Tomàs Carmen, Cañellas Francisca, Rodríguez Virginia, Picornell Antònia, Lafau Oriol, Nadal Marcos, Roca Miquel, Serrano M Jesús, Castro José A, Ramon M Misericòrdia
Laboratory of Genetics, Department of Biology, University Institute of Health Sciences (IUNICS), and Juan March Hospital, Palma de Mallorca, Spain.
Psychiatr Genet. 2006 Aug;16(4):145-51. doi: 10.1097/01.ypg.0000218614.42762.b0.
Genetically, bipolar disorder is a complex genetic illness, in which both genes and environmental factors play an important role in pathogenesis. Linkage studies have reported suggestive evidence for genomic regions, especially on chromosome 18, but in most cases they have been inconclusive. A total of 12 pedigrees, from the islands of Majorca and Minorca (Balearic Archipelago), with a high expression of mental illness, have been studied. A scan of 29 polymorphic short tandem repeat markers was performed, spanning chromosomes 17 and 18 for bipolar and other affective disorder susceptibility loci. Narrow (only bipolar I disorder) and broad (bipolar plus other affective disorders) diagnosis criteria were employed. The loci D18S63, D18S452, D18S53, D18S61, D18S1161 and D17S831 showed LOD score values of less than -2. Thus, the positive linkage found by other authors on the regions 18p11.2 and 18p11.3 has not been reproduced in the families studied. The data obtained in chromosome 17 suggested two possible regions that could contain a bipolar disorder susceptibility gene: 17q11 (D17S1857, D17S798) and especially 17q24-qter (D17S949, D17S928). The maximum significant linkage was to D17S949 (17q24), following a recessive mode of inheritance. We have also found a positive LOD score value for D18S478 marker located in the region 18q12.
从基因角度来看,双相情感障碍是一种复杂的遗传性疾病,基因和环境因素在其发病机制中都起着重要作用。连锁研究报告了基因组区域存在提示性证据,特别是在18号染色体上,但在大多数情况下,这些证据并不确凿。我们对来自马略卡岛和梅诺卡岛(巴利阿里群岛)的12个精神疾病高发家系进行了研究。对29个多态性短串联重复标记进行了扫描,覆盖17号和18号染色体,以寻找双相情感障碍及其他情感障碍的易感基因座。采用了狭义(仅双相I型障碍)和广义(双相情感障碍加其他情感障碍)诊断标准。基因座D18S63、D18S452、D18S53、D18S61、D18S1161和D17S831的对数优势(LOD)分值小于-2。因此,其他作者在18p11.2和18p11.3区域发现的阳性连锁在本研究家族中未得到重现。在17号染色体上获得的数据表明,有两个可能包含双相情感障碍易感基因的区域:17q11(D17S1857、D17S798),尤其是17q24 - qter(D17S949、D17S928)。最大显著连锁位于D17S949(17q24),呈隐性遗传模式。我们还发现位于18q12区域的D18S47标记的LOD分值为阳性。