The Zucker Hillside Hospital, Psychiatry Research, Northwell Health, Glen Oaks, New York, USA.
Department of Clinical Pharmacology, St Olav University Hospital, Trondheim, Norway.
Prog Neuropsychopharmacol Biol Psychiatry. 2021 Apr 20;107:110228. doi: 10.1016/j.pnpbp.2020.110228. Epub 2021 Jan 2.
Data regarding the ability of antidepressants to enter fetal, newborn and infant fluids have become gradually available, but mechanisms of antidepressant transfer remain poorly understood. Here we calculated penetration ratios in an array of matrices from combined samples of pregnant/breastfeeding women taking antidepressants.
We performed a systematic literature search of PubMed and EMBASE to identify studies with concentrations of antidepressants from maternal blood, amniotic fluid, umbilical cord blood and/or breast milk. Penetration ratios were calculated by dividing the concentrations in amniotic fluid, umbilical cord plasma or breast milk by the maternal plasma concentration. When data from multiple studies were available, we calculated combined penetration ratios, weighting the study mean by study size.
Eighty-five eligible studies were identified. For amniotic fluid, the highest penetration ratios were estimated for venlafaxine (mean 2.77, range 0.43-4.70 for the active moiety) and citalopram (mean 2.03, range 0.35-6.97), while the lowest ratios were for fluvoxamine (mean 0.10) and fluoxetine (mean 0.11, range 0.02-0.20 for the active moiety). For umbilical cord plasma, nortriptyline had the highest ratio (mean 2.97, range 0.25-26.43) followed by bupropion (mean 1.14, range 0.3-5.08). For breast milk, the highest ratios were observed for venlafaxine (mean 2.59, range 0.85-4.85), mianserin (mean 2.22, range 0.80-3.64) and escitalopram (mean 2.19, range 1.68-3.00).
We observed considerable variability across antidepressants regarding their ability to enter fetal, newborn and infant fluids. Measuring antidepressant concentrations in a maternal blood sample can provide a reliable estimate of fetal/infant exposure, although further evidence for concentration-dependent effects is required.
有关抗抑郁药进入胎儿、新生儿和婴儿体液能力的数据逐渐得到证实,但抗抑郁药转移的机制仍知之甚少。在这里,我们计算了来自服用抗抑郁药的孕妇/哺乳期妇女的合并样本中一系列基质的穿透比。
我们对 PubMed 和 EMBASE 进行了系统文献检索,以确定具有母体血液、羊水、脐血和/或母乳中抗抑郁药浓度的研究。穿透比通过将羊水、脐血浆或母乳中的浓度除以母体血浆浓度来计算。当有多个研究的数据可用时,我们通过研究规模对研究平均值进行加权,计算出合并穿透比。
确定了 85 项合格的研究。对于羊水,文拉法辛(活性部分的平均 2.77,范围 0.43-4.70)和西酞普兰(平均 2.03,范围 0.35-6.97)的估计穿透比最高,而氟伏沙明(平均 0.10)和氟西汀(平均 0.11,活性部分的范围为 0.02-0.20)的比值最低。对于脐血浆,去甲替林的比值最高(平均 2.97,范围 0.25-26.43),其次是安非他酮(平均 1.14,范围 0.3-5.08)。对于母乳,文拉法辛(平均 2.59,范围 0.85-4.85)、米氮平(平均 2.22,范围 0.80-3.64)和依西酞普兰(平均 2.19,范围 1.68-3.00)的比值最高。
我们观察到抗抑郁药进入胎儿、新生儿和婴儿体液的能力存在相当大的差异。测量母体血液样本中的抗抑郁药浓度可以可靠估计胎儿/婴儿暴露情况,尽管需要进一步的证据来证明浓度依赖性效应。