早期使用 SGLT2 抑制剂可减少糖尿病肾病的恶化:一项回顾性队列研究。

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL American journal of translational research Pub Date : 2024-09-15 eCollection Date: 2024-01-01 DOI:10.62347/ARYA8831
Shaowei Pang, Xiaoli Li
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引用次数: 0

摘要

目的评估钠-葡萄糖共转运体2(SGLT2)抑制剂在预防糖尿病肾病进展方面的潜力,为临床实践提供指导,以改善糖尿病患者的肾脏健康管理策略:对宝鸡高新医院2023年3月至2024年3月收治的178例糖尿病肾病患者进行回顾性分析。其中,88例早期接受SGLT2抑制剂达帕格列净治疗的患者被纳入早期SGLT2-i组,90例晚期接受SGLT2抑制剂达帕格列净治疗的患者被纳入晚期SGLT2-i组。比较了两组患者的临床数据、总体疗效、不良反应、血糖、肾功能、血脂水平和炎症指标:治疗前,两组患者的血糖指标无差异(P>0.05)。治疗后,两组的餐后 2 小时血糖(2hPG)、空腹血浆葡萄糖(FPG)和糖化血红蛋白(HbA1c)均有所下降,其中早期 SGLT2-i 组的血糖值明显低于晚期 SGLT2-i 组(所有 P 均小于 0.05)。同样,两组患者在治疗前的肾功能指标也没有差异(均为 P > 0.05)。但在治疗后,早期 SGLT2-i 组与晚期 SGLT2-i 组相比有更明显的改善(P < 0.05)。炎症指标和血脂水平的变化趋势相似。早期SGLT2-i组的总体有效率高于晚期SGLT2-i组(92.05% vs. 78.89%,P < 0.05),而两组的不良反应发生率无统计学差异(6.82% vs. 10.00%,P > 0.05):结论:糖尿病肾病患者早期使用 SGLT2 抑制剂可有效控制血糖和血脂水平,改善肾功能,减轻炎症反应,且不良反应发生率较低。这表明其安全性很高,在延缓疾病进展方面发挥着重要作用。因此,值得考虑在这一患者群体中进行临床推广和使用。
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Early use of SGLT2 inhibitors reduces the progression of diabetic kidney disease: a retrospective cohort study.

Objective: To evaluate the potential of sodium-glucose cotransporter 2 (SGLT2) inhibitors in preventing the progression of diabetic kidney disease and to provide guidance for clinical practice to improve renal health management strategies for diabetic patients.

Methods: A retrospective analysis was conducted on 178 patients with diabetic kidney disease admitted to Baoji High Tech Hospital from March 2023 to March 2024. Of these, 88 patients who received early treatment with the SGLT2 inhibitor dapagliflozin were included in the early SGLT2-i group, while 90 patients receiving later treatment with SGLT2 inhibitor dapagliflozin were included in the late SGLT2-i group. Clinical data, overall effectiveness, adverse reactions, blood glucose, renal function, lipid levels, and inflammatory markers were compared between the two groups.

Results: Prior to treatment, there were no differences in blood glucose indicators between the two groups (all P > 0.05). Following treatment, both groups showed reductions in 2-hour postprandial blood glucose (2hPG), fasting plasma glucose (FPG), and glycosylated hemoglobin (HbA1c), with the early SGLT2-i group demonstrating significantly lower values compared to the late SGLT2-i group (all P < 0.05). Similarly, there were no differences in renal function indicators between the two groups before treatment (all P > 0.05). However, following treatment, the early SGLT2-i group showed more noticeable improvements compared to the late SGLT2-i group (P < 0.05). Inflammatory markers and lipid levels followed similar patterns. The overall effectiveness of the early SGLT2-i group was higher than that of the late SGLT2-i group (92.05% vs. 78.89%, P < 0.05), while the incidence of adverse reactions did not differ statistically between the two groups (6.82% vs. 10.00%, P > 0.05).

Conclusion: Early use of SGLT2 inhibitors in diabetic kidney disease patients effectively controls blood glucose and lipid levels, improves renal function, reduces inflammatory responses, and exhibits a low incidence of adverse reactions. This demonstrates high safety and an important role in delaying disease progression. Therefore, it is worth considering clinical promotion and use for this patient population.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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