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<journal-meta>
<journal-id journal-id-type="publisher-id">CC</journal-id>
<journal-id journal-id-type="nlm-ta">Cardiol Croat</journal-id>
<journal-title-group>
<journal-title>Cardiologia Croatica</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Cardiol. Croat.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">1848-543X</issn>
<issn pub-type="epub">1848-5448</issn>
<publisher><publisher-name>Croatian Cardiac Society</publisher-name></publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">CC_13(5-6)_200</article-id>
<article-id pub-id-type="doi">10.15836/ccar2018.200</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Extended Abstract</subject></subj-group>
</article-categories>
<title-group>
<article-title>Global longitudinal strain and red cell distribution width in patients with mild, moderate and severe aortic stenosis, preserved left ventricular ejection fraction and unestablished coronary artery diseases: improving prediction of left ventricle dysfunction with a simple test</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2637-9691</contrib-id><name><surname>Jurin</surname><given-names>Ivana</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9644-9739</contrib-id><name><surname>&#x0160;u&#x0161;njar</surname><given-names>Dubravka</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6602-699X</contrib-id><name><surname>Varvodi&#x0107;</surname><given-names>Josip</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7735-6721</contrib-id><name><surname>Rude&#x017E;</surname><given-names>Igor</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9688-8582</contrib-id><name><surname>Pai&#x0107;</surname><given-names>Frane</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3768-9134</contrib-id><name><surname>Had&#x017E;ibegovi&#x0107;</surname><given-names>Irzal</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1">*</xref></contrib>
<aff id="aff1"><label>1</label><institution>University Hospital Dubrava</institution>, <addr-line>Zagreb</addr-line>, <country>Croatia</country></aff>
<aff id="aff2"><label>2</label><institution>University of Zagreb School of Medicine</institution>, <addr-line>Zagreb</addr-line>, <country>Croatia</country></aff>
</contrib-group>
<author-notes>
<corresp id="cor1"><label>*</label>ADDRESS FOR CORRESPONDENCE: Irzal Had&#x017E;ibegovi&#x0107;, Klini&#x010D;ka bolnica Dubrava, Avenija Gojka &#x0160;u&#x0161;ka 6, HR-10000 Zagreb, Croatia. / E-mail: <email xlink:href="irzalh@gmail.com">irzalh@gmail.com</email></corresp></author-notes>
<pub-date pub-type="epub-ppub"><month>06</month><year>2018</year></pub-date>
<volume>13</volume>
<issue>5-6</issue>
<fpage>200</fpage>
<lpage>200</lpage>
<history>
<date date-type="received"><day>01</day><month>05</month><year>2018</year></date><date date-type="accepted"><day>10</day><month>05</month><year>2018</year></date>
</history>
<permissions>
<copyright-year>2018</copyright-year>
<copyright-holder>Croatian Cardiac Society</copyright-holder>
</permissions>
<kwd-group kwd-group-type="author"><title>Keywords: </title><kwd>global longitudinal strain</kwd><kwd>aortic stenosis</kwd><kwd>red cell distribution width</kwd></kwd-group>
</article-meta>
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<body>
<p><bold>Background</bold>: Patients with preserved left ventricular ejection fraction (EF) and aortic stenosis have often increased global longitudinal strain as a sign of intrinsic left ventricular impairment. Heart failure due to left ventricular deformation is also shown to be predicted with simple blood count test like red cell distribution width (RDW). We evaluated the correlation of GLS and RDW patients with different severity stage of aortic stenosis and signs of left ventricular strain.</p>
<p><bold>Methods</bold>: We recorded relevant clinical, laboratory, and echocardiographic parameters, and measured global longitudinal strain (GLS) in 83 patients with EF &gt; 45% and mild, moderate, and severe aortic stenosis (AS) in whom coronary artery disease was previously excluded. GLS was obtained using 2D speckle tracking echocardiography. RDW was easily obtained from full blood count that is routinely measured.</p>
<p><bold>Results:</bold> Mean velocity and aortic valve area was 2.73 m/s and 1.72 cm<sup>2</sup>, 3.37 m/s and 1,33 cm<sup>2</sup>, and 4.62 m/s and 0.74 cm<sup>2</sup> in patients with mild, moderate and severe AS, respectively. Mean GLS was -18.82%, -17.7% and -16.85% in patients with mild, moderate and severe AS, and did not differ significantly. Patients with severe aortic stenosis had significantly higher left ventricular mass index and NT-pro BNP levels compared to patients with mild and moderate AS (186.66 g/m<sup>2</sup> vs 133.57 and 169.57 g/m<sup>2</sup>, and 2644.69 pg/ml vs 312.71 vs 403.2 pg/ml, respectively). Among patients with mild aortic stenosis regression analysis showed significant positive correlation of GLS with RDW (beta 0.590, R square 0.34, p=0.005). That correlation was not confirmed for GLS and NT-pro BNP.</p>
<p><bold>Conclusion</bold>: GLS did not differ significantly among patients with different severity of AS, although patients with severe AS had highest values of GLS. Among patients with moderate AS, RDW showed to be a good predictor of impaired left ventricular function measured by GLS, and therefore it could be further evaluated as a tool in early selection for treatment of patients with moderate AS, preserved EF and no coronary artery disease.</p>
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