{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,23]],"date-time":"2025-08-23T05:16:21Z","timestamp":1755926181985,"version":"3.37.3"},"reference-count":42,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2018,3,25]],"date-time":"2018-03-25T00:00:00Z","timestamp":1521936000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Echocardiography"],"published-print":{"date-parts":[[2018,7]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Left ventricular noncompaction (<jats:styled-content style=\"fixed-case\">LVNC<\/jats:styled-content>) is associated with progressive <jats:styled-content style=\"fixed-case\">LV<\/jats:styled-content> systolic dysfunction and dilated cardiomyopathy. We aimed to investigate the echocardiographic and clinical characteristics associated with <jats:styled-content style=\"fixed-case\">LV<\/jats:styled-content> ejection fraction (<jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>) and moderate or greater systolic dysfunction in patients with <jats:styled-content style=\"fixed-case\">LVNC<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Our institutional echocardiography database was retrospectively reviewed between 2008 and 2014, and 62 patients with <jats:styled-content style=\"fixed-case\">LVNC<\/jats:styled-content> were identified. Forty\u2010three (69%) had moderate or greater <jats:styled-content style=\"fixed-case\">LV<\/jats:styled-content> systolic dysfunction (<jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>\u00a0\u2264\u00a040%) and were compared with 19 (31%) patients with preserved or mildly reduced <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content> (&gt;40%). Linear regression analyses were utilized to identify markers associated with <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>The mean age was 63\u00a0\u00b1\u00a017\u00a0years and noncompacted\u2010to\u2010compacted ratio was 2.3\u00a0\u00b1\u00a00.5, and was larger in patients with <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>\u00a0\u2264\u00a040% (2.4 vs 2.1; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.02). Patients with <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>\u00a0\u2264\u00a040% were older, had more congestive heart failure, significant <jats:styled-content style=\"fixed-case\">QRS<\/jats:styled-content> interval prolongation, and greater <jats:styled-content style=\"fixed-case\">LV<\/jats:styled-content> remodeling and worse mean global longitudinal strain (<jats:styled-content style=\"fixed-case\">GLS<\/jats:styled-content>). Multivariate regression analysis revealed increased age (standardized regression coefficient (\u03b2)\u00a0=\u00a0\u22120.17; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.04) and <jats:styled-content style=\"fixed-case\">QRS<\/jats:styled-content> duration (\u03b2\u00a0=\u00a0\u22120.13; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.08), congestive heart failure (\u03b2\u00a0=\u00a0\u22120.18; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.04), and worsened <jats:styled-content style=\"fixed-case\">GLS<\/jats:styled-content> (\u03b2\u00a0=\u00a0\u22120.40; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.001) were independently associated with decreased <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content> in the cohort (overall model fit <jats:italic>R<\/jats:italic><jats:sup>2\u00a0<\/jats:sup>=\u00a00.71; <jats:italic>P<\/jats:italic>\u00a0&lt;\u00a0.0001). Increased age (\u03b2\u00a0=\u00a0\u22120.49; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.01) and <jats:styled-content style=\"fixed-case\">QRS<\/jats:styled-content> duration (\u03b2\u00a0=\u00a0\u22120.50; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.002), and worsened <jats:styled-content style=\"fixed-case\">GLS<\/jats:styled-content> (\u03b2\u00a0=\u00a0\u22120.33; <jats:italic>P<\/jats:italic>\u00a0=\u00a0.04), were also associated with a lower <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content> in patients with <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content>\u00a0&gt;\u00a040%.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The independent markers associated with <jats:styled-content style=\"fixed-case\">LVEF<\/jats:styled-content> and moderate or greater <jats:styled-content style=\"fixed-case\">LV<\/jats:styled-content> systolic dysfunction in patients with <jats:styled-content style=\"fixed-case\">LVNC<\/jats:styled-content>, in particular <jats:styled-content style=\"fixed-case\">GLS<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">QRS<\/jats:styled-content> duration, may detect high\u2010risk candidates for more aggressive clinical surveillance and medical therapy.<\/jats:p><\/jats:sec>","DOI":"10.1111\/echo.13873","type":"journal-article","created":{"date-parts":[[2018,3,26]],"date-time":"2018-03-26T01:26:36Z","timestamp":1522027596000},"page":"941-948","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Echocardiographic and clinical markers of left ventricular ejection fraction and moderate or greater systolic dysfunction in left ventricular noncompaction cardiomyopathy"],"prefix":"10.1111","volume":"35","author":[{"given":"Ivan A.","family":"Arenas","sequence":"first","affiliation":[{"name":"Echocardiography Laboratory Division of Cardiology Columbia University 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