{"title":"SGLT2 抑制剂会在治疗后立即增加慢性肾病患者的低血清镁水平。","authors":"Kosuke Osawa, Masaki Ohya, Shuto Yamamoto, Yuri Nakashima, Yusuke Tanaka, Yukiko Yamano, Taisuke Takatsuka, Shin-Ichi Araki","doi":"10.1007/s10157-024-02590-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown in clinical trials to increase serum Mg<sup>2+</sup> levels in patients with type 2 diabetes mellitus. However, it is unclear whether this effect is similarly observed in patients with chronic kidney disease (CKD) and whether such an increase is observed immediately after treatment.</p><p><strong>Methods: </strong>Our retrospective observational study included the 62 patients with CKD who started SGLT2 inhibitor therapy at our institution between 2017 and 2022 and who had complete data on serum Mg<sup>2+</sup> measurements at baseline and at 1, 3, and 6 months after treatment. Patients were divided into three subgroups, stratified by serum Mg<sup>2+</sup> levels at baseline. We evaluated the changes in serum Mg<sup>2+</sup> levels from baseline to 6 months after treatment and the factors associated with these changes.</p><p><strong>Results: </strong>Median eGFR and mean serum Mg<sup>2+</sup> at baseline were 33.5 mL/min/1.73 m<sup>2</sup> and 2.03 mg/dL, respectively. Treatment with SGLT2 inhibitors significantly increased serum Mg<sup>2+</sup> levels immediately from 1 month after treatment compared with those at baseline and persisted over 6 months, with an overall mean change of 0.13 mg/dL from baseline to 6 months. This increased effect was observed in the low and middle tertile subgroups, but not in the high tertile subgroup. Multivariate linear regression analysis revealed that baseline serum Mg<sup>2+</sup> levels and sodium-chloride differences, as a parameter of acid-base status, were independently associated with these changes.</p><p><strong>Conclusions: </strong>SGLT2 inhibitors increased serum Mg<sup>2+</sup> levels in patients with CKD, particularly those with lower baseline Mg<sup>2+</sup> levels, potentially improving their prognosis.</p>","PeriodicalId":10349,"journal":{"name":"Clinical and Experimental Nephrology","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"SGLT2 inhibitors increase low serum magnesium levels in patients with chronic kidney disease immediately after treatment.\",\"authors\":\"Kosuke Osawa, Masaki Ohya, Shuto Yamamoto, Yuri Nakashima, Yusuke Tanaka, Yukiko Yamano, Taisuke Takatsuka, Shin-Ichi Araki\",\"doi\":\"10.1007/s10157-024-02590-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown in clinical trials to increase serum Mg<sup>2+</sup> levels in patients with type 2 diabetes mellitus. However, it is unclear whether this effect is similarly observed in patients with chronic kidney disease (CKD) and whether such an increase is observed immediately after treatment.</p><p><strong>Methods: </strong>Our retrospective observational study included the 62 patients with CKD who started SGLT2 inhibitor therapy at our institution between 2017 and 2022 and who had complete data on serum Mg<sup>2+</sup> measurements at baseline and at 1, 3, and 6 months after treatment. Patients were divided into three subgroups, stratified by serum Mg<sup>2+</sup> levels at baseline. We evaluated the changes in serum Mg<sup>2+</sup> levels from baseline to 6 months after treatment and the factors associated with these changes.</p><p><strong>Results: </strong>Median eGFR and mean serum Mg<sup>2+</sup> at baseline were 33.5 mL/min/1.73 m<sup>2</sup> and 2.03 mg/dL, respectively. Treatment with SGLT2 inhibitors significantly increased serum Mg<sup>2+</sup> levels immediately from 1 month after treatment compared with those at baseline and persisted over 6 months, with an overall mean change of 0.13 mg/dL from baseline to 6 months. This increased effect was observed in the low and middle tertile subgroups, but not in the high tertile subgroup. Multivariate linear regression analysis revealed that baseline serum Mg<sup>2+</sup> levels and sodium-chloride differences, as a parameter of acid-base status, were independently associated with these changes.</p><p><strong>Conclusions: </strong>SGLT2 inhibitors increased serum Mg<sup>2+</sup> levels in patients with CKD, particularly those with lower baseline Mg<sup>2+</sup> levels, potentially improving their prognosis.</p>\",\"PeriodicalId\":10349,\"journal\":{\"name\":\"Clinical and Experimental Nephrology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Experimental Nephrology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10157-024-02590-8\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Nephrology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10157-024-02590-8","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
SGLT2 inhibitors increase low serum magnesium levels in patients with chronic kidney disease immediately after treatment.
Background: Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been shown in clinical trials to increase serum Mg2+ levels in patients with type 2 diabetes mellitus. However, it is unclear whether this effect is similarly observed in patients with chronic kidney disease (CKD) and whether such an increase is observed immediately after treatment.
Methods: Our retrospective observational study included the 62 patients with CKD who started SGLT2 inhibitor therapy at our institution between 2017 and 2022 and who had complete data on serum Mg2+ measurements at baseline and at 1, 3, and 6 months after treatment. Patients were divided into three subgroups, stratified by serum Mg2+ levels at baseline. We evaluated the changes in serum Mg2+ levels from baseline to 6 months after treatment and the factors associated with these changes.
Results: Median eGFR and mean serum Mg2+ at baseline were 33.5 mL/min/1.73 m2 and 2.03 mg/dL, respectively. Treatment with SGLT2 inhibitors significantly increased serum Mg2+ levels immediately from 1 month after treatment compared with those at baseline and persisted over 6 months, with an overall mean change of 0.13 mg/dL from baseline to 6 months. This increased effect was observed in the low and middle tertile subgroups, but not in the high tertile subgroup. Multivariate linear regression analysis revealed that baseline serum Mg2+ levels and sodium-chloride differences, as a parameter of acid-base status, were independently associated with these changes.
Conclusions: SGLT2 inhibitors increased serum Mg2+ levels in patients with CKD, particularly those with lower baseline Mg2+ levels, potentially improving their prognosis.
期刊介绍:
Clinical and Experimental Nephrology is a peer-reviewed monthly journal, officially published by the Japanese Society of Nephrology (JSN) to provide an international forum for the discussion of research and issues relating to the study of nephrology. Out of respect for the founders of the JSN, the title of this journal uses the term “nephrology,” a word created and brought into use with the establishment of the JSN (Japanese Journal of Nephrology, Vol. 2, No. 1, 1960). The journal publishes articles on all aspects of nephrology, including basic, experimental, and clinical research, so as to share the latest research findings and ideas not only with members of the JSN, but with all researchers who wish to contribute to a better understanding of recent advances in nephrology. The journal is unique in that it introduces to an international readership original reports from Japan and also the clinical standards discussed and agreed by JSN.