Kvien T K, Møller P, Dale K
Scand J Rheumatol. 1985;14(1):47-50. doi: 10.3109/03009748509102016.
Ten consecutive patients with juvenile ankylosing spondylitis were investigated in a prospective study. At least one of the parents of each patient had a positive history of probable or definite ankylosing spondylitis, Reiter's syndrome, or acute anterior uveitis. The patients and their parents were examined clinically and were HLA-typed. Nine of the 10 patients exhibited the genetic marker HLA B27, but only one patient was homozygous for HLA B27. This prevalence of homozygosity among HLA B27 positive persons could be expected to occur by chance alone. Based on the limited material studied, we cautiously conclude that HLA B27 homozygosity is probably not responsible for disease onset in childhood.
在一项前瞻性研究中,对连续10例青少年强直性脊柱炎患者进行了调查。每位患者至少有一位父母有可能或确诊的强直性脊柱炎、赖特综合征或急性前葡萄膜炎的阳性病史。对患者及其父母进行了临床检查并进行了HLA分型。10例患者中有9例表现出基因标记HLA B27,但只有1例患者为HLA B27纯合子。这种HLA B27阳性者中纯合子的患病率仅靠偶然因素就可能出现。基于所研究的有限资料,我们谨慎地得出结论,HLA B27纯合性可能不是儿童期疾病发病的原因。