Ewald H, Degn B, Mors O, Kruse T A
Department of Psychiatric Demography, Psychiatric Hospital in Aarhus, Denmark.
Mol Psychiatry. 1998 Sep;3(5):442-8. doi: 10.1038/sj.mp.4000420.
Significant evidence for linkage between bipolar affective disorder and markers on chromosome 4p16 has been reported in Scottish families. Linkage analyses using 16 DNA markers covering more than 50 cM from chromosome 4pter-4p12, including candidate genes encoding the dopamine D5 receptor and an adrenergic receptor (2C), were performed in two Danish families with bipolar affective disorder. Assuming homogeneity in the two families, the highest lod score found in the two-point linkage analyses was 2.00 at 0.03 recombination fraction for D4S394, i.e. the marker which also was most significant in the original Scottish study. Simulation showed that such a lod score would only occur six out of 10,000 times with an unlinked marker. Though the present study thus replicates the Scottish findings according to the criteria suggested by Lander and Kruglyak, caution is warranted as the mode of inheritance which yielded the highest lod score in the two studies was different. Final proof of a disease locus in the Scottish and our study has to await the identification of a DNA sequence of functional significance for bipolar disorder.
在苏格兰家庭中,已有大量证据表明双相情感障碍与4号染色体p16区域的标记物之间存在连锁关系。在两个患有双相情感障碍的丹麦家庭中,使用了16个DNA标记进行连锁分析,这些标记覆盖了4号染色体从pter到p12区域超过50厘摩的范围,包括编码多巴胺D5受体和一种肾上腺素能受体(2C)的候选基因。假设这两个家庭具有同质性,在两点连锁分析中发现的最高对数优势分数在D4S394的重组率为0.03时为2.00,D4S394也就是在最初的苏格兰研究中最显著的标记物。模拟显示,对于一个不连锁的标记物,这样的对数优势分数在10000次中只会出现6次。因此,尽管根据兰德和克鲁格利亚克提出的标准,本研究重复了苏格兰的研究结果,但由于两项研究中产生最高对数优势分数的遗传模式不同,仍需谨慎。苏格兰和我们研究中疾病位点的最终证据,必须等待鉴定出对双相情感障碍具有功能意义的DNA序列。