{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,18]],"date-time":"2026-06-18T23:33:35Z","timestamp":1781825615900,"version":"3.54.5"},"reference-count":27,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"9","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2020,5,5]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              Proprotein convertase subtilisin\/kexin type 9 inhibitors (\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i) are used to reduce low\u2010density lipoprotein (\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              ) cholesterol.\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i use after initiation, as well as persistence with or alterations to other\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010lowering therapy after\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation, is not well understood.\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              We conducted a retrospective study of alirocumab or evolocumab (\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i) new users from July 2015 to December 2017 in the MarketScan Early View database of US commercial insurance beneficiaries. We determined the prevalence of\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i interruption (\u226530\u2010day gap in supply) and\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010lowering therapy use in the year after\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation. The average age of 6151 patients initiating\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i therapy was 63\u00a0years, 44.4% were women, and 76.8% had atherosclerotic cardiovascular disease. Overall, 52.2% (95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 50.8%\u201353.7%) of patients had an interruption in\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i therapy in the first year after treatment initiation and 62.5% remained on\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i therapy at 1\u2010year postinitiation. Also, 27.7% of patients were taking a statin at the time of\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation, with only 22.4% on statin therapy at 1\u00a0year after\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation. Ezetimibe use decreased from 20.9% at the time of\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation to 12.0% a year later. By 1\u00a0year after\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation, 44.0% of patients had experienced an interruption in all\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010lowering therapies, and 26.6% were no longer on any\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010lowering therapies.\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              After\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i initiation, statins were often discontinued, whereas more than half of patients experienced an interruption in\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i therapy. These results suggest that many new\n              <jats:styled-content style=\"fixed-case\">PCSK<\/jats:styled-content>\n              9i users may remain at high risk for cardiovascular events because of interruptions in\n              <jats:styled-content style=\"fixed-case\">LDL<\/jats:styled-content>\n              \u2010lowering therapy.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.119.014347","type":"journal-article","created":{"date-parts":[[2020,4,24]],"date-time":"2020-04-24T09:01:05Z","timestamp":1587718865000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":22,"title":["Use of Low\u2010Density Lipoprotein\u2013Lowering Therapies Before and After PCSK9 Inhibitor Initiation"],"prefix":"10.1161","volume":"9","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9841-2393","authenticated-orcid":false,"given":"Jennifer A.","family":"Rymer","sequence":"first","affiliation":[{"name":"Duke Clinical Research Institute Durham NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katherine E.","family":"Mues","sequence":"additional","affiliation":[{"name":"Center for Observational Research Amgen Inc Thousand Oaks CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Keri L.","family":"Monda","sequence":"additional","affiliation":[{"name":"Center for Observational Research Amgen Inc Thousand Oaks CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emily W.","family":"Bratton","sequence":"additional","affiliation":[{"name":"IQVIA, Real\u2010World Evidence Solutions Durham NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Heidi S.","family":"Wirtz","sequence":"additional","affiliation":[{"name":"Center for Observational Research Amgen Inc Thousand Oaks CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ted","family":"Okerson","sequence":"additional","affiliation":[{"name":"Center for Observational Research Amgen Inc Thousand Oaks CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert A.","family":"Overman","sequence":"additional","affiliation":[{"name":"NoviSci, Inc Durham NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. Alan","family":"Brookhart","sequence":"additional","affiliation":[{"name":"NoviSci, Inc Durham NC"},{"name":"University of North Carolina at Chapel Hill Chapel Hill NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paul","family":"Muntner","sequence":"additional","affiliation":[{"name":"Department of Epidemiology University of Alabama at Birmingham AL"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tracy Y.","family":"Wang","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute Durham NC"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"e_1_3_1_2_2","unstructured":"FDA Approval of Evolocumab . Available at: https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/label\/2017\/125522s014lbl.pdf. 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