Loading…
Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis
Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we investigated whether the IL23R variant (rs1884444) is associated with...
Saved in:
Published in: | BMC rheumatology 2024-04, Vol.8 (1), p.14-14, Article 14 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c487t-74252c09839ecf0acd271a3f73218e2c3b53c081a3712700cc9d296d14cb03cb3 |
container_end_page | 14 |
container_issue | 1 |
container_start_page | 14 |
container_title | BMC rheumatology |
container_volume | 8 |
creator | Mellati, Atiyeh Soltani, Samaneh Kazemi, Tohid Ahmadzadeh, Nooshin Akhtari, Maryam Madreseh, Elham Jamshidi, Ahmadreza Farhadi, Elham Mahmoudi, Mahdi |
description | Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we investigated whether the IL23R variant (rs1884444) is associated with AS in the Iranian population.
In this research, we analyzed rs1884444 in a group of 425 patients with AS and 400 matched controls. For DNA extraction, the phenol/chloroform technique was utilized. Peripheral blood mononuclear cells (PBMCs) were obtained from the whole blood of 39 patients and 43 healthy controls and total RNA was extracted. Genotyping was performed by amplification-refractory mutation system (ARMS)-PCR method. Afterward, the expression level of IL23R was analyzed by the real-time quantitative (Q)-PCR method.
We observed no significant association between the distribution of alleles and genotypes of rs1884444 and susceptibility to AS. In addition, the expression level of IL23R did not differ between PBMCs from AS patients compared to the control group (P = 0.167). Furthermore, the relative expression level of IL23R was positively correlated with the BASDAI (P |
doi_str_mv | 10.1186/s41927-024-00383-w |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_69ae0f6a2f744b5b9b19ca07f71c5bd0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_69ae0f6a2f744b5b9b19ca07f71c5bd0</doaj_id><sourcerecordid>3038426384</sourcerecordid><originalsourceid>FETCH-LOGICAL-c487t-74252c09839ecf0acd271a3f73218e2c3b53c081a3712700cc9d296d14cb03cb3</originalsourceid><addsrcrecordid>eNpVkk1v1DAQhiMEolXpH-CAfCyHwPgjsX1CqFBYaSUucLYcZ7LrktjBznZZiR9ft1uq1gfbmpn3sUfzVtVbCh8oVe3HLKhmsgYmagCueL1_UZ2yhkFNgbUvn9xPqvOcrwGAUa415a-rE65aaLgWp9W_L7hgmnywi4-BxIGs1jXjJKHDeYmJ4N85Yc53SRt6ssGAZI7jYYpp3vo8kYuUqVKirPfEB7JKNngbyFyAGJZM9n7ZFunvwxizDxuS5xj6w-gXn99UrwY7Zjx_OM-qX1dff15-r9c_vq0uP69rJ5RcailKLw604hrdANb1TFLLB8kZVcgc7xruQJWQpEwCOKd7ptueCtcBdx0_q1ZHbh_ttZmTn2w6mGi9uQ_EtDE2Ld6NaFptEYbWskEK0TWd7qh2FuQgqWu6Hgrr05E177oJe1d6THZ8Bn2eCX5rNvHGUAogtW4L4eKBkOKfHebFTD47HEcbMO6y4WWcgrVlK6XsWOpSzDnh8PgOBXNnA3O0gSk2MPc2MPsievf0h4-S_0Pnt_mKrzw</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3038426384</pqid></control><display><type>article</type><title>Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis</title><source>PMC (PubMed Central)</source><source>Publicly Available Content (ProQuest)</source><creator>Mellati, Atiyeh ; Soltani, Samaneh ; Kazemi, Tohid ; Ahmadzadeh, Nooshin ; Akhtari, Maryam ; Madreseh, Elham ; Jamshidi, Ahmadreza ; Farhadi, Elham ; Mahmoudi, Mahdi</creator><creatorcontrib>Mellati, Atiyeh ; Soltani, Samaneh ; Kazemi, Tohid ; Ahmadzadeh, Nooshin ; Akhtari, Maryam ; Madreseh, Elham ; Jamshidi, Ahmadreza ; Farhadi, Elham ; Mahmoudi, Mahdi</creatorcontrib><description>Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we investigated whether the IL23R variant (rs1884444) is associated with AS in the Iranian population.
In this research, we analyzed rs1884444 in a group of 425 patients with AS and 400 matched controls. For DNA extraction, the phenol/chloroform technique was utilized. Peripheral blood mononuclear cells (PBMCs) were obtained from the whole blood of 39 patients and 43 healthy controls and total RNA was extracted. Genotyping was performed by amplification-refractory mutation system (ARMS)-PCR method. Afterward, the expression level of IL23R was analyzed by the real-time quantitative (Q)-PCR method.
We observed no significant association between the distribution of alleles and genotypes of rs1884444 and susceptibility to AS. In addition, the expression level of IL23R did not differ between PBMCs from AS patients compared to the control group (P = 0.167). Furthermore, the relative expression level of IL23R was positively correlated with the BASDAI (P < 0.01) and BASFI (P < 0.05) scores of the patients.
It appears that IL23R polymorphism (rs1884444) and the level of gene expression might not contribute to the susceptibility to AS in the Iranian population. The correlation of IL23R expression with the level of BASDAI and BASFI scores in patients may be due to the role of the IL-23/IL-23R signaling cascade in inflammation and exert a critical role in the development of AS.</description><identifier>ISSN: 2520-1026</identifier><identifier>EISSN: 2520-1026</identifier><identifier>DOI: 10.1186/s41927-024-00383-w</identifier><identifier>PMID: 38605394</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Ankylosing spondylitis ; ARMS-PCR ; Gene expression ; IL-23 receptor</subject><ispartof>BMC rheumatology, 2024-04, Vol.8 (1), p.14-14, Article 14</ispartof><rights>2024. The Author(s).</rights><rights>The Author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c487t-74252c09839ecf0acd271a3f73218e2c3b53c081a3712700cc9d296d14cb03cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11007996/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11007996/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38605394$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mellati, Atiyeh</creatorcontrib><creatorcontrib>Soltani, Samaneh</creatorcontrib><creatorcontrib>Kazemi, Tohid</creatorcontrib><creatorcontrib>Ahmadzadeh, Nooshin</creatorcontrib><creatorcontrib>Akhtari, Maryam</creatorcontrib><creatorcontrib>Madreseh, Elham</creatorcontrib><creatorcontrib>Jamshidi, Ahmadreza</creatorcontrib><creatorcontrib>Farhadi, Elham</creatorcontrib><creatorcontrib>Mahmoudi, Mahdi</creatorcontrib><title>Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis</title><title>BMC rheumatology</title><addtitle>BMC Rheumatol</addtitle><description>Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we investigated whether the IL23R variant (rs1884444) is associated with AS in the Iranian population.
In this research, we analyzed rs1884444 in a group of 425 patients with AS and 400 matched controls. For DNA extraction, the phenol/chloroform technique was utilized. Peripheral blood mononuclear cells (PBMCs) were obtained from the whole blood of 39 patients and 43 healthy controls and total RNA was extracted. Genotyping was performed by amplification-refractory mutation system (ARMS)-PCR method. Afterward, the expression level of IL23R was analyzed by the real-time quantitative (Q)-PCR method.
We observed no significant association between the distribution of alleles and genotypes of rs1884444 and susceptibility to AS. In addition, the expression level of IL23R did not differ between PBMCs from AS patients compared to the control group (P = 0.167). Furthermore, the relative expression level of IL23R was positively correlated with the BASDAI (P < 0.01) and BASFI (P < 0.05) scores of the patients.
It appears that IL23R polymorphism (rs1884444) and the level of gene expression might not contribute to the susceptibility to AS in the Iranian population. The correlation of IL23R expression with the level of BASDAI and BASFI scores in patients may be due to the role of the IL-23/IL-23R signaling cascade in inflammation and exert a critical role in the development of AS.</description><subject>Ankylosing spondylitis</subject><subject>ARMS-PCR</subject><subject>Gene expression</subject><subject>IL-23 receptor</subject><issn>2520-1026</issn><issn>2520-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkk1v1DAQhiMEolXpH-CAfCyHwPgjsX1CqFBYaSUucLYcZ7LrktjBznZZiR9ft1uq1gfbmpn3sUfzVtVbCh8oVe3HLKhmsgYmagCueL1_UZ2yhkFNgbUvn9xPqvOcrwGAUa415a-rE65aaLgWp9W_L7hgmnywi4-BxIGs1jXjJKHDeYmJ4N85Yc53SRt6ssGAZI7jYYpp3vo8kYuUqVKirPfEB7JKNngbyFyAGJZM9n7ZFunvwxizDxuS5xj6w-gXn99UrwY7Zjx_OM-qX1dff15-r9c_vq0uP69rJ5RcailKLw604hrdANb1TFLLB8kZVcgc7xruQJWQpEwCOKd7ptueCtcBdx0_q1ZHbh_ttZmTn2w6mGi9uQ_EtDE2Ld6NaFptEYbWskEK0TWd7qh2FuQgqWu6Hgrr05E177oJe1d6THZ8Bn2eCX5rNvHGUAogtW4L4eKBkOKfHebFTD47HEcbMO6y4WWcgrVlK6XsWOpSzDnh8PgOBXNnA3O0gSk2MPc2MPsievf0h4-S_0Pnt_mKrzw</recordid><startdate>20240411</startdate><enddate>20240411</enddate><creator>Mellati, Atiyeh</creator><creator>Soltani, Samaneh</creator><creator>Kazemi, Tohid</creator><creator>Ahmadzadeh, Nooshin</creator><creator>Akhtari, Maryam</creator><creator>Madreseh, Elham</creator><creator>Jamshidi, Ahmadreza</creator><creator>Farhadi, Elham</creator><creator>Mahmoudi, Mahdi</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240411</creationdate><title>Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis</title><author>Mellati, Atiyeh ; Soltani, Samaneh ; Kazemi, Tohid ; Ahmadzadeh, Nooshin ; Akhtari, Maryam ; Madreseh, Elham ; Jamshidi, Ahmadreza ; Farhadi, Elham ; Mahmoudi, Mahdi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-74252c09839ecf0acd271a3f73218e2c3b53c081a3712700cc9d296d14cb03cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Ankylosing spondylitis</topic><topic>ARMS-PCR</topic><topic>Gene expression</topic><topic>IL-23 receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mellati, Atiyeh</creatorcontrib><creatorcontrib>Soltani, Samaneh</creatorcontrib><creatorcontrib>Kazemi, Tohid</creatorcontrib><creatorcontrib>Ahmadzadeh, Nooshin</creatorcontrib><creatorcontrib>Akhtari, Maryam</creatorcontrib><creatorcontrib>Madreseh, Elham</creatorcontrib><creatorcontrib>Jamshidi, Ahmadreza</creatorcontrib><creatorcontrib>Farhadi, Elham</creatorcontrib><creatorcontrib>Mahmoudi, Mahdi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mellati, Atiyeh</au><au>Soltani, Samaneh</au><au>Kazemi, Tohid</au><au>Ahmadzadeh, Nooshin</au><au>Akhtari, Maryam</au><au>Madreseh, Elham</au><au>Jamshidi, Ahmadreza</au><au>Farhadi, Elham</au><au>Mahmoudi, Mahdi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis</atitle><jtitle>BMC rheumatology</jtitle><addtitle>BMC Rheumatol</addtitle><date>2024-04-11</date><risdate>2024</risdate><volume>8</volume><issue>1</issue><spage>14</spage><epage>14</epage><pages>14-14</pages><artnum>14</artnum><issn>2520-1026</issn><eissn>2520-1026</eissn><abstract>Through investigating genetic variations, it has been demonstrated that single nucleotide polymorphisms (SNPs) in the IL-23 receptor (IL23R) gene have a critical role in the pathophysiology of ankylosing spondylitis (AS). Here, we investigated whether the IL23R variant (rs1884444) is associated with AS in the Iranian population.
In this research, we analyzed rs1884444 in a group of 425 patients with AS and 400 matched controls. For DNA extraction, the phenol/chloroform technique was utilized. Peripheral blood mononuclear cells (PBMCs) were obtained from the whole blood of 39 patients and 43 healthy controls and total RNA was extracted. Genotyping was performed by amplification-refractory mutation system (ARMS)-PCR method. Afterward, the expression level of IL23R was analyzed by the real-time quantitative (Q)-PCR method.
We observed no significant association between the distribution of alleles and genotypes of rs1884444 and susceptibility to AS. In addition, the expression level of IL23R did not differ between PBMCs from AS patients compared to the control group (P = 0.167). Furthermore, the relative expression level of IL23R was positively correlated with the BASDAI (P < 0.01) and BASFI (P < 0.05) scores of the patients.
It appears that IL23R polymorphism (rs1884444) and the level of gene expression might not contribute to the susceptibility to AS in the Iranian population. The correlation of IL23R expression with the level of BASDAI and BASFI scores in patients may be due to the role of the IL-23/IL-23R signaling cascade in inflammation and exert a critical role in the development of AS.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>38605394</pmid><doi>10.1186/s41927-024-00383-w</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2520-1026 |
ispartof | BMC rheumatology, 2024-04, Vol.8 (1), p.14-14, Article 14 |
issn | 2520-1026 2520-1026 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_69ae0f6a2f744b5b9b19ca07f71c5bd0 |
source | PMC (PubMed Central); Publicly Available Content (ProQuest) |
subjects | Ankylosing spondylitis ARMS-PCR Gene expression IL-23 receptor |
title | Determination of IL-23 receptor expression and gene polymorphism (rs1884444) in Iranian patients with ankylosing spondylitis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A38%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Determination%20of%20IL-23%20receptor%20expression%20and%20gene%20polymorphism%20(rs1884444)%20in%20Iranian%20patients%20with%20ankylosing%20spondylitis&rft.jtitle=BMC%20rheumatology&rft.au=Mellati,%20Atiyeh&rft.date=2024-04-11&rft.volume=8&rft.issue=1&rft.spage=14&rft.epage=14&rft.pages=14-14&rft.artnum=14&rft.issn=2520-1026&rft.eissn=2520-1026&rft_id=info:doi/10.1186/s41927-024-00383-w&rft_dat=%3Cproquest_doaj_%3E3038426384%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c487t-74252c09839ecf0acd271a3f73218e2c3b53c081a3712700cc9d296d14cb03cb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3038426384&rft_id=info:pmid/38605394&rfr_iscdi=true |