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The Incidence of IgG4-Related and Inflammatory Abdominal Aortic Aneurysm Is Rare in a 101 Patient Cohort
Abdominal aortic aneurysms (AAA) are the most frequent aortic dilation, with considerable morbidity and mortality. Inflammatory (infl) and IgG4-positive AAAs represent specific subtypes of unclear incidence and clinical significance. Here, histologic and serologic analyses with retrospective clinica...
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Published in: | Journal of clinical medicine 2023-06, Vol.12 (12), p.4029 |
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creator | Nackenhorst, Maja Carina Kapalla, Marvin Weidle, Simon Kirchhoff, Felix Zschäpitz, David Sieber, Sabine Reeps, Christian Eckstein, Hans-Henning Schneider, Heike Thaler, Markus Moog, Philipp Busch, Albert Sachs, Nadja |
description | Abdominal aortic aneurysms (AAA) are the most frequent aortic dilation, with considerable morbidity and mortality. Inflammatory (infl) and IgG4-positive AAAs represent specific subtypes of unclear incidence and clinical significance. Here, histologic and serologic analyses with retrospective clinical data acquisition are investigated via detailed histology, including morphologic (HE, EvG: inflammatory subtype, angiogenesis, and fibrosis) and immunhistochemic analyses (IgG and IgG4). In addition, complement factors C3/C4 and immunoglobulins IgG, IgG2, IgG4 and IgE were measured in serum samples and clinical data uses patients' metrics, as well as through semi-automated morphometric analysis (diameter, volume, angulation and vessel tortuosity). A total of 101 eligible patients showed five (5%) IgG4 positive (all scored 1) and seven (7%) inflammatory AAAs. An increased degree of inflammation was seen in IgG4 positive and inflAAA, respectively. However, serologic analysis revealed no increased levels of IgG or IgG4. The operative procedure time was not different for those cases and the short-term clinical outcomes were equal for the entire AAA cohort. Overall, the incidence of inflammatory and IgG4-positive AAA samples seems very low based on histologic and serum analyses. Both entities must be considered distinct disease phenotypes. Short-term operative outcomes were not different for both sub-cohorts. |
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Inflammatory (infl) and IgG4-positive AAAs represent specific subtypes of unclear incidence and clinical significance. Here, histologic and serologic analyses with retrospective clinical data acquisition are investigated via detailed histology, including morphologic (HE, EvG: inflammatory subtype, angiogenesis, and fibrosis) and immunhistochemic analyses (IgG and IgG4). In addition, complement factors C3/C4 and immunoglobulins IgG, IgG2, IgG4 and IgE were measured in serum samples and clinical data uses patients' metrics, as well as through semi-automated morphometric analysis (diameter, volume, angulation and vessel tortuosity). A total of 101 eligible patients showed five (5%) IgG4 positive (all scored 1) and seven (7%) inflammatory AAAs. An increased degree of inflammation was seen in IgG4 positive and inflAAA, respectively. However, serologic analysis revealed no increased levels of IgG or IgG4. The operative procedure time was not different for those cases and the short-term clinical outcomes were equal for the entire AAA cohort. Overall, the incidence of inflammatory and IgG4-positive AAA samples seems very low based on histologic and serum analyses. Both entities must be considered distinct disease phenotypes. Short-term operative outcomes were not different for both sub-cohorts.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm12124029</identifier><identifier>PMID: 37373722</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abdominal aneurysm ; Antibodies ; Aortic aneurysms ; Cardiovascular disease ; Chronic obstructive pulmonary disease ; Clinical medicine ; Clinical outcomes ; Diagnosis ; Health aspects ; Histology ; Hospitals ; Immunoglobulin G ; Inflammation ; Ischemia ; Laboratories ; Leukocytes ; Measurement ; Mortality ; Open source software ; Patients ; Risk factors ; Statistics ; Vein & artery diseases</subject><ispartof>Journal of clinical medicine, 2023-06, Vol.12 (12), p.4029</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c435t-3e73f6b96363e35547d72be735c13de9a6512da201a96fdcabe5fd6cc177ca8b3</cites><orcidid>0009-0005-2649-4082 ; 0000-0003-2374-0338 ; 0000-0001-8031-017X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2829816068/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2829816068?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37373722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nackenhorst, Maja Carina</creatorcontrib><creatorcontrib>Kapalla, Marvin</creatorcontrib><creatorcontrib>Weidle, Simon</creatorcontrib><creatorcontrib>Kirchhoff, Felix</creatorcontrib><creatorcontrib>Zschäpitz, David</creatorcontrib><creatorcontrib>Sieber, Sabine</creatorcontrib><creatorcontrib>Reeps, Christian</creatorcontrib><creatorcontrib>Eckstein, Hans-Henning</creatorcontrib><creatorcontrib>Schneider, Heike</creatorcontrib><creatorcontrib>Thaler, Markus</creatorcontrib><creatorcontrib>Moog, Philipp</creatorcontrib><creatorcontrib>Busch, Albert</creatorcontrib><creatorcontrib>Sachs, Nadja</creatorcontrib><title>The Incidence of IgG4-Related and Inflammatory Abdominal Aortic Aneurysm Is Rare in a 101 Patient Cohort</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>Abdominal aortic aneurysms (AAA) are the most frequent aortic dilation, with considerable morbidity and mortality. Inflammatory (infl) and IgG4-positive AAAs represent specific subtypes of unclear incidence and clinical significance. Here, histologic and serologic analyses with retrospective clinical data acquisition are investigated via detailed histology, including morphologic (HE, EvG: inflammatory subtype, angiogenesis, and fibrosis) and immunhistochemic analyses (IgG and IgG4). In addition, complement factors C3/C4 and immunoglobulins IgG, IgG2, IgG4 and IgE were measured in serum samples and clinical data uses patients' metrics, as well as through semi-automated morphometric analysis (diameter, volume, angulation and vessel tortuosity). A total of 101 eligible patients showed five (5%) IgG4 positive (all scored 1) and seven (7%) inflammatory AAAs. An increased degree of inflammation was seen in IgG4 positive and inflAAA, respectively. However, serologic analysis revealed no increased levels of IgG or IgG4. The operative procedure time was not different for those cases and the short-term clinical outcomes were equal for the entire AAA cohort. Overall, the incidence of inflammatory and IgG4-positive AAA samples seems very low based on histologic and serum analyses. Both entities must be considered distinct disease phenotypes. Short-term operative outcomes were not different for both sub-cohorts.</description><subject>Abdominal aneurysm</subject><subject>Antibodies</subject><subject>Aortic aneurysms</subject><subject>Cardiovascular disease</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Clinical medicine</subject><subject>Clinical outcomes</subject><subject>Diagnosis</subject><subject>Health aspects</subject><subject>Histology</subject><subject>Hospitals</subject><subject>Immunoglobulin G</subject><subject>Inflammation</subject><subject>Ischemia</subject><subject>Laboratories</subject><subject>Leukocytes</subject><subject>Measurement</subject><subject>Mortality</subject><subject>Open source software</subject><subject>Patients</subject><subject>Risk factors</subject><subject>Statistics</subject><subject>Vein & artery diseases</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkkFr3DAQhU1paUKaU-9F0EuhOJU0tmSfilnaZCHQEtKzkKXxrhZbSiU7sP--WpImm1LNQWLmmyfpMUXxntELgJZ-2ZmJccYryttXxSmnUpYUGnh9dD4pzlPa0byapuJMvi1OQB6C89Nie7tFsvbGWfQGSRjIenNZlTc46hkt0d7m6jDqadJziHvS9TZMzuuRdCHOzpDO4xL3aSLrRG50ROI80YRRRn7q2aGfySpsM_queDPoMeH5435W_Pr-7XZ1VV7_uFyvuuvSVFDPJaCEQfStAAEIdV1JK3mfk7VhYLHVombcak6ZbsVgje6xHqwwhklpdNPDWfH1Qfdu6Se0Jr8g6lHdRTfpuFdBO_Wy4t1WbcK9YtnCpuVNVvj0qBDD7wXTrCaXDI6j9hiWpDJChagqqDL68R90F5aY3TlQWY4JKppnaqNHVM4PIV9sDqKqk3UDUAuATF38h8phcXImeBxczr9o-PzQYGJIKeLw9ElG1WE41NFwZPrDsS9P7N9RgD97lbIG</recordid><startdate>20230613</startdate><enddate>20230613</enddate><creator>Nackenhorst, Maja Carina</creator><creator>Kapalla, Marvin</creator><creator>Weidle, Simon</creator><creator>Kirchhoff, Felix</creator><creator>Zschäpitz, David</creator><creator>Sieber, Sabine</creator><creator>Reeps, Christian</creator><creator>Eckstein, Hans-Henning</creator><creator>Schneider, Heike</creator><creator>Thaler, Markus</creator><creator>Moog, Philipp</creator><creator>Busch, Albert</creator><creator>Sachs, Nadja</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0009-0005-2649-4082</orcidid><orcidid>https://orcid.org/0000-0003-2374-0338</orcidid><orcidid>https://orcid.org/0000-0001-8031-017X</orcidid></search><sort><creationdate>20230613</creationdate><title>The Incidence of IgG4-Related and Inflammatory Abdominal Aortic Aneurysm Is Rare in a 101 Patient Cohort</title><author>Nackenhorst, Maja Carina ; 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Inflammatory (infl) and IgG4-positive AAAs represent specific subtypes of unclear incidence and clinical significance. Here, histologic and serologic analyses with retrospective clinical data acquisition are investigated via detailed histology, including morphologic (HE, EvG: inflammatory subtype, angiogenesis, and fibrosis) and immunhistochemic analyses (IgG and IgG4). In addition, complement factors C3/C4 and immunoglobulins IgG, IgG2, IgG4 and IgE were measured in serum samples and clinical data uses patients' metrics, as well as through semi-automated morphometric analysis (diameter, volume, angulation and vessel tortuosity). A total of 101 eligible patients showed five (5%) IgG4 positive (all scored 1) and seven (7%) inflammatory AAAs. An increased degree of inflammation was seen in IgG4 positive and inflAAA, respectively. However, serologic analysis revealed no increased levels of IgG or IgG4. The operative procedure time was not different for those cases and the short-term clinical outcomes were equal for the entire AAA cohort. Overall, the incidence of inflammatory and IgG4-positive AAA samples seems very low based on histologic and serum analyses. Both entities must be considered distinct disease phenotypes. Short-term operative outcomes were not different for both sub-cohorts.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37373722</pmid><doi>10.3390/jcm12124029</doi><orcidid>https://orcid.org/0009-0005-2649-4082</orcidid><orcidid>https://orcid.org/0000-0003-2374-0338</orcidid><orcidid>https://orcid.org/0000-0001-8031-017X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdominal aneurysm Antibodies Aortic aneurysms Cardiovascular disease Chronic obstructive pulmonary disease Clinical medicine Clinical outcomes Diagnosis Health aspects Histology Hospitals Immunoglobulin G Inflammation Ischemia Laboratories Leukocytes Measurement Mortality Open source software Patients Risk factors Statistics Vein & artery diseases |
title | The Incidence of IgG4-Related and Inflammatory Abdominal Aortic Aneurysm Is Rare in a 101 Patient Cohort |
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