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Effects of SGLT-2 inhibitors on diabetic ketoacidosis: A meta-analysis of randomised controlled trials.

Authors :
Monami, Matteo
Nreu, Besmir
Zannoni, Stefania
Lualdi, Carlotta
Mannucci, Edoardo
Source :
Diabetes Research & Clinical Practice. Aug2017, Vol. 130, p53-60. 8p.
Publication Year :
2017

Abstract

<bold>Aims: </bold>Diabetic ketoacidosis (DKA) associated with SGLT-2 inhibitors (SGLT-2i) is a possible adverse event. In fact, SGLT-2i are capable of stimulating the release of glucagon and ketone re-absorption in the renal tubuli, thus increasing the concentration of ketone bodies.<bold>Methods: </bold>A Medline search for SGLT2i (dapagliflozin, empagliflozin, canagliflozin, ipragliflozin, ertugliflozin, luseogliflozin) was performed, collecting all randomized trials with a duration of treatment≥12weeks, enrolling patients with type 2 diabetes, and comparing a SGLT2i with placebo or other comparators. The principal outcome was the effect of SGLT2i on ketoacidosis as serious adverse event.<bold>Results: </bold>Out of 72 trials reporting information on DKA, 9 reported at least one event of ketoacidosis; those eight trials enrolled 10,157 and 5396 in SGLT-2 inhibitors and comparator groups, respectively. No signal of increased risk for ketoacidosis was observed for SGLT2 inhibitors as a class (MH-OR [95% CI] 1.14 [0.45-2.88], p=0.78) or as individual molecule. The sensitivity analysis with continuity correction (inputing one event each in drug and comparator arms of each trial with zero events) suggested a reduced incidence of ketoacidosis in patients treated with SGLT-2 inhibitors (MH-OR 0.65 [0.47-0.90]; p=0.01).<bold>Conclusions: </bold>The results of clinical trials summarized in the present meta-analysis reassure us that, when the drug is properly prescribed, the risk of DKA is negligible. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01688227
Volume :
130
Database :
Academic Search Index
Journal :
Diabetes Research & Clinical Practice
Publication Type :
Academic Journal
Accession number :
124301985
Full Text :
https://doi.org/10.1016/j.diabres.2017.04.017