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It is not known whether the\n                      <jats:italic>JAK2V617F<\/jats:italic>\n                      mutation is associated with increased cardiac calcification.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Aim<\/jats:title>\n                    <jats:p>\n                      To investigate if a higher\n                      <jats:italic>JAK2V617F<\/jats:italic>\n                      variant allele frequency (\n                      <jats:italic>VAF<\/jats:italic>\n                      ) is associated with severe coronary atherosclerosis and the presence of aortic valve calcification (AVC).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Patients with MPNs were examined by cardiac computer tomography to establish coronary artery calcium score (CACS) and AVC score. The first\n                      <jats:italic>VAF<\/jats:italic>\n                      after diagnosis was registered. Severe coronary atherosclerosis was defined as a CACS &gt;400 and AVC was defined as an AVC score &gt;0.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among 161 patients, 137 were\n                      <jats:italic>JAK2V617F<\/jats:italic>\n                      mutation\u2010positive, with a median\n                      <jats:italic>VAF<\/jats:italic>\n                      of 26% (interquartile range 12%\u201352%). A\n                      <jats:italic>VAF<\/jats:italic>\n                      in the upper quartile range was associated with a CACS &gt;400 [odds ratio (OR) 15.96, 95% confidence interval [CI] 2.13\u2013119.53,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u2009.0070], after adjustment for cardiovascular risk factors and MPN subtype. An association was not found for the presence of AVC (OR 2.30, 95% CI 0.47\u201311.33,\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.31).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      In patients with MPNs, there is a significant association between having a\n                      <jats:italic>VAF<\/jats:italic>\n                      in the upper quartile (&gt;52%), and severe coronary atherosclerosis, defined as a CACS &gt;400. The presence of AVC is not associated with\n                      <jats:italic>VAF<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/ejh.14019","type":"journal-article","created":{"date-parts":[[2023,6,8]],"date-time":"2023-06-08T00:37:42Z","timestamp":1686184662000},"page":"400-406","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["High\n                    <i>JAK2V617F variant allele frequency<\/i>\n                    is associated with coronary artery but not aortic valve calcifications in patients with Philadelphia\u2010negative myeloproliferative neoplasms"],"prefix":"10.1111","volume":"111","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7514-9083","authenticated-orcid":false,"given":"Camilla Nordheim","family":"Solli","sequence":"first","affiliation":[{"name":"Department of Cardiology Zealand University Hospital  Roskilde 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