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Prior observational studies suggest paradoxically better outcomes in hypercholesterolemic patients who sustain an acute myocardial infarction (\n                      <jats:styled-content style=\"fixed-case\">AMI<\/jats:styled-content>\n                      ), one of several known recurrent risk paradoxes. To date, the association of directly measured remnant lipoprotein cholesterol (\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C) with survival after an\n                      <jats:styled-content style=\"fixed-case\">AMI<\/jats:styled-content>\n                      has not been examined.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Hypothesis<\/jats:title>\n                    <jats:p>\n                      Higher\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C levels may be paradoxically associated with lower mortality.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We examined 2465\n                      <jats:styled-content style=\"fixed-case\">AMI<\/jats:styled-content>\n                      survivors in a prospective, 24\u2010center\n                      <jats:styled-content style=\"fixed-case\">US<\/jats:styled-content>\n                      study of\n                      <jats:styled-content style=\"fixed-case\">AMI<\/jats:styled-content>\n                      outcomes. Lipoprotein cholesterol subfractions were directly measured by ultracentrifugation. RLP\u2010C was defined as intermediate\u2010density lipoprotein cholesterol (\n                      <jats:styled-content style=\"fixed-case\">IDL<\/jats:styled-content>\n                      \u2010C) + very\u2010low\u2010density lipoprotein cholesterol subfraction 3 (\n                      <jats:styled-content style=\"fixed-case\">\n                        VLDL\n                        <jats:sub>3<\/jats:sub>\n                      <\/jats:styled-content>\n                      \u2010C). Given a linear relationship between\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C and mortality, we examined\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C by tertiles and continuously. Cox regression hazard ratios (\n                      <jats:styled-content style=\"fixed-case\">HRs<\/jats:styled-content>\n                      ) were adjusted for the Global Registry of Acute Coronary Events (\n                      <jats:styled-content style=\"fixed-case\">GRACE<\/jats:styled-content>\n                      ) score and 23 other covariates.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Participants were age 58 \u00b1 12 years (mean \u00b1\n                      <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>\n                      ), and 68% were men. After 2 years of follow\u2010up, 226 (9%) participants died. The mortality proportion was 12.4% in the lowest tertile of\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C (0\u201315 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      ), 8.5% in the middle tertile (16\u201323 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      ), and 6.8% in the highest tertile (24\u2013120 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      ;\n                      <jats:italic>P<\/jats:italic>\n                      &lt; 0.001). A 1\u2010\n                      <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>\n                      increase in\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C (11 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      ) predicted a 24% lower adjusted risk of 2\u2010year mortality (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      : 0.76, 95% confidence interval [\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      ]: 0.64\u20100.91). Similar results were found for a 1\u2010\n                      <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>\n                      increase in\n                      <jats:styled-content style=\"fixed-case\">IDL<\/jats:styled-content>\n                      \u2010C (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      per 8 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      : 0.80, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      : 0.67\u20100.96),\n                      <jats:styled-content style=\"fixed-case\">\n                        VLDL\n                        <jats:sub>3<\/jats:sub>\n                      <\/jats:styled-content>\n                      \u2010C (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      per 4 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      : 0.74, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      : 0.61\u20100.89), and very\u2010low\u2010density lipoprotein cholesterol (\n                      <jats:styled-content style=\"fixed-case\">VLDL<\/jats:styled-content>\n                      \u2010C;\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      per 8 mg\/\n                      <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n                      : 0.69, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      : 0.55\u20100.85).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Higher\n                      <jats:styled-content style=\"fixed-case\">RLP<\/jats:styled-content>\n                      \u2010C levels were associated with lower mortality 2 years after\n                      <jats:styled-content style=\"fixed-case\">AMI<\/jats:styled-content>\n                      despite rigorous adjustment for known confounders. Unknown protective factors or a lead\u2010time bias likely explains the paradox.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/clc.22470","type":"journal-article","created":{"date-parts":[[2015,10,13]],"date-time":"2015-10-13T13:53:17Z","timestamp":1444744397000},"page":"660-667","source":"Crossref","is-referenced-by-count":21,"title":["Remnant Lipoprotein Cholesterol and Mortality After Acute Myocardial Infarction: Further Evidence for a Hypercholesterolemia Paradox From the TRIUMPH Registry"],"prefix":"10.1002","volume":"38","author":[{"given":"Seth S.","family":"Martin","sequence":"first","affiliation":[{"name":"Johns Hopkins Ciccarone Center for the Prevention of Heart Disease  Baltimore Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kamil F.","family":"Faridi","sequence":"additional","affiliation":[{"name":"Johns Hopkins Ciccarone Center for the Prevention of Heart Disease  Baltimore 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