Key result
Dapagliflozin added to conventional therapy significantly improved LVEF, decreased LVEDD, and reduced levels of inflammatory factors and myocardial fibrosis markers at 4 weeks (P<0.05).
Why the study?
To explore the effect of dapagliflozin on myocardial fibrosis and inflammatory factor levels in patients with heart failure.
Does dapagliflozin reduce inflammatory factors and improve indicators of myocardial fibrosis and cardiac function in patients with T2DM and acute or exacerbated chronic left heart failure?
Does dapagliflozin reduce inflammatory factors and improve indicators of myocardial fibrosis and cardiac function in patients with T2DM and acute or exacerbated chronic left heart failure?
p-value: p=<0.05
Dapagliflozin added to conventional therapy significantly reduces inflammatory markers and improves surrogate markers of cardiac function and fibrosis at 4 weeks in patients with T2DM and acute or exacerbated chronic left heart failure.
s anti-fibrotic and anti-inflammatory effects in acute heart failure;.
Objective. To explore the effect of dapagliflozin on the myocardial fibrosis and the levels of inflammatory factors in heart failure patients. Methods. 60 patients with T2DM who were diagnosed as acute left heart failure or acute exacerbation of chronic left heart failure in the Department of Cardiology of our hospital from November 1, 2020, to December 31, 2021, during hospitalization were the study subjects. According to the treatment regimen, they were divided into the experimental group (EG) which received dapagliflozin and conventional drugs and the control group (CG) which received conventional drugs, with 30 cases in each group to compare and analyze the clinical indicators such as myocardial fibrosis and inflammatory factors. Results. The levels of TNF-α, IL-1β, IL-6, and hs-CRP in the two groups were decreased gradually after treatment, and the levels of TNF-α, IL-1β, IL-6, and hs-CRP in the EG were visibly lower compared with those in the CG at week 4 of treatment ( <a:math xmlns:a="http://www.w3.org/1998/Math/MathML" id="M1"> <a:mi>P</a:mi> <a:mo><</a:mo> <a:mn>0.05</a:mn> </a:math> ). The cardiac function evaluation of patients showed that the levels of LVEF and LVEDD in both groups were gradually improved after treatment, with a significant difference from the fourth week. In other words, compared with the CG, the LVEF level in the EG was obviously higher ( <c:math xmlns:c="http://www.w3.org/1998/Math/MathML" id="M2"> <c:mi>P</c:mi> <c:mo><</c:mo> <c:mn>0.05</c:mn> </c:math> ), the LVEDD level was distinctly lower ( <e:math xmlns:e="http://www.w3.org/1998/Math/MathML" id="M3"> <e:mi>P</e:mi> <e:mo><</e:mo> <e:mn>0.05</e:mn> </e:math> ), and the levels of ST2, BNP, and MCP-1 in the EG were clearly lower at week 4 of treatment ( <g:math xmlns:g="http://www.w3.org/1998/Math/MathML" id="M4"> <g:mi>P</g:mi> <g:mo><</g:mo> <g:mn>0.05</g:mn> </g:math> ) with a statistical significance in difference. Conclusion. Dapagliflozin has a definite curative effect in heart failure patients with type 2 diabetes mellitus, which can effectively reduce the inflammatory response of patients and inhibit the myocardial fibrosis, and has a potential value in improving cardiac function and promoting prognosis.
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Wang et al. (2022) studied Heart failure with type 2 diabetes mellitus (n=60). Dapagliflozin vs. Conventional drugs was evaluated on Levels of inflammatory factors (TNF-α, IL-1β, IL-6, hs-CRP), cardiac function (LVEF, LVEDD), and myocardial fibrosis markers (ST2, BNP, MCP-1) (p=<0.05). Dapagliflozin added to conventional therapy significantly improved LVEF, decreased LVEDD, and reduced levels of inflammatory factors and myocardial fibrosis markers at 4 weeks (P<0.05).
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