Hebebrand J, Hennighausen K
Klinik für Kinder- und Jugendpsychiatrie, Philipps-Universität, Marburg, Federal Republic of Germany.
Hum Genet. 1992 Nov;90(3):289-93. doi: 10.1007/BF00220081.
High lod scores were obtained in several X-linkage studies of bipolar illness under the assumption that a subgroup of manic depression follows an X-linked dominant mode of inheritance. We have previously shown that the segregation patterns do not substantiate this assumption. We now statistically address the lack of evidence for X-linked inheritance by sex-dependently analyzing segregation ratios and clinical data presented in eight positive X-linkage studies. Accordingly, affected males have significantly fewer offspring, a lower mean age and a higher bipolar to unipolar ratio than affected females. There are two possible explanations for these findings: either the X-linked subgroup of bipolar illness has unique features that have not been accounted for clinically, or (more probably) the pedigree structures could also (and might be more likely to) result from ascertaining kindreds following autosomal or multifactorial inheritance only, with exclusion of kindreds encompassing male to male transmission.
在双相情感障碍的多项X连锁研究中,基于躁郁症的一个亚组遵循X连锁显性遗传模式这一假设,获得了较高的连锁值。我们之前已经表明,分离模式并不能证实这一假设。我们现在通过性别依赖性分析八项阳性X连锁研究中呈现的分离比率和临床数据,从统计学角度探讨缺乏X连锁遗传证据的问题。因此,与受影响的女性相比,受影响的男性后代显著更少,平均年龄更低,双相情感障碍与单相情感障碍的比例更高。对于这些发现有两种可能的解释:要么双相情感障碍的X连锁亚组具有临床上未考虑到的独特特征,要么(更有可能)家系结构也可能(并且更有可能)仅在确定遵循常染色体或多因素遗传的亲属时出现,而排除了包含男性到男性传递的亲属。