Källén Bengt A J, Otterblad Olausson Petra, Danielsson Bengt R
Tornblad Institute, Lund University, Biskospgatan 7, SE-22362 Lund, Sweden.
Reprod Toxicol. 2005 Jul-Aug;20(2):209-14. doi: 10.1016/j.reprotox.2005.01.010.
The possible teratogenic effect of erythromycin therapy, noted previously, was studied. Women who had taken erythromycin or penicillin V in early pregnancy and their infants were studied, using the Swedish Medical Birth Register where information on drug use during pregnancy was recorded based on interviews in early pregnancy. The risk for any congenital malformation after erythromycin therapy (but not after penicillin V therapy) was increased (odds ratio 1.24, 95% confidence interval: 1.01-1.51) and this was due to an effect on cardiovascular malformations (odds ratio 1.92, 95% CI: 1.37-2.68). There was also an indicated increased risk for pyloric stenosis (risk ratio 3.0, 95% CI: 1.1-8.5 after exposure in early pregnancy). Various explanations to the finding are discussed, one of them linked to the fact that erythromycin inhibits a specific cardiac potassium channel (IKr) which seems to play a major role in cardiac rhythm regulation in the early embryo. Potent blocking drugs cause as a class effect cardiac defects in animal experiments.
此前已注意到的红霉素治疗可能的致畸作用得到了研究。对在妊娠早期服用过红霉素或青霉素V的女性及其婴儿进行了研究,利用瑞典医学出生登记册,其中关于孕期用药的信息是基于妊娠早期的访谈记录的。红霉素治疗后(而非青霉素V治疗后)出现任何先天性畸形的风险增加(比值比1.24,95%置信区间:1.01 - 1.51),这是由于对心血管畸形的影响(比值比1.92,95%置信区间:1.37 - 2.68)。还表明幽门狭窄风险增加(妊娠早期暴露后风险比3.0,95%置信区间:1.1 - 8.5)。对该发现进行了各种解释的讨论,其中之一与红霉素抑制一种特定的心脏钾通道(IKr)这一事实有关,该通道似乎在早期胚胎的心律调节中起主要作用。在动物实验中,强效阻断药物作为一类效应会导致心脏缺陷。