[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]。

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
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引用次数: 0

摘要

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

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.

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