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印度北部系统性红斑狼疮患者CTLA4基因多态性及其与疾病发生、临床表现、血清标志物和细胞因子水平的关联

CTLA4 Gene Polymorphism and its Association with Disease Occurrence, Clinical Manifestations, Serum Markers and Cytokine Levels in SLE Patients from North India.

作者信息

Kailashiya Vikas, Singh Usha, Kailashiya Jyotsna

机构信息

Department of Pathology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

Department of Biochemistry, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

出版信息

Indian J Dermatol. 2022 May-Jun;67(3):311. doi: 10.4103/ijd.ijd_82_22.

Abstract

BACKGROUND

Cytotoxic T lymphocyte-associated protein-4 (CTLA-4) or CD152 is an inhibitory receptor expressed constitutively on CD4+CD25+ T regulatory lymphocytes (Treg) and transiently on activated CD4+ and CD8+ T lymphocytes. Association of gene polymorphisms with Systemic Lupus Erythematosus (SLE) has been reported in south Indians, but not in north Indians. This study aims to investigate gene polymorphism and its association with the occurrence of SLE, its clinical manifestation and serological markers in north Indians.

METHODS

This cross sectional study was done in a tertiary health care centre in north India. Patients reporting to the hospital and diagnosed with systemic lupus erythematosus were included in study. +49 A/G (snp- rs231775) gene polymorphism was analysed in 41 SLE patients and 21 matched healthy controls by real time PCR method. ANA (Antinuclear Antibody), anti dsDNA, Interferon-γ (IFN- γ), TGF-β, IL-10 were measured by ELISA kits. Complement (C3 and C4) and immunoglobulins (IgA, IgG, IgM) estimation were done with the turbidometry method. Chi-square test was used for comparison between groups and odds ratio with 95% confidence interval was calculated to estimate the associated risk.

RESULTS

A/A genotype was most common (51.2%) followed by the A/G genotype (46.3%) and G/G genotype (2.4%, detected in only 1 patient). The frequency of A allele was 74.4%, while of G allele was only 25.6%. A/G genotype SLE patients showed a higher risk (odds ratio 37.5, 95% CI- 6.048-232.51) of developing edema compared to A/A genotype patients. There was no statistically significant association of various genotypes with the occurrence of SLE and serum markers.

CONCLUSIONS

A/A was the most common genotype in both SLE patients and healthy controls of north India. Contrary to the previous report in south Indians, there was no statistically significant association between genotype and occurrence of SLE in north Indians. Only the presence of generalised edema was found significantly associated with the A/G genotype.

摘要

背景

细胞毒性T淋巴细胞相关蛋白4(CTLA - 4)或CD152是一种抑制性受体,在CD4 + CD25 +调节性T淋巴细胞(Treg)上持续表达,在活化的CD4 +和CD8 + T淋巴细胞上短暂表达。在南印度人中已报道基因多态性与系统性红斑狼疮(SLE)有关,但在北印度人中尚未见报道。本研究旨在调查北印度人中基因多态性及其与SLE发生、临床表现和血清学标志物的关系。

方法

本横断面研究在印度北部的一家三级医疗保健中心进行。纳入到医院就诊并被诊断为系统性红斑狼疮的患者。采用实时PCR方法对41例SLE患者和21例匹配的健康对照进行+49 A/G(snp - rs231775)基因多态性分析。采用ELISA试剂盒检测抗核抗体(ANA)、抗双链DNA、干扰素 - γ(IFN - γ)、转化生长因子 - β(TGF - β)、白细胞介素 - 10。采用比浊法检测补体(C3和C4)和免疫球蛋白(IgA、IgG、IgM)。采用卡方检验进行组间比较,并计算95%置信区间的比值比以估计相关风险。

结果

A/A基因型最为常见(51.2%),其次是A/G基因型(46.3%),G/G基因型(2.4%,仅在1例患者中检测到)。A等位基因频率为74.4%,而G等位基因频率仅为25.6%。与A/A基因型患者相比,A/G基因型SLE患者发生水肿的风险更高(比值比37.5,95% CI - 6.048 - 232.51)。各种基因型与SLE的发生及血清标志物之间无统计学显著关联。

结论

A/A是印度北部SLE患者和健康对照中最常见的基因型。与之前南印度人的报道相反,在北印度人中基因型与SLE的发生之间无统计学显著关联。仅发现全身性水肿的存在与A/G基因型显著相关。

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