Correlation Between Changes in the Serum Magnesium Concentration and Visceral Fat Volume in Patients With Type 2 Diabetes Receiving Luseogliflozin: A Sub-Analysis of Data From the LIGHT Study

IF 0.6 Q4 ENDOCRINOLOGY & METABOLISM Journal of Endocrinology and Metabolism Pub Date : 2021-04-25 DOI:10.14740/JEM.V11I2.738
T. Yanagawa, H. Matsuda, M. Sugawara, M. Fukuda, Takashi Sasaki
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Abstract

Background: Sodium-glucose cotransporter 2 (SGLT-2) inhibitors have been reported to more effectively suppress cardiovascular events (CVEs) in patients with type 2 diabetes. The underlying mechanism, however, remains unknown. SGLT-2 inhibitors have the unique beneficial effect of ameliorating hypomagnesemia, which is a well-known independent risk factor for CVE. However, the mechanism by which SGLT-2 inhibitors increase the serum magnesium (Mg) levels also remains unknown. We hypothesized that SGLT-2 inhibitor-induced visceral fat loss might also be correlated with the serum Mg levels. Methods: We conducted a sub-analysis of the data of 31 patients with type 2 diabetes who were treated with luseogliflozin in the LIGHT study. The correlations between changes in the serum Mg concentration (Delta Mg) and the baseline patient characteristics/changes in the values of clinical parameters at 24 weeks were analyzed by multiple regression analysis. Results: The Delta Mg was significantly associated with the baseline serum Mg concentration (beta = -0.47, 95% confidence interval (CI): -0.84 - -0.13; P = 0.01) and Delta visceral fat volume (VFV) (beta = -0.33, -0.59 - -0.09; P = 0.03). Conclusions: We found that elevation of serum Mg concentrations after SGLT-2 inhibitor treatment was associated with two factors; low serum Mg concentrations before the start of treatment and decrease in the VFV after treatment. J Endocrinol Metab. 2021;11(2):35-41 doi: https://doi.org/10.14740/jem738
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接受Luseogliflozin治疗的2型糖尿病患者血清镁浓度变化与内脏脂肪量的相关性:LIGHT研究数据的亚分析
背景:据报道,钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂可更有效地抑制2型糖尿病患者的心血管事件(CVE)。然而,其根本机制仍然未知。SGLT-2抑制剂具有改善低镁血症的独特有益作用,低镁血症是CVE的一个众所周知的独立危险因素。然而,SGLT-2抑制剂增加血清镁(Mg)水平的机制仍然未知。我们假设SGLT-2抑制剂诱导的内脏脂肪损失也可能和血清镁水平相关。方法:我们对LIGHT研究中31例接受甘西奥利嗪治疗的2型糖尿病患者的数据进行了亚分析。通过多元回归分析分析血清镁浓度(ΔMg)变化与基线患者特征/24周时临床参数值变化之间的相关性。结果:ΔMg与基线血清Mg浓度显著相关(β=-0.47,95%可信区间(CI):-0.84-0.13;P=0.01)和Δ内脏脂肪体积(VFV)(β=0.33,-0.59-0.09;P=0.03)。结论:SGLT-2抑制剂治疗后血清镁浓度升高与两个因素有关;治疗开始前血清Mg浓度低,治疗后VFV降低。内分泌代谢杂志。2021年;11(2):35-41 doi:https://doi.org/10.14740/jem738
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来源期刊
Journal of Endocrinology and Metabolism
Journal of Endocrinology and Metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
0.70
自引率
0.00%
发文量
21
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