Chakravarti A, Halloran S L, Bale S J, Tucker M A
Genet Epidemiol. 1986;3(6):407-15. doi: 10.1002/gepi.1370030605.
Forty-one multiplex families, from published sources and new data from the National Cancer Institute, segregating for Hodgkin's disease and HLA, have been studied. A reanalysis of these data strongly suggests a recessive mode of inheritance for susceptibility to Hodgkin's disease. The HLA haplotype sharing data between affected relatives demonstrate that approximately 60% of cases in multiplex families are due to an HLA-linked susceptibility gene, the remaining 40% being due to other familial factors. The data clearly support the hypothesis of etiological heterogeneity for Hodgkin's disease, with both HLA-linked and HLA-unlinked factors being responsible. Finally, there is an increased concordance of histological types between affected relatives, but this concordance seems independent of HLA sharing.
对来自已发表资料以及美国国立癌症研究所新数据的41个多重家庭进行了研究,这些家庭中霍奇金病和HLA呈分离状态。对这些数据的重新分析有力地表明,霍奇金病易感性的遗传模式为隐性遗传。患病亲属之间的HLA单倍型共享数据表明,多重家庭中约60%的病例归因于与HLA相关的易感性基因,其余40%归因于其他家族因素。这些数据明确支持霍奇金病病因异质性的假说,即与HLA相关和与HLA不相关的因素均起作用。最后,患病亲属之间组织学类型的一致性增加,但这种一致性似乎与HLA共享无关。