[HLA genotypes associated with gastrointestinal symptoms in patients with spondyloarthritis without inflammatory bowel disease].

Maria Alejandra Meneses-Toro, Omar Javier Calixto, Viviana Parra-Izquierdo, Cristian Flórez-Sarmiento, Juliette de Ávila de-Quiroga, Alejandro Ramos-Casallas, Lorena Chila-Moreno, Juan Manuel Bello-Gualtero, Wilson Bautista-Molano, Consuelo Romero-Sanchez
{"title":"[HLA genotypes associated with gastrointestinal symptoms in patients with spondyloarthritis without inflammatory bowel disease].","authors":"Maria Alejandra Meneses-Toro, Omar Javier Calixto, Viviana Parra-Izquierdo, Cristian Flórez-Sarmiento, Juliette de Ávila de-Quiroga, Alejandro Ramos-Casallas, Lorena Chila-Moreno, Juan Manuel Bello-Gualtero, Wilson Bautista-Molano, Consuelo Romero-Sanchez","doi":"10.29262/ram.v71i1.1371","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to establish the association between HLA-A, B, DR genotypes and gastrointestinal variables in patients with SpA without inflammatory bowel disease (IBD).</p><p><strong>Methods: </strong>Retrospective study of 91 patients with SpA and 401 healthy controls, with typing by Illumina Sequencing/PacBio and LIFECODES HLA-PCR/SSO multiplex sequencing technology. The presence of gastrointestinal symptoms was evaluated by administering a survey, and those who presented 2 or more symptoms were taken for clinical evaluation by rheumatology and gastroenterology, colonoscopy and histopathological study. (Ethics committee approval).</p><p><strong>Results: </strong>The 59,3% of the patients were men, with a mean age of 43,9±11.4 years; 80,2% were classified as ankylosing spondylitis. 14, 28 and 19 genotypes for the HLA-A*, HLA-B* and HLA-DR* loci were identified in both groups, of which a relationship with gastrointestinal symptoms was identified: <i>A*26, A*29</i> and <i>B*27</i> were associated to abdominal pain, <i>DRB1*11</i> and <i>DRB1*16</i> with abdominal distention, <i>A*30, B*38, DRB1*13</i> and <i>DRB1*14</i> with weight loss, <i>B*40</i> with diarrhea >4 weeks, and presence of mucus in the stools with <i>A*02</i> and <i>DRB1*11</i> (p<0.05). Furthermore, the presence of <i>B*15</i> had a statistical relationship with intolerance to some food, highlighting the <i>B*27</i> genotype in relation to grains and dairy products, <i>A*23</i> with grains, vegetables and meats, and <i>B*49</i> with vegetables and dairy (p<0.05). Regarding the endoscopic variables, macroscopic changes were found in the ileum mucosa related to <i>A*02, B*48, DRB1*14</i> and the relationship between <i>B*27</i> and ulcers at this level should be highlighted. Macroscopic changes in the sigmoid colon with <i>B*48</i> and the rectum with <i>A*30</i>. In microscopic changes, inflammatory alterations of the ileum are mentioned with genotypes <i>DRB1*07, DRB1*13</i> and <i>DRB1*14</i>, a genotype that is related to changes in the ileum both endoscopically and histologically (p<0.05).</p><p><strong>Conclusions: </strong>These findings indicate a potential genetic predisposition related to HLA genotypes that may increase the likelihood of food intolerance, gastrointestinal symptoms, and even visible and microscopic changes, specifically in the ileal tissue. The study highlights the presence of B*27 and other noteworthy HLA class I and class II genes (such as DRB1*14) in the diverse Colombian population.</p>","PeriodicalId":101421,"journal":{"name":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","volume":"71 1","pages":"66"},"PeriodicalIF":0.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29262/ram.v71i1.1371","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: This study aimed to establish the association between HLA-A, B, DR genotypes and gastrointestinal variables in patients with SpA without inflammatory bowel disease (IBD).

Methods: Retrospective study of 91 patients with SpA and 401 healthy controls, with typing by Illumina Sequencing/PacBio and LIFECODES HLA-PCR/SSO multiplex sequencing technology. The presence of gastrointestinal symptoms was evaluated by administering a survey, and those who presented 2 or more symptoms were taken for clinical evaluation by rheumatology and gastroenterology, colonoscopy and histopathological study. (Ethics committee approval).

Results: The 59,3% of the patients were men, with a mean age of 43,9±11.4 years; 80,2% were classified as ankylosing spondylitis. 14, 28 and 19 genotypes for the HLA-A*, HLA-B* and HLA-DR* loci were identified in both groups, of which a relationship with gastrointestinal symptoms was identified: A*26, A*29 and B*27 were associated to abdominal pain, DRB1*11 and DRB1*16 with abdominal distention, A*30, B*38, DRB1*13 and DRB1*14 with weight loss, B*40 with diarrhea >4 weeks, and presence of mucus in the stools with A*02 and DRB1*11 (p<0.05). Furthermore, the presence of B*15 had a statistical relationship with intolerance to some food, highlighting the B*27 genotype in relation to grains and dairy products, A*23 with grains, vegetables and meats, and B*49 with vegetables and dairy (p<0.05). Regarding the endoscopic variables, macroscopic changes were found in the ileum mucosa related to A*02, B*48, DRB1*14 and the relationship between B*27 and ulcers at this level should be highlighted. Macroscopic changes in the sigmoid colon with B*48 and the rectum with A*30. In microscopic changes, inflammatory alterations of the ileum are mentioned with genotypes DRB1*07, DRB1*13 and DRB1*14, a genotype that is related to changes in the ileum both endoscopically and histologically (p<0.05).

Conclusions: These findings indicate a potential genetic predisposition related to HLA genotypes that may increase the likelihood of food intolerance, gastrointestinal symptoms, and even visible and microscopic changes, specifically in the ileal tissue. The study highlights the presence of B*27 and other noteworthy HLA class I and class II genes (such as DRB1*14) in the diverse Colombian population.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[HLA基因型与无炎症性肠病的脊柱关节炎患者的胃肠道症状相关]。
研究目的本研究旨在确定无炎症性肠病(IBD)的SpA患者的HLA-A、B、DR基因型与胃肠道变量之间的关联:对91名SpA患者和401名健康对照者进行回顾性研究,采用Illumina测序/PacBio和LIFECODES HLA-PCR/SSO多重测序技术进行分型。通过问卷调查评估是否存在胃肠道症状,并对出现 2 种或 2 种以上症状的患者进行风湿病学和胃肠病学临床评估、结肠镜检查和组织病理学研究。(结果:59.3%的患者为男性,平均年龄(43.9±11.4)岁;80.2%的患者被归类为强直性脊柱炎。两组患者的 HLA-A*、HLA-B* 和 HLA-DR* 基因座分别有 14、28 和 19 种基因型,其中有一种与胃肠道症状有关:A*26、A*29 和 B*27 与腹痛有关,DRB1*11 和 DRB1*16 与腹胀有关,A*30、B*38、DRB1*13 和 DRB1*14 与体重减轻有关,B*40 与腹泻 >4 周有关,A*02 和 DRB1*11 与粪便中出现粘液有关(pB*15 与对某些食物不耐受有统计学关系)、应强调 B*27 基因型与谷物和乳制品的关系,A*23 与谷物、蔬菜和肉类的关系,以及 B*49 与蔬菜和乳制品的关系(pA*02、B*48、DRB1*14 和 B*27 与溃疡的关系应在这一层面加以强调)。B*48 的乙状结肠和 A*30 的直肠的宏观变化。在微观变化中,回肠的炎症性改变与 DRB1*07、DRB1*13 和 DRB1*14 基因型有关,这种基因型与回肠在内窥镜和组织学上的变化有关(P 结论:这些研究结果表明,与 HLA 基因型有关的潜在遗传易感性可能会增加食物不耐受、胃肠道症状、甚至可见和显微变化(尤其是回肠组织)的可能性。这项研究突出表明,在多样化的哥伦比亚人群中存在 B*27 和其他值得注意的 HLA I 类和 II 类基因(如 DRB1*14)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Adenovirus-related acute liver failure treated with intravenous immunoglobulin]. [Allergic contact dermatitis due to Furacin®]. [Chronic urticaria as an atypical reaction after a vespid bite]. [Epidemiological profile of allergic respiratory disease in Mexican children]. [Knowledge of mothers of children under 5 years of age about vaccination schedule].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1