Vrgoc Goran, Vrbanec Jurica, Eftedal Randi K, Dembic Petra L, Balen Sanja, Dembic Zlatko, Jotanovic Zdravko
Molecular Genetics Laboratory, Faculty of Dental, Department of Oral Biology, University of Oslo, Oslo, Norway.
Department of Orthopedic Surgery, University Hospital "Sveti Duh,", Sveti Duh 64, 10000, Zagreb, Croatia.
J Orthop Res. 2018 Jun;36(6):1684-1693. doi: 10.1002/jor.23823. Epub 2017 Dec 19.
Primary osteoarthritis (OA) is the most common type of a joint disease. It has a polygenic risk inheritance pattern and affects older people. The etiology of this disease is not fully understood. The aim of this study was to investigate the associations between polymorphisms in pro-inflammatory interleukin-17 (IL17A and IL17F) and anti-inflammatory Toll-like Receptor 10 (TLR10) genes with the risk for development of advanced stage hip and knee primary OA in the Croatian population. A total of 500 OA patients and 597 controls were genotyped for IL17A SNP (rs2275913), IL17F SNPs (rs763780 and rs1889570), and TLR10 (rs11096957) genes. The allelic and genotypic frequencies of IL17F SNP (rs763780) showed statistically significant differences in comparisons of controls with hip-but not knee-OA patients. The major allele (T) of rs763780 was associated with the lower risk for developing hip OA (p = 7.9 × 10 , OR = 0.45, 95%CI = 0.27-0.74), whereas the minor allele (C) was associated with susceptibility to hip OA (p = 7.9 × 10 , OR = 2.24, 95%CI = 1.35-3.72). The genotype T/T was associated with the protection to hip OA (p = 3.9 × 10 , OR = 0.41, 95%CI = 0.24-0.70), and, lastly, the genotype T/C was associated with the higher risk to acquiring hip OA (p = 2.6 × 10 , OR = 2.50, 95%CI = 1.47-4.25). TLR10 SNP rs11096957 was found significantly associated with predisposition to hip OA (p = 0.04, OR = 1.41, 95%CI = 1.02-1.94) but not knee OA. Our findings suggest that hip OA in Croatian population might have a different genetic risk regarding the IL17 and TLR10 gene locus than knee OA. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 36:1684-1693, 2018.
原发性骨关节炎(OA)是最常见的关节疾病类型。它具有多基因风险遗传模式,且影响老年人。这种疾病的病因尚未完全明确。本研究的目的是调查促炎白细胞介素-17(IL17A和IL17F)及抗炎Toll样受体10(TLR10)基因多态性与克罗地亚人群中晚期髋和膝原发性OA发病风险之间的关联。对总共500例OA患者和597例对照进行了IL17A单核苷酸多态性(SNP,rs2275913)、IL17F SNPs(rs763780和rs1889570)以及TLR10(rs11096957)基因的基因分型。在对照与髋部OA患者(而非膝部OA患者)的比较中,IL17F SNP(rs763780)的等位基因和基因型频率显示出统计学上的显著差异。rs763780的主要等位基因(T)与髋部OA发病风险较低相关(p = 7.9×10 ,比值比[OR] = 0.45,95%置信区间[CI] = 0.27 - 0.74),而次要等位基因(C)与髋部OA易感性相关(p = 7.9×l0 ,OR = 2.24,95%CI = 1.35 - 3.72)。基因型T/T与髋部OA的保护作用相关(p = 3.9×10 ,OR = 0.41,95%CI = 0.24 - 0.70),最后,基因型T/C与患髋部OA的较高风险相关(p = !2.6×10 ,OR = 2.50,95%CI = 1.47 - 4.25)。发现TLR10 SNP rs11096957与髋部OA的易感性显著相关(p = 0.04,OR = 1.41,95%CI = 1.02 - 1.94),但与膝部OA无关。我们的研究结果表明,克罗地亚人群中的髋部OA在IL17和TLR10基因位点可能具有与膝部OA不同的遗传风险。©2017骨科学研究协会。由威利期刊公司出版。《矫形外科学研究》36:1684 - 1693,2018年。 (注:原文中部分p值后的乘号及次方表述不完整,翻译时保留原文格式)