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Multiparametric ultrasound liver examination in cardiological overweight patients: determining the cause of fibrosis and severity of steatosis

https://doi.org/10.15829/1560-4071-2025-6163

EDN: XYHCSX

Abstract

Aim. To evaluate the feasibility of using multiparametric liver ultrasound to determine the pathophysiological causes of increased stiffness in patients with cardio-metabolic risks.

Material and methods. A study was conducted involving 104 cardiology patients, including 48 men (46,2%) and 56 women (53,8%), aged 49 to 73 years, of Caucasian ethnicity. Inclusion criteria included chronic heart failure stage IIB (II, III functional classes according to NYHA), main and additional criteria of metabolic syndrome containing cardiometabolic risks for the development of metabolically associated fatty liver disease. All patients were examined according to a unified diagnostic algorithm consisting of two stages: Stage 1 — clinical and laboratory assessment, Stage 2 — instrumental assessment using liver ultrasound methods (B-mode, color Doppler imaging, two-dimensional shear wave elastography, quantitative steatometry).

Results. A scoring system has been proposed to assess the predominant contribution to liver fibrosis development based on data from multiparametric ultrasound examination of the liver. Total score 0-8: predominant liver involvement — in this case, characteristic signs of liver involvement, such as increased echogenicity and absence of significant venous vessel dilation, are observed. Total score 9-14: combined involvement — the signs include both liver-related changes (e.g., steatosis) and signs of venous congestion. Total score 15-16: predominant cardiovascular involvement — in this case, significant venous vessel dilation and other signs of congestive hepatopathy are the main features, indicating venous congestion as the primary cause of liver changes.

Conclusion. Multiparametric ultrasound examination of the liver combined with the developed scoring system can be used to differentiate the causes of increased liver stiffness and the severity of liver steatosis in patients with cardiometabolic risks. Standardization of the ultrasound protocol improves the reproducibility of the method.

About the Authors

D. Yu. Shestakova
Smolensk State Medical University
Russian Federation

Smolensk


Competing Interests:

None



A. V. Borsukov
Smolensk State Medical University
Russian Federation

Smolensk


Competing Interests:

None



A. I. Skutar
Smolensk State Medical University
Russian Federation

Smolensk


Competing Interests:

None



A. R. Akhmedova
Smolensk State Medical University
Russian Federation

Smolensk


Competing Interests:

None



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Supplementary files

  • For the first time, a scoring system has been proposed to assess the contribution of various factors (metabolic and cardiogenic) to increased liver stiffness in patients with cardiometabolic risks.
  • Multiparametric ultrasound examination of the liver (B-mode, elastography, steatometry) allows you to differentiate the causes of changes in liver stiffness: steatosis, fibrosis, venous congestion or a combination thereof.
  • The use of a scoring system ensures the accuracy and reproducibility of diagnosis, which contributes to a more personalized approach to the treatment of patients with metabolically associated steatosis liver disease.
  • The results of the study confirm the value of ultra­sound diagnostic methods for determining the severity of changes in the liver associated with venous congestion in patients with chronic heart failure.
  • The developed ultrasound examination protocol can become the basis for standardization of diagnostics in clinical practice and scientific research.

Review

For citations:


Shestakova D.Yu., Borsukov A.V., Skutar A.I., Akhmedova A.R. Multiparametric ultrasound liver examination in cardiological overweight patients: determining the cause of fibrosis and severity of steatosis. Russian Journal of Cardiology. 2025;30(1):6163. (In Russ.) https://doi.org/10.15829/1560-4071-2025-6163. EDN: XYHCSX

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ISSN 1560-4071 (Print)
ISSN 2618-7620 (Online)