Vallada H P, Vasques L, Curtis D, Zatz M, Kirov G, Lauriano V, Gentil V, Murray R M, McGuffin P, Owen M, Gill M, Craddock N, Collier D A
Department of Psychological Medicine, Institute of Psychiatry, London, UK.
Psychiatr Genet. 1998 Autumn;8(3):183-6. doi: 10.1097/00041444-199800830-00008.
Since 1969, several classical linkage studies suggested an X-chromosome locus for bipolar affective disorder. However, methods using highly polymorphic DNA markers have provided conflicting evidence for linkage, and an X-chromosomal locus for bipolar disorder remains controversial. More recently, Pekkarinen et al. (1995) found a maximum LOD score of 3.54 at the marker DXS994 in a large bipolar Finnish kindred. In the present study, we attempted to replicate this finding using 43 families multiply affected by bipolar affective disorder. These families were selected for the absence of male-to-male transmission of the disease, and were genotyped for two microsatellte markers, DXS1227 and DXS1062 (which is about 2 cM telomeric to DXS994). Linkage to this region was excluded either using a two-point lod score method with two plausible genetic models, or by a model-free lod score analysis which does not require specification of a particular mode of transmission. We conclude that there is no evidence of a common major gene for bipolar affective disorder at Xq25-q27 in our set of families.
自1969年以来,多项经典连锁研究表明双相情感障碍存在一个X染色体位点。然而,使用高度多态性DNA标记的方法得出了相互矛盾的连锁证据,双相情感障碍的X染色体位点仍存在争议。最近,佩卡里宁等人(1995年)在一个芬兰双相情感障碍大家族中发现,标记DXS994处的最大对数优势(LOD)得分为3.54。在本研究中,我们试图使用43个受双相情感障碍多重影响的家族来重复这一发现。选择这些家族是因为不存在疾病的男性对男性传递,并对两个微卫星标记DXS1227和DXS1062(位于DXS994端粒约2厘摩处)进行基因分型。使用具有两种合理遗传模型的两点LOD评分方法,或通过无需指定特定传递模式的无模型LOD评分分析,排除了与该区域的连锁。我们得出结论,在我们的这组家族中,没有证据表明Xq25 - q27存在双相情感障碍的常见主基因。