Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis: An experience from a multicenter study in Saudi Arabia

Objectives: To understand the most common type and clinical manifestations of associated vasculitis (AAV) in the Saudi Arabia. Methods: This retrospective study was conducted at King Fahad Medical City and the Security Forces Hospital Program, Riyadh, Saudi Arabia, between January 2014 and May 2022....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Saudi medical journal 2023-05, Vol.44 (5), p.486-491
Hauptverfasser: Alfuwayris, Jumanah J, Almulhim, Amal M, Almansour, Mohammed A, Albadi, Marzouq A, Alhomood, Ibrahim A, Alblewi, Faisal, Althemery, Abdullah U
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 491
container_issue 5
container_start_page 486
container_title Saudi medical journal
container_volume 44
creator Alfuwayris, Jumanah J
Almulhim, Amal M
Almansour, Mohammed A
Albadi, Marzouq A
Alhomood, Ibrahim A
Alblewi, Faisal
Althemery, Abdullah U
description Objectives: To understand the most common type and clinical manifestations of associated vasculitis (AAV) in the Saudi Arabia. Methods: This retrospective study was conducted at King Fahad Medical City and the Security Forces Hospital Program, Riyadh, Saudi Arabia, between January 2014 and May 2022. Patients aged >18 years were included in the study and diagnosed based on clinical manifestations, serology, or histopathology according to the EMA algorithm. Univariate analysis was carried out to compare different groups; a series of independent samples t-tests was applied for continuous data. Results: A total of 53 patients were enrolled: eosinophilic granulomatosis with polyangiitis (EGPA), granulomatosis with polyangiitis (GPA), and microscopic polyangiitis (MPA). Overall, proteinase-3 was the most prevalent (52.8%), and myeloperoxidase, myeloperoxidase MPO was the least prevalent antineutrophil cytoplasmic antibody (ANCA)-type (18.9%) among patients; other patients showed negative ANCA test results. The clinical manifestations differed significantly between EGPA and GPA groups in pulmonary, neurological, cardiological, and renal signs and symptoms (p
doi_str_mv 10.15537/smj.2023.44.5.20220818
format Article
fullrecord <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_gale_infotracmisc_A758626892</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A758626892</galeid><sourcerecordid>A758626892</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1482-786023264e24f614f7679501003cef44de15c6d11298c058bdee3c348ace15393</originalsourceid><addsrcrecordid>eNptUE1LAzEQDaJgrf4GFzzvmu9kj6X4BQUv9hzS2URTdjdlkwr996ZWD4LMYYZ57w1vHkK3BDdECKbu07BtKKas4bwRx4liTfQZmhEpdM2IEudohplqa0E1v0RXKW0xZlJiOUPrZRyGOFbQhzGA7audzdlNYxV9ZcccRrfPU9x9hL6CQ4673qYhwDe0id2hqm1KEYLNrqs-bYJ9H3JI1-jC2z65m58-R-vHh7flc716fXpZLlY1EK5prbQsvqnkjnIvCfdKqlZgUtyB85x3jgiQHSG01YCF3nTOMWBcWygIa9kc3Z3uvtvemTD6mCcLQ0hgFkpoSaVuaWE1_7BKda78EkfnQ9n_EaiTAKaY0uS82U1hsNPBEGy-QzcldHMM3XBuhPkNnX0BzeF1tw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis: An experience from a multicenter study in Saudi Arabia</title><source>PubMed Central Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Alfuwayris, Jumanah J ; Almulhim, Amal M ; Almansour, Mohammed A ; Albadi, Marzouq A ; Alhomood, Ibrahim A ; Alblewi, Faisal ; Althemery, Abdullah U</creator><creatorcontrib>Alfuwayris, Jumanah J ; Almulhim, Amal M ; Almansour, Mohammed A ; Albadi, Marzouq A ; Alhomood, Ibrahim A ; Alblewi, Faisal ; Althemery, Abdullah U</creatorcontrib><description>Objectives: To understand the most common type and clinical manifestations of associated vasculitis (AAV) in the Saudi Arabia. Methods: This retrospective study was conducted at King Fahad Medical City and the Security Forces Hospital Program, Riyadh, Saudi Arabia, between January 2014 and May 2022. Patients aged &gt;18 years were included in the study and diagnosed based on clinical manifestations, serology, or histopathology according to the EMA algorithm. Univariate analysis was carried out to compare different groups; a series of independent samples t-tests was applied for continuous data. Results: A total of 53 patients were enrolled: eosinophilic granulomatosis with polyangiitis (EGPA), granulomatosis with polyangiitis (GPA), and microscopic polyangiitis (MPA). Overall, proteinase-3 was the most prevalent (52.8%), and myeloperoxidase, myeloperoxidase MPO was the least prevalent antineutrophil cytoplasmic antibody (ANCA)-type (18.9%) among patients; other patients showed negative ANCA test results. The clinical manifestations differed significantly between EGPA and GPA groups in pulmonary, neurological, cardiological, and renal signs and symptoms (p&lt;0.05); there was a higher incidence of the former 3 in the EGPA group. Although upper airway was predominant in all groups, there was no statistical difference between both groups. Conclusion: This study validated international reports on AAV clinical manifestations in the Saudi population. The GPA was associated with more upper airway and pulmonary signs and symptoms. Further investigation is needed to understand the treatments and quality of life of patients with AAV. Keywords: antineutrophil cytoplasmic antibody, AN CA-associated vasculitis, autoimmune disorder, Saudi Arabia, clinical manifestations [phrase omitted]</description><identifier>ISSN: 0379-5284</identifier><identifier>EISSN: 1658-3175</identifier><identifier>DOI: 10.15537/smj.2023.44.5.20220818</identifier><language>eng</language><publisher>Saudi Medical Journal</publisher><subject>Autoantibodies ; Autoimmune diseases ; Complications and side effects ; Development and progression ; Health aspects ; Vasculitis</subject><ispartof>Saudi medical journal, 2023-05, Vol.44 (5), p.486-491</ispartof><rights>COPYRIGHT 2023 Saudi Medical Journal</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids></links><search><creatorcontrib>Alfuwayris, Jumanah J</creatorcontrib><creatorcontrib>Almulhim, Amal M</creatorcontrib><creatorcontrib>Almansour, Mohammed A</creatorcontrib><creatorcontrib>Albadi, Marzouq A</creatorcontrib><creatorcontrib>Alhomood, Ibrahim A</creatorcontrib><creatorcontrib>Alblewi, Faisal</creatorcontrib><creatorcontrib>Althemery, Abdullah U</creatorcontrib><title>Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis: An experience from a multicenter study in Saudi Arabia</title><title>Saudi medical journal</title><description>Objectives: To understand the most common type and clinical manifestations of associated vasculitis (AAV) in the Saudi Arabia. Methods: This retrospective study was conducted at King Fahad Medical City and the Security Forces Hospital Program, Riyadh, Saudi Arabia, between January 2014 and May 2022. Patients aged &gt;18 years were included in the study and diagnosed based on clinical manifestations, serology, or histopathology according to the EMA algorithm. Univariate analysis was carried out to compare different groups; a series of independent samples t-tests was applied for continuous data. Results: A total of 53 patients were enrolled: eosinophilic granulomatosis with polyangiitis (EGPA), granulomatosis with polyangiitis (GPA), and microscopic polyangiitis (MPA). Overall, proteinase-3 was the most prevalent (52.8%), and myeloperoxidase, myeloperoxidase MPO was the least prevalent antineutrophil cytoplasmic antibody (ANCA)-type (18.9%) among patients; other patients showed negative ANCA test results. The clinical manifestations differed significantly between EGPA and GPA groups in pulmonary, neurological, cardiological, and renal signs and symptoms (p&lt;0.05); there was a higher incidence of the former 3 in the EGPA group. Although upper airway was predominant in all groups, there was no statistical difference between both groups. Conclusion: This study validated international reports on AAV clinical manifestations in the Saudi population. The GPA was associated with more upper airway and pulmonary signs and symptoms. Further investigation is needed to understand the treatments and quality of life of patients with AAV. Keywords: antineutrophil cytoplasmic antibody, AN CA-associated vasculitis, autoimmune disorder, Saudi Arabia, clinical manifestations [phrase omitted]</description><subject>Autoantibodies</subject><subject>Autoimmune diseases</subject><subject>Complications and side effects</subject><subject>Development and progression</subject><subject>Health aspects</subject><subject>Vasculitis</subject><issn>0379-5284</issn><issn>1658-3175</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNptUE1LAzEQDaJgrf4GFzzvmu9kj6X4BQUv9hzS2URTdjdlkwr996ZWD4LMYYZ57w1vHkK3BDdECKbu07BtKKas4bwRx4liTfQZmhEpdM2IEudohplqa0E1v0RXKW0xZlJiOUPrZRyGOFbQhzGA7audzdlNYxV9ZcccRrfPU9x9hL6CQ4673qYhwDe0id2hqm1KEYLNrqs-bYJ9H3JI1-jC2z65m58-R-vHh7flc716fXpZLlY1EK5prbQsvqnkjnIvCfdKqlZgUtyB85x3jgiQHSG01YCF3nTOMWBcWygIa9kc3Z3uvtvemTD6mCcLQ0hgFkpoSaVuaWE1_7BKda78EkfnQ9n_EaiTAKaY0uS82U1hsNPBEGy-QzcldHMM3XBuhPkNnX0BzeF1tw</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Alfuwayris, Jumanah J</creator><creator>Almulhim, Amal M</creator><creator>Almansour, Mohammed A</creator><creator>Albadi, Marzouq A</creator><creator>Alhomood, Ibrahim A</creator><creator>Alblewi, Faisal</creator><creator>Althemery, Abdullah U</creator><general>Saudi Medical Journal</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230501</creationdate><title>Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis</title><author>Alfuwayris, Jumanah J ; Almulhim, Amal M ; Almansour, Mohammed A ; Albadi, Marzouq A ; Alhomood, Ibrahim A ; Alblewi, Faisal ; Althemery, Abdullah U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1482-786023264e24f614f7679501003cef44de15c6d11298c058bdee3c348ace15393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Autoantibodies</topic><topic>Autoimmune diseases</topic><topic>Complications and side effects</topic><topic>Development and progression</topic><topic>Health aspects</topic><topic>Vasculitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alfuwayris, Jumanah J</creatorcontrib><creatorcontrib>Almulhim, Amal M</creatorcontrib><creatorcontrib>Almansour, Mohammed A</creatorcontrib><creatorcontrib>Albadi, Marzouq A</creatorcontrib><creatorcontrib>Alhomood, Ibrahim A</creatorcontrib><creatorcontrib>Alblewi, Faisal</creatorcontrib><creatorcontrib>Althemery, Abdullah U</creatorcontrib><collection>CrossRef</collection><jtitle>Saudi medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alfuwayris, Jumanah J</au><au>Almulhim, Amal M</au><au>Almansour, Mohammed A</au><au>Albadi, Marzouq A</au><au>Alhomood, Ibrahim A</au><au>Alblewi, Faisal</au><au>Althemery, Abdullah U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis: An experience from a multicenter study in Saudi Arabia</atitle><jtitle>Saudi medical journal</jtitle><date>2023-05-01</date><risdate>2023</risdate><volume>44</volume><issue>5</issue><spage>486</spage><epage>491</epage><pages>486-491</pages><issn>0379-5284</issn><eissn>1658-3175</eissn><abstract>Objectives: To understand the most common type and clinical manifestations of associated vasculitis (AAV) in the Saudi Arabia. Methods: This retrospective study was conducted at King Fahad Medical City and the Security Forces Hospital Program, Riyadh, Saudi Arabia, between January 2014 and May 2022. Patients aged &gt;18 years were included in the study and diagnosed based on clinical manifestations, serology, or histopathology according to the EMA algorithm. Univariate analysis was carried out to compare different groups; a series of independent samples t-tests was applied for continuous data. Results: A total of 53 patients were enrolled: eosinophilic granulomatosis with polyangiitis (EGPA), granulomatosis with polyangiitis (GPA), and microscopic polyangiitis (MPA). Overall, proteinase-3 was the most prevalent (52.8%), and myeloperoxidase, myeloperoxidase MPO was the least prevalent antineutrophil cytoplasmic antibody (ANCA)-type (18.9%) among patients; other patients showed negative ANCA test results. The clinical manifestations differed significantly between EGPA and GPA groups in pulmonary, neurological, cardiological, and renal signs and symptoms (p&lt;0.05); there was a higher incidence of the former 3 in the EGPA group. Although upper airway was predominant in all groups, there was no statistical difference between both groups. Conclusion: This study validated international reports on AAV clinical manifestations in the Saudi population. The GPA was associated with more upper airway and pulmonary signs and symptoms. Further investigation is needed to understand the treatments and quality of life of patients with AAV. Keywords: antineutrophil cytoplasmic antibody, AN CA-associated vasculitis, autoimmune disorder, Saudi Arabia, clinical manifestations [phrase omitted]</abstract><pub>Saudi Medical Journal</pub><doi>10.15537/smj.2023.44.5.20220818</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0379-5284
ispartof Saudi medical journal, 2023-05, Vol.44 (5), p.486-491
issn 0379-5284
1658-3175
language eng
recordid cdi_gale_infotracmisc_A758626892
source PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Autoantibodies
Autoimmune diseases
Complications and side effects
Development and progression
Health aspects
Vasculitis
title Common clinical pattern of antineutrophil cytoplasmic antibody -associated vasculitis: An experience from a multicenter study in Saudi Arabia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-06T20%3A38%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Common%20clinical%20pattern%20of%20antineutrophil%20cytoplasmic%20antibody%20-associated%20vasculitis:%20An%20experience%20from%20a%20multicenter%20study%20in%20Saudi%20Arabia&rft.jtitle=Saudi%20medical%20journal&rft.au=Alfuwayris,%20Jumanah%20J&rft.date=2023-05-01&rft.volume=44&rft.issue=5&rft.spage=486&rft.epage=491&rft.pages=486-491&rft.issn=0379-5284&rft.eissn=1658-3175&rft_id=info:doi/10.15537/smj.2023.44.5.20220818&rft_dat=%3Cgale_cross%3EA758626892%3C/gale_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A758626892&rfr_iscdi=true