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Data were collected on cardiometabolic and safety outcomes and synthesized using network meta\u2010analyses.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 38 trials (23 997 participants) were included. Compared with placebo, all\n                      <jats:styled-content style=\"fixed-case\">SGLT2<\/jats:styled-content>\n                      inhibitors reduced glycated haemoglobin (\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      ), fasting plasma glucose (\n                      <jats:styled-content style=\"fixed-case\">FPG<\/jats:styled-content>\n                      ), body weight and blood pressure, and slightly increased\n                      <jats:styled-content style=\"fixed-case\">HDL<\/jats:styled-content>\n                      cholesterol. Canagliflozin 300 mg reduced\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">FPG<\/jats:styled-content>\n                      and systolic blood pressure and increased\n                      <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n                      cholesterol to a greater extent compared with other inhibitors at any dose. At their highest doses, canagliflozin 300 mg reduced:\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      by 0.2% [95% confidence interval (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ) 0.1\u20130.3] versus both dapagliflozin 10 mg and empagliflozin 25 mg;\n                      <jats:styled-content style=\"fixed-case\">FPG<\/jats:styled-content>\n                      by 0.6 mmol\/l (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.3\u20130.9) and 0.5 mmol\/l (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.1\u20130.8) versus dapagliflozin and empagliflozin, respectively; and systolic blood pressure by 2\n                      <jats:styled-content style=\"fixed-case\">mmHg<\/jats:styled-content>\n                      (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      1.0\u20133.0) versus dapagliflozin; and increased\n                      <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n                      cholesterol by 0.13 mmol\/l (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.03\u20130.23) and 0.15 mmol\/l (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.06\u20130.23) versus dapagliflozin and empagliflozin, respectively. The highest doses of inhibitors had similar effects on body weight reduction. Canagliflozin 300 and 100 mg increased the risk of hypoglycaemia versus placebo, dapagliflozin 10 mg and empagliflozin 10 mg [odds ratios (\n                      <jats:styled-content style=\"fixed-case\">ORs<\/jats:styled-content>\n                      ) 1.4\u20131.6]. Dapagliflozin 10 mg increased the risk of urinary tract infection versus placebo and empagliflozin 25 mg (\n                      <jats:styled-content style=\"fixed-case\">ORs<\/jats:styled-content>\n                      1.4). All inhibitors similarly increased the risk of genital infection (\n                      <jats:styled-content style=\"fixed-case\">ORs<\/jats:styled-content>\n                      4\u20136 versus placebo).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Although they increase the risk of genital infection,\n                      <jats:styled-content style=\"fixed-case\">SGLT2<\/jats:styled-content>\n                      inhibitors are effective in improving cardiometabolic markers in type 2 diabetes, with canagliflozin 300 mg performing better in this respect than other inhibitors. Further studies will clarify whether these differences are likely to translate into differing long\u2010term outcomes.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12670","type":"journal-article","created":{"date-parts":[[2016,4,10]],"date-time":"2016-04-10T08:24:13Z","timestamp":1460276653000},"page":"783-794","source":"Crossref","is-referenced-by-count":431,"title":["Efficacy and safety of sodium\u2010glucose co\u2010transporter\u20102 inhibitors in type 2 diabetes mellitus: systematic review and network meta\u2010analysis"],"prefix":"10.1111","volume":"18","author":[{"given":"F.","family":"Zaccardi","sequence":"first","affiliation":[{"name":"Diabetes Research Centre, University of Leicester  Leicester UK"},{"name":"Diabetes Research Center, Leicester Diabetes Centre, UHL NHS Trust  Leicester UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D. 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