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多例类风湿关节炎患者家庭中的人类白细胞抗原分型

HLA typing in families with multiple cases of rheumatoid arthritis.

作者信息

Strotzer M, Menninger H, Scholz S, Albert E D

机构信息

I. Clinic of Internal Medicine, Rheumatologic Center of Bavarian Red Cross, Bad Abbach, Federal Republic of Germany.

出版信息

Ann Rheum Dis. 1991 May;50(5):298-300. doi: 10.1136/ard.50.5.298.

Abstract

Thirty one white patients from 14 families with multiple cases of rheumatoid arthritis (RA) and 42 of their healthy relatives were completely HLA typed. In contrast with class I antigens, the class II antigens DR1 and DR4 were significantly more common in the patients than in a group of 200 healthy local white controls (DR1: 32% v 12%; DR4: 48% v 28%, in patients and controls respectively). Owing to the small number of cases the data from this study were combined with those of published reports. Examination of patients for DR1 and DR4 homozygosity and DR1/4 heterozygosity showed an increase of DR1 homozygous patients, which was not statistically significant. There was no striking deviation from random expectation in haplotype sharing of affected sib pairs. These results are compatible with a dominant influence of DR1 and DR4 in the mode of inheritance. The nearly random haplotype sharing and the molecular relation between DR1 and DR4 support the hypothesis of a direct influence of these antigens in the pathogenesis of RA. Only 68% of the patients in this study possessed either DR1 or DR4, possibly indicating a subtype of RA which is independent of HLA. Clinical and serological variables were measured and indicated no significant difference between DR1 (or DR4) positive and DR1 (or DR4) negative disease. In this small group of patients the clinical course of RA seemed to be determined mainly by other genetic or environmental factors.

摘要

对来自14个有多例类风湿性关节炎(RA)病例的家庭的31名白人患者及其42名健康亲属进行了完整的HLA分型。与I类抗原不同,II类抗原DR1和DR4在患者中比200名当地健康白人对照组更为常见(DR1:患者组为32%,对照组为12%;DR4:患者组为48%,对照组为28%)。由于病例数量较少,本研究的数据与已发表报告的数据合并。对患者进行DR1和DR4纯合性以及DR1/4杂合性检测,结果显示DR1纯合患者有所增加,但无统计学意义。受累同胞对的单倍型共享情况与随机预期无明显偏差。这些结果与DR1和DR4在遗传模式中的显性影响相符。近乎随机的单倍型共享以及DR1和DR4之间的分子关系支持了这些抗原在RA发病机制中直接起作用的假说。本研究中只有68%的患者携带DR1或DR4,这可能表明存在一种独立于HLA的RA亚型。对临床和血清学变量进行了测量,结果显示DR1(或DR4)阳性和DR1(或DR4)阴性疾病之间无显著差异。在这一小群患者中,RA的临床病程似乎主要由其他遗传或环境因素决定。

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HLA antigens and rheumatoid arthritis.
Arthritis Rheum. 1983 Aug;26(8):1053-4. doi: 10.1002/art.1780260820.
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HLA haplotypes in multiple case families with rheumatoid arthritis.
Clin Rheumatol. 1984 Dec;3(4):557. doi: 10.1007/BF02031286.

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