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									<identifier>oai:www.peertechzpublications.org:10.17352/ijcem.000025</identifier>
									<datestamp>2017-09-19</datestamp>
									<setSpec>PTZ.IJCEM:VOL3</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Protein S100A8/A9: A Potential New Biomarker for Pancreatic Diseases
										</dc:title><dc:creator>El Gammal AT</dc:creator><dc:creator> Sturm JH</dc:creator><dc:creator> Pinnschmidt HO</dc:creator><dc:creator> Hofmann BT</dc:creator><dc:creator> Bellon E</dc:creator><dc:creator> et al</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Objectives:&lt;/strong&gt; S100A8/A9&amp;nbsp; expression&amp;nbsp; has&amp;nbsp; been&amp;nbsp; linked&amp;nbsp; to&amp;nbsp; carcinogenesis&amp;nbsp; and&amp;nbsp; inflammation.We hypothesized&amp;nbsp; that&amp;nbsp; S100A8/A9&amp;nbsp; protein&amp;nbsp; serum&amp;nbsp; levels&amp;nbsp; are&amp;nbsp; a&amp;nbsp; useful&amp;nbsp; stratification&amp;nbsp; marker&amp;nbsp; for&amp;nbsp; patients&amp;nbsp; with pancreatic&amp;nbsp; ductal&amp;nbsp; adenocarcinoma&amp;nbsp; (PDAC),&amp;nbsp; intraductal&amp;nbsp; papillary&amp;nbsp; mucinous&amp;nbsp; neoplasm&amp;nbsp; (IPMN)&amp;nbsp; or&amp;nbsp; chronic pancreatitis (CP). &lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods:&lt;/strong&gt; S100A8/A9 serum levels were analysed in PDAC, CP and IPMN patients and compared to S100A8/A9 healthy donor controls (HD) using ELISA. S100A8/A9 levels and clinical data were statistically analysed. &lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results:&lt;/strong&gt; Out&amp;nbsp; of134&amp;nbsp; patients&amp;nbsp; included,&amp;nbsp; 84&amp;nbsp; were&amp;nbsp; diagnosed&amp;nbsp; with&amp;nbsp; PDAC&amp;nbsp; (46%),&amp;nbsp; 30&amp;nbsp; patients with&amp;nbsp; IPMN&amp;nbsp; (16%) and 20 patients with CP (11%), 50 patients were HD (27%). When compared to HD (343.3 ng/ml), S100A8/A9 serum concentration was elevated in PDAC (402.0 ng/ml, p = 0.001) and CP patients (426.51 ng/ml p &amp;lt; 0.001). Also, S100A8/A9 levels were elevated in PDAC compared to IPMN group (369.0 ng/ml p&amp;nbsp; =&amp;nbsp; 0.026)&amp;nbsp; and&amp;nbsp; in&amp;nbsp; CP&amp;nbsp; compared&amp;nbsp; to&amp;nbsp; IPMN&amp;nbsp; group&amp;nbsp; (p&amp;nbsp; =&amp;nbsp; 0.001).&amp;nbsp; A&amp;nbsp; multivariate&amp;nbsp; model&amp;nbsp; including&amp;nbsp; age,&amp;nbsp; gender, leukocyte levels, C-reactive protein (CrP), S100A8/A9 and CA 19-9 concentrations reported a diagnostic sensitivity of 74.8%.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; S100A8/A9 serum levels are increased in patients with PDAC, CP, and IPM might be useful to distinguish malignant and inflammatory diseases from normal and non-malignant pathological conditions.&lt;br&gt;&lt;/p&gt;&lt;br&gt;</dc:description>
										<dc:publisher>International Journal of Clinical Endocrinology and Metabolism - Peertechz Publications</dc:publisher>
										<dc:date>2017-09-19</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/ijcem.000025</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © El Gammal AT et al.</dc:rights>
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