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<art>
   <ui>cc2149</ui>
   <ji>CCJ</ji>
   <fm>
      <dochead>Meeting abstract</dochead>
      <bibl>
         <title>
            <p>Role of parathyroid-hormone-related peptide in volume or pressure loaded pulmonary vasculature</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Zimmermann</snm>
               <fnm>R</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Kreuder</snm>
               <fnm>J</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Sokolova</snm>
               <fnm>J</fnm>
               <insr iid="I2"/>
            </au>
            <au id="A4">
               <snm>Michel-Behnke</snm>
               <fnm>I</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A5">
               <snm>Schranz</snm>
               <fnm>D</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A6">
               <snm>Schl&#252;ter</snm>
               <fnm>KD</fnm>
               <insr iid="I2"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Paediatric Cardiology, University of Giessen, Germany</p>
            </ins>
            <ins id="I2">
               <p>Department of Physiology, University of Giessen, Germany</p>
            </ins>
         </insg>
         <source>Critical Care</source>
         <supplement>
            <title>
               <p>4th International Symposium on the Pathophysiology of Cardiopulmonary Bypass: Endothelial Damage. Abstracts</p>
            </title>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>4th International Symposium on the Pathophysiology of Cardiopulmonary Bypass: Endothelial Damage. Abstracts</p>
            </title>
            <location>Munich, Germany</location>
            <date-range>29 November 2002</date-range>
         </conference>
         <issn>1364-8535</issn>
         <pubdate>2003</pubdate>
         <volume>7</volume>
         <issue>Suppl 1</issue>
         <fpage>3</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/cc2149</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>18</day>
               <month>2</month>
               <year>2003</year>
            </date>
         </pub>
      </history>
   </fm>
   <bdy>
      <sec>
         <st>
            <p>Objectives</p>
         </st>
         <p>Parathyroid-hormone-related peptide (PTHrP) is a paracrine factor expressed throughout the body with vasodilatative qualities. <it>In vitro</it>, PTHrP is released from the endothelium via a mechano-sensitive mechanism. <it>In vivo </it>data on changes in PTHrP release were collected in two pediatric patient groups.</p>
      </sec>
      <sec>
         <st>
            <p>Methods</p>
         </st>
         <p>(A) Twenty patients (median age 6.1 years), pre- and postinterventional closure of an atrial septal defect (ASD), preclosure Qp/Qs 2.1 &#177; 0.24. (B) Twenty patients (median age 8.1 years) with pulmonary hypertension (PHT), Rp/Rs 0.36&#8211;1.79. (A) Blood samples from pulmonary artery (PA), left atrium (LA), systemic artery (SA) and superior vena cava (SVC); and (B) from PA and SA (baseline, after oxygen and after nebulized iloprost). Determination of PTHrP concentrations ([PTHrP]) by quantitative immunoblot, normalized to SA-[PTHrP], compared by Mann&#8211;Whitney U-test. Assessment of average peak (blood flow) velocity (APV) in the PA with intraluminal flow wire (FloMap, Cardiometrics).</p>
      </sec>
      <sec>
         <st>
            <p>Results PHT</p>
         </st>
         <p>In all 11/20 patients with significant oxygen- or ilo-prost-induced drop in Rp/Rs, a significant difference in baseline [PTHrP] was found (PA +43.4 &#177; 6.1% [<it>P </it>= 0.05] compared with SA). After pressure drop (induced by oxygen/iloprost) [PTHrP] decreased from PA/SA-[PTHrP] of 1.49 &#177; 0.27 &#8594; 1.02 &#177; 0.17 (<it>P </it>= 0.02) and 1.51 &#177; 0.21 &#8594; 0.88 &#177; 0.16 (<it>P </it>= 0.0001), respectively. In all patients with lack of inducible vascular reactivity (9/20) no difference was seen in [PTHrP] before (-6.5 &#177; 2.0%) or after drug application. In addition, an increase in APV after infusion of the endothelium-dependent vasodilator acetylcholine was only seen in patients with significant pressure-induced PTHrP release.</p>
      </sec>
      <sec>
         <st>
            <p>Results ASD</p>
         </st>
         <p>Preclosure [PTHrP] was 55 &#177; 14.4% higher in the PA than in the SA, further decreasing with distance from the PA: +11.5% &#177; 5.5% in the LA and -4.1 &#177; 6.4% in the SVC. Postclosure, the [PTHrP] decreased from +55% to +14.9 &#177; 4.1%.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusions</p>
         </st>
         <p>There is a clear <it>in vivo </it>correlation between volume (ASD) and pressure (PHT) load and [PTHrP] in the PA system, with an acute decrease in [PTHrP] following drop in volume and/or pressure. In children with PHT, PTHrP may be useful for assessing PA endothelial function and may play a role as a diagnostic or prognostic marker. In patients with ASD the [PTHrP] gradient indicates a release from the right heart and/or proximal PA.</p>
      </sec>
   </bdy>
</art>
