathophysiology, diagnosis, and treatment. Eur Heart J Cardiovasc Imaging. 2024;25(11):1525-36. DOI: 10.1093/ehjci/jeae178. PMID: 39018386.

Zhu L, Wang Y, Zhao S, Lu M. Detection of myocardial fibrosis: where we stand. Front Cardiovasc Med. 2022;9:926378. DOI: 10.3389/fcvm.2022.926378. PMID: 36247487.

Nagueh SF, Sanborn DY, Oh JK, Anderson B, Billick K, Derumeaux G, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography and for heart failure with preserved ejection fraction diagnosis: an update from the American Society of Echocardiography. J Am Soc Echocardiogr. 2025;38(7):537-69. DOI: 10.1016/j.echo.2025.03.011. PMID: 40617625.

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