AB017。在土耳其人群中是否存在与病态肥胖相关的特定HLA等位基因

IF 0.5 4区 医学 Q4 SURGERY
Fusun Ozmen, Gul Ozge Ergen, Mehmet Mahir Özmen
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引用次数: 0

摘要

背景:病态肥胖是一种多因素疾病,与遗传和环境因素有关。脂肪组织重塑是由脂肪肥大和免疫细胞激活引起的。人类白细胞抗原(HLA)基因座也与一些炎症性和自身免疫性疾病有关。HLA分子向T细胞提供肽并引发炎症。本研究旨在分析HLA I类和II类等位基因与病态肥胖疾病的相关性。方法:对80例(10M)接受肥胖手术的BMI为51(40-68)kg/M的病态肥胖患者进行HLA I类和II类等位基因频率调查。对照人群由100名健康捐献者组成。采用PCR-SSO方法在低分辨率水平上进行HLA基因分型。采用卡方检验和Fisher精确检验进行统计评价。结果:在评估HLA I类等位基因时,两组共检测到18个HLA-A、25个HLA-B和12个HLA-C等位基因。我们发现,在肥胖组和对照组中,所有HLA I类基因座的等位基因频率非常相似,尽管患者群体中的HLA-B*45(8%)(P=0.001)和HLA-C*15(10%)(P=0.04)等位基因的频率显著高于对照组。本研究共鉴定出18个不同的HLAⅡ类等位基因。患者群体中的某些HLA等位基因频率,包括HLADRB1*03(13.13%)、-DRB1*04(22.5%)、-DRB1*08(5.63%)、-DRB1*09(1.25%)、-DRB1*12(1.88%)、-Dlb1*14(6.25%)、-Drob1*16(6.88%)高于对照组,只有-DRB1*33和-DRB1*44频率达到统计学意义(分别为P=0.05和P=0.012),HLA-DRB1*13(5%,P=0.001)和HLA-DQB1*06(8.75%,P=0.006)等位基因在患者中频率较低,与健康对照组有显著差异。结论:目前的研究表明,某些HLA等位基因在患者群体中较高。HLA I类和II类分子分别将外源肽呈递给CD8 T细胞和CD4+T细胞,并促进适应性免疫系统的激活。我们的结论是,由于这些等位基因可能对引发脂肪组织炎症很重要,它们可能与病态肥胖有关。尽管呈递肽在病态肥胖中与HLA等位基因一样重要。然而,还需要新的研究,包括HLA分子肽T细胞受体和更大的患者群体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AB017. OP17 Are there any specific HLA alleles related to morbid obesity in Turkish population
Background: Morbid obesity is a multifactorial disease and associated with genetic and environmental factors. Adipose tissue remodeling is created with adiposity hypertrophia and activation of immune cells. Human Leukocyte Antigen (HLA) loci are also related to some inflammatory and autoimmune diseases. HLA molecules present peptids to T cells and triger the inflammation. The present study aims to analyze the association HLA class I and class II alleles with morbid obesity disease. Methods: HLA class I and class II alleles frequency was investigated in 80 (10 M) morbidly obese patients with 51 (40–68) kg/m BMI who underwent obesity surgery. The control population was created from 100 healthy donors. HLA genotyping was performed using the PCR-SSO method at the low-resolution level. Chi-square and Fisher’s exact test were used for statistical evaluation. Results: When evaluated HLA class I alleles, eighteen HLA-A, twenty five HLA-B and twelve HLA-C different alleles were detected in two groups. We found that alleles frequency were very similar for all HLA class I loci in obese and control groups, although HLA-B*45 (8%) (P=0.001) and HLA*C*15 (10%) (P=0.04) alleles frequency in the patient population were significantly higher than the control group. Eighteen different HLA class II alleles were identified in this study. The certain HLA alleles frequencies in the patient population including HLADRB1*03 (13.13%), -DRB1*04 (22.5%), -DRB1*08 (5.63%), -DRB1*09 (1.25%), -DRB1*12 (1.88%), -DRB1*14 (6.25%), -DRB1*16 (6.88%) were higher than the controls, only -DRB1*03 and -DRB1*04 frequencies reached statistical significance (respectively, P=0.05 and P=0.012). HLA-DRB1*01 (5%, P=0.029), HLA-DRB1*13 (5%, P=0.001) and HLA-DQB1*06 (8.75%, P=0.006) alleles were lower frequency alleles in patients and differed significantly from the healthy controls. Conclusions: Present study demonstrates that certain HLA alleles were found to be higher in the patient population. HLA class I and class II molecules present the foreign peptides to CD8 T cells and CD4+ T cells, respectively and promote to activation of the adaptive immune system. We conclude that as these alleles might be important for triggering the inflammation in adipose tissue, they might be associated with morbid obesity. Although presenting peptides are important as much as HLA alleles in morbid obesity. However, new researches including HLA molecule-peptid-T Cell Receptor and larger patient population are needed.
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CiteScore
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