Gladman Dafna D, Farewell Vernon T, Pellett Fawnda, Schentag Cathy, Rahman Proton
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Hum Immunol. 2003 Sep;64(9):887-9. doi: 10.1016/s0198-8859(03)00162-9.
Psoriatic arthritis (PsA) is an inflammatory arthritis that may affect as many as 30% of patients with psoriasis (Ps). Genetic factors play an important role in the susceptibility to and the expression of PsA. The objective of this study was to identify whether haplotype sharing among affected sibling pairs of individuals with PsA is increased compared with unaffected sibling pairs. We collected 182 sibling pairs of probands affected with PsA. Extracted genomic DNA was amplified in polymerase chain reactions using locus specific primers homologous to nucleotide sequences for each of the HLA-A, -B, -C, -DR, and -DQ loci. Polymerase chain reaction amplicons were identified by reverse line blot assay using sequence-specific oligonucleotide probes. Evidence for excessive haplotype sharing was examined through Green and Woodrow's test. Results indicate that of the 182 sibling pairs, 46 were affected by PsA, 48 by Ps, and 88 were unaffected. The sharing of 2, 1, and 0 haplotypes for the PsA affected sibling pairs was 14, 27, and 5, respectively (p = 0.04); whereas the haplotype sharing for the Ps affected sibling pairs was 12, 26, and 10, respectively (p = 0.38). In conclusion, the human leukocyte antigen region on chromosome 6p is implicated as one of the candidate regions in PsA.
银屑病关节炎(PsA)是一种炎症性关节炎,可能影响多达30%的银屑病(Ps)患者。遗传因素在PsA的易感性和表达中起重要作用。本研究的目的是确定与未患病的同胞对相比,患PsA的同胞对之间的单倍型共享是否增加。我们收集了182对患PsA的先证者同胞对。提取的基因组DNA在聚合酶链反应中使用与HLA - A、- B、- C、- DR和 - DQ位点的核苷酸序列同源的位点特异性引物进行扩增。聚合酶链反应扩增产物通过使用序列特异性寡核苷酸探针的反向线印迹分析进行鉴定。通过格林和伍德罗检验检查单倍型过度共享的证据。结果表明,在182对同胞对中,46对受PsA影响,48对受Ps影响,88对未受影响。患PsA的同胞对共享2个、1个和0个单倍型的比例分别为14、27和5(p = 0.04);而患Ps的同胞对的单倍型共享比例分别为12、26和10(p = 0.38)。总之,6号染色体短臂上的人类白细胞抗原区域被认为是PsA的候选区域之一。