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糖尿病母亲所生婴儿的畸形

Malformations in infants of diabetic mothers.

作者信息

Mills J L

出版信息

Teratology. 1982 Jun;25(3):385-94. doi: 10.1002/tera.1420250316.

Abstract

Maternal insulin-dependent diabetes has long been associated with congenital malformations. As other causes of mortality and morbidity have been eliminated or reduced, malformations have become increasingly prominent. Although there is not universal agreement, the great majority of investigators find a two- to threefold increase in malformations in infants of insulin-dependent diabetic mothers. This increase is not seen in infants of gestational diabetics. It probably is not present in women whose diabetes can be controlled by diet or oral hypoglycemic agents. The risk does not appear to be primarily genetic since diabetic fathers do not have an increased number of malformed offspring. Most studies show a generalized increase in malformations involving multiple organ systems. Multiple malformations seem to be more common in diabetic than nondiabetic infants. Caudal regression has the strongest association with diabetes, occurring roughly 200 times more frequently in infants of diabetic mothers than in other infants. The teratogenic mechanism in diabetes is not known. Hyperglycemia may be important but human studies focusing on the period of organogenesis are lacking. Hypoglycemia has also been suggested based mainly on animal experiments. Insulin appears unlikely. Numerous other factors including vascular disease, hypoxia, ketone and amino acid abnormalities, glycosylation of proteins, or hormone imbalances could be teratogenic. None has been studied in sufficient detail to make a judgment. A large-scale prospective study is required to determine early fetal loss rates, correlate metabolic status during organogenesis with outcome, and assess the effect of diabetic control on malformation rates.

摘要

母体胰岛素依赖型糖尿病长期以来一直与先天性畸形有关。随着其他死亡和发病原因已被消除或减少,畸形问题变得日益突出。尽管并非所有人都达成共识,但绝大多数研究者发现,胰岛素依赖型糖尿病母亲所生婴儿的畸形率增加了两到三倍。妊娠期糖尿病母亲所生婴儿未出现这种增加情况。糖尿病可通过饮食或口服降糖药控制的女性所生婴儿可能也不存在这种风险。这种风险似乎并非主要由基因引起,因为糖尿病父亲所生后代的畸形数量并未增加。大多数研究表明,涉及多个器官系统的畸形普遍增加。糖尿病婴儿似乎比非糖尿病婴儿更容易出现多发畸形。尾椎退化与糖尿病的关联最为密切,糖尿病母亲所生婴儿出现尾椎退化的频率大约是其他婴儿的200倍。糖尿病的致畸机制尚不清楚。高血糖可能很重要,但缺乏针对器官形成期的人体研究。主要基于动物实验也有人提出低血糖可能致畸。胰岛素似乎不太可能。包括血管疾病、缺氧、酮体和氨基酸异常、蛋白质糖基化或激素失衡在内的许多其他因素都可能致畸。但对这些因素均未进行充分详细的研究以做出判断。需要开展大规模前瞻性研究,以确定早期胎儿丢失率,将器官形成期的代谢状态与结局相关联,并评估糖尿病控制对畸形率的影响。

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