{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T00:48:13Z","timestamp":1787014093528,"version":"build-2736575974"},"reference-count":45,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2016,12,5]],"date-time":"2016-12-05T00:00:00Z","timestamp":1480896000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/100008349","name":"Boehringer Ingelheim","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100008349","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100002429","name":"Amgen","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100002429","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2017,2]]},"abstract":"<jats:sec>\n                    <jats:title>Aims<\/jats:title>\n                    <jats:p>\n                      Since 2005, several 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                      ) have been approved to treat people with type 2 diabetes. These agents are considered for use at the same point in the treatment paradigm as basal insulins. A comprehensive comparison of these drug classes, therefore, can help inform treatment decisions. This systematic review and meta\u2010analysis assessed the clinical efficacy and safety 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                      compared with basal insulins.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and methods<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">MEDLINE<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">EMBASE<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">CENTRAL<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">PubMed<\/jats:styled-content>\n                      databases were searched. Randomized clinical trials (\n                      <jats:styled-content style=\"fixed-case\">RCTs<\/jats:styled-content>\n                      ) of \u226516 weeks\u2019 duration comparing\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                      vs basal insulins in adults with type 2 diabetes inadequately controlled with oral antihyperglycemic drugs were included. Data on the change from baseline to 26 weeks (\u00b110 weeks) of treatment in hemoglobin A1c (\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      ) and weight, as well as the proportion of patients experiencing hypoglycaemia, were extracted. Fixed\u2010effect pairwise meta\u2010analyses were conducted where data were available from \u22652 studies.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Fifteen\n                      <jats:styled-content style=\"fixed-case\">RCTs<\/jats:styled-content>\n                      were identified and 11 were meta\u2010analysed. The once\u2010weekly\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                      , exenatide long acting release (\n                      <jats:styled-content style=\"fixed-case\">LAR<\/jats:styled-content>\n                      ) and dulaglutide, led to greater, statistically significant mean\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      reductions vs basal insulins (exenatide: \u22120.31% [95% confidence interval \u22120.42, \u22120.19], dulaglutide: \u22120.39% [\u22120.49, \u22120.29]) whilst once\u2010daily liraglutide and twice\u2010daily exenatide did not (liraglutide: 0.06% [\u22120.06, 0.18], exenatide: 0.01% [\u22120.11, 0.13]). Mean weight reduction was seen with all\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                      while mean weight gain was seen with basal insulins. Interpretation of the analysis of hypoglycaemia was limited by inconsistent definitions and reporting. Because of the limited number of available studies sensitivity analyses to explore heterogeneity could not be conducted.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Although weight reduction is seen with all\n                      <jats:styled-content style=\"fixed-case\">GLP\u20101 RA<\/jats:styled-content>\n                      \u2019s, only the once\u2010weekly agents, exenatide\n                      <jats:styled-content style=\"fixed-case\">LAR<\/jats:styled-content>\n                      and dulaglutide, demonstrate significant\n                      <jats:styled-content style=\"fixed-case\">HbA1c<\/jats:styled-content>\n                      reductions when compared to basal insulins.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12805","type":"journal-article","created":{"date-parts":[[2016,10,13]],"date-time":"2016-10-13T01:39:24Z","timestamp":1476322764000},"page":"228-238","source":"Crossref","is-referenced-by-count":91,"title":["Glucagon\u2010like peptide\u20101 receptor agonists compared with basal insulins for the treatment of type 2 diabetes mellitus:\n                    <scp>a<\/scp>\n                    systematic review and meta\u2010analysis"],"prefix":"10.1111","volume":"19","author":[{"given":"Sonal","family":"Singh","sequence":"first","affiliation":[{"name":"Johns Hopkins University School of Medicine  Baltimore Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"suffix":"Jr.","given":"Eugene E.","family":"Wright","sequence":"additional","affiliation":[{"name":"Department of Medicine Duke University Medical Center at the Southern Regional Area Health Education Center (AHEC)  Fayetteville North Carolina"},{"name":"Department of Community and Family Medicine Duke University Medical Center at the Southern Regional Area Health Education Center (AHEC)  Fayetteville North Carolina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anita Y. 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