Frecker M, Mercer G, Skanes V M, Farid N R
Thyroid Research Laboratory, Memorial University of Newfoundland, Canada.
Autoimmunity. 1988;1(4):307-15. doi: 10.3109/08916938809010684.
We investigated the influence of gene mapping within the major histocompatibility complex on the susceptibility to Graves' eye disease. We studied 133 randomly selected patients with Graves' disease, many of whom had eye disease. HLA B8 and DR3 carried the greatest risk for disease but the difference between the two patient groups was not statistically significant. An earlier finding that Hungarian patients with a subset of B8, (B8 + DR7 +) had a greatly enhanced risk for eye disease was confirmed in Newfoundland patients. HLA B8 and DR7 are probably carried on different homologous chromosomes and their interaction enhances eye disease. HLA-DR4 was negatively correlated with eye disease. In particular, a subset of DR4 (B35 + DR4 +) appears to protect against eye disease. We have also derived the haplotypes of 22 probands, half of whom had eye disease. The haplotype data emphasized the high frequency of HLA A1 B8 DR3 C4AQO and C4B1 in both patient groups, 15% of the haplotypes in the group with eye disease and 25% in that without eye disease. Forty-one percent of haplotypes in the eye disease group and 32% in the no eye disease group were either C4AQO or C4BQO. In one proband with eye disease B8 and DR7 were carried on separate chromosomes. The phenotype DR4, C4A3 C4B1 was found in 3/20 haplotypes of patients without eye disease but in 0/20 of patients with eye disease. This finding is in keeping with the increased frequency of the DR4 C4A3 C4B1 in the patient group with no eye disease when 94 patients were phenotyped.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了主要组织相容性复合体内的基因定位对格雷夫斯眼病易感性的影响。我们研究了133名随机选取的格雷夫斯病患者,其中许多人患有眼部疾病。HLA B8和DR3携带的患病风险最高,但两组患者之间的差异无统计学意义。一项早期研究发现,匈牙利患有B8子集(B8 + DR7 +)的患者患眼病的风险大大增加,这一发现在纽芬兰患者中得到了证实。HLA B8和DR7可能位于不同的同源染色体上,它们的相互作用会加重眼病。HLA-DR4与眼病呈负相关。特别是,DR4的一个子集(B35 + DR4 +)似乎可预防眼病。我们还推导了22名先证者的单倍型,其中一半患有眼病。单倍型数据强调了HLA A1 B8 DR3 C4AQO和C4B1在两组患者中的高频率,在患有眼病的组中为15%的单倍型,在无眼病的组中为25%。眼病组中41%的单倍型和无眼病组中32%的单倍型要么是C4AQO要么是C4BQO。在一名患有眼病的先证者中,B8和DR7位于不同的染色体上。在无眼病患者的20个单倍型中有3个发现了DR4、C4A3 C4B1的表型,但在患有眼病的患者中20个单倍型中均未发现。当对94名患者进行表型分析时,这一发现与无眼病患者组中DR4 C4A3 C4B1频率增加一致。(摘要截选至250词)