Gilger J W, Pennington B F, Harbeck R J, DeFries J C, Kotzin B, Green P, Smith S
University of Kansas, 3031 Dole Human Development Center, Lawrence, KS 66045, USA.
Brain Cogn. 1998 Apr;36(3):310-33. doi: 10.1006/brcg.1997.0972.
We conducted a study of the association between developmental reading disability (DRD) and immune disorders (ID) using both survey and immunoassay data in two separate samples of families. One sample was made up of twins and their parents and was ascertained through a population-based sampling scheme. The other sample was a set of extended pedigrees selected for apparent autosomal dominant transmission of DRD. We failed to find an association between DRD and ID in either sample, regardless of the method used to assess immune system function. Even though our twin sample provided evidence that both DRD and immune conditions were significantly heritable, there was no evidence for a genetic correlation between ID and DRD nor was there any clear indication that a special subgroup of individuals may be comorbid for these conditions because of genetic reasons. How these negative findings can be reconciled with the developmental hypothesis of Geschwind, Behan, Galaburda, and colleagues, and how they may relate to the gene locus influencing DRD that has been recently located in the HLA region of the short arm of chromosome 6 is discussed.
我们利用两个独立的家庭样本中的调查数据和免疫测定数据,对发育性阅读障碍(DRD)与免疫紊乱(ID)之间的关联进行了研究。一个样本由双胞胎及其父母组成,通过基于人群的抽样方案确定。另一个样本是一组扩展家系,因其明显的常染色体显性遗传DRD而被选取。无论使用何种方法评估免疫系统功能,我们在两个样本中均未发现DRD与ID之间存在关联。尽管我们的双胞胎样本提供了证据表明DRD和免疫状况都具有显著的遗传性,但没有证据表明ID与DRD之间存在遗传相关性,也没有任何明确迹象表明由于遗传原因,可能有一个特殊的个体亚组会同时患有这两种疾病。本文讨论了这些阴性结果如何与Geschwind、Behan、Galaburda及其同事的发育假说相协调,以及它们如何与最近位于6号染色体短臂HLA区域的影响DRD的基因座相关。