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Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes
BACKGROUND: Despite the number of medications for type 2 diabetes, many people with the condition do not achieve good glycaemic control. Some existing glucose-lowering agents have adverse effects such as weight gain or hypoglycaemia. Type 2 diabetes tends to be a progressive disease, and most patien...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488745/ https://www.ncbi.nlm.nih.gov/pubmed/23087012 http://dx.doi.org/10.1136/bmjopen-2012-001007 |
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author | Clar, Christine Gill, James Alexander Court, Rachel Waugh, Norman |
author_facet | Clar, Christine Gill, James Alexander Court, Rachel Waugh, Norman |
author_sort | Clar, Christine |
collection | PubMed |
description | BACKGROUND: Despite the number of medications for type 2 diabetes, many people with the condition do not achieve good glycaemic control. Some existing glucose-lowering agents have adverse effects such as weight gain or hypoglycaemia. Type 2 diabetes tends to be a progressive disease, and most patients require treatment with combinations of glucose-lowering agents. The sodium glucose co-transporter 2 (SGLT2) receptor inhibitors are a new class of glucose-lowering agents. OBJECTIVE: To assess the clinical effectiveness and safety of the SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes. DATA SOURCES: MEDLINE, Embase, Cochrane Library (all sections); Science Citation Index; trial registries; conference abstracts; drug regulatory authorities; bibliographies of retrieved papers. INCLUSION CRITERIA: Randomised controlled trials of SGLT2 receptor inhibitors compared with placebo or active comparator in type 2 diabetes in dual or combination therapy. METHODS: Systematic review. Quality assessment used the Cochrane risk of bias score. RESULTS: Seven trials, published in full, assessed dapagliflozin and one assessed canagliflozin. Trial quality appeared good. Dapagliflozin 10 mg reduced HbA1c by −0.54% (weighted mean differences (WMD), 95% CI −0.67 to −0.40) compared to placebo, but there was no difference compared to glipizide. Canagliflozin reduced HbA1c slightly more than sitagliptin (up to −0.21% vs sitagliptin). Both dapagliflozin and canagliflozin led to weight loss (dapagliflozin WMD −1.81 kg (95% CI −2.04 to −1.57), canagliflozin up to −2.3 kg compared to placebo). LIMITATIONS: Long-term trial extensions suggested that effects were maintained over time. Data on canagliflozin are currently available from only one paper. Costs of the drugs are not known so cost-effectiveness cannot be assessed. More data on safety are needed, with the Food and Drug Administration having concerns about breast and bladder cancers. CONCLUSIONS: Dapagliflozin appears effective in reducing HbA1c and weight in type 2 diabetes, although more safety data are needed. |
format | Online Article Text |
id | pubmed-3488745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34887452012-11-05 Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes Clar, Christine Gill, James Alexander Court, Rachel Waugh, Norman BMJ Open Diabetes and Endocrinology BACKGROUND: Despite the number of medications for type 2 diabetes, many people with the condition do not achieve good glycaemic control. Some existing glucose-lowering agents have adverse effects such as weight gain or hypoglycaemia. Type 2 diabetes tends to be a progressive disease, and most patients require treatment with combinations of glucose-lowering agents. The sodium glucose co-transporter 2 (SGLT2) receptor inhibitors are a new class of glucose-lowering agents. OBJECTIVE: To assess the clinical effectiveness and safety of the SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes. DATA SOURCES: MEDLINE, Embase, Cochrane Library (all sections); Science Citation Index; trial registries; conference abstracts; drug regulatory authorities; bibliographies of retrieved papers. INCLUSION CRITERIA: Randomised controlled trials of SGLT2 receptor inhibitors compared with placebo or active comparator in type 2 diabetes in dual or combination therapy. METHODS: Systematic review. Quality assessment used the Cochrane risk of bias score. RESULTS: Seven trials, published in full, assessed dapagliflozin and one assessed canagliflozin. Trial quality appeared good. Dapagliflozin 10 mg reduced HbA1c by −0.54% (weighted mean differences (WMD), 95% CI −0.67 to −0.40) compared to placebo, but there was no difference compared to glipizide. Canagliflozin reduced HbA1c slightly more than sitagliptin (up to −0.21% vs sitagliptin). Both dapagliflozin and canagliflozin led to weight loss (dapagliflozin WMD −1.81 kg (95% CI −2.04 to −1.57), canagliflozin up to −2.3 kg compared to placebo). LIMITATIONS: Long-term trial extensions suggested that effects were maintained over time. Data on canagliflozin are currently available from only one paper. Costs of the drugs are not known so cost-effectiveness cannot be assessed. More data on safety are needed, with the Food and Drug Administration having concerns about breast and bladder cancers. CONCLUSIONS: Dapagliflozin appears effective in reducing HbA1c and weight in type 2 diabetes, although more safety data are needed. BMJ Publishing Group 2012 2012-10-18 /pmc/articles/PMC3488745/ /pubmed/23087012 http://dx.doi.org/10.1136/bmjopen-2012-001007 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Diabetes and Endocrinology Clar, Christine Gill, James Alexander Court, Rachel Waugh, Norman Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title | Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title_full | Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title_fullStr | Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title_full_unstemmed | Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title_short | Systematic review of SGLT2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
title_sort | systematic review of sglt2 receptor inhibitors in dual or triple therapy in type 2 diabetes |
topic | Diabetes and Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488745/ https://www.ncbi.nlm.nih.gov/pubmed/23087012 http://dx.doi.org/10.1136/bmjopen-2012-001007 |
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