{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T10:29:24Z","timestamp":1784543364625,"version":"3.55.0"},"reference-count":57,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2016,8,31]],"date-time":"2016-08-31T00:00:00Z","timestamp":1472601600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Merck Frosst"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2016,12]]},"abstract":"<jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>\n                      To gain further insight into intestinal cholesterol homeostasis in dyslipidaemic men with insulin resistance (\n                      <jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content>\n                      ) by examining the impact of treatment with ezetimibe on the expression of key genes involved in cholesterol synthesis and\n                      <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n                      receptor (\n                      <jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>\n                      )\u2010mediated uptake of lipoproteins.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      A total of 25 men with dyslipidaemia and\n                      <jats:styled-content style=\"fixed-case\">IR<\/jats:styled-content>\n                      were recruited to participate in this double\u2010blind, randomized, crossover, placebo\u2010controlled trial. Participants received 10 mg\/day ezetimibe or placebo for periods of 12 weeks each. Intestinal gene expression was measured by quantitative\n                      <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\n                      in duodenal biopsy samples collected by gastroduodenoscopy at the end of each treatment.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 20 participants completed the protocol. Treatment with ezetimibe significantly increased intestinal\n                      <jats:styled-content style=\"fixed-case\">LDLR<\/jats:styled-content>\n                      (+16.2%;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.01), 3\u2010hydroxy\u20103\u2010methyl\u2010glutaryl\u2010\n                      <jats:styled-content style=\"fixed-case\">CoA<\/jats:styled-content>\n                      reductase (\n                      <jats:styled-content style=\"fixed-case\">HMG\u2010CoAR<\/jats:styled-content>\n                      ; +14.0%;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.04) and acetyl\u2010\n                      <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                      oenzyme\n                      <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>\n                      acetyltransferase 2 (\n                      <jats:styled-content style=\"fixed-case\">ACAT<\/jats:styled-content>\n                      \u20102)\n                      <jats:styled-content style=\"fixed-case\">mRNA<\/jats:styled-content>\n                      expression (+12.5%;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.03). Changes in sterol regulatory element\u2010binding transcription factor 2 (\n                      <jats:styled-content style=\"fixed-case\">SREBP<\/jats:styled-content>\n                      \u20102) expression were significantly correlated with changes in\n                      <jats:styled-content style=\"fixed-case\">HMG\u2010CoAR<\/jats:styled-content>\n                      (r\u2009=\u20090.55;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u2009.05),\n                      <jats:styled-content style=\"fixed-case\">ACAT<\/jats:styled-content>\n                      \u20102 (r\u2009=\u20090.69;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u2009.001) and proprotein convertase substilisin\/kexin type 9 (\n                      <jats:styled-content style=\"fixed-case\">PCSK9<\/jats:styled-content>\n                      ) expression (r\u2009=\u20090.45;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009&lt;\u2009.05).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      These results show that inhibition of intestinal cholesterol absorption by ezetimibe increases expression of the\n                      <jats:styled-content style=\"fixed-case\">LDLR<\/jats:styled-content>\n                      gene, supporting the concept that increased\n                      <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n                      clearance with ezetimibe treatment occurs not only in the liver but also in the small intestine.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12749","type":"journal-article","created":{"date-parts":[[2016,7,27]],"date-time":"2016-07-27T03:54:16Z","timestamp":1469591656000},"page":"1226-1235","source":"Crossref","is-referenced-by-count":11,"title":["Ezetimibe increases intestinal expression of the\n                    <scp>LDL<\/scp>\n                    receptor gene in dyslipidaemic men with insulin resistance"],"prefix":"10.1111","volume":"18","author":[{"given":"Jean\u2010Philippe","family":"Drouin\u2010Chartier","sequence":"first","affiliation":[{"name":"Department of Medicine, Institute of Nutrition and Functional Foods Laval University  Quebec City Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andr\u00e9 J.","family":"Tremblay","sequence":"additional","affiliation":[{"name":"Department of Medicine, Institute of Nutrition and Functional Foods Laval University  Quebec City 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