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Association of single-nucleotide polymorphisms in HLA class II/III region with knee osteoarthritis.

机译:HLA II / III类区域的单核苷酸多态性与膝骨关节炎的关联。

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OBJECTIVE: A genome-wide association study and a replication using Japanese, Spanish and Greek Caucasian populations have recently indicated two single-nucleotide polymorphisms (SNPs) (rs7775228 and rs10947262) associated with knee Osteoarthritis (OA) susceptibility. We have further evaluated the association in knee OA subjects from Han Chinese and Australian Caucasian origin. METHODS: Two independent case-control association studies were performed using Han Chinese and Australian Caucasian populations. The two SNPs were genotyped in patients who had primary symptomatic knee OA with radiographic confirmation and/or received total knee replacement surgery as well as in matched controls. They were subjected to statistic analyses. RESULTS: A total of 991 OA patients and 1536 controls were genotyped. No significant difference was detected in genotype or allele frequencies of the two SNPs between knee OA and control groups in the two populations (all P>0.05). The association was also negative even after stratification by sex, body mass index (BMI) and Kellgren/Lawrence scores. The significant heterogeneity was detected between Chinese and Japanese (both P<0.05). In the Caucasian samples, no significant heterogeneity was detected (both P>0.05). The result of meta-analysis showed significant association between knee OA and rs10947262 in total subjects [summary OR=1.26, 95%confidence intervals (CI)=1.07-1.27, P=3 x 10(-8)] and in Caucasian samples (summary OR=1.28, 95%CI=1.04-1.57, P=0.02). CONCLUSION: We demonstrated no association between the two SNPs in human leukocyte antigen (HLA) class II/III region and knee OA in Han Chinese population. A significant association was detected between SNP rs10947262 and knee OA in Caucasian subjects. Further replication studies are required to identify the impact of controversial association.
机译:目的:全基因组关联研究和使用日本,西班牙和希腊高加索人群的复制最近表明,两种单核苷酸多态性(SNP)(rs7775228和rs10947262)与膝骨关节炎(OA)易感性有关。我们进一步评估了汉族和澳大利亚高加索族膝关节炎患者的相关性。方法:使用汉族和澳大利亚高加索人群进行了两项独立的病例对照协会研究。在有影像学检查并/或接受全膝关节置换手术的原发性症状性膝OA患者中,对两种SNPs进行基因分型,并在对照中进行。他们接受了统计分析。结果:共有991例OA患者和1536例对照组进行了基因分型。在两个人群中,膝OA和对照组之间两个SNP的基因型或等位基因频率均未检测到显着差异(均P> 0.05)。即使在按性别,体重指数(BMI)和Kellgren / Lawrence分数分层后,该关联也为负值。在中文和日文之间检测到显着异质性(均P <0.05)。在白种人样本中,未检测到明显的异质性(均P> 0.05)。荟萃分析的结果显示,在所有受试者中,膝骨关节炎和rs10947262之间存在显着相关性[摘要OR = 1.26,95%置信区间(CI)= 1.07-1.27,P = 3 x 10(-8)]和白种人样本中(摘要OR = 1.28,95%CI = 1.04-1.57,P = 0.02)。结论:我们证明汉族人群中人类白细胞抗原(HLA)II / III类区域中的两个SNP与膝盖OA之间没有关联。在白种人受试者中,SNP rs10947262与膝盖OA之间存在显着关联。需要进一步的复制研究来确定有争议的关联的影响。

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