{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T02:39:06Z","timestamp":1790995146840,"version":"4.1.0"},"reference-count":26,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"18","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2018,9,18]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              In statin trials, men and women derived similar relative risk reductions in cardiovascular events per 39\u00a0mg\/\n              <jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>\n              low\u2010density lipoprotein cholesterol (\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C) reduction. We explored whether lower\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C levels and greater\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C percentage reductions than those achieved with statins are associated with reduced major adverse cardiovascular event (\n              <jats:styled-content style=\"fixed-case\">MACE<\/jats:styled-content>\n              ) rates in women as well as men.\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              Data pooled from 10 phase 3\n              <jats:styled-content style=\"fixed-case\">ODYSSEY<\/jats:styled-content>\n              randomized trials (n=4983) comparing alirocumab with control (placebo\/ezetimibe) were assessed for association between 39\u00a0mg\/dL lower on\u2010treatment\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C and percentage\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C change from baseline, and\n              <jats:styled-content style=\"fixed-case\">MACE<\/jats:styled-content>\n              risk by sex, using multivariable Cox regression. Mean baseline\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C was 135\u00a0mg\/dL (women) and 121\u00a0mg\/dL (men). Average on\u2010treatment\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C levels with alirocumab, ezetimibe, and placebo were 71, 114, and 134\u00a0mg\/dL, respectively, in women (n=1882) and 52, 93, and 122\u00a0mg\/dL, respectively, in men (n=3090). Overall, 36.5% and 58.7% of women and men, respectively, achieved on\u2010treatment\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C &lt;50\u00a0mg\/dL. Each 39\u00a0mg\/dL lower\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C was associated with a 33% and 22%\u00a0lower risk of\n              <jats:styled-content style=\"fixed-case\">MACE<\/jats:styled-content>\n              in women (\n              <jats:italic>P<\/jats:italic>\n              =0.0209) and men (\n              <jats:italic>P<\/jats:italic>\n              =0.0307), respectively, with no significant between\u2010sex difference (\n              <jats:italic>P<\/jats:italic>\n              for heterogeneity=0.4597). Results were similar when analyzed per 50%\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C reduction, 24% (\n              <jats:italic>P<\/jats:italic>\n              =0.1094) and 29% (\n              <jats:italic>P<\/jats:italic>\n              =0.0125) lower\n              <jats:styled-content style=\"fixed-case\">MACE<\/jats:styled-content>\n              risk in women and men, respectively (\n              <jats:italic>P<\/jats:italic>\n              for heterogeneity=0.7499). Alirocumab was generally well tolerated in both sexes.\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              The present analysis reinforces the notion that both sexes derive a similar cardiovascular benefit from\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C lowering. Although women had slightly higher on\u2010treatment\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C than men, both sexes showed a similar lower\n              <jats:styled-content style=\"fixed-case\">MACE<\/jats:styled-content>\n              risk with lower\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010C.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.118.009221","type":"journal-article","created":{"date-parts":[[2018,9,16]],"date-time":"2018-09-16T15:02:17Z","timestamp":1537110137000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":28,"title":["Lower On\u2010Treatment Low\u2010Density Lipoprotein Cholesterol and Major Adverse Cardiovascular Events in Women and Men: Pooled Analysis of 10 ODYSSEY Phase 3 Alirocumab Trials"],"prefix":"10.1161","volume":"7","author":[{"given":"Antonio J.","family":"Vallejo\u2010Vaz","sequence":"first","affiliation":[{"name":"Imperial Centre for Cardiovascular Disease Prevention Department of Primary Care and Public Health Imperial College London United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Henry N.","family":"Ginsberg","sequence":"additional","affiliation":[{"name":"Columbia University New York NY"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael H.","family":"Davidson","sequence":"additional","affiliation":[{"name":"Department of Medicine University of Chicago Medicine Chicago IL"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert H.","family":"Eckel","sequence":"additional","affiliation":[{"name":"University of Colorado Anschutz Medical Campus Aurora CO"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christopher P.","family":"Cannon","sequence":"additional","affiliation":[{"name":"Cardiovascular Medicine Innovation Brigham and Women's Hospital Boston MA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. Veronica","family":"Lee","sequence":"additional","affiliation":[{"name":"Sanofi Bridgewater NJ"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laurence","family":"Bessac","sequence":"additional","affiliation":[{"name":"Sanofi Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert","family":"Pordy","sequence":"additional","affiliation":[{"name":"Regeneron Pharmaceuticals, Inc. Tarrytown NY"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexia","family":"Letierce","sequence":"additional","affiliation":[{"name":"Sanofi Chilly\u2010Mazarin France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kausik K.","family":"Ray","sequence":"additional","affiliation":[{"name":"Imperial Centre for Cardiovascular Disease Prevention Department of Primary Care and Public Health Imperial College London United Kingdom"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1161\/CIRCULATIONAHA.110.968792"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.jacc.2013.11.002"},{"key":"e_1_3_2_4_2","doi-asserted-by":"publisher","DOI":"10.1093\/eurheartj\/ehw272"},{"key":"e_1_3_2_5_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(14)61368-4"},{"key":"e_1_3_2_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.jacc.2016.03.519"},{"key":"e_1_3_2_7_2","first-page":"2245","article-title":"European Society of Cardiology\/European Atherosclerosis Society Task Force consensus statement on proprotein convertase subtilisin\/kexin type 9 inhibitors: practical guidance for use in patients at very high cardiovascular risk","volume":"38","author":"Landmesser U","year":"2017","unstructured":"Landmesser U, Chapman MJ, Farnier M, Gencer B, Gielen S, Hovingh GK, Luscher TF, Sinning D, Tokgozoglu L, Wiklund O, Zamorano JL, Pinto FJ, Catapano AL; European Society of Cardiology, European Atherosclerosis Society . 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