Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E
Department of Genetics and Pathology, Uppsala University, S-751, 23 Uppsala, Sweden.
Am J Hum Genet. 2001 Jul;69(1):96-105. doi: 10.1086/321288. Epub 2001 May 25.
We have completed a genome scan of a 12-generation, 3,400-member pedigree with schizophrenia. Samples from 210 individuals were collected from the pedigree. We performed an "affecteds-only" genome-scan analysis using 43 members of the pedigree. The affected individuals included 29 patients with schizophrenia, 10 with schizoaffective disorders, and 4 with psychosis not otherwise specified. Two sets of white-European allele frequencies were used-one from a Swedish control population (46 unrelated individuals) and one from the pedigree (210 individuals). All analyses pointed to the same region: D6S264, located at 6q25.2, showed a maximum LOD score of 3.45 when allele frequencies in the Swedish control population were used, compared with a maximum LOD score of 2.59 when the pedigree's allele frequencies were used. We analyzed additional markers in the 6q25 region and found a maximum LOD score of 6.6 with marker D6S253, as well as a 6-cM haplotype (markers D6S253-D6S264) that segregated, after 12 generations, with the majority of the affected individuals. Multipoint analysis was performed with the markers in the 6q25 region, and a maximum LOD score of 7.7 was obtained. To evaluate the significance of the genome scan, we simulated the complete analysis under the assumption of no linkage. The results showed that a LOD score >2.2 should be considered as suggestive of linkage, whereas a LOD score >3.7 should be considered as significant. These results suggest that a common ancestral region was inherited by the affected individuals in this large pedigree.
我们对一个有精神分裂症的12代、3400名成员的家系进行了全基因组扫描。从该家系中收集了210名个体的样本。我们使用该家系中的43名成员进行了“仅针对患者”的全基因组扫描分析。受影响个体包括29名精神分裂症患者、10名精神分裂症情感障碍患者和4名未另行指定的精神病患者。使用了两组白人欧洲等位基因频率——一组来自瑞典对照人群(46名无亲属关系的个体),另一组来自该家系(210名个体)。所有分析都指向同一区域:位于6q25.2的D6S264,使用瑞典对照人群的等位基因频率时,最大对数优势(LOD)得分为3.45,而使用该家系的等位基因频率时,最大LOD得分为2.59。我们分析了6q25区域的其他标记,发现标记D6S253的最大LOD得分为6.6,以及一个6厘摩(cM)的单倍型(标记D6S253 - D6S264),经过12代后,该单倍型与大多数受影响个体分离。对6q25区域的标记进行了多点分析,获得的最大LOD得分为7.7。为了评估全基因组扫描的显著性,我们在无连锁的假设下模拟了完整分析。结果表明,LOD得分>2.2应被视为提示连锁,而LOD得分>3.7应被视为显著。这些结果表明,这个大型家系中的受影响个体继承了一个共同的祖先区域。