Impact of the etiology and Vitamin D receptor TaqI rs731236 gene polymorphism on the severity of acute pancreatitis

Background/Purpose This work aimed to assess the impact of different etiologies of acute pancreatitis (AP) and vitamin D receptor (VDR) TaqI rs731236 gene polymorphism on the severity of AP. Methods This case‐control study included 70 patients with AP and 40 healthy controls. Etiologies of AP were i...

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Veröffentlicht in:Journal of hepato-biliary-pancreatic sciences 2020-11, Vol.27 (11), p.896-906
Hauptverfasser: El‐Mahdy, Reham I, Ramadan, Haidi Karam‐Allah, Mohammed, Hanan Sharaf EL_Deen, Ahmed, Entsar H, Mokhtar, Abeer A, Hosni, Amal
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container_end_page 906
container_issue 11
container_start_page 896
container_title Journal of hepato-biliary-pancreatic sciences
container_volume 27
creator El‐Mahdy, Reham I
Ramadan, Haidi Karam‐Allah
Mohammed, Hanan Sharaf EL_Deen
Ahmed, Entsar H
Mokhtar, Abeer A
Hosni, Amal
description Background/Purpose This work aimed to assess the impact of different etiologies of acute pancreatitis (AP) and vitamin D receptor (VDR) TaqI rs731236 gene polymorphism on the severity of AP. Methods This case‐control study included 70 patients with AP and 40 healthy controls. Etiologies of AP were identified by imaging, ANA, cytomegalovirus (CMV) IgM, coxsackie B virus IgM, and IgG4. Genotyping of VDR TaqI rs731236 polymorphism, Laboratory tests and severity scores using Ranson, BISAP, Atlanta and APACHE II scores were determined. Results The age in AP patients was 36.03 ± 10.76, and females were 85.7%. The etiologies of AP were as follows: biliary (51.4%), coxsackievirus (22.9%), autoimmune (14.3%), post‐ERCP (8.6%) and 2.9% were idiopathic. The TT genotype of VDR polymorphism was significantly more common in AP than control (P = .001) and allele T dominated in AP group (OR = 2; 95% CI: 0.665–5.64). Most cases showed low severity scores with significant differences among etiologies and VDR genotypes. Biliary pancreatitis showed highest percentages of severe AP. However, etiologies and VDR polymorphism were not predictors of severity. Conclusion Etiology of AP could have impact on the disease severity. VDR gene polymorphism increases the risk of AP. Neither the etiology nor VDR gene polymorphism could predict AP severity. Highlight This case‐control study showed the predominance of the TT genotype of vitamin D receptor TaqI rs731236 gene polymorphism in severe acute pancreatitis. While the etiology of acute pancreatitis may affect disease severity, El‐Mahdy and colleagues revealed that neither the etiology nor vitamin D receptor TaqI rs731236 gene polymorphism predicted severity.
doi_str_mv 10.1002/jhbp.817
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Methods This case‐control study included 70 patients with AP and 40 healthy controls. Etiologies of AP were identified by imaging, ANA, cytomegalovirus (CMV) IgM, coxsackie B virus IgM, and IgG4. Genotyping of VDR TaqI rs731236 polymorphism, Laboratory tests and severity scores using Ranson, BISAP, Atlanta and APACHE II scores were determined. Results The age in AP patients was 36.03 ± 10.76, and females were 85.7%. The etiologies of AP were as follows: biliary (51.4%), coxsackievirus (22.9%), autoimmune (14.3%), post‐ERCP (8.6%) and 2.9% were idiopathic. The TT genotype of VDR polymorphism was significantly more common in AP than control (P = .001) and allele T dominated in AP group (OR = 2; 95% CI: 0.665–5.64). Most cases showed low severity scores with significant differences among etiologies and VDR genotypes. Biliary pancreatitis showed highest percentages of severe AP. However, etiologies and VDR polymorphism were not predictors of severity. Conclusion Etiology of AP could have impact on the disease severity. VDR gene polymorphism increases the risk of AP. Neither the etiology nor VDR gene polymorphism could predict AP severity. Highlight This case‐control study showed the predominance of the TT genotype of vitamin D receptor TaqI rs731236 gene polymorphism in severe acute pancreatitis. While the etiology of acute pancreatitis may affect disease severity, El‐Mahdy and colleagues revealed that neither the etiology nor vitamin D receptor TaqI rs731236 gene polymorphism predicted severity.</description><identifier>ISSN: 1868-6974</identifier><identifier>EISSN: 1868-6982</identifier><identifier>DOI: 10.1002/jhbp.817</identifier><identifier>PMID: 32780933</identifier><language>eng</language><publisher>Japan: Wiley Subscription Services, Inc</publisher><subject>Acute Disease ; acute pancreatitis ; Case-Control Studies ; Cytomegalovirus ; Etiology ; Female ; gene polymorphism ; Genetic Predisposition to Disease ; Humans ; Pancreatitis ; Pancreatitis - genetics ; Polymorphism ; Polymorphism, Genetic ; predictors ; Receptors, Calcitriol - genetics ; vitamin D</subject><ispartof>Journal of hepato-biliary-pancreatic sciences, 2020-11, Vol.27 (11), p.896-906</ispartof><rights>2020 Japanese Society of Hepato‐Biliary‐Pancreatic Surgery</rights><rights>2020 Japanese Society of Hepato-Biliary-Pancreatic Surgery.</rights><rights>Copyright © 2020 Japanese Society of Hepato‐Biliary‐Pancreatic Surgery</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3737-2ea0f728d8c7610480a43f71de430951e4fc3ab26f6a14393e3b3fdc6553390d3</citedby><cites>FETCH-LOGICAL-c3737-2ea0f728d8c7610480a43f71de430951e4fc3ab26f6a14393e3b3fdc6553390d3</cites><orcidid>0000-0003-4144-1868</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjhbp.817$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhbp.817$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32780933$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El‐Mahdy, Reham I</creatorcontrib><creatorcontrib>Ramadan, Haidi Karam‐Allah</creatorcontrib><creatorcontrib>Mohammed, Hanan Sharaf EL_Deen</creatorcontrib><creatorcontrib>Ahmed, Entsar H</creatorcontrib><creatorcontrib>Mokhtar, Abeer A</creatorcontrib><creatorcontrib>Hosni, Amal</creatorcontrib><title>Impact of the etiology and Vitamin D receptor TaqI rs731236 gene polymorphism on the severity of acute pancreatitis</title><title>Journal of hepato-biliary-pancreatic sciences</title><addtitle>J Hepatobiliary Pancreat Sci</addtitle><description>Background/Purpose This work aimed to assess the impact of different etiologies of acute pancreatitis (AP) and vitamin D receptor (VDR) TaqI rs731236 gene polymorphism on the severity of AP. Methods This case‐control study included 70 patients with AP and 40 healthy controls. Etiologies of AP were identified by imaging, ANA, cytomegalovirus (CMV) IgM, coxsackie B virus IgM, and IgG4. Genotyping of VDR TaqI rs731236 polymorphism, Laboratory tests and severity scores using Ranson, BISAP, Atlanta and APACHE II scores were determined. Results The age in AP patients was 36.03 ± 10.76, and females were 85.7%. The etiologies of AP were as follows: biliary (51.4%), coxsackievirus (22.9%), autoimmune (14.3%), post‐ERCP (8.6%) and 2.9% were idiopathic. The TT genotype of VDR polymorphism was significantly more common in AP than control (P = .001) and allele T dominated in AP group (OR = 2; 95% CI: 0.665–5.64). Most cases showed low severity scores with significant differences among etiologies and VDR genotypes. Biliary pancreatitis showed highest percentages of severe AP. However, etiologies and VDR polymorphism were not predictors of severity. Conclusion Etiology of AP could have impact on the disease severity. VDR gene polymorphism increases the risk of AP. Neither the etiology nor VDR gene polymorphism could predict AP severity. Highlight This case‐control study showed the predominance of the TT genotype of vitamin D receptor TaqI rs731236 gene polymorphism in severe acute pancreatitis. 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Methods This case‐control study included 70 patients with AP and 40 healthy controls. Etiologies of AP were identified by imaging, ANA, cytomegalovirus (CMV) IgM, coxsackie B virus IgM, and IgG4. Genotyping of VDR TaqI rs731236 polymorphism, Laboratory tests and severity scores using Ranson, BISAP, Atlanta and APACHE II scores were determined. Results The age in AP patients was 36.03 ± 10.76, and females were 85.7%. The etiologies of AP were as follows: biliary (51.4%), coxsackievirus (22.9%), autoimmune (14.3%), post‐ERCP (8.6%) and 2.9% were idiopathic. The TT genotype of VDR polymorphism was significantly more common in AP than control (P = .001) and allele T dominated in AP group (OR = 2; 95% CI: 0.665–5.64). Most cases showed low severity scores with significant differences among etiologies and VDR genotypes. Biliary pancreatitis showed highest percentages of severe AP. However, etiologies and VDR polymorphism were not predictors of severity. Conclusion Etiology of AP could have impact on the disease severity. VDR gene polymorphism increases the risk of AP. Neither the etiology nor VDR gene polymorphism could predict AP severity. Highlight This case‐control study showed the predominance of the TT genotype of vitamin D receptor TaqI rs731236 gene polymorphism in severe acute pancreatitis. While the etiology of acute pancreatitis may affect disease severity, El‐Mahdy and colleagues revealed that neither the etiology nor vitamin D receptor TaqI rs731236 gene polymorphism predicted severity.</abstract><cop>Japan</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32780933</pmid><doi>10.1002/jhbp.817</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-4144-1868</orcidid></addata></record>
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subjects Acute Disease
acute pancreatitis
Case-Control Studies
Cytomegalovirus
Etiology
Female
gene polymorphism
Genetic Predisposition to Disease
Humans
Pancreatitis
Pancreatitis - genetics
Polymorphism
Polymorphism, Genetic
predictors
Receptors, Calcitriol - genetics
vitamin D
title Impact of the etiology and Vitamin D receptor TaqI rs731236 gene polymorphism on the severity of acute pancreatitis
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