SGLT2 inhibition: efficacy and safety in type 2 diabetes treatment
Abstract
Introduction Inhibitors of sodium-glucose cotransporters type 2 (SGLT2) offer a new opportunity for the management of type 2 diabetes mellitus. These agents reduce hyperglycemia by decreasing the renal glucose threshold and thereby increasing urinary glucose excretion. Subsequent reduction of glucotoxicity improves beta-cell sensitivity to glucose and tissue insulin sensitivity. Areas covered This article analyzes the efficacy and safety data of canagliflozin, dapagliflozin and empagliflozin in randomized controlled trials of 24 - 104 weeks duration, compared with placebo or an active comparator, in patients treated with diet/exercise, metformin, dual oral therapy or insulin. Expert opinion SGLT2 inhibitors significantly and consistently reduce glycated hemoglobin, with a minimal risk of hypoglycemia. The improvement of glucose control is similar or slightly better compared with metformin, sulfonylureas or sitagliptin, with the add-on value of significant reductions in body weight and blood pressure. However, caution is recommended in fragile elderly patients and patients with chronic kidney disease. An increased risk of genital mycotic infections is observed, but urinary tract infections are rare. Concern about an unexpected risk of euglycemic ketoacidosis has been recently reported. A possible renal protection deserves further attention. A remarkable reduction in cardiovascular mortality was reported in EMPA-REG OUTCOME with empagliflozin.
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SGLT-2 inhibitors can lower body weight in individuals with obesity.
“SGLT-2 inhibitors can also able to lower the body weight of individuals with obesity (74–76).”
SGLT-2 inhibitors lower the renal glucose threshold and raise urine glucose excretion, thereby lessening hyperglycemia.
“Due to their ability to lower the renal glucose threshold and raise urine glucose excretion, these medicines lessen hyperglycemia.”
SGLT-2 inhibitors (empagliflozin and dapagliflozin) are most beneficial as adjunct medication in addition to metformin in patients with a history of cardiovascular or renal disease that needs further HbA1c reduction.
“Sodium glucosinolate co-transporter 2 (SGLT-2) inhibitors (empagliflozin and dapagliflozin) are the most beneficial as an adjunct medication in addition to metformin in patients with a history of cardiovascular or renal disease that needs further HbA1c reduction.”
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References 124 · Cited by 70
- Authors
- Scheen, A. J.
- Affiliations
- University of Liège (BE)
- Corresponding author
- Scheen, André J.
- ORCID
- Scheen, André J.
- Venue
- Expert Opinion on Drug Safety
- Publisher
- Informa Healthcare
- Published
- 2015-10-29
- Volume
- 14
- Issue
- 12
- Pages
- 1879-1904
- ISSN
- 1474-0338 (ISSN-L)
- 1744-764X
- OpenAlex
- W2198388354
- Cited by
- 70
- References
- 124
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 8 · 2023: 3 · 2022: 5 · 2021: 2 · 2020: 4 · 2019: 7 · 2018: 9 · 2017: 15 · 2016: 15
- FWCI
- 1.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Expert Opinion on Drug Safety (publishedVersion)
- PubMed (publishedVersion)
- ORBi (University of Liège) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
- Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
- Keywords
- SGLT2 inhibitors, type 2 diabetes, canagliflozin, dapagliflozin, empagliflozin, HbA1c, hypoglycemia, weight loss, blood pressure reduction, genital mycotic infections, euglycemic diabetic ketoacidosis, chronic kidney disease, renal protection, cardiovascular mortality, EMPA-REG OUTCOME, metformin comparison
- MeSH terms
- Canagliflozin, Sodium-Glucose Transporter 2 Inhibitors, Aged, Benzhydryl Compounds, Blood Glucose, Diabetes Mellitus, Type 2, Glucose, Glucosides, Humans, Hypoglycemic Agents, Insulin Resistance, Randomized Controlled Trials as Topic, Sodium-Glucose Transporter 2
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