Correction of hypomagnesemia by dapagliflozin in patients with type 2 diabetes: A post hoc analysis of 10 randomized, placebo-controlled trialsShow others and affiliations
2019 (English)In: Journal of diabetes and its complications, ISSN 1056-8727, E-ISSN 1873-460X, Vol. 33, no 10, article id 107402Article in journal (Refereed) Published
Abstract [en]
Aims: Hypomagnesemia (serum magnesium [Mg] <0.74 mmol/L [<1.8 mg/dL]) is commonly observed in patients with type 2 diabetes (T2D). This study investigated the effect of treatment with dapagliflozin 10 mg on Mg concentrations in patients with T2D. Methods: In this post hoc analysis, we used pooled data from 10 placebo-controlled studies of dapagliflozin over 24 weeks of treatment in patients with T2D. We evaluated the change in Mg in patients receiving dapagliflozin vs. placebo overall, and in subgroups with baseline hypomagnesemia and normal/hypermagnesemia (≥0.74 mmol/L [≥1.8 mg/dL]). We determined the proportion of patients with baseline hypomagnesemia who achieved Mg ≥0.74 mmol/L (≥1.8 mg/dL). Results: A total of 4398 patients with T2D were included. The mean change from baseline to week 24 in Mg was significantly larger with dapagliflozin vs. placebo; difference, 0.06 mmol/L (95% confidence interval [CI]: 0.05, 0.06). The proportion of patients with Mg within the population reference range after 24 weeks of treatment was significantly higher with dapagliflozin vs. placebo; difference, 47.8% (95% CI: 41.4, 53.9). The proportion of patients displaying hypermagnesemia did not increase with dapagliflozin treatment. Conclusions: Treatment with dapagliflozin 10 mg resulted in correction of Mg concentrations in patients with T2D and hypomagnesemia.
Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 33, no 10, article id 107402
Keywords [en]
Dapagliflozin, Hypomagnesemia, Post hoc analysis, Randomized controlled trials, SGLT2 inhibitor, Type 2 diabetes
National Category
Endocrinology and Diabetes
Research subject
Bioinformatics
Identifiers
URN: urn:nbn:se:his:diva-17521DOI: 10.1016/j.jdiacomp.2019.06.007ISI: 000488886900007PubMedID: 31375422Scopus ID: 2-s2.0-85069912043OAI: oai:DiVA.org:his-17521DiVA, id: diva2:1341995
2019-08-122019-08-122025-09-29Bibliographically approved