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Study on the Early Renal Function Protective Effect and Inflammatory Impact of ARNI Combined with SGLT2i in Patients with Ischemic Cardiomyopathy |
WU Zhenhua, MIAO Pengfei, TANG Jianhua, et al |
Linfen Central Hospital, Shanxi Linfen 041000, China |
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Abstract Objective: To explore the early renal function protective effect and inflammatory impact of angiotensin receptor neprilysin inhibitor (ARNI) combined with sodium-glucose co-transporter 2 inhibitor (SGLT2i) in patients with ischemic cardiomyopathy (ICM). Methods: A total of 128 ICM patients who were admitted to our hospital between December 2022 and February 2024 were selected as the study subjects and randomly divided into four groups: control group (standard medication, n=32), ARNI group (ARNI treatment, n=32), SGLT2i group (SGLT2i treatment, n=32), and combined group (ARNI + SGLT2i treatment, n=32). Kidney function indicators [urinary microalbumin (mALB), serum cystatin C (CysC)], brain natriuretic peptide (BNP), 6-minute walk test (6MWT), and inflammatory markers [interleukin (IL)-1β, IL-6, C-reactive protein (CRP), tumor necrosis factor-α (TNF-α)] were compared before and after treatment, and adverse reaction incidence was recorded. Results: After treatment, kidney function indicators (mALB and CysC) decreased in all groups, with the ARNI, SGLT2i, and combined groups showing a greater reduction in mALB and CysC compared to the control group, and the combined group showing the greatest reduction compared to the ARNI and SGLT2i groups (P<0.05). After treatment, BNP levels decreased and 6MWT improved in all groups, with the ARNI, SGLT2i, and combined groups showing a greater decrease in BNP and greater improvement in 6MWT than the control group, and the combined group showing the greatest decrease in BNP and the greatest improvement in 6MWT compared to the ARNI and SGLT2i groups (P<0.05). After treatment, inflammatory markers (TNF-α, IL-6, CRP, IL-1β) decreased in all groups, with the ARNI, SGLT2i, and combined groups showing a greater decrease in inflammatory markers than the control group, and the combined group showing the greatest reduction in inflammatory markers compared to the ARNI and SGLT2i groups (P<0.05). There were no significant differences in the overall incidence of adverse reactions among the four groups (P>0.05). Conclusion: ARNI combined with SGLT2i is more effective than monotherapy in treating ICM, effectively protecting early renal function, enhancing vasodilation ability and exercise tolerance, improving systemic inflammation, and showing good safety, with great potential for broader application.
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[1] Pastena P,Frye JT,Ho C,et al.Ischemic cardiomyopathy:epidemiology,pathophysiology,outcomes,and therapeutic options[J].Heart Fail Rev,2024,29(1):287-299. [2] Tsukamoto S,Uehara T,Azushima K,et al.Updates for cardio-kidney protective effects by angiotensin receptor-neprilysin inhibitor:requirement for additional evidence of kidney protection[J].Am Heart Assoc,2023,12(8):29565. [3] Cho IJ,Kang SM.Angiotensin receptor-neprilysin inhibitor in patients with heart failure and chronic kidney disease[J].Kidney Res Clin Pract,2021,40(4):555-565. [4] Andreea MM,Surabhi S,Razvan-Ionut P,et al.Sodium-glucose cotransporter 2 (SGLT2i) inhibitors:harms or unexpected benefits[J].Medicina (Kaunas),2023,59(4):742. [5] Towbin JA,McKenna WJ,Abrams DJ,et al.2019 HRS expert consensus statement on evaluation,risk stratification,and management of arrhythmogenic cardiomyopathy[J].Heart Rhythm,2019,16(11):301-372. [6] 姜洋.沙库巴曲缬沙坦对缺血性心肌病与扩张型心肌病心力衰竭患者疗效及安全性的比较[J].中国冶金工业医学杂志,2022,39(5):590-592. [7] 李静,边云飞.SGLT2抑制剂治疗射血分数保留的心力衰竭作用机制的研究进展[J].中西医结合心脑血管病杂志,2023,21(17):3193-3196. [8] 李志家,李佩仪.血管紧张素受体脑啡肽酶抑制剂和血管紧张素转化酶抑制剂在老年缺血性心肌病患者中的效果分析[J].中国社区医师,2021,37(19):23-24. [9] Bozkurt B,Nair AP,Misra A,et al.Neprilysin inhibitors in heart failure:the science,mechanism of action,clinical studies,and unanswered questions[J].JACC Basic Transl Sci,2022,8(1):88-105. [10] Iordan L,Gaita L,Timar R,et al.The renoprotective mechanisms of sodium-glucose cotransporter-2 inhibitors (SGLT2i)-A narrative review[J].Int Mol Sci,2024,25(13):7057. [11] Lee YC,Lin JK,Ko D,et al.Frailty and uptake of angiotensin receptor neprilysin inhibitor for heart failure with reduced ejection fraction[J].Am Geriatr Soc,2023,71(10):3110-3121. [12] Chen Y,He Q,Mo DC,et al.The angiotensin receptor and neprilysin inhibitor,LCZ696,in heart failure:a meta-analysis of randomized controlled trials[J].Medicine (Baltimore),2022,101(41):30904. |
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