{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T00:29:36Z","timestamp":1791851376809,"version":"4.3.4"},"reference-count":47,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["CJASN"],"published-print":{"date-parts":[[2017,2]]},"abstract":"<jats:sec>\n                    <jats:title>Background and objectives<\/jats:title>\n                    <jats:p>\n                      Patients receiving hemodialysis are at risk of cardiovascular events. A novel blood test (\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      test) determines the individual calcification propensity of blood.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design, setting, participants, &amp; measurements<\/jats:title>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      was determined in 2785 baseline serum samples of patients receiving hemodialysis enrolled in the Evaluation of Cinacalcet Therapy to Lower Cardiovascular Events (EVOLVE) trial and the\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      results were related to patient outcomes.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Serum albumin, bicarbonate, HDL cholesterol, and creatinine were the main factors positively\/directly and phosphate was the main factor negatively\/inversely associated with\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      . The primary composite end point (all-cause mortality, myocardial infarction [MI], hospitalization for unstable angina, heart failure, or peripheral vascular event [PVE]) was reached in 1350 patients after a median follow-up time of 619 days. After adjustments for confounding, a lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      was independently associated with a higher risk of the primary composite end point as a continuous measure (hazard ratio [HR] per 1 SD lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      , 1.15; 95% confidence interval [95% CI], 1.08 to 1.22;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001). Furthermore, lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      was associated with a higher risk in all-cause mortality (HR per 1 SD lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      , 1.10; 95% CI, 1.02 to 1.17;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.001), MI (HR per 1 SD lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      , 1.38; 95% CI, 1.19 to 1.60;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001), and PVE (HR per 1 SD lower\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      , 1.22; 95% CI, 1.05 to 1.42;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.01).\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      improved risk prediction (integrated discrimination improvement and net reclassification improvement,\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt;0.001 and\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      =0.001) of the primary composite end point.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Blood calcification propensity was independently associated with the primary composite end point, all-cause mortality, MI, and PVE in the EVOLVE study and improved risk prediction. Prospective trials should clarify whether\n                      <jats:italic toggle=\"yes\">T<\/jats:italic>\n                      <jats:sub>50<\/jats:sub>\n                      -guided therapies improve outcomes.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.2215\/cjn.04720416","type":"journal-article","created":{"date-parts":[[2016,12,9]],"date-time":"2016-12-09T22:21:54Z","timestamp":1481322114000},"page":"315-322","source":"Crossref","is-referenced-by-count":143,"title":["Blood Calcification Propensity, Cardiovascular Events, and Survival in Patients Receiving Hemodialysis in the EVOLVE Trial"],"prefix":"10.2215","volume":"12","author":[{"given":"Andreas","family":"Pasch","sequence":"first","affiliation":[{"name":"University of Bern, Bern, Switzerland;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Geoffrey A.","family":"Block","sequence":"additional","affiliation":[{"name":"Denver Nephrologists, Denver, Colorado;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthias","family":"Bachtler","sequence":"additional","affiliation":[{"name":"University of Bern, Bern, Switzerland;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Edward R.","family":"Smith","sequence":"additional","affiliation":[{"name":"The Royal Melbourne Hospital, Victoria, Melbourne, Australia;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wilhelm","family":"Jahnen-Dechent","sequence":"additional","affiliation":[{"name":"Rheinisch-Westfaelische Technische Hochschule University of Aachen, Aachen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Spyridon","family":"Arampatzis","sequence":"additional","affiliation":[{"name":"University of Bern, Bern, Switzerland;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Glenn M.","family":"Chertow","sequence":"additional","affiliation":[{"name":"Stanford University School of Medicine, Palo Alto, California;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Parfrey","sequence":"additional","affiliation":[{"name":"Health Sciences Center, St. John\u2019s, Newfoundland, Canada; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaoye","family":"Ma","sequence":"additional","affiliation":[{"name":"Amgen, Thousand Oaks, California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juergen","family":"Floege","sequence":"additional","affiliation":[{"name":"Rheinisch-Westfaelische Technische Hochschule University of Aachen, Aachen, Germany;"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2016,12,9]]},"reference":[{"key":"B1-20230813","doi-asserted-by":"crossref","first-page":"1296","DOI":"10.1056\/NEJMoa041031","article-title":"Chronic kidney disease and the risks of death, cardiovascular events, and 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