{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,26]],"date-time":"2026-03-26T09:13:43Z","timestamp":1774516423330,"version":"3.50.1"},"reference-count":31,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"11","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2018,6,5]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              Antihyperglycemic therapies may increase the risk of cardiovascular events including hospitalization for heart failure. There is a paucity of data evaluating the cardiovascular safety of antihyperglycemic therapies in the high\u2010risk period following an acute coronary syndrome (\n              <jats:styled-content style=\"fixed-case\">ACS<\/jats:styled-content>\n              ).\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Methods and Results<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              The\n              <jats:styled-content style=\"fixed-case\">EXAMINE<\/jats:styled-content>\n              (Examination of Cardiovascular Outcomes with Alogliptin versus Standard of Care) trial randomized 5380 patients who were 15 to 90\u00a0days post\n              <jats:styled-content style=\"fixed-case\">ACS<\/jats:styled-content>\n              to the dipeptidyl dipeptidase\u2010IV (\n              <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n              \u2010\n              <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content>\n              ) inhibitor alogliptin versus placebo; mean follow\u2010up was 18\u00a0months. Using a landmark analysis, we assessed the (1) burden of cardiovascular events from randomization to 6\u00a0months (early period) and from 6\u00a0months to the end of follow\u2010up (late period) and (2) the risk of cardiovascular events associated with early (up to 6\u00a0months) and chronic (6\u00a0months to end of follow\u2010up)\n              <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n              \u2010\n              <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content>\n              inhibition with alogliptin. Patients with early versus late events had similar baseline demographic profiles. Overall, 42.1% of the composite of cardiovascular death\/myocardial infarction\/stroke and 47.5% of hospitalization for heart failure occurred in the early period. Early\n              <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n              \u2010\n              <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content>\n              inhibition did not increase the risk of early cardiovascular death\/myocardial infarction\/stroke (hazard ratio 0.96, 95% confidence interval, 0.76\u20131.21) or hospitalization for heart failure (1.23, 95% confidence interval, 0.84\u20131.82). Similarly, chronic\n              <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n              \u2010\n              <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content>\n              inhibition did not increase the risk of late cardiovascular death\/myocardial infarction\/stroke (hazard ratio 1.03, 95% confidence interval, 0.89\u20131.26) or hospitalization for heart failure (hazard ratio 1.02, 95% confidence interval, 0.85\u20131.22).\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              Early after an\n              <jats:styled-content style=\"fixed-case\">ACS<\/jats:styled-content>\n              , patients with type 2 diabetes mellitus experience a significant burden of\n              <jats:styled-content style=\"fixed-case\">HF<\/jats:styled-content>\n              events and recurrent\n              <jats:styled-content style=\"fixed-case\">ACS<\/jats:styled-content>\n              .\n              <jats:styled-content style=\"fixed-case\">DPP<\/jats:styled-content>\n              \u2010\n              <jats:styled-content style=\"fixed-case\">IV<\/jats:styled-content>\n              inhibition with alogliptin appears to be safe even in the high\u2010risk period following an\n              <jats:styled-content style=\"fixed-case\">ACS<\/jats:styled-content>\n              .\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.117.007649","type":"journal-article","created":{"date-parts":[[2018,5,16]],"date-time":"2018-05-16T09:15:16Z","timestamp":1526462116000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":13,"title":["Early and Chronic Dipeptidyl\u2010Peptidase\u2010IV Inhibition and Cardiovascular Events in Patients With Type 2 Diabetes Mellitus After an Acute Coronary Syndrome: A Landmark Analysis of 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