Fonseca-Camarillo Gabriela, Furuzawa-Carballeda Janette, Priego-Ranero Ángel A, Barreto-Zúñiga Rafael, Martínez-Benítez Braulio, Yamamoto-Furusho Jesús K
Inflammatory Bowel Disease Clinic, Department of Gastroenterology, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City 14080, CP, Mexico.
Department of Immunology, Instituto Nacional de Cardiología, Ignacio Chávez, Mexico City 14080, CP, Mexico.
Metabolites. 2024 Dec 1;14(12):662. doi: 10.3390/metabo14120662.
The expression of selenium-binding protein 1 (SELENBP1), a molecule responsible for the absorption of selenium in the colon, is crucial for its immunoregulatory effect, but this phenomenon has not been studied in patients with UC. The present study aimed to determine the clinical outcome of SELENBP1 expression in colonic tissue from patients with UC.
The relative mRNA expression of SELENBP1 was analyzed in 34 patients with UC and 20 controls. Statistical analyses were performed with SPSS 19.
SELENBP1 gene expression was significantly lower in patients with active UC than those with UC in remission ( = 0.003) and within the controls ( = 0.04). Overexpression of the SELENBP1 gene was associated with a more benign clinical course characterized by initial activity and more than two years of prolonged remission (OR 23.7, = 0.003) and an intermittent clinical course (OR 47.5, = 0.001), mild histological activity (OR 0.11; 95% CI: 1.00-1.41, = 0.05) and severe histological activity (OR 0.08, 95% CI: 0.008-0.866, = 0.02). SELENBP1-positive cells were found mainly in the submucosa's inflammatory infiltrate and muscular and adventitia's internal layers from patients with active UC compared to those in the control group ( ≤ 0.001).
The upregulation of SELENBP1 was associated with a benign clinical course of UC. This is the first report suggesting the immunoregulatory role of SELENBP1 in patients with UC.
硒结合蛋白1(SELENBP1)是一种负责结肠中硒吸收的分子,其表达对免疫调节作用至关重要,但尚未在溃疡性结肠炎(UC)患者中对此现象进行研究。本研究旨在确定UC患者结肠组织中SELENBP1表达的临床结果。
分析了34例UC患者和20例对照中SELENBP1的相对mRNA表达。使用SPSS 19进行统计分析。
活动期UC患者的SELENBP1基因表达显著低于缓解期UC患者(P = 0.003)和对照组(P = 0.04)。SELENBP1基因的过表达与更良性的临床病程相关,其特征为初始活动和超过两年的长期缓解(OR 23.7,P = 0.003)以及间歇性临床病程(OR 47.5,P = 0.001)、轻度组织学活动(OR = 0.11;95%CI:0.01 - 1.41,P = 0.05)和重度组织学活动(OR 0.08,95%CI:0.008 - 0.866,P = 0.02)。与对照组相比,活动期UC患者的SELENBP1阳性细胞主要存在于黏膜下层的炎性浸润以及肌肉层和外膜内层(P≤0.001)。
SELENBP1的上调与UC的良性临床病程相关。这是首次报道提示SELENBP1在UC患者中的免疫调节作用。