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Bone mineral density and parameters of bone metabolism in men with heart failure of various origins

https://doi.org/10.15829/1728-8800-2023-3694

EDN: FXUPOZ

Abstract

AimTo evaluate bone mineral density (BMD) and parameters of bone metabolism in men with heart failure (HF) of various origins.

Material and methods. The study included 100 men aged 20-70 years. The main group consisted of 60 men with HF, while the control group — 40 men without HF. BMD was measured using dual energy X-ray absorptiometry. The levels of C-terminal telopeptide type I collagen (CTx) and N-terminal propeptide type 1 procollagen (P1NP) were determined in blood serum by electrochemiluminescence immunoassay.

ResultsAnalysis in the group with HF showed a significant inverse correlation for the BMD of the spine, femoral neck and proximal femur with HF class, the independent nature of which was confirmed by multivariate regression analysis: BMD L1-L4 (β=-0,135, p=0,001), femoral neck (β=
-0,122, p=0,001), proximal femur (β=-0,127, p=0,001). However, the average values of BMD in all measured areas did not differ in the main and control groups. The mean P1NP level was significantly lower in the HF group compared to the control group — 42,5±15,0 vs 52,6±19,8 ng/ml (p=0,007). The bone resorption marker CTx was independently associated with HF stage (β=0,137, p=0,001) and N-terminal pro-brain natriuretic peptide level (β=0,128, p=0,001), and also negatively correlated with the left ventricular ejection fraction (r=-0,36, p<0,01) and positively — with left ventricular end-diastolic volume (r=0,34, p<0,01).

ConclusionIn men with HF, BMD is inversely related to HF class, which acts as an independent factor in reducing bone mass. There were no differences in the frequency of low bone mass in men with HF and in the control group. A significant decrease in bone formation marker in patients with HF compared with the control group and an association of bone resorption marker with HF severity were noted.

About the Authors

E. K. Yaralieva
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



I. A. Skripnikova
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



R. P. Myasnikov
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



O. V. Kulikova
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



V. E. Novikov
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



M. A. Myagkova
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



V. A. Vygodin
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



O. M. Drapkina
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



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Supplementary files

What is already known about the subject?

  • In a small number of available studies, there is a decrease in bone mineral density (BMD) and an increase in osteoporosis incidence in patients with heart failure (HF). This is explained by the authors common risk factors for osteoporotic fractures and HF, as well as possible common links in pathogenesis.

What might this study add?

  • This study was carefully selected to minimize the common risk factors for HF and osteoporosis that are known to lead to decreased bone mass and increased risk of fracture. However, despite this, a significant inverse relationship was found between BMD parameters and HF class, which is consistent with previous studies on the possible negative impact of the underlying disease on BMD.

Review

For citations:


Yaralieva E.K., Skripnikova I.A., Myasnikov R.P., Kulikova O.V., Novikov V.E., Myagkova M.A., Vygodin V.A., Drapkina O.M. Bone mineral density and parameters of bone metabolism in men with heart failure of various origins. Cardiovascular Therapy and Prevention. 2023;22(8):3694. (In Russ.) https://doi.org/10.15829/1728-8800-2023-3694. EDN: FXUPOZ

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