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   <subfield code="a">10.1007/s10620-010-1303-5</subfield>
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   <subfield code="a">Serum Markers and Intestinal Mucosal Injury in Chronic Gastrointestinal Ischemia</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Désirée van Noord, Peter Mensink, Robert de Knegt, Martine Ouwendijk, Jan Francke, Anneke van Vuuren, Bettina Hansen, Ernst Kuipers]</subfield>
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   <subfield code="a">Background: Diagnosing chronic gastrointestinal ischemia (CGI) is a challenging problem in clinical practice. Serum markers for CGI would be of great diagnostic value as a non-invasive test method. Aims: This study investigated serum markers in patients with well-defined ischemia. Furthermore, intestinal mucosal injury was also evaluated in CGI patients. Methods: Consecutive patients suspected of CGI were prospectively enrolled and underwent a diagnostic work-up consisting of gastrointestinal tonometry and either CT or MR angiography. Blood samples for analysis of intestinal fatty acid-binding protein (I-FABP), D-dimer, lactate dehydrogenase (LDH), leucocyte counts, C-reactive protein (CRP), and L-lactate were drawn before and after a standard meal. Intestinal mucosal injury was assessed with glutamine, citrulline and arginine in blood samples and compared to a sugar absorption test (SAT). Test reproducibility was validated in healthy subjects. Results: Forty patients and nine healthy subjects were included. Ischemia was diagnosed in 32 patients (80%). I-FABP, leucocyte counts, LDH, CRP, glutamine, citrulline, arginine and SAT levels did not differ between patients with and without ischemia. L-lactate concentration showed a significant elevation in ischemia patients as compared to non-ischemia patients. In ischemia patients, D-dimer levels showed a significant elevation postprandially as compared to D-dimer levels at baseline. However, these ischemia patients did not show intestinal mucosal injury. Conclusions: I-FABP, leucocyte counts, LDH and CRP levels are not clinically useful for the diagnosis of CGI. However, postprandial rises in L-lactate and D-dimer serum levels can serve as non-invasive indicators of CGI.</subfield>
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   <subfield code="a">The Author(s), 2010</subfield>
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   <subfield code="a">Early serum markers</subfield>
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   <subfield code="a">Late serum markers</subfield>
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   <subfield code="a">Chronic gastrointestinal ischemia</subfield>
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   <subfield code="a">Intestinal mucosal injury</subfield>
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   <subfield code="a">D -dimer</subfield>
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   <subfield code="a">L -lactate</subfield>
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   <subfield code="a">CA : Celiac artery</subfield>
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   <subfield code="a">CGI : Chronic gastrointestinal ischemia</subfield>
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   <subfield code="a">CRP : C-reactive protein</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">CTA : Computed tomography angiography</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">I-FABP : Intestinal fatty acid binding protein</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">IMA : Inferior mesenteric artery</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">LDH : Lactate dehydrogenase</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MRA : Magnetic resonance angiography</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">NOMI : Non-occlusive mesenteric ischemia</subfield>
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   <subfield code="a">SAT : Sugar absorption test</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SMA : Superior mesenteric artery</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">TM : 24-hour gastric and jejunal tonometry</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">van Noord</subfield>
   <subfield code="D">Désirée</subfield>
   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">Mensink</subfield>
   <subfield code="D">Peter</subfield>
   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">de Knegt</subfield>
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   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">Ouwendijk</subfield>
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   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">Francke</subfield>
   <subfield code="D">Jan</subfield>
   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">van Vuuren</subfield>
   <subfield code="D">Anneke</subfield>
   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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   <subfield code="u">Department of Gastroenterology and Hepatology, Erasmus MC—University Medical Center, ‘s-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands</subfield>
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