ВАЖНО! Правила приравнивания журналов, входящих в международные базы данных к журналам перечня ВАК.
Ответ на официальный запрос в ВАК журнала Кардиология.

Preview

Kardiologiia

Advanced search

Clinical significance of different assesment methods of myocardial fibrosis in patients with hypertrophic cardiomyopathy.

https://doi.org/10.18087/cardio.2020.3.n561

Abstract

Objective To evaluate prospects for clinical use of circulating biomarkers for characterizing fibrotic changes in the myocardium of patients with hypertrophic cardiomyopathy (HCMP) with left ventricular (LV) outflow tract obstruction.

Materials and Methods This was a prospective study with a 12-month follow-up period. The study included 47 patients (29 females and 18 males) with obstructive HCMP who were selected for septal reduction. Echocardiography (EchoCG), cardiac magnetic resonance imaging (MRI) and measurements of serum C-reactive protein, N-terminal pro-brain natriuretic peptide, and relevant circulating markers of fibrosis (TGF-β1, MMP-2,-9, TIMP-1, galectin-3, sST2, CITP, PICP, and PIIINP) were performed for all patients. All patients were evaluated at baseline and at 7 days, 6 and 12 months following surgical treatment. Morphometrical analysis of intraoperative biopsy samples was performed for evaluation of the degree of fibrotic changes. Patients received beta-blockers (95.7%), angiotensin-converting enzyme inhibitors/angiotensin receptor blockers (34%), loop diuretics (68.1%), aldosterone antagonists (34%), and statins (66%).

Results Women with HCMP were older and more frequently had additional risk factors (arterial hypertension). Men had a higher risk of sudden cardiac death. Histological study of intraoperative myocardial biopsy samples showed that the area of fibrotic changes was 13.9±6.9%. According to cardiac MRI mean area of delayed contrast enhancement was 8.7±3.3% of LV myocardial mass. No association was established between traditional cardiovascular risk factors and severity of myocardial fibrotic changes or levels of circulating fibrosis markers. Perhaps that was due to the modifying effect of the drug therapy received by HCMP patients. According to EchoCG maximum pressure gradient in the LV outflow tract before the surgical treatment was 88 (55; 192) mm Hg, and interventricular septal thickness was 22 (16; 32) mm. A considerable decrease (p=0.0002) in the LV outflow tract gradient was observed after myectomy in all patients. At the same time, the left ventricular dimension, which tended to decrease in the early postoperative period, returned to baseline values by the 6th month of follow-up.

Conclusion The study confirmed the increase in relevant circulating markers of fibrosis in patients with obstructive HCMP. At the same time, no correlation was observed between levels of circulating biomarkers and severity of fibrosis according to data of histology and cardiac MRI, which was probably due to the modifying effect of drug therapy and limited sampling.

About the Authors

V. V. Zaitsev
Almazov National Medical Research Centre
Russian Federation
cardiologist of Almazov National Medical Research Centre


A. V. Gurshchenkov
Almazov National Medical Research Centre
Russian Federation
cardiovascular surgeon of the department of cardiovascular surgery, PhD, assistant of the department of surgical diseases Almazov National Medical Research Centre


L. B. Mitrofanova
Almazov National Medical Research Centre
Russian Federation
DSc,Chief Researcher, Head of Research Laboratory of Pathomorphology


A. V. Ryzhkov
Almazov National Medical Research Centre
Russian Federation
head of MRI department of Almazov National Medical Research Centre


E. E. Kazakova
Almazov National Medical Research Centre
Russian Federation
doctor of clinical diagnostic laboratory of Almazov National Medical Research Centre


K. D. Badaev
Pavlov First Saint Petersburg State Medical University
Russian Federation
student of  the Pavlov First Saint Petersburg State Medical University


M. L. Gordeev
Almazov National Medical Research Centre
Russian Federation
DSc, professor, head of the Research Department for Cardiothoracic Surgery, head of the department of surgical diseases of  Almazov National Medical Research Centre


O. M. Moiseeva
Almazov National Medical Research Centre
Russian Federation
DSc, Director of the Institute of Heart and Vessels,
Chief Researcher of Non-Coronary Heart Disease Research Department  of Almazov National Medical Research Centre


References

1. Kim JB, Porreca GJ, Song L, Greenway SC, Gorham JM, Church GM et al. Polony Multiplex Analysis of Gene Expression (PMAGE) in Mouse Hypertrophic Cardiomyopathy. Science. 2007;316(5830):1481–4. DOI: 10.1126/science.1137325

2. Hundley WG, Bluemke DA, Finn JP, Flamm SD, Fogel MA, Friedrich MG et al. ACCF/ACR/AHA/NASCI/SCMR 2010 Expert Consensus Document on Cardiovascular Magnetic Resonance: A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents. Circulation. 2010;121(22):2462–508. DOI: 10.1161/CIR.0b013e3181d44a8f

3. Geske JB, Ong KC, Siontis KC, Hebl VB, Ackerman MJ, Hodge DO et al. Women with hypertrophic cardiomyopathy have worse survival. European Heart Journal. 2017;38(46):3434–40. DOI: 10.1093/eurheartj/ehx527

4. Meghji Z, Nguyen A, Fatima B, Geske JB, Nishimura RA, Ommen SR et al. Survival Differences in Women and Men After Septal Myectomy for Obstructive Hypertrophic Cardiomyopathy. JAMA Cardiology. 2019;4(3):237. DOI: 10.1001/jamacardio.2019.0084

5. Nijenkamp LLAM, Bollen IAE, van Velzen HG, Regan JA, van Slegten­horst M, Niessen HWM et al. Sex Differences at the Time of Myecto­my in Hy­per­trophic Cardiomyopathy. Circulation: Heart Failure. 2018;11(6):e004133. DOI: 10.1161/CIRCHEARTFAILURE.117.004133

6. Frangogiannis NG. Cardiac fibrosis: Cell biological mechanisms, molecular pathways and therapeutic opportunities. Molecular Aspects of Medicine. 2019; 65:70–99. DOI: 10.1016/j.mam.2018.07.001

7. Münch J, Avanesov M, Bannas P, Säring D, Krämer E, Mearini G et al. Serum Matrix Metalloproteinases as Quantitative Biomarkers for Myocardial Fibrosis and Sudden Cardiac Death Risk Stratification in Patients with Hypertrophic Cardiomyopathy. Journal of Cardiac Failure. 2016;22(10):845–50. DOI: 10.1016/j.cardfail.2016.03.010

8. Ayça B, Sahin I, Kucuk SH, Akin F, Kafadar D, Avşar M et al. Increased Transforming Growth Factor-β Levels Associated with Cardiac Adverse Events in Hypertrophic Cardiomyopathy: High TGF-β worsens prognosis in HCM. Clinical Cardiology. 2015;38(6):371–7. DOI: 10.1002/clc.22404

9. Gehlken C, Suthahar N, Meijers WC, de Boer RA. Galectin-3 in Heart Failure: An Update of the Last 3 Years. Heart Failure Clinics. 2018;14(1):75–92. DOI: 10.1016/j.hfc.2017.08.009

10. Thomas MR, Lip GYH. Novel Risk Markers and Risk Assessments for Cardiovascular Disease. Circulation Research. 2017;120(1): 133–49. DOI: 10.1161/CIRCRESAHA.116.309955

11. Marian AJ, Braunwald E. Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy. Circulation Research. 2017;121(7):749–70. DOI: 10.1161/CIRCRESAHA.117.311059

12. Chan RH, Maron BJ, Olivotto I, Pencina MJ, Assenza GE, Haas T et al. Prognostic Value of Quantitative Contrast-Enhanced Cardiovascular Magnetic Resonance for the Evaluation of Sudden Death Risk in Patients with Hypertrophic Cardiomyopathy. Circulation. 2014;130(6):484–95. DOI: 10.1161/CIRCULATIONAHA.113.007094

13. Priori SG, Blomström-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J et al. 2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC). European Heart Journal. 2015;36(41):2793–867. DOI: 10.1093/eurheartj/ehv316


Review

For citations:


Zaitsev V.V., Gurshchenkov A.V., Mitrofanova L.B., Ryzhkov A.V., Kazakova E.E., Badaev K.D., Gordeev M.L., Moiseeva O.M. Clinical significance of different assesment methods of myocardial fibrosis in patients with hypertrophic cardiomyopathy. Kardiologiia. 2020;60(3):44-50. https://doi.org/10.18087/cardio.2020.3.n561

Views: 1905


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


ISSN 0022-9040 (Print)
ISSN 2412-5660 (Online)