James N M
Arch Gen Psychiatry. 1977 Jun;34(6):715-7. doi: 10.1001/archpsyc.1977.01770180101009.
A group of 46 bipolar probands was divided equally into those with early (before age 30) and later onset. The only significant difference found was a higher morbidity risk for the relatives of the early-onset group. Slater's model for a polygenic transmission was found compatible with this group, but insufficient data prevented its application in the older-onset group. In all other respects, however, no significant differences were found. Age of onset of illness may be unhelpful in elucidating the genetic basis of affective disorder. Further progress will depend on the development of more sensitive mathematical models and the finding of specific genetic markers.
一组46名双相情感障碍先证者被平均分为早发组(30岁之前发病)和晚发组。唯一发现的显著差异是早发组亲属的发病风险更高。发现斯莱特的多基因传递模型与该组相符,但数据不足阻碍了其在晚发组中的应用。然而,在所有其他方面,未发现显著差异。疾病的发病年龄可能无助于阐明情感障碍的遗传基础。进一步的进展将取决于更敏感的数学模型的开发以及特定遗传标记的发现。