PMID- 38495948 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240319 IS - 1179-5514 (Print) IS - 1179-5514 (Electronic) IS - 1179-5514 (Linking) VI - 17 DP - 2024 TI - Safety and Effectiveness of Sodium-Glucose Co-transporter 2 Inhibitors on Glycemic Control in Patients with Type 2 Diabetes Mellitus Fasting during Ramadan: A Review. PG - 11795514241238058 LID - 10.1177/11795514241238058 [doi] LID - 11795514241238058 AB - This review evaluates the current evidence on the safety and efficacy of sodium-glucose cotransporter 2 (SGLT2) inhibitors for patients with type 2 diabetes mellitus (T2DM) fasting during Ramadan. All studies included in the review were conducted in Asia and the Middle East. Overall, the evidence suggests that SGLT2 inhibitors are a safe and effective treatment option for most T2DM patients fasting during Ramadan. The average incidence of symptomatic hypoglycemia is 12.5%, but ranges from 0.7% to 27%, depending on the study population and concomitant use of other medications. The risk of hypoglycemia is increased when SGLT2 inhibitors are used in combination with insulin and/or sulfonylureas. Therefore, patients taking SGLT2 inhibitors in combination with insulin and/or sulfonylureas can take steps to mitigate this risk, such as having their insulin and/or sulfonylurea doses adjusted and being closely monitored for hypoglycemia. Patients taking SGLT2 inhibitors may be at increased risk of dehydration. To mitigate the risk of dehydration, patients should be advised to consume adequate fluids during the fast-breaking hours. Further research is warranted to validate these findings and extend their applicability to high-risk populations and other regions of the world. CI - (c) The Author(s) 2024. FAU - Nakhleh, Afif AU - Nakhleh A AUID- ORCID: 0000-0003-1206-1516 AD - Diabetes and Endocrinology Clinic, Maccabi Healthcare Services, Haifa, Israel. AD - Institute of Endocrinology, Diabetes and Metabolism, Rambam Health Care Campus, Haifa, Israel. AD - The Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel. FAU - Mazareeb, Jomana AU - Mazareeb J AD - Diabetes and Endocrinology Clinic, Maccabi Healthcare Services, Haifa, Israel. FAU - Darawshi, Said AU - Darawshi S AD - Institute of Endocrinology, Diabetes and Metabolism, Rambam Health Care Campus, Haifa, Israel. FAU - Masri, Amin AU - Masri A AD - Institute of Endocrinology, Diabetes and Metabolism, Rambam Health Care Campus, Haifa, Israel. FAU - Shehadeh, Naim AU - Shehadeh N AD - Diabetes and Endocrinology Clinic, Maccabi Healthcare Services, Haifa, Israel. AD - Institute of Endocrinology, Diabetes and Metabolism, Rambam Health Care Campus, Haifa, Israel. AD - The Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel. LA - eng PT - Journal Article PT - Review DEP - 20240314 PL - United States TA - Clin Med Insights Endocrinol Diabetes JT - Clinical medicine insights. Endocrinology and diabetes JID - 101578235 PMC - PMC10943741 OAB - Safety and effectiveness of sodium-glucose co-transporter 2 inhibitors on glycemic control in patients with type 2 diabetes mellitus fasting during Ramadan: a review This review delves into the existing evidence regarding the safety and efficacy of sodium-glucose co-transporter 2 (SGLT2) inhibitors for patients with type 2 diabetes mellitus (T2DM) who observe Ramadan fasting. The studies reviewed were conducted exclusively in Asia and the Middle East. Overall, the gathered evidence suggests that SGLT2 inhibitors constitute a safe and effective treatment option for most T2DM patients fasting during Ramadan. While a slightly elevated risk of dehydration compared to other medications may exist, this is generally well-tolerated. To mitigate the risk of dehydration, patients should be advised to consume adequate fluids during the fast-breaking hours. However, further research is warranted to validate these findings and extend their applicability to high-risk populations and other world regions. OABL- eng OTO - NOTNLM OT - Ramadan OT - SGLT2 inhibitors OT - fasting COIS- The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2024/03/18 06:43 MHDA- 2024/03/18 06:44 PMCR- 2024/03/14 CRDT- 2024/03/18 04:30 PHST- 2023/11/13 00:00 [received] PHST- 2024/02/13 00:00 [accepted] PHST- 2024/03/18 06:44 [medline] PHST- 2024/03/18 06:43 [pubmed] PHST- 2024/03/18 04:30 [entrez] PHST- 2024/03/14 00:00 [pmc-release] AID - 10.1177_11795514241238058 [pii] AID - 10.1177/11795514241238058 [doi] PST - epublish SO - Clin Med Insights Endocrinol Diabetes. 2024 Mar 14;17:11795514241238058. doi: 10.1177/11795514241238058. eCollection 2024.