{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T00:30:45Z","timestamp":1791851445378,"version":"4.3.4"},"reference-count":39,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"12","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["ATVB"],"published-print":{"date-parts":[[2024,12]]},"abstract":"<jats:sec>\n            <jats:title>BACKGROUND:<\/jats:title>\n            <jats:p>Chronic kidney disease confers a high risk of atherosclerotic cardiovascular disease (ASCVD), partly due to hyperlipidemia. Although statins reduce the risk of ASCVD in chronic kidney disease, residual risk persists. We investigated whether higher remnant cholesterol is associated with an increased risk of ASCVD in statin users and nonusers with impaired renal function.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>METHODS:<\/jats:title>\n            <jats:p>\n              We included 107\u2009925 individuals from CGPS (Copenhagen General Population Study) initiated in 2003 to 2015, of whom 10\u2009427 had impaired renal function (estimated glomerular filtration rate, &lt;60 mL\/min per 1.73 m\n              <jats:sup>2<\/jats:sup>\n              ). Remnant cholesterol was calculated from a standard lipid profile. ASCVD was myocardial infarction, coronary heart disease death, ischemic stroke, coronary artery bypass graft, or percutaneous coronary intervention extracted from Danish nationwide health registries from baseline through 2018; individuals with events before the start of follow-up were excluded from relevant analysis.\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>RESULTS:<\/jats:title>\n            <jats:p>In individuals with impaired renal function during up to 15 years of follow-up, 597 were diagnosed with myocardial infarction, 618 with ischemic stroke, and 1182 with ASCVD. In these individuals, a 1-mmol\/L (39 mg\/dL) higher remnant cholesterol level was associated with multivariable-adjusted hazard ratios of 1.22 (95% CI, 1.05\u20131.42) for myocardial infarction, 1.16 (95% CI, 0.97\u20131.38) for ischemic stroke, and 1.21 (95% CI, 1.08\u20131.36) for ASCVD. Corresponding hazard ratios for ASCVD were 1.40 (95% CI, 1.07\u20131.83) in statin users and 1.16 (95% CI, 1.01\u20131.34) in nonusers. Of the 1.36-fold excess risk of ASCVD in impaired versus normal renal function, elevated remnant cholesterol and elevated LDL (low-density lipoprotein) cholesterol explained 25% (95% CI, 2.5%\u201347%) and 0% in statin users and 8.3% (95% CI, 2.4%\u201314%) and 14% (95% CI, 6.4%\u201322%) in nonusers, respectively.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>CONCLUSIONS:<\/jats:title>\n            <jats:p>Our results suggest that higher remnant cholesterol is a good marker of increased risk of ASCVD in individuals with impaired renal function, while higher LDL cholesterol may not be. Patients with chronic kidney disease who have high levels of remnant cholesterol are identifiable through higher non-HDL (high-density lipoprotein) cholesterol or apoB levels.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/atvbaha.124.321387","type":"journal-article","created":{"date-parts":[[2024,10,24]],"date-time":"2024-10-24T09:00:37Z","timestamp":1729760437000},"page":"2647-2658","update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":23,"title":["Impaired Renal Function With Higher Remnant Cholesterol Related to Risk of Atherosclerotic Cardiovascular Disease: A Cohort Study"],"prefix":"10.1161","volume":"44","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9817-409X","authenticated-orcid":true,"given":"Daniel","family":"El\u00edas-L\u00f3pez","sequence":"first","affiliation":[{"name":"Department of Clinical Biochemistry (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"The Copenhagen General Population Study (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"Department of Endocrinology and Metabolism and Research Center of Metabolic Diseases, National Institute of Medical Sciences and Nutrition Salvador Zubir\u00e1n, M\u00e9xico City, M\u00e9xico (D.E.-L.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0435-1110","authenticated-orcid":true,"given":"Signe","family":"Vedel-Krogh","sequence":"additional","affiliation":[{"name":"Department of Clinical Biochemistry (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"The Copenhagen General Population Study (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark (S.V.-K., B.N.W., B.G.N.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9562-2897","authenticated-orcid":true,"given":"Camilla Jannie","family":"Kobylecki","sequence":"additional","affiliation":[{"name":"Department of Clinical Biochemistry (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"The Copenhagen General Population Study (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1913-7472","authenticated-orcid":true,"given":"Benjamin Nilsson","family":"Wadstr\u00f6m","sequence":"additional","affiliation":[{"name":"Department of Clinical Biochemistry (D.E.-L., S.V.-K., C.J.K., B.N.W., B.G.N.), Copenhagen University Hospital, Herlev Gentofte, Denmark."},{"name":"The Copenhagen General Population Study (D.E.-L., S.V.-K., 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