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人类白细胞抗原B27与强直性脊柱炎的遗传学

HLA B27 and the genetics of ankylosing spondylitis.

作者信息

Woodrow J C, Eastmond C J

出版信息

Ann Rheum Dis. 1978 Dec;37(6):504-9. doi: 10.1136/ard.37.6.504.

Abstract

One hundred and twenty-eight of 145 patients with ankylosing spondylitis (AS) were found to be HLA B27 positive. Five patients had evidence of a sero-negative peripheral arthritis resembling peripheral psoriatic arthritis and 3 of these were B27 negative. One further B27 negative patients had a sister with ankylosing spondylitis and ulcerative colitis and a mother with ulcerative colitis. There was evidence of a somewhat later age of onset of symptoms in B27 negative patients. These findings are interpreted as suggesting some degree of clinical and genetic heterogeneity in ankylosing spondylitis with genes for psoriasis and inflammatory bowel disease being important in some individuals, particularly those who are B27 negative. Twenty-five first-degree relatives with ankylosing spondylitis were all B27 positive. The only instance of disassociation of B27 and spondylitis in a family was where the proband had ulcerative colitis as well as spondylitis. Of 13 B27 positive fathers 3 could be diagnosed as having definite ankylosing spondylitis (23%). These findings are thought to provide evidence against the concept that the gene for ankylosing spondylitis is not B27 but a closely linked gene and favour the occurrence of an environmental event affecting approximately one-fifth of B27 positive males to result in disease.

摘要

145例强直性脊柱炎(AS)患者中,128例HLA B27呈阳性。5例患者有血清阴性外周关节炎的证据,类似于外周型银屑病关节炎,其中3例B27呈阴性。另有1例B27阴性患者,其姐姐患有强直性脊柱炎和溃疡性结肠炎,母亲患有溃疡性结肠炎。有证据表明,B27阴性患者的症状出现年龄稍晚。这些发现被解释为提示强直性脊柱炎存在一定程度的临床和遗传异质性,银屑病和炎症性肠病的基因在某些个体中很重要,特别是那些B27阴性的个体。25名患有强直性脊柱炎的一级亲属均为B27阳性。在一个家族中,B27与脊柱炎分离的唯一情况是先证者同时患有溃疡性结肠炎和脊柱炎。在13名B27阳性的父亲中,3名可被诊断为患有明确的强直性脊柱炎(23%)。这些发现被认为提供了证据,反对强直性脊柱炎基因不是B27而是一个紧密连锁基因的概念,并支持存在一种环境事件,影响约五分之一的B27阳性男性从而导致疾病的发生。

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本文引用的文献

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Ankylosing spondylitis and HL-A 27.强直性脊柱炎与人类白细胞抗原27
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Tissue Antigens. 1975 Oct;6(4):262-4. doi: 10.1111/j.1399-0039.1975.tb00641.x.
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