Magnus P, Magnus E M, Berg K
Clin Genet. 1986 Sep;30(3):167-72. doi: 10.1111/j.1399-0004.1986.tb00590.x.
In an attempt to identify biochemical components of the genetic predisposition to neural tube defects (NTDs), levels of folate, cobalamin, apo-transcobalamins I and II and alpha-fetoprotein were studied in midtrimester amniotic fluid from 24 pregnant women who had previously had a child with NTD. The control group consisted of 76 mothers, subjected to amniocentesis for reasons other than risk of NTD in offspring. Only pregnancies with normal outcome were included. No differences were found between groups for levels of folate, cobalamin or alpha-fetoprotein. Folate intake or metabolism did not appear to differ between groups. In contrast, the level of apo-transcobalamin I was doubled and the level of apo-transcobalamin II tripled in amniotic fluid from women who had had a child with NTD compared with the control group. Since the variation in apo-transcobalamin II in adults is to a high degree genetically determined, the present results may suggest that the genetic predisposition to NTD is associated with variation in this protein. Further studies are needed to substantiate or reject this possibility.
为了确定神经管缺陷(NTDs)遗传易感性的生化成分,对24名曾生育过患神经管缺陷孩子的孕妇孕中期羊水样本中的叶酸、钴胺素、脱辅基转钴胺素I和II以及甲胎蛋白水平进行了研究。对照组由76名母亲组成,她们因后代神经管缺陷风险以外的原因接受了羊膜穿刺术。仅纳入结局正常的妊娠。两组间叶酸、钴胺素或甲胎蛋白水平未发现差异。两组间叶酸摄入或代谢情况似乎也无差异。相比之下,与对照组相比,曾生育过患神经管缺陷孩子的女性羊水中脱辅基转钴胺素I水平翻倍,脱辅基转钴胺素II水平增至三倍。由于成年人脱辅基转钴胺素II的变异在很大程度上由基因决定,目前的结果可能表明神经管缺陷的遗传易感性与该蛋白的变异有关。需要进一步研究来证实或排除这种可能性。