Weight-independent amelioration of adipokine profile by enavogliflozin, a selective SGLT2 inhibitor, in patients with type 2 diabetes.

IF 10.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Young Sang Lyu, Hansol Lee, Kyung-Soo Kim, Sangmo Hong, Cheol-Young Park
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引用次数: 0

Abstract

Background and objective: The metabolic benefits of sodium-glucose co-transporter 2 inhibitors in clinical application are well established; however, there is dearth of knowledge on their impact on adipokine regulation. This study investigated the effect of enavogliflozin on adiponectin and leptin in patients with type 2 diabetes.

Methods: This secondary analysis of a phase III randomized, double-blind, placebo-controlled trial evaluated changes in serum adiponectin and leptin over 24 weeks. Analysis of covariance was used with baseline values and weight change as covariates to examine whether the effects of enavogliflozin persisted after adjusting for weight change. Correlations between adipokine changes and key metabolic parameters were also assessed.

Results: Over the 24 weeks, the enavogliflozin group showed increased adiponectin levels with a least squares (LS) mean difference of 0.98 mg/L compared with the placebo group, while leptin levels showed a significant decrease with an LS mean difference of -2.99 µg/L. Enavogliflozin significantly reduced leptin levels over 24 weeks after adjusting for weight change; however, adiponectin changes were not significant after adjusting for weight change. Adiponectin levels significantly increased across weight loss categories, but leptin showed no significant differences. Leptin changes over 24 weeks significantly were positively correlated with changes in homeostasis model assessment of insulin resistance and homeostasis model assessment of β-cell function but significantly negatively correlated with changes in serum ketone and urinary glucose-to-creatinine ratio.

Conclusions: Enavogliflozin treatment decreased leptin over 24 weeks in patients with type 2 diabetes, and this effect remained significant after adjusting for weight change, suggesting an improved adipokine profile. Reductions in leptin were also associated with improvements in insulin resistance and increases in serum ketone levels. These results highlight enavogliflozin as a potential treatment beyond glycemic control, offering additional benefits in managing metabolic dysregulation associated with type 2 diabetes.

Trial registration: Not applicable (post hoc analysis).

Abstract Image

选择性SGLT2抑制剂enavoglilozin对2型糖尿病患者中脂肪因子谱的非体重依赖性改善
背景与目的:钠-葡萄糖共转运蛋白2抑制剂在临床应用中的代谢益处已得到充分证实;然而,关于它们对脂肪因子调节的影响的知识缺乏。本研究探讨依那格列净对2型糖尿病患者脂联素和瘦素的影响。方法:这项III期随机、双盲、安慰剂对照试验的二级分析评估了24周内血清脂联素和瘦素的变化。采用协方差分析,以基线值和体重变化为协变量,检验在调整体重变化后,依那格列净的效果是否持续。脂肪因子变化与关键代谢参数之间的相关性也被评估。结果:在24周内,依纳格列净组与安慰剂组相比,脂联素水平升高,最小二乘(LS)平均差为0.98 mg/L,而瘦素水平显著降低,LS平均差为-2.99µg/L。依纳格列净在调整体重变化后24周内显著降低瘦素水平;然而,在调整体重变化后,脂联素的变化并不显著。脂联素水平在减肥组中显著增加,但瘦素没有显著差异。24周瘦素变化与胰岛素抵抗的稳态模型评估和β细胞功能的稳态模型评估的变化呈显著正相关,而与血清酮和尿糖/肌酐比值的变化呈显著负相关。结论:enavoglilozin治疗24周后,2型糖尿病患者的瘦素下降,并且在调整体重变化后,这种效果仍然显著,表明脂肪因子谱得到改善。瘦素的减少也与胰岛素抵抗的改善和血清酮水平的增加有关。这些结果突出了enavoglilozin作为一种潜在的治疗血糖控制之外的治疗方法,在管理与2型糖尿病相关的代谢失调方面提供了额外的益处。试验注册:不适用(事后分析)。
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来源期刊
Cardiovascular Diabetology
Cardiovascular Diabetology 医学-内分泌学与代谢
CiteScore
12.30
自引率
15.10%
发文量
240
审稿时长
1 months
期刊介绍: Cardiovascular Diabetology is a journal that welcomes manuscripts exploring various aspects of the relationship between diabetes, cardiovascular health, and the metabolic syndrome. We invite submissions related to clinical studies, genetic investigations, experimental research, pharmacological studies, epidemiological analyses, and molecular biology research in this field.
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