Woo P, O'Brien J, Robson M, Ansell B M
Division of Rheumatology, MRC Clinical Research Centre, Harrow, Middlesex.
Lancet. 1987 Oct 3;2(8562):767-9. doi: 10.1016/s0140-6736(87)92501-3.
A genetic marker of susceptibility to systemic amyloidosis has been identified. A DNA polymorphic site, 5' to the serum amyloid P component gene, has been found to be significantly associated with amyloidosis in juvenile arthritic patients. When genomic DNA was cut with the restriction enzyme MspI and probed with the cDNA for serum amyloid P component, homozygosity for the 5.6 kb restriction fragment length polymorphic (RFLP) band was absent in all 28 amyloid patients. Furthermore, the proportion who were homozygous for the 8.8 kb RFLP band was greater (p = 0.008) than that among 89 normal subjects. The distribution of this polymorphic site among 19 juvenile arthritic patients without amyloidosis was the same as that in the normal group. Thus the 8.8 kb RFLP band represents a genetic predisposition to reactive amyloidosis in juvenile arthritis and may apply to amyloidosis associated with more common inflammatory conditions.
一种全身性淀粉样变性易感性的基因标记已被识别。已发现血清淀粉样蛋白P成分基因5'端的一个DNA多态性位点与青少年关节炎患者的淀粉样变性显著相关。当用限制性内切酶MspI切割基因组DNA并用血清淀粉样蛋白P成分的cDNA进行探针杂交时,所有28例淀粉样变性患者均不存在5.6 kb限制性片段长度多态性(RFLP)条带的纯合性。此外,8.8 kb RFLP条带纯合子的比例高于89名正常受试者(p = 0.008)。该多态性位点在19例无淀粉样变性的青少年关节炎患者中的分布与正常组相同。因此,8.8 kb RFLP条带代表青少年关节炎中反应性淀粉样变性的遗传易感性,可能也适用于与更常见炎症性疾病相关的淀粉样变性。