{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T16:45:41Z","timestamp":1790009141282,"version":"4.0.1"},"reference-count":39,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2016,5,2]],"date-time":"2016-05-02T00:00:00Z","timestamp":1462147200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100006691","name":"Harvard Medical School","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100006691","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2016,8]]},"abstract":"<jats:sec>\n                    <jats:title>Aims<\/jats:title>\n                    <jats:p>\n                      To evaluate the comparative cardiovascular disease (\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      ) safety of glucagon\u2010like peptide\u20101 receptor agonists (\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RAs<\/jats:styled-content>\n                      ) in head\u2010to\u2010head comparisons with dipeptidyl peptidase\u20104 (\n                      <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n                      \u20104) inhibitors, sulphonylureas or insulin, when added to metformin, as used in \u2018real\u2010world\u2019 patients with type 2 diabetes mellitus (\n                      <jats:styled-content style=\"fixed-case\">T2DM<\/jats:styled-content>\n                      ).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Within a large\n                      <jats:styled-content style=\"fixed-case\">US<\/jats:styled-content>\n                      commercial health plan database linked to laboratory test results, we identified three pairwise 1 : 1 propensity\u2010score\u2010matched cohorts of patients with\n                      <jats:styled-content style=\"fixed-case\">T2DM<\/jats:styled-content>\n                      aged \u226518 years treated with metformin who initiated a\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RA<\/jats:styled-content>\n                      or a comparator, i.e.\n                      <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n                      \u20104 inhibitor (n = 35 534), second\u2010generation sulphonylureas (n = 28 138) or insulin (n = 47 068), between 2005 and 2013. We examined the association between drug initiation and a composite\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      endpoint, comprising hospitalizations for acute myocardial infarction, unstable angina, stroke or coronary revascularization.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      During the course of 1 year, there were 13.9 and 13.7\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      events per 1000 person\u2010years among propensity\u2010score\u2010matched initiators of\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RAs<\/jats:styled-content>\n                      versus\n                      <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n                      \u20104 inhibitors [hazard ratio (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      ) 1.02; 95% confidence interval (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ) 0.84\u20131.24]; and 12.1 versus 14.0 events among initiators of\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RAs<\/jats:styled-content>\n                      versus sulphonylureas (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      0.86; 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.69\u20131.08). The effect estimates for\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RAs<\/jats:styled-content>\n                      versus insulin were sensitive to the adjustment for glycated haemoglobin, after which the\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      was 1.01 (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      0.73\u20131.41). Results were robust across several sensitivity analyses, including an as\u2010treated analysis considering up to 8.7 years of follow\u2010up.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      This large study, performing head\u2010to\u2010head comparisons of\n                      <jats:styled-content style=\"fixed-case\">GLP<\/jats:styled-content>\n                      \u20101\n                      <jats:styled-content style=\"fixed-case\">RAs<\/jats:styled-content>\n                      with other antidiabetic agents in real\u2010world patients, provides estimates of relative safety precise enough to exclude large differences in\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      risk and adds further understanding to results from recent clinical trials.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12665","type":"journal-article","created":{"date-parts":[[2016,3,22]],"date-time":"2016-03-22T09:05:09Z","timestamp":1458637509000},"page":"755-765","source":"Crossref","is-referenced-by-count":27,"title":["Comparative cardiovascular safety of glucagon\u2010like peptide\u20101 receptor agonists versus other antidiabetic drugs in routine care: a cohort study"],"prefix":"10.1111","volume":"18","author":[{"given":"E.","family":"Patorno","sequence":"first","affiliation":[{"name":"Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine Brigham and Women's Hospital, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B. M.","family":"Everett","sequence":"additional","affiliation":[{"name":"Divisions of Cardiovascular and Preventive Medicine, Department of Medicine Brigham and Women's Hospital, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. B.","family":"Goldfine","sequence":"additional","affiliation":[{"name":"Clinical Research Joslin Diabetes Center, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. J.","family":"Glynn","sequence":"additional","affiliation":[{"name":"Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine Brigham and Women's Hospital, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.","family":"Liu","sequence":"additional","affiliation":[{"name":"Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine Brigham and Women's Hospital, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.","family":"Gopalakrishnan","sequence":"additional","affiliation":[{"name":"Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine Brigham and Women's Hospital, Harvard Medical School  Boston MA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. 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