{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,13]],"date-time":"2025-12-13T06:48:26Z","timestamp":1765608506010,"version":"build-2065373602"},"reference-count":36,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2016,1,28]],"date-time":"2016-01-28T00:00:00Z","timestamp":1453939200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100000925","name":"National Health and Medical Research Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100000925","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Diabetes Obesity Metabolism"],"published-print":{"date-parts":[[2016,4]]},"abstract":"<jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>\n                      To investigate the effects of extended\u2010release (\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      ) niacin on apolipoprotein B\u201048 (\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048) kinetics in statin\u2010treated patients with type 2 diabetes (\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                      A total of 12 men with\n                      <jats:styled-content style=\"fixed-case\">T2DM<\/jats:styled-content>\n                      were randomized to rosuvastatin or rosuvastatin plus\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin for 12 weeks and then crossed to the alternate therapy. Postprandial metabolic studies were performed at the end of each treatment period.\n                      <jats:styled-content style=\"fixed-case\">D3<\/jats:styled-content>\n                      \u2010leucine tracer was administered as subjects consumed a high\u2010fat liquid meal.\n                      <jats:styled-content style=\"fixed-case\">ApoB<\/jats:styled-content>\n                      \u201048 kinetics were determined using stable isotope tracer kinetics with fractional catabolic rates (\n                      <jats:styled-content style=\"fixed-case\">FCRs<\/jats:styled-content>\n                      ) and secretion rates derived using a non\u2010steady\u2010state compartmental model. Area\u2010under\u2010the\u2010curve (\n                      <jats:styled-content style=\"fixed-case\">AUC<\/jats:styled-content>\n                      ) and incremental\n                      <jats:styled-content style=\"fixed-case\">AUC<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">iAUC<\/jats:styled-content>\n                      ) for plasma triglyceride and\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048 were also calculated over the 10\u2010h period after ingestion of the fat meal.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In statin\u2010treated patients with\n                      <jats:styled-content style=\"fixed-case\">T2DM<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048 concentration was lower with\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin (8.24 \u00b1 1.98 vs 5.48 \u00b1 1.14 mg\/l, p = 0.03) compared with statin alone. Postprandial triglyceride and\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048\n                      <jats:styled-content style=\"fixed-case\">AUC<\/jats:styled-content>\n                      were also significantly lower on\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin treatment (\u201015 and \u201026%, respectively; p &lt; 0.05), without any change to triglyceride and\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048\n                      <jats:styled-content style=\"fixed-case\">iAUC<\/jats:styled-content>\n                      .\n                      <jats:styled-content style=\"fixed-case\">ApoB<\/jats:styled-content>\n                      \u201048 secretion rate in the basal state (3.21 \u00b1 0.34 vs 2.50 \u00b1 0.31 mg\/kg\/day; p = 0.04) and number of\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048\u2010containing particles secreted in response to the fat load (1.35 \u00b1 0.19 vs 0.84 \u00b1 0.12 mg\/kg; p = 0.02) were lower on\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin.\n                      <jats:styled-content style=\"fixed-case\">ApoB<\/jats:styled-content>\n                      \u201048\n                      <jats:styled-content style=\"fixed-case\">FCR<\/jats:styled-content>\n                      was not altered with\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin (8.78 \u00b1 1.04 vs 9.17 \u00b1 1.26 pools\/day; p = 0.79).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">ER<\/jats:styled-content>\n                      niacin reduces\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048 concentration by lowering fasting and postprandial\n                      <jats:styled-content style=\"fixed-case\">apoB<\/jats:styled-content>\n                      \u201048 secretion rate. This effect may be beneficial for lowering atherogenic postprandial lipoproteins and may provide cardiovascular disease risk benefit in patients with\n                      <jats:styled-content style=\"fixed-case\">T2DM<\/jats:styled-content>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/dom.12622","type":"journal-article","created":{"date-parts":[[2015,12,18]],"date-time":"2015-12-18T03:04:59Z","timestamp":1450407899000},"page":"384-391","source":"Crossref","is-referenced-by-count":11,"title":["Effect of niacin on triglyceride\u2010rich lipoprotein apolipoprotein B\u201048 kinetics in statin\u2010treated patients with type 2 diabetes"],"prefix":"10.1111","volume":"18","author":[{"given":"J.","family":"Pang","sequence":"first","affiliation":[{"name":"Metabolic Research Centre, School of Medicine and Pharmacology University of Western Australia  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D. C.","family":"Chan","sequence":"additional","affiliation":[{"name":"Metabolic Research Centre, School of Medicine and Pharmacology University of Western Australia  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S. J.","family":"Hamilton","sequence":"additional","affiliation":[{"name":"Metabolic Research Centre, School of Medicine and Pharmacology University of Western Australia  Perth Western Australia Australia"},{"name":"Combined Universities Centre for Rural Health, University of Western Australia  Geraldton Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"V. S.","family":"Tenneti","sequence":"additional","affiliation":[{"name":"Metabolic Research Centre, School of Medicine and Pharmacology University of Western Australia  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G. F.","family":"Watts","sequence":"additional","affiliation":[{"name":"Metabolic Research Centre, School of Medicine and Pharmacology University of Western Australia  Perth Western Australia Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P. H. 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