HLA polymorphisms in South Tunisian systemic sclerosis patients: a case-control study.

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Aida Charfi, Raida Ben Salah, Olfa Frikha, Nadia Mahfoudh, Arwa Kamoun, Yosra Bouattour, Lilia Gaddour, Feiza Hakim, Zouhir Bahloul, Hafedh Makni
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引用次数: 0

Abstract

Objective: Systemic sclerosis (SSc) is a complex autoimmune connective tissue disease. Genetic factors may play a pivotal role in determining susceptibility to these disorders. HLA associations with SSc, especially HLA class II, were investigated in different populations but not in Tunisia. Our aim was to study HLA profile in South Tunisian patients with SSc.

Methods: We conducted a case-control study on 19 SSc patients and 123 healthy controls. HLA class I (HLA-A and -B) typing was performed using a microlymphocytotoxicity complement-dependent technique followed by polymerase chain reaction sequence specific primer (PCR-SSP). HLA class II DRB1/DQB1 of all patients and controls was genotyped using the PCR-SSP technique. Statistical analysis was performed using SPSS software and R language.

Results: Nineteen SSc patients and 123 healthy controls were included. The HLA-DRB1*11 was associated with the genetic susceptibility to SSc (corrected p-value (pc) = 0.005; OR = 5.56; 95% CI = [2-15.4]). The HLA-DQB1*03:01 had also increased the risk of SSc in our study (pc = 0.002; OR = 5.9; 95% CI = [2-16.8]). Concerning HLA class I typing, we found a significant association between HLA-B53 and SSc (pc = 0.01; OR = 9; 95% CI = [2.53-31.99]). The association of HLA-B53 was independent of HLA-DRB1*11 in binary logistic regression test (HLA-B53: p = 0.01; HLA-DRB1*11: p = 0.008). Concerning the haplotype study, a significant difference in the distribution of the haplotype B53-DRB1*11 was found between patients and controls (13.15% in SSc patients vs. 0.8% in controls; p = 1.33 10-5; HaploScore = 4.35).

Conclusion: Our results showed that in South Tunisia SSc is associated with HLA-DRB1*11 and DQB1*03:01 alleles. A susceptibility to SSc was found in positive HLA-B53 patients. This association of HLA alleles with SSc needs further study. Key Points •HLA-DR and DQ alleles represent the most common associations reported in Systemic Sclerosis (SSc). •In this study, in addition to the known association with HLA-DRB1*11, we identified an association with HLA-B53 in a cohort of 19 South Tunisian patients.

HLA多态性在南突尼斯系统性硬化症患者:一个病例对照研究。
目的:系统性硬化症(SSc)是一种复杂的自身免疫性结缔组织疾病。遗传因素可能在决定这些疾病的易感性方面起关键作用。HLA与SSc的关系,特别是HLAⅱ类,在不同人群中进行了调查,但在突尼斯没有。我们的目的是研究南突尼斯SSc患者的HLA谱。方法:对19例SSc患者和123名健康对照者进行病例对照研究。HLA I类(HLA- a和-B)分型采用微淋巴细胞毒性补体依赖技术,随后采用聚合酶链反应序列特异性引物(PCR-SSP)进行分型。采用PCR-SSP技术对所有患者和对照组的HLAⅱ型DRB1/DQB1进行基因分型。采用SPSS软件和R语言进行统计分析。结果:纳入SSc患者19例,健康对照123例。HLA-DRB1*11与SSc遗传易感性相关(校正p值(pc) = 0.005;或= 5.56;95% ci =[2-15.4])。在我们的研究中,HLA-DQB1*03:01也增加了SSc的风险(pc = 0.002; OR = 5.9; 95% CI =[2-16.8])。HLA- b53分型与SSc有显著相关性(pc = 0.01; OR = 9; 95% CI =[2.53-31.99])。经二元logistic回归检验,HLA-B53的相关性与HLA-DRB1*11无关(HLA-B53: p = 0.01; HLA-DRB1*11: p = 0.008)。在单倍型研究中,B53-DRB1*11单倍型在患者和对照组之间的分布有显著差异(SSc患者为13.15%,对照组为0.8%;p = 1.33 10-5; HaploScore = 4.35)。结论:南突尼斯地区SSc与HLA-DRB1*11和DQB1*03:01等位基因相关。HLA-B53阳性患者对SSc有易感性。HLA等位基因与SSc的关系有待进一步研究。•HLA-DR和DQ等位基因代表了系统性硬化症(SSc)中最常见的关联。•在这项研究中,除了已知的与HLA-DRB1*11的关联外,我们还在19名南突尼斯患者的队列中发现了与HLA-B53的关联。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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