Preview

Cardiovascular Therapy and Prevention

Advanced search

Associations of NT-proBNP and hepcidin levels with clinical and laboratory parameters in patients with heart failure with various severity of left ventricular systolic dysfunction

https://doi.org/10.15829/1728-8800-2020-2587

Abstract

Data on hepcidin levels in patients with heart failure (HF) are contradictory and do not make clear its contribution to the progression of multiple organ failure. There remain a number of issues about the prognostic significance of the N-terminal pro-brain natriuretic peptide (NT-proBNP) in HF with preserved ejection fraction (EF). The authors suggested the relationships between these markers in decompensated HF, as well as their associations with other clinical and laboratory parameters.

Aim. To identify the association of NT-proBNP and hepcidin levels with clinical and laboratory parameters in patients with HF with various severity of left ventricular (LV) systolic dysfunction.

Material and methods. The study included 68 patients (29 women, 39 men; mean age — 72,3±11,7 years) hospitalized due to decompensated HF. Patients were divided into three groups: reduced (HFrEF) (n=20), mid-range (HFmrEF) (n=23), and preserved EF (HFpEF) (n=24). Upon admission, along with standard diagnostic tests, all patients were examined for NT-proBNP and hepcidin levels by enzyme-linked immunosorbent assay. Statistical processing was carried out using the software package Statistica 8.0.

Results. NT-proBNP levels in the entire sample was 315,9 [129,9; 576,1] pg/ml. Significantly higher concentrations of NT-proBNP were found in patients with lower EF: 433,05 (346,8-892,6) pg/ml for HFrEF, 289,97 (185,9-345,3) pg/ml for HFmrEF pg/ml and 214,98 (207,37-562,31) pg/ ml for HFpEF (p<0,05). At the same time, hepcidin levels in the HFrEF group (31,63 ng/ml [22,0; 71,6]) was significantly higher than in the HFmrEF (23,89 ng/ml [21,1; 27,9]) (p<0,05) and HFpEF (26,91 ng/ml [18,6; 31,1]) (p<0,05). In HFpEF patients, there was a correlation of hepcidin level with body mass index (r=0,47, p<0,05) and chronic obstructive airway diseases (r=0,44, p<0,05). A correlation of hepcidin level with cardiac arrhythmias (r=0,61, p<0,05) was revealed in the HFmrEF group. In the HFrEF group, there were correlations of a significantly increased level of NT-proBNP (median — 433,05; 95% confidence interval: 346,8-892,6) with indicators of disease severity and multiple organ dysfunction: decrease in systolic blood pressure, cardiorenal syndrome, decrease in hemoglobin level and mean corpuscular hemoglobin concentration, characteristic of iron-deficiency anemia.

Conclusion. Patients with lower EF showed higher NT-proBNP values and a trend towards higher hepcidin levels. Relationships of hepcidin and NT-proBNP levels with following clinical parameters were found: body mass index, presence of obstructive airway diseases, cardiac arrhythmias, as well as low cardiac output syndrome, cardiorenal syndrome and anemia.

About the Authors

V. I. Podzolkov
I. M. Sechenov First Moscow State Medical University
Russian Federation
Moscow


N. A. Dragomiretskaya
I. M. Sechenov First Moscow State Medical University
Russian Federation
Moscow


S. K. Stolbova
I. M. Sechenov First Moscow State Medical University
Russian Federation
Moscow


I. S. Rusinov
I. M. Sechenov First Moscow State Medical University
Russian Federation
Moscow


References

1. Mareev VY, Fomin IV, Ageev FT, et al. Russian Heart Failure Society, Russian Society of Cardiology. Russian Scientific Medical Society of Internal Medicine Guidelines for Heart failure: chronic (CHF) and acute decompensated (ADHF). Diagnosis, prevention and treatment. Kardiologiia. 2018;58(6S):8-158. (In Russ.) doi:10.18087/cardio.2475.

2. Fomin IV. Chronic heart failure in Russian Federation: what do we know and what to do. Russian Journal of Cardiology. 2016;(8):7-13. (In Russ.) doi:10.15829/1560-4071-2016-8-7-13.

3. Zaphiriou A, Robb S, Murray-Thomas T, et al. The diagnostic accuracy of plasma BNP and NT-proBNP in patients referred from primary care with suspected heart failure: Results of the UK natriuretic peptide study. Eur J Heart Fail. 2005;7(4):537-41. doi:10.1016/j.ejheart.2005.01.022.

4. Maisel A, Mueller C, Adams K, et al. State of the art: Using natriuretic peptide levels in clinical practice. Eur J Heart Fail. 2008:10(9):824-39. doi:10.1016/j.ejheart.2008.07.014.

5. Leto L, Testa M, Feola M. The predictive value of plasma biomarkers in discharged heart failure patients: role of plasma NT-proBNP. Minerva Cardioangiol. 2016; 64(2):157-64.

6. Govender AP, Rodseth RN, Biccard BM. Natriuretic peptidedirected medical therapy: a systematic review. Perioper Med (Lond). 2020;9:5. doi:10.1186/s13741-019-0134-y.

7. Stienen S, Salah KCS, Moons AH, et al. NT-proBNP (N-Terminal pro-B-Type Natriuretic Peptide)-Guided Therapy in Acute Decompensated Heart Failure: PRIMA II Randomized Controlled Trial (Can NT-ProBNP-Guided Therapy During Hospital Admission for Acute Decompensated Heart Failure Reduce Mortality and Readmissions?). Circulation. 2018;137(16):1671-83. doi:10.1161/CIRCULATIONAHA.117.029882.

8. Ganz T, Nemeth E. Hepcidin and iron homeostasis. Biochim Biophys Acta 2012;1823:1434-43. doi:10.1016/j.bbamcr.2012.01.014.

9. Divakaran V. Hepcidin in anemia of chronic heart failure. Am J Hematol. 2011;86(1):107-9. doi:10.1002/ajh.21902.

10. Wang CY, Babitt JL. Hepcidin regulation in the anemia of inflammation. Curr Opin Hematol. 2016;23(3):189-97. doi:10.097/MOH.0000000000000236.

11. Saprina VT, Zima AP, Musina NN, et al. Pathogenetic aspects of hepcidin metabolism and ferrocinetics dysregulation in carbohydrate metabolism disorders. Diabetes mellitus. 2018;6(21): 506-12. (In Russ.) doi:10.14341/DM9378.

12. Jankowska EA, Malyszko J, Ardehali H, et al. Iron status in patients with chronic heart failure. Eur Heart J. 2013;34(11):827- 34. doi:10.1093/eurheartj/ehs377.

13. Solomakhina NI, Nakhodnova ES, Gitel EP, Belenkov YN. Hepcidin and its relationship with inflammation in old and older patients with anemia of chronic disease associated with CHF. Kardiologiia. 2018;58(2S):4-11. (In Russ.) doi:10.18087/cardio.2457.

14. Аgusti AG. Systemic effects of chronic obstructive pulmonary disease. Proc Am Thorac Soc. 2005;2:367-70. doi:10.1513/pats.200504-026SR.

15. Karoli NA, Borodkin AV, Rebrov AP. Features of the clinic and diagnosis of chronic heart failure in patients with chronic obstructive pulmonary disease. Kardiologiia. 2019;59(2S):47-55. (In Russ.) doi:10.18087/cardio.2486.

16. Ohno Y, Hanawa H, Jiao S, et al. Liver congestion in heart failure contributes to inappropriately increased serum hepcidin despite anemia J Exp Med. 2015;235:69-79. doi:10.1620/tjem.235.69.

17. Vuppalanchi R, Troutt JS, Konrad RJ, Ghabril M. Serum hepcidin levels are associated with obesity but not liver diseasе. Obesity. 2014;22(3):836-41. doi:10.1002/oby.20403.

18. Horwich TB, Fonarow GC, Clark AL. Obesity and the Obesity Paradox in Heart Failure. Prog Cardiovasc Dis. 2018;61(2):151-6. doi:10.1016/j.pcad.2018.05.005.

19. Elagizi A, Kachur S, Lavie CJ, et al. An Overview and Update on Obesity and the Obesity Paradox in Cardiovascular Diseases. Prog Cardiovasc Dis. 2018;61(2):142-50. doi:10.1016/j.pcad.2018.07.003.

20. Jamali R, Razavizade M, Arj A, Aarabi MH. Serum adipokines might predict liver histology findings in non-alcoholic fatty liver disease. World J Gastroenterol. 2016;22(21):5096-103. doi:10.3748/wjg.v22.i21.5096.


Review

For citations:


Podzolkov V.I., Dragomiretskaya N.A., Stolbova S.K., Rusinov I.S. Associations of NT-proBNP and hepcidin levels with clinical and laboratory parameters in patients with heart failure with various severity of left ventricular systolic dysfunction. Cardiovascular Therapy and Prevention. 2020;19(4):2587. https://doi.org/10.15829/1728-8800-2020-2587

Views: 1115


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


ISSN 1728-8800 (Print)
ISSN 2619-0125 (Online)