Department of Orthopaedic, The Yongchuan Hospital of Chongqing Medical University, Chongqing, China (mainland).
Med Sci Monit. 2020 Feb 21;26:e916935. doi: 10.12659/MSM.916935.
BACKGROUND The aim of this case-control study was to evaluate the correlation of caspase recruitment domain-containing protein 8 (CARD8) gene rs2043211 (exon) and rs7253718 (intron) polymorphisms with the susceptibility of ankylosing spondylitis (AS) in the Chinese Han population. MATERIAL AND METHODS CARD8 polymorphisms were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 118 AS patients and 122 healthy persons. Linkage disequilibrium (LD) and haplotype analysis were carried out using Haploview software. Distribution differences of genotypes, alleles and haplotypes between the case and control groups were tested by chi-square test. Relative risk of AS was expressed by odds ratios (ORs) and 95% confidence intervals (CIs). Logistic regression analysis was used to adjust the results of association by clinical parameters. RESULTS For rs2043211, distribution of variant allele T was obviously different between AS patients and healthy controls (P=0.046). It indicated that T allele might increase the susceptibility of AS (OR=1.441, 95%CI=1.006-2.065). Adjusted by clinical characteristics, the significance of difference was slightly decreased (P=0.050, OR=1.439, 95%CI=0.999-2.072). Strong LD existed between rs2043211 and rs7253718 polymorphisms, and rs2043211T-rs7253718G haplotype was significantly associated with increased AS susceptibility (OR=1.787, 95%CI=1.165-2.740). In subgroup analysis, we found that the TT genotype and T allele of rs2043211 significantly increased the risk of AS in males (TT versus AA: OR=2.554, 95%CI=1.079-6.049; T versus A: OR=1.661, 95%CI=1.067-2.586), but not females. CONCLUSIONS CARD8 polymorphisms are likely to be associated with the elevated susceptibility of AS. Present results should be confirmed in the future studies.
本病例对照研究旨在评估半胱氨酸天冬氨酸蛋白酶募集域蛋白 8(CARD8)基因 rs2043211(外显子)和 rs7253718(内含子)多态性与中国汉族人群强直性脊柱炎(AS)易感性的相关性。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对 118 例 AS 患者和 122 例健康对照者的 CARD8 多态性进行基因分型。采用 Haploview 软件进行连锁不平衡(LD)和单倍型分析。采用卡方检验比较病例组和对照组基因型、等位基因和单倍型的分布差异。采用比值比(ORs)和 95%置信区间(CIs)表示 AS 的相对风险。采用 logistic 回归分析调整临床参数对关联结果的影响。
rs2043211 中,变异等位基因 T 在 AS 患者和健康对照组中的分布差异有统计学意义(P=0.046)。这表明 T 等位基因可能增加 AS 的易感性(OR=1.441,95%CI=1.006-2.065)。调整临床特征后,差异的显著性略有降低(P=0.050,OR=1.439,95%CI=0.999-2.072)。rs2043211 与 rs7253718 多态性之间存在强连锁不平衡,rs2043211T-rs7253718G 单倍型与 AS 易感性增加显著相关(OR=1.787,95%CI=1.165-2.740)。在亚组分析中,我们发现 rs2043211 的 TT 基因型和 T 等位基因显著增加了男性 AS 的发病风险(TT 与 AA:OR=2.554,95%CI=1.079-6.049;T 与 A:OR=1.661,95%CI=1.067-2.586),但在女性中无此相关性。
CARD8 多态性可能与 AS 易感性升高有关。本研究结果有待进一步研究验证。