Haines J L, Panter S S, Rich S S, Eaton J W, Tsai M Y, Anderson V E
Am J Med Genet. 1986 Aug;24(4):723-34. doi: 10.1002/ajmg.1320240417.
The multisib (MS) sampling strategy was used for detecting possible genetic influences on a complex and heterogeneous disorder. The MS strategy increases the likelihood of selecting pedigrees for single genetic factors and allows the efficient analysis of data. The collection of complete pedigrees will procure additional data, but at a large marginal expense. The MS ascertainment procedure was applied to seizure disorders by examination of taurine excretion levels and by conducting two-dimensional gel electrophoresis of plasma proteins. Reduced taurine excretion (proposed to be genetically controlled) was found to associate with seizures, particularly in those individuals with a generalized spike and wave (GSW) EEg, or in families with a GSW-seizure history. Examination of two-dimensional gels showed hypohaptoglobinemia in several seizure patients [Panter et al, 1984]. The frequency of hypohaptoglobinemia is greatly increased in familial seizure cases, and may also be genetically controlled. Thus the MS strategy has proven successful in identifying kindreds in which specific physiological alterations may contribute toward the complex phenotype of seizures.
多同胞(MS)抽样策略用于检测对复杂异质性疾病可能的遗传影响。MS策略增加了为单一遗传因素选择家系的可能性,并允许对数据进行有效分析。收集完整家系会获得额外数据,但边际成本很高。通过检测牛磺酸排泄水平和对血浆蛋白进行二维凝胶电泳,将MS确定程序应用于癫痫发作疾病。发现牛磺酸排泄减少(推测受遗传控制)与癫痫发作有关,特别是在那些有全身性棘波和慢波(GSW)脑电图的个体中,或在有GSW癫痫发作病史的家庭中。二维凝胶检查显示,一些癫痫患者存在低结合珠蛋白血症[潘特等人,1984年]。在家族性癫痫病例中,低结合珠蛋白血症的频率大大增加,也可能受遗传控制。因此,MS策略已被证明在识别特定生理改变可能导致癫痫复杂表型的亲属关系方面是成功的。