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Клиническо-диагностическое значение экстрацеллюлярного объема в разные периоды инфаркта миокарда левого желудочка
Клиническо-диагностическое значение экстрацеллюлярного объема в разные периоды инфаркта миокарда левого желудочка
Олейников В.Э., Вдовкин А.В., Донецкая Н.А., Салямова Л.И., Чернова А.А. Клиническо-диагностическое значение экстрацеллюлярного объема в разные периоды инфаркта миокарда левого желудочка. Терапевтический архив. 2026;98(4):231–236. DOI: 10.26442/00403660.2026.04.203577
© ООО «КОНСИЛИУМ МЕДИКУМ», 2026 г.
© ООО «КОНСИЛИУМ МЕДИКУМ», 2026 г.
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Аннотация
В обзоре представлены данные о патофизиологических процессах, отражающихся на объеме внеклеточного пространства (Extracellular Volume – ECV) в остром и хроническом периодах инфаркта миокарда. Обсуждается влияние совокупности острых повреждений миокарда на повышение ECV, что делает его мощным независимым предиктором неблагоприятного ремоделирования левого желудочка, риска серьезных сердечно-сосудистых событий и аритмий. Представлены актуальные методики оценки ECV. Показано, что, несмотря на ограничения, связанные с неспецифичностью и необходимостью стандартизации методик, ECV-картирование превосходит традиционные подходы в оценке размера инфаркта и стратификации риска, открывая пути для индивидуального контроля эффективности лечения. Обзор охватывает как фундаментальные валидационные работы, так и новейшие исследования, посвященные патофизиологическому обоснованию метода, методическим аспектам реализации, клиническим подходам, посвященным изучению ECV, в том числе для оценки антиремоделирующей терапии.
Ключевые слова: инфаркт миокарда, объем внеклеточного пространства, магнитно-резонансная томография сердца, компьютерная томография сердца
Keywords: myocardial infarction, extracellular volume, cardiac magnetic resonance, cardiac computed tomography
Ключевые слова: инфаркт миокарда, объем внеклеточного пространства, магнитно-резонансная томография сердца, компьютерная томография сердца
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Keywords: myocardial infarction, extracellular volume, cardiac magnetic resonance, cardiac computed tomography
Полный текст
Список литературы
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2. Xu B, Li W, You Z, et al. Risk factors for left ventricular remodeling after myocardial infarction: A meta-analysis. Medicine (Baltimore). 2024;103(46):e40496. DOI:10.1097/MD.0000000000040496
3. Frangogiannis NG. Cardiac fibrosis. Cardiovasc Res. 2021;117(6):1450-88. DOI:10.1093/cvr/cvaa324
4. Chen L, Qiu B, Du X, et al. Establishment of a synthetic ECV model and its prognostic value in diabetes patients with acute myocardial infarction. Front Endocrinol. 2025;16:1534236. DOI:10.3389/fendo.2025.1534236
5. Martuszewski A, Paluszkiewicz P, Poręba R, et al. Clinical Significance of Extracellular Volume of Myocardium (ECV) Assessed by Computed Tomography: A Systematic Review and Meta-Analysis. J Clin Med. 2025;14(6):2066. DOI:10.3390/jcm14062066
6. Zhu GJ, Qureshi S, Hedges W, et al. Cardiac ECV mapping: Underlying concepts and clinical applications. Meta-Radiology. 2025;3:100168. DOI:10.1016/j.metrad.2025.100168
7. Cundari G, Galea N, Mergen V, et al. Myocardial extracellular volume quantification with computed tomography-current status and future outlook. Insights Imaging. 2023;14(1):156. DOI:10.1186/s13244-023-01506-6
8. Matusik PS, Mikrut K, Bryll A, et al. Cardiac Magnetic Resonance Imaging in Diagnostics and Cardiovascular Risk Assessment. Diagnostics (Basel). 2025;15(2):178. DOI:10.3390/diagnostics15020178
9. Stoeck CT, von Deuster C, Fuetterer M, et al. Cardiovascular magnetic resonance imaging of functional and microstructural changes of the heart in a longitudinal pig model of acute to chronic myocardial infarction. J Cardiovasc Magn Reson. 2021;23(1):103. DOI:10.1186/s12968-021-00794-5
10. Zhang SJ, Chang D, Jin JY, et al. Myocardial Extracellular Volume Fraction Measured by Cardiac Magnetic Resonance Imaging Negatively Correlates With Cardiomyocyte Breadth in a Healthy Porcine Model. Front Cardiovasc Med. 2022;9:791963. DOI:10.3389/fcvm.2022.791963
11. Buck KM, Rogers HT, Gregorich ZR, et al. Extracellular matrix alterations in chronic ischemic cardiomyopathy revealed by quantitative proteomics. JCI Insight. 2025;10(21):e196933. DOI:10.1172/jci.insight.196933
12. Gunata M, Parlakpinar H. A review of myocardial ischaemia/reperfusion injury: Pathophysiology, experimental models, biomarkers, genetics and pharmacological treatment. Cell Biochem Funct. 2021;39(2):190-217. DOI:10.1002/cbf.3587
13. Byrne RA, Rossello X, Coughlan JJ, et al. 2023 ESC Guidelines for the management of acute coronary syndromes. Eur Heart J Acute Cardiovasc Care. 2024;13(1):55-161. DOI:10.1093/ehjacc/zuad107
14. Yong J, Tao J, Wang K, et al. Post-myocardial Infarction Cardiac Remodeling: Multidimensional Mechanisms and Clinical Prospects of Stem Cell Therapy. Stem Cell Rev Rep. 2025;21(5):1369-427. DOI:10.1007/s12015-025-10888-7
15. Ma Y. Role of Neutrophils in Cardiac Injury and Repair Following Myocardial Infarction. Cells. 2021;10(7):1676. DOI:10.3390/cells10071676
16. Yang Z, Zhang Z, Feng S, et al. Cross-talk between cardiac lymphatics and immune cells regulates inflammatory response and cardiac recovery after myocardial infarction. Front Immunol. 2025;16:1557250. DOI:10.3389/fimmu.2025.1557250
17. Ren LL, Miao H, Wang YN, et al. TGF-β as A Master Regulator of Aging-Associated Tissue Fibrosis. Aging Dis. 2023;14(5):1633-50. DOI:10.14336/AD.2023.0222
18. Umbarkar P, Ejantkar S, Tousif S, et al. Mechanisms of Fibroblast Activation and Myocardial Fibrosis: Lessons Learned from FB-Specific Conditional Mouse Models. Cells. 2021;10(9):2412. DOI:10.3390/cells10092412
19. Poddi S, Lefter CL, Linardi D, et al. 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
20. De Meester de Ravenstein C, Bouzin C, Lazam S, et al. Histological Validation of measurement of diffuse interstitial myocardial fibrosis by myocardial extravascular volume fraction from Modified Look-Locker imaging (MOLLI) T1 mapping at 3T. J Cardiovasc Magn Reson. 2015;17(1):48. DOI:10.1186/s12968-015-0150-0
21. Messroghli DR, Moon JC, Ferreira VM, et al. Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI). J Cardiovasc Magn Reson. 2017;19(1):75. DOI:10.1186/s12968-017-0389-8
22. Ishiyama M, Kurita T, Nakamura S, et al. Prognostic importance of acute phase extracellular volume evaluated by cardiac magnetic resonance imaging for patients with acute myocardial infarction. Int J Cardiovasc Imaging. 2021;37(11):3285-97. DOI:10.1007/s10554-021-02321-0
23. Chen H, Erley J, Muellerleile K, et al. Contrast-enhanced cardiac MRI is superior to non-contrast mapping to predict left ventricular remodeling at 6 months after acute myocardial infarction. Eur Radiol. 2024;34(3):1863-74. DOI:10.1007/s00330-023-10100-9
24. Calvieri C, Riva A, Sturla F, et al. Left Ventricular Adverse Remodeling in Ischemic Heart Disease: Emerging Cardiac Magnetic Resonance Imaging Biomarkers. J Clin Med. 2023;12(1):334. DOI:10.3390/jcm12010334
25. Ralota KK, Layland J, Han Win KT, et al. Myocardial Viability: Evolving Insights and Challenges in Revascularization and Functional Recovery. J Cardiovasc Dev Dis. 2025;12(3):106. DOI:10.3390/jcdd12030106
26. Garg P, Broadbent DA, Swoboda PP, et al. Acute Infarct Extracellular Volume Mapping to Quantify Myocardial Area at Risk and Chronic Infarct Size on Cardiovascular Magnetic Resonance Imaging. Circ Cardiovasc Imaging. 2017;10(7):e006182. DOI:10.1161/CIRCIMAGING.117.006182
27. Segre CAW, de Lemos JA, Assunção Junior AN, et al. Chronic troponin elevation assessed by myocardial T1 mapping in patients with stable coronary artery disease. Medicine (Baltimore). 2023;102(16):e33548. DOI:10.1097/MD.0000000000033548
28. Kato S, Misumi Y, Horita N, et al. Clinical Utility of Computed Tomography-Derived Myocardial Extracellular Volume Fraction: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2024;17(5):516-28. DOI:10.1016/j.jcmg.2023.10.008
29. Black N, Bradley J, Schelbert EB, Bonnett LJ, et al. Remote myocardial fibrosis predicts adverse outcome in patients with myocardial infarction on clinical cardiovascular magnetic resonance imaging. J Cardiovasc Magn Reson. 2024;26(2):101064. DOI:10.1016/j.jocmr.2024.101064
30. Liang K, Nakou E, Del Buono MG, et al. The Role of Cardiac Magnetic Resonance in Myocardial Infarction and Non-obstructive Coronary Arteries. Front Cardiovasc Med. 2022;8:821067. DOI:10.3389/fcvm.2021.821067
31. Cadour F, Quemeneur M, Biere L, et al. Prognostic value of cardiovascular magnetic resonance T1 mapping and extracellular volume fraction in nonischemic dilated cardiomyopathy. J Cardiovasc Magn Reson. 2023;25(1):7. DOI:10.1186/s12968-023-00919-y
32. Chen L, Qiu B, Du X, et al. Association Between Extracellular Volume Assessed by Cardiac MRI and New-Onset Atrial Fibrillation in Patients With ST-Segment Elevation Myocardial Infarction. Korean J Radiol. 2025;26(6):546-56. DOI:10.3348/kjr.2025.0070
33. Chen Y, Zheng X, Jin H, et al. Role of Myocardial Extracellular Volume Fraction Measured with Magnetic Resonance Imaging in the Prediction of Left Ventricular Functional Outcome after Revascularization of Chronic Total Occlusion of Coronary Arteries. Korean J Radiol. 2019;20(1):83-93. DOI:10.3348/kjr.2018.0069
34. Benz DC, Gräni C, Antiochos P, et al. Cardiac magnetic resonance biomarkers as surrogate endpoints in cardiovascular trials for myocardial diseases. Eur Heart J. 2023;44(45):4738-47. DOI:10.1093/eurheartj/ehad510
35. Juhasz V, Quinaglia T, Drobni ZD, et al. Atorvastatin and Myocardial Extracellular Volume Expansion During Anthracycline-Based Chemotherapy. JACC CardioOncol. 2025;7(2):125-37. DOI:10.1016/j.jaccao.2024.11.008
36. Schneider CA, Pfister R. Treatment of heart failure with preserved ejection fraction with SGLT2 inhibitors: new therapy standard? Herz. 2022;47(5):395-400. DOI:10.1007/s00059-022-05134-6
37. Tu C, Shen H, Liu R, et al. Myocardial extracellular volume derived from contrast-enhanced chest computed tomography for longitudinal evaluation of cardiotoxicity in patients with breast cancer treated with anthracyclines. Insights Imaging. 2022;13:85. DOI:10.1186/s13244-022-01224-5
38. Stukalova OV, Gupalo EM, Chumachenko PV, et al. The value of cardiovascular magnetic resonance in myocarditis with different clinical presentation. Therapeutic Archive. 2019;91(4):28-36 (in Russian). DOI:10.26442/00403660.2019.04.000078
39. Kiamanesh O, Toma M. The State of the Heart Biopsy: A Clinical Review. CJC Open. 2020;3(4):524-31. DOI:10.1016/j.cjco.2020.11.017
40. Almaskhanova AA, Melkozerov KV, Przhiyalkovskaya EG, et al. Advantages of using T1-mapping in cardiac magnetic resonance imaging in patients with acromegaly. Terapevticheskii Arkhiv (Ter. Arkh.). 2024;96(10):950-6 (in Russian). DOI:10.26442/00403660.2024.10.202871
41. Terenicheva MA, Stukalova OV, Shakhnovich RM, et al. The role of cardiac magnetic resonance imaging (cardiovascular magnetic resonance) in defining the prognosis of patients with acute ST-segment elevation myocardial infarction. Part 1. Indications and contraindications to cardiovascular magnetic resonance. Terapevticheskii Arkhiv (Ter. Arkh.). 2021;93(4):497-501 (in Russian). DOI:10.26442/00403660.2021.04.200687
42. Muthalaly RG, Abrahams T, Lin A, et al. Myocardial extracellular volume measurement using cardiac computed tomography. Int J Cardiovasc Imaging. 2024;40(11):2237-45. DOI:10.1007/s10554-024-03226-4
43. Camacho-Mondragon CG, Ibarrola-Peña JC, Lira-Lozano D, et al. Clinical Applications of Cardiac Computed Tomography: A Focused Review for the Clinical Cardiologists. J Cardiovasc Dev Dis. 2025;12(10):375. DOI:10.3390/jcdd12100375
44. Lorenzatti DA, Filtz A, Piña P, et al. Comparison of dual-energy iodine and standard subtraction methods for myocardial extracellular volume quantification using cardiac computed tomography. J Cardiovasc Comput Tomogr. 2025;19(4):483-7. DOI:10.1016/j.jcct.2025.03.009
45. Han D, Lin A, Kuronuma K, et al. Cardiac Computed Tomography for Quantification of Myocardial Extracellular Volume Fraction: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2023;16(10):1306-17. DOI:10.1016/j.jcmg.2023.03.021
46. Hagar MT, Moore WG, Vecsey-Nagy M, et al. Synthetic hematocrit-based extracellular volume quantification from photon-counting CT: Validation against MRI and systematic bias correction. Eur J Radiol. 2025;191:112321. DOI:10.1016/j.ejrad.2025.112321
47. Mergen V, Sartoretti T, Klotz E, et al. Extracellular volume quantification with cardiac late enhancement scanning using dual-source photon-counting detector CT. Invest Radiol. 2022;57:406-11. DOI:10.1097/RLI.0000000000000851
48. Oyama-Manabe N, Oda S, Ohta Y, et al. Myocardial late enhancement and extracellular volume with single-energy, dual-energy, and photon-counting computed tomography. J Cardiovasc Comput Tomogr. 2024;18(1):3-10. DOI:10.1016/j.jcct.2023.12.006
49. Dragomiretskaya NA, Volchkov II, Belov AK, et al. A fresh angle on myocardial fibrosis processes: cold and hot phenotypes. Pathogenesis features and potential therapeutic strategies. Russian Journal of Cardiology. 2025;30(9S):6397 (in Russian). DOI:10.15829/1560-4071-2025-6397
50. Kushol R, Wilman AH, Kalra S, et al. DSMRI: Domain Shift Analyzer for Multi-Center MRI Datasets. Diagnostics. 2023;13(18):2947. DOI:10.3390/diagnostics13182947
51. Terenicheva MA, Stukalova OV, Shakhnovich RM, et al. The role of cardiac magnetic resonance imaging in defining the prognosis of patients with acute ST-segment elevation myocardial infarction. Part 2. Assessment of the disease prognosis. Terapevticheskii Arkhiv (Ter. Arkh.). 2022;94(4):552-7 (in Russian). DOI:10.26442/00403660.2022.04.201458
2. Xu B, Li W, You Z, et al. Risk factors for left ventricular remodeling after myocardial infarction: A meta-analysis. Medicine (Baltimore). 2024;103(46):e40496. DOI:10.1097/MD.0000000000040496
3. Frangogiannis NG. Cardiac fibrosis. Cardiovasc Res. 2021;117(6):1450-88. DOI:10.1093/cvr/cvaa324
4. Chen L, Qiu B, Du X, et al. Establishment of a synthetic ECV model and its prognostic value in diabetes patients with acute myocardial infarction. Front Endocrinol. 2025;16:1534236. DOI:10.3389/fendo.2025.1534236
5. Martuszewski A, Paluszkiewicz P, Poręba R, et al. Clinical Significance of Extracellular Volume of Myocardium (ECV) Assessed by Computed Tomography: A Systematic Review and Meta-Analysis. J Clin Med. 2025;14(6):2066. DOI:10.3390/jcm14062066
6. Zhu GJ, Qureshi S, Hedges W, et al. Cardiac ECV mapping: Underlying concepts and clinical applications. Meta-Radiology. 2025;3:100168. DOI:10.1016/j.metrad.2025.100168
7. Cundari G, Galea N, Mergen V, et al. Myocardial extracellular volume quantification with computed tomography-current status and future outlook. Insights Imaging. 2023;14(1):156. DOI:10.1186/s13244-023-01506-6
8. Matusik PS, Mikrut K, Bryll A, et al. Cardiac Magnetic Resonance Imaging in Diagnostics and Cardiovascular Risk Assessment. Diagnostics (Basel). 2025;15(2):178. DOI:10.3390/diagnostics15020178
9. Stoeck CT, von Deuster C, Fuetterer M, et al. Cardiovascular magnetic resonance imaging of functional and microstructural changes of the heart in a longitudinal pig model of acute to chronic myocardial infarction. J Cardiovasc Magn Reson. 2021;23(1):103. DOI:10.1186/s12968-021-00794-5
10. Zhang SJ, Chang D, Jin JY, et al. Myocardial Extracellular Volume Fraction Measured by Cardiac Magnetic Resonance Imaging Negatively Correlates With Cardiomyocyte Breadth in a Healthy Porcine Model. Front Cardiovasc Med. 2022;9:791963. DOI:10.3389/fcvm.2022.791963
11. Buck KM, Rogers HT, Gregorich ZR, et al. Extracellular matrix alterations in chronic ischemic cardiomyopathy revealed by quantitative proteomics. JCI Insight. 2025;10(21):e196933. DOI:10.1172/jci.insight.196933
12. Gunata M, Parlakpinar H. A review of myocardial ischaemia/reperfusion injury: Pathophysiology, experimental models, biomarkers, genetics and pharmacological treatment. Cell Biochem Funct. 2021;39(2):190-217. DOI:10.1002/cbf.3587
13. Byrne RA, Rossello X, Coughlan JJ, et al. 2023 ESC Guidelines for the management of acute coronary syndromes. Eur Heart J Acute Cardiovasc Care. 2024;13(1):55-161. DOI:10.1093/ehjacc/zuad107
14. Yong J, Tao J, Wang K, et al. Post-myocardial Infarction Cardiac Remodeling: Multidimensional Mechanisms and Clinical Prospects of Stem Cell Therapy. Stem Cell Rev Rep. 2025;21(5):1369-427. DOI:10.1007/s12015-025-10888-7
15. Ma Y. Role of Neutrophils in Cardiac Injury and Repair Following Myocardial Infarction. Cells. 2021;10(7):1676. DOI:10.3390/cells10071676
16. Yang Z, Zhang Z, Feng S, et al. Cross-talk between cardiac lymphatics and immune cells regulates inflammatory response and cardiac recovery after myocardial infarction. Front Immunol. 2025;16:1557250. DOI:10.3389/fimmu.2025.1557250
17. Ren LL, Miao H, Wang YN, et al. TGF-β as A Master Regulator of Aging-Associated Tissue Fibrosis. Aging Dis. 2023;14(5):1633-50. DOI:10.14336/AD.2023.0222
18. Umbarkar P, Ejantkar S, Tousif S, et al. Mechanisms of Fibroblast Activation and Myocardial Fibrosis: Lessons Learned from FB-Specific Conditional Mouse Models. Cells. 2021;10(9):2412. DOI:10.3390/cells10092412
19. Poddi S, Lefter CL, Linardi D, et al. 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
20. De Meester de Ravenstein C, Bouzin C, Lazam S, et al. Histological Validation of measurement of diffuse interstitial myocardial fibrosis by myocardial extravascular volume fraction from Modified Look-Locker imaging (MOLLI) T1 mapping at 3T. J Cardiovasc Magn Reson. 2015;17(1):48. DOI:10.1186/s12968-015-0150-0
21. Messroghli DR, Moon JC, Ferreira VM, et al. Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI). J Cardiovasc Magn Reson. 2017;19(1):75. DOI:10.1186/s12968-017-0389-8
22. Ishiyama M, Kurita T, Nakamura S, et al. Prognostic importance of acute phase extracellular volume evaluated by cardiac magnetic resonance imaging for patients with acute myocardial infarction. Int J Cardiovasc Imaging. 2021;37(11):3285-97. DOI:10.1007/s10554-021-02321-0
23. Chen H, Erley J, Muellerleile K, et al. Contrast-enhanced cardiac MRI is superior to non-contrast mapping to predict left ventricular remodeling at 6 months after acute myocardial infarction. Eur Radiol. 2024;34(3):1863-74. DOI:10.1007/s00330-023-10100-9
24. Calvieri C, Riva A, Sturla F, et al. Left Ventricular Adverse Remodeling in Ischemic Heart Disease: Emerging Cardiac Magnetic Resonance Imaging Biomarkers. J Clin Med. 2023;12(1):334. DOI:10.3390/jcm12010334
25. Ralota KK, Layland J, Han Win KT, et al. Myocardial Viability: Evolving Insights and Challenges in Revascularization and Functional Recovery. J Cardiovasc Dev Dis. 2025;12(3):106. DOI:10.3390/jcdd12030106
26. Garg P, Broadbent DA, Swoboda PP, et al. Acute Infarct Extracellular Volume Mapping to Quantify Myocardial Area at Risk and Chronic Infarct Size on Cardiovascular Magnetic Resonance Imaging. Circ Cardiovasc Imaging. 2017;10(7):e006182. DOI:10.1161/CIRCIMAGING.117.006182
27. Segre CAW, de Lemos JA, Assunção Junior AN, et al. Chronic troponin elevation assessed by myocardial T1 mapping in patients with stable coronary artery disease. Medicine (Baltimore). 2023;102(16):e33548. DOI:10.1097/MD.0000000000033548
28. Kato S, Misumi Y, Horita N, et al. Clinical Utility of Computed Tomography-Derived Myocardial Extracellular Volume Fraction: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2024;17(5):516-28. DOI:10.1016/j.jcmg.2023.10.008
29. Black N, Bradley J, Schelbert EB, Bonnett LJ, et al. Remote myocardial fibrosis predicts adverse outcome in patients with myocardial infarction on clinical cardiovascular magnetic resonance imaging. J Cardiovasc Magn Reson. 2024;26(2):101064. DOI:10.1016/j.jocmr.2024.101064
30. Liang K, Nakou E, Del Buono MG, et al. The Role of Cardiac Magnetic Resonance in Myocardial Infarction and Non-obstructive Coronary Arteries. Front Cardiovasc Med. 2022;8:821067. DOI:10.3389/fcvm.2021.821067
31. Cadour F, Quemeneur M, Biere L, et al. Prognostic value of cardiovascular magnetic resonance T1 mapping and extracellular volume fraction in nonischemic dilated cardiomyopathy. J Cardiovasc Magn Reson. 2023;25(1):7. DOI:10.1186/s12968-023-00919-y
32. Chen L, Qiu B, Du X, et al. Association Between Extracellular Volume Assessed by Cardiac MRI and New-Onset Atrial Fibrillation in Patients With ST-Segment Elevation Myocardial Infarction. Korean J Radiol. 2025;26(6):546-56. DOI:10.3348/kjr.2025.0070
33. Chen Y, Zheng X, Jin H, et al. Role of Myocardial Extracellular Volume Fraction Measured with Magnetic Resonance Imaging in the Prediction of Left Ventricular Functional Outcome after Revascularization of Chronic Total Occlusion of Coronary Arteries. Korean J Radiol. 2019;20(1):83-93. DOI:10.3348/kjr.2018.0069
34. Benz DC, Gräni C, Antiochos P, et al. Cardiac magnetic resonance biomarkers as surrogate endpoints in cardiovascular trials for myocardial diseases. Eur Heart J. 2023;44(45):4738-47. DOI:10.1093/eurheartj/ehad510
35. Juhasz V, Quinaglia T, Drobni ZD, et al. Atorvastatin and Myocardial Extracellular Volume Expansion During Anthracycline-Based Chemotherapy. JACC CardioOncol. 2025;7(2):125-37. DOI:10.1016/j.jaccao.2024.11.008
36. Schneider CA, Pfister R. Treatment of heart failure with preserved ejection fraction with SGLT2 inhibitors: new therapy standard? Herz. 2022;47(5):395-400. DOI:10.1007/s00059-022-05134-6
37. Tu C, Shen H, Liu R, et al. Myocardial extracellular volume derived from contrast-enhanced chest computed tomography for longitudinal evaluation of cardiotoxicity in patients with breast cancer treated with anthracyclines. Insights Imaging. 2022;13:85. DOI:10.1186/s13244-022-01224-5
38. Стукалова О.В., Гупало Е.М., Чумаченко П.В., и др. Возможности магнитно-резонансной томографии сердца с контрастированием в диагностике миокардита различного клинического течения. Терапевтический архив. 2019;91(4):28-36 [Stukalova OV, Gupalo EM, Chumachenko PV, et al. The value of cardiovascular magnetic resonance in myocarditis with different clinical presentation. Therapeutic Archive. 2019;91(4):28-36 (in Russian)]. DOI:10.26442/00403660.2019.04.000078
39. Kiamanesh O, Toma M. The State of the Heart Biopsy: A Clinical Review. CJC Open. 2020;3(4):524-31. DOI:10.1016/j.cjco.2020.11.017
40. Алмасханова А.А., Мелкозеров К.В., Пржиялковская Е.Г., и др. Преимущества применения T1-картирования при магнитно-резонансной томографии сердца у пациентов с акромегалией. Терапевтический архив. 2024;96(10):950-6 [Almaskhanova AA, Melkozerov KV, Przhiyalkovskaya EG, et al. Advantages of using T1-mapping in cardiac magnetic resonance imaging in patients with acromegaly. Terapevticheskii Arkhiv (Ter. Arkh.). 2024;96(10):950-6 (in Russian)]. DOI:10.26442/00403660.2024.10.202871
41. Тереничева М.А., Стукалова О.В., Шахнович Р.М., и др. Роль магнитно-резонансной томографии сердца в определении прогноза больных с острым инфарктом миокарда с подъемом сегмента ST. Часть 1. Показания и противопоказания к исследованию. Основные методики. Терапевтический архив. 2021;93(4):497-501 [Terenicheva MA, Stukalova OV, Shakhnovich RM, et al. The role of cardiac magnetic resonance imaging (cardiovascular magnetic resonance) in defining the prognosis of patients with acute ST-segment elevation myocardial infarction. Part 1. Indications and contraindications to cardiovascular magnetic resonance. Terapevticheskii Arkhiv (Ter. Arkh.). 2021;93(4):497-501 (in Russian)]. DOI:10.26442/00403660.2021.04.200687
42. Muthalaly RG, Abrahams T, Lin A, et al. Myocardial extracellular volume measurement using cardiac computed tomography. Int J Cardiovasc Imaging. 2024;40(11):2237-45. DOI:10.1007/s10554-024-03226-4
43. Camacho-Mondragon CG, Ibarrola-Peña JC, Lira-Lozano D, et al. Clinical Applications of Cardiac Computed Tomography: A Focused Review for the Clinical Cardiologists. J Cardiovasc Dev Dis. 2025;12(10):375. DOI:10.3390/jcdd12100375
44. Lorenzatti DA, Filtz A, Piña P, et al. Comparison of dual-energy iodine and standard subtraction methods for myocardial extracellular volume quantification using cardiac computed tomography. J Cardiovasc Comput Tomogr. 2025;19(4):483-7. DOI:10.1016/j.jcct.2025.03.009
45. Han D, Lin A, Kuronuma K, et al. Cardiac Computed Tomography for Quantification of Myocardial Extracellular Volume Fraction: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2023;16(10):1306-17. DOI:10.1016/j.jcmg.2023.03.021
46. Hagar MT, Moore WG, Vecsey-Nagy M, et al. Synthetic hematocrit-based extracellular volume quantification from photon-counting CT: Validation against MRI and systematic bias correction. Eur J Radiol. 2025;191:112321. DOI:10.1016/j.ejrad.2025.112321
47. Mergen V, Sartoretti T, Klotz E, et al. Extracellular volume quantification with cardiac late enhancement scanning using dual-source photon-counting detector CT. Invest Radiol. 2022;57:406-11. DOI:10.1097/RLI.0000000000000851
48. Oyama-Manabe N, Oda S, Ohta Y, et al. Myocardial late enhancement and extracellular volume with single-energy, dual-energy, and photon-counting computed tomography. J Cardiovasc Comput Tomogr. 2024;18(1):3-10. DOI:10.1016/j.jcct.2023.12.006
49. Драгомирецкая Н.А., Волчков И.И., Белов А.К., и др. Новый взгляд на процессы фиброза миокарда: «холодный» и «горячи» фенотипы. Особенности патогенеза и потенциальные терапевтические стратегии. Российский кардиологический журнал. 2025;30(9S):6397 [Dragomiretskaya NA, Volchkov II, Belov AK, et al. A fresh angle on myocardial fibrosis processes: cold and hot phenotypes. Pathogenesis features and potential therapeutic strategies. Russian Journal of Cardiology. 2025;30(9S):6397 (in Russian)]. DOI:10.15829/1560-4071-2025-6397
50. Kushol R, Wilman AH, Kalra S, et al. DSMRI: Domain Shift Analyzer for Multi-Center MRI Datasets. Diagnostics. 2023;13(18):2947. DOI:10.3390/diagnostics13182947
51. Тереничева М.А., Стукалова О.В., Шахнович Р.М., и др. Роль магнитно-резонансной томографии сердца в определении прогноза больных с острым инфарктом миокарда с подъемом сегмента ST. Часть 2. Оценка прогноза заболевания. Терапевтический архив. 2022;94(4):552-7 [Terenicheva MA, Stukalova OV, Shakhnovich RM, et al. The role of cardiac magnetic resonance imaging in defining the prognosis of patients with acute ST-segment elevation myocardial infarction. Part 2. Assessment of the disease prognosis. Terapevticheskii Arkhiv (Ter. Arkh.). 2022;94(4):552-7 (in Russian)]. DOI:10.26442/00403660.2022.04.201458
________________________________________________
2. Xu B, Li W, You Z, et al. Risk factors for left ventricular remodeling after myocardial infarction: A meta-analysis. Medicine (Baltimore). 2024;103(46):e40496. DOI:10.1097/MD.0000000000040496
3. Frangogiannis NG. Cardiac fibrosis. Cardiovasc Res. 2021;117(6):1450-88. DOI:10.1093/cvr/cvaa324
4. Chen L, Qiu B, Du X, et al. Establishment of a synthetic ECV model and its prognostic value in diabetes patients with acute myocardial infarction. Front Endocrinol. 2025;16:1534236. DOI:10.3389/fendo.2025.1534236
5. Martuszewski A, Paluszkiewicz P, Poręba R, et al. Clinical Significance of Extracellular Volume of Myocardium (ECV) Assessed by Computed Tomography: A Systematic Review and Meta-Analysis. J Clin Med. 2025;14(6):2066. DOI:10.3390/jcm14062066
6. Zhu GJ, Qureshi S, Hedges W, et al. Cardiac ECV mapping: Underlying concepts and clinical applications. Meta-Radiology. 2025;3:100168. DOI:10.1016/j.metrad.2025.100168
7. Cundari G, Galea N, Mergen V, et al. Myocardial extracellular volume quantification with computed tomography-current status and future outlook. Insights Imaging. 2023;14(1):156. DOI:10.1186/s13244-023-01506-6
8. Matusik PS, Mikrut K, Bryll A, et al. Cardiac Magnetic Resonance Imaging in Diagnostics and Cardiovascular Risk Assessment. Diagnostics (Basel). 2025;15(2):178. DOI:10.3390/diagnostics15020178
9. Stoeck CT, von Deuster C, Fuetterer M, et al. Cardiovascular magnetic resonance imaging of functional and microstructural changes of the heart in a longitudinal pig model of acute to chronic myocardial infarction. J Cardiovasc Magn Reson. 2021;23(1):103. DOI:10.1186/s12968-021-00794-5
10. Zhang SJ, Chang D, Jin JY, et al. Myocardial Extracellular Volume Fraction Measured by Cardiac Magnetic Resonance Imaging Negatively Correlates With Cardiomyocyte Breadth in a Healthy Porcine Model. Front Cardiovasc Med. 2022;9:791963. DOI:10.3389/fcvm.2022.791963
11. Buck KM, Rogers HT, Gregorich ZR, et al. Extracellular matrix alterations in chronic ischemic cardiomyopathy revealed by quantitative proteomics. JCI Insight. 2025;10(21):e196933. DOI:10.1172/jci.insight.196933
12. Gunata M, Parlakpinar H. A review of myocardial ischaemia/reperfusion injury: Pathophysiology, experimental models, biomarkers, genetics and pharmacological treatment. Cell Biochem Funct. 2021;39(2):190-217. DOI:10.1002/cbf.3587
13. Byrne RA, Rossello X, Coughlan JJ, et al. 2023 ESC Guidelines for the management of acute coronary syndromes. Eur Heart J Acute Cardiovasc Care. 2024;13(1):55-161. DOI:10.1093/ehjacc/zuad107
14. Yong J, Tao J, Wang K, et al. Post-myocardial Infarction Cardiac Remodeling: Multidimensional Mechanisms and Clinical Prospects of Stem Cell Therapy. Stem Cell Rev Rep. 2025;21(5):1369-427. DOI:10.1007/s12015-025-10888-7
15. Ma Y. Role of Neutrophils in Cardiac Injury and Repair Following Myocardial Infarction. Cells. 2021;10(7):1676. DOI:10.3390/cells10071676
16. Yang Z, Zhang Z, Feng S, et al. Cross-talk between cardiac lymphatics and immune cells regulates inflammatory response and cardiac recovery after myocardial infarction. Front Immunol. 2025;16:1557250. DOI:10.3389/fimmu.2025.1557250
17. Ren LL, Miao H, Wang YN, et al. TGF-β as A Master Regulator of Aging-Associated Tissue Fibrosis. Aging Dis. 2023;14(5):1633-50. DOI:10.14336/AD.2023.0222
18. Umbarkar P, Ejantkar S, Tousif S, et al. Mechanisms of Fibroblast Activation and Myocardial Fibrosis: Lessons Learned from FB-Specific Conditional Mouse Models. Cells. 2021;10(9):2412. DOI:10.3390/cells10092412
19. Poddi S, Lefter CL, Linardi D, et al. 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
20. De Meester de Ravenstein C, Bouzin C, Lazam S, et al. Histological Validation of measurement of diffuse interstitial myocardial fibrosis by myocardial extravascular volume fraction from Modified Look-Locker imaging (MOLLI) T1 mapping at 3T. J Cardiovasc Magn Reson. 2015;17(1):48. DOI:10.1186/s12968-015-0150-0
21. Messroghli DR, Moon JC, Ferreira VM, et al. Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI). J Cardiovasc Magn Reson. 2017;19(1):75. DOI:10.1186/s12968-017-0389-8
22. Ishiyama M, Kurita T, Nakamura S, et al. Prognostic importance of acute phase extracellular volume evaluated by cardiac magnetic resonance imaging for patients with acute myocardial infarction. Int J Cardiovasc Imaging. 2021;37(11):3285-97. DOI:10.1007/s10554-021-02321-0
23. Chen H, Erley J, Muellerleile K, et al. Contrast-enhanced cardiac MRI is superior to non-contrast mapping to predict left ventricular remodeling at 6 months after acute myocardial infarction. Eur Radiol. 2024;34(3):1863-74. DOI:10.1007/s00330-023-10100-9
24. Calvieri C, Riva A, Sturla F, et al. Left Ventricular Adverse Remodeling in Ischemic Heart Disease: Emerging Cardiac Magnetic Resonance Imaging Biomarkers. J Clin Med. 2023;12(1):334. DOI:10.3390/jcm12010334
25. Ralota KK, Layland J, Han Win KT, et al. Myocardial Viability: Evolving Insights and Challenges in Revascularization and Functional Recovery. J Cardiovasc Dev Dis. 2025;12(3):106. DOI:10.3390/jcdd12030106
26. Garg P, Broadbent DA, Swoboda PP, et al. Acute Infarct Extracellular Volume Mapping to Quantify Myocardial Area at Risk and Chronic Infarct Size on Cardiovascular Magnetic Resonance Imaging. Circ Cardiovasc Imaging. 2017;10(7):e006182. DOI:10.1161/CIRCIMAGING.117.006182
27. Segre CAW, de Lemos JA, Assunção Junior AN, et al. Chronic troponin elevation assessed by myocardial T1 mapping in patients with stable coronary artery disease. Medicine (Baltimore). 2023;102(16):e33548. DOI:10.1097/MD.0000000000033548
28. Kato S, Misumi Y, Horita N, et al. Clinical Utility of Computed Tomography-Derived Myocardial Extracellular Volume Fraction: A Systematic Review and Meta-Analysis. JACC Cardiovasc Imaging. 2024;17(5):516-28. DOI:10.1016/j.jcmg.2023.10.008
29. Black N, Bradley J, Schelbert EB, Bonnett LJ, et al. Remote myocardial fibrosis predicts adverse outcome in patients with myocardial infarction on clinical cardiovascular magnetic resonance imaging. J Cardiovasc Magn Reson. 2024;26(2):101064. DOI:10.1016/j.jocmr.2024.101064
30. Liang K, Nakou E, Del Buono MG, et al. The Role of Cardiac Magnetic Resonance in Myocardial Infarction and Non-obstructive Coronary Arteries. Front Cardiovasc Med. 2022;8:821067. DOI:10.3389/fcvm.2021.821067
31. Cadour F, Quemeneur M, Biere L, et al. Prognostic value of cardiovascular magnetic resonance T1 mapping and extracellular volume fraction in nonischemic dilated cardiomyopathy. J Cardiovasc Magn Reson. 2023;25(1):7. DOI:10.1186/s12968-023-00919-y
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Авторы
В.Э. Олейников*1, А.В. Вдовкин2, Н.А. Донецкая2, Л.И. Салямова1, А.А. Чернова1
1ФГБОУ ВО «Пензенский государственный университет», Пенза, Россия;
2ГБУЗ «Пензенская областная клиническая больница им. Н.Н. Бурденко», Пенза, Россия
*v.oleynikof@gmail.com
1Penza State University, Penza, Russia;
2Burdenko Penza Regional Clinical Hospital, Penza, Russia
*v.oleynikof@gmail.com
1ФГБОУ ВО «Пензенский государственный университет», Пенза, Россия;
2ГБУЗ «Пензенская областная клиническая больница им. Н.Н. Бурденко», Пенза, Россия
*v.oleynikof@gmail.com
________________________________________________
1Penza State University, Penza, Russia;
2Burdenko Penza Regional Clinical Hospital, Penza, Russia
*v.oleynikof@gmail.com
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