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Stratification by age of onset with 30 years as age limit is an effective means of identifying PSORS1-associated psoriasis in patients with psoriatic arthritis.

机译:以发病年龄(年龄限制为30岁)进行分层是鉴定银屑病关节炎患者中PSORS1相关牛皮癣的有效手段。

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OBJECTIVES: To determine which of the following is the best method to identify PSORS1-associated psoriasis in patients with psoriatic arthritis (PsA): age at disease onset or positive family history of disease. METHODS: A total of 71 patients with PsA who met the CASPAR criteria were recruited on a randomized basis. The patients were stratified according to age at disease onset, with cutoff points at 25, 30, 35 and 40years of age. The alleles of locus Cw were analyzed by PCR-based methods, and their distribution was compared to that of 177 healthy blood donors. RESULTS: HLA-Cw*0602-PSORS1- was associated with disease risk (56% vs. 18%) OR 5.8, 95%CI: 3.2-10.7, P=0.00001. A close relationship was established between this allele and onset of psoriasis under 30years of age (68% vs. 24%) OR 6.4, 95%CI: 2.3-18.2, P=0.0003. The relationship in turn lost significance above this age limit. An association was found between a family history of psoriasis and disease risk, though there was no specific cutoff point according to age at onset of the disease. Sixty-four percent of the subjects with positive family history were HLA-Cw*06 (+) compared to 44% of those without a family history, OR 2.3, 95% CI: 0.82-6.36, P=0.08. CONCLUSIONS: In patients with PsA, the susceptibility effect of HLA-Cw*06 declines with increasing age of onset. Disease onset under or above 30years of age may contribute to differentiate type I vs. type II psoriasis in PsA populations, while the family history have a lesser contribution to such stratification.
机译:目的:确定以下哪种方法是鉴定患有银屑病关节炎(PsA)的PSORS1相关牛皮癣的最佳方法:发病年龄或发病家族史。方法:随机招募了符合CASPAR标准的71例PsA患者。根据疾病发作的年龄对患者进行分层,分界点分别为25、30、35和40岁。通过基于PCR的方法分析了Cw基因座的等位基因,并将其分布与177位健康献血者的分布进行了比较。结果:HLA-Cw * 0602-PSORS1-与疾病风险相关(56%比18%)或5.8,95%CI:3.2-10.7,P = 0.00001。在30岁以下(68%比24%)或6.4、95%CI:2.3-18.2,P = 0.0003,此等位基因与牛皮癣的发作之间建立了密切的关系。在超过这个年龄限制后,这种关系反过来失去了意义。尽管没有根据疾病发病年龄的具体分界点,但在牛皮癣家族病史和疾病风险之间发现了关联。家族史阳性的受试者中有64%为HLA-Cw * 06(+),而没有家族史的受试者为44%,或2.3,95%CI:0.82-6.36,P = 0.08。结论:在PsA患者中,HLA-Cw * 06的药敏作用随着发病年龄的增加而降低。在PsA人群中,年龄在30岁以下或30岁以上的疾病可能有助于区分I型和II型牛皮癣,而家族史对这种分层的影响较小。

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