Genetic Variations in TLR7 and Their Role in Systemic Lupus Erythematosus: A Systematic Review and Meta-analysis.

IF 1.5 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Indian Journal of Clinical Biochemistry Pub Date : 2026-10-01 Epub Date: 2025-01-13 DOI:10.1007/s12291-024-01294-w
Lisie L Patnayak, Seema Shah, Suprava Patel, Rachita Nanda, Eli Mohapatra
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引用次数: 0

Abstract

Systemic Lupus Erythematosus (SLE) is a complex autoimmune disease with multi-systemic involvement. It is characterized by the excessive production of auto-antibodies and immune complex deposition which occurs due to improper functioning of TLR7 (toll-like receptor 7). This systematic review and meta-analysis aims to study the genetic polymorphism in TLR7 and its risk to the development of SLE. PubMed, Scopus and Cochrane central were searched for articles published till August 2023 that examined TLR7 polymorphism in SLE. Case-control, cohort, and cross-sectional studies reporting clear data on genotype frequency were selected. Odds Ratio (OR) and 95% confidence interval was calculated for each study, and publication risk was calculated using Egger's test. Although we started with 8 (single nucleotide polymorphism) SNPs for systematic review, meta-analysis was done on 3 SNPs based on the inclusion criteria. A total of 10 studies involving 10,917 cases and 10,945 controls for rs3853839, rs179008, and rs179010 were included in our meta-analysis. The pooled analysis showed no association of TLR7 gene polymorphism and SLE susceptibility for rs3853839, rs179008, and rs179010 in all models including allelic, homozygous, heterozygotes, dominant, and recessive models. Notably no heterogeneity was reported for rs179008. In contrast allelic, homozygous, dominant and recessive models of rs3853839 showed significant heterogeneity of p < 0.05. Overall, our meta-analysis suggests that these TLR7 genetic variants do not influence the development of SLE.

TLR7基因变异及其在系统性红斑狼疮中的作用:系统综述和荟萃分析。
系统性红斑狼疮(SLE)是一种复杂的多系统自身免疫性疾病。它的特点是由于TLR7 (toll样受体7)功能不正常而导致自身抗体过量产生和免疫复合物沉积。本系统综述和荟萃分析旨在研究TLR7基因多态性及其与SLE发展的风险。检索PubMed、Scopus和Cochrane central截至2023年8月发表的关于SLE中TLR7多态性的文章。选择了报告基因型频率明确数据的病例对照、队列和横断面研究。计算各研究的优势比(OR)和95%置信区间,采用Egger检验计算发表风险。虽然我们从8个(单核苷酸多态性)snp开始进行系统评价,但根据纳入标准对3个snp进行了荟萃分析。我们的荟萃分析共纳入了10项研究,涉及rs3853839、rs179008和rs179010的10,917例病例和10,945例对照。合并分析显示,包括等位基因、纯合子、杂合子、显性和隐性模型在内的所有模型中,rs3853839、rs179008和rs179010的TLR7基因多态性与SLE易感性均无相关性。值得注意的是,rs179008没有异质性报告。相比之下,rs3853839等位基因的纯合子、显性和隐性模型显示p
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来源期刊
Indian Journal of Clinical Biochemistry
Indian Journal of Clinical Biochemistry BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
4.50
自引率
4.80%
发文量
74
期刊介绍: The primary mission of the journal is to promote improvement in the health and well-being of community through the development and practice of clinical biochemistry and dissemination of knowledge and recent advances in this discipline among professionals, diagnostics industry, government and non-government organizations. Indian Journal of Clinical Biochemistry (IJCB) publishes peer reviewed articles that contribute to the existing knowledge in all fields of Clinical biochemistry, either experimental or theoretical, particularly deal with the applications of biochemistry, molecular biology, genetics, biotechnology, and immunology to the diagnosis, treatment, monitoring and prevention of human diseases. The articles published also include those covering the analytical and molecular diagnostic techniques, instrumentation, data processing, quality assurance and accreditation aspects of the clinical investigations in which chemistry has played a major role, or laboratory animal studies with biochemical and clinical relevance.
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