Visscher B R, Detels R, Dudley J, Haile R W, Malmgren R M, Terasaki P I, Park M S
Neurology. 1979 Oct;29(10):1354-60. doi: 10.1212/wnl.29.10.1354.
Previous studies of histocompatibility (HLA) types in multiple sclerosis (MS) families did not provide convincing proof of an HLA-linked susceptibility factor. In 12 families we studied, all MS cases in each family shared at least one chromosome. The probability of this occurring in the absence of genetic linkage is approximately 0.001. The estimated penetrance is 5 percent, implying that the genetic susceptibility factor may be a necessary but not a sufficient cause of MS. Additional studies are needed to identify other differences between affected and unaffected susceptible individuals.
先前对多发性硬化症(MS)家族中组织相容性(HLA)类型的研究并未提供HLA相关易感性因素的令人信服的证据。在我们研究的12个家族中,每个家族中的所有MS病例至少共享一条染色体。在不存在基因连锁的情况下发生这种情况的概率约为0.001。估计的外显率为5%,这意味着遗传易感性因素可能是MS的必要但非充分病因。需要进一步的研究来确定患病和未患病的易感个体之间的其他差异。