Can we improve the outcome of pregnancies with low serum PAPP-A in the first trimester?

IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY Journal of Maternal-Fetal & Neonatal Medicine Pub Date : 2024-12-01 Epub Date: 2024-03-19 DOI:10.1080/14767058.2024.2326303
Valentina Tsibizova, Baydaa Al-Sannan, Anna Fedorova, Igor Govorov, Arun Meyyazhagan, Gian Carlo Di Renzo
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Abstract

Objective: This study aimed to assess the impact of micronized progesterone (VMP4) supplementation on pregnancies with low serum pregnancy-associated plasma protein-A (PAPP-A) multiples of the median (MoM) values during first-trimester screening.

Methods: Out of 8933 patients evaluated, 116 pregnant women with low PAPP-A concentrations in their blood and no fetal chromosomal anomalies (CAs) were included. Three groups were formed: group 1 received VMP4 from 11 to 16 weeks (29 women, 25%), group 2 received VMP4 from 11 to 36 weeks (25 women, 21.5%), and group 3 (62 women, 53.5%) served as controls without receiving progesterone.

Results: Results indicated that group 3 had higher rates of complications, including miscarriages (16.37%), preterm delivery (17.8%), and fetal developmental abnormalities (19.4%). Birthweight variations were elevated in pregnancies without progesterone, contrasting with lower variations in VMP4 groups. Group 2, receiving VMP4 until 36 weeks, reported the lowest incidence of abortion and preterm birth (PB), along with the highest mean birth weight.

Conclusions: The conclusion suggests that 200 mg per day of VMP4 up to 36 weeks of supplementation led to fewer placental-related complications in women with very low PAPP-A at first-trimester screening (0.399 MoM). By reporting lower rates of miscarriages, PBs, and fetal developmental abnormalities in the micronized progesterone-treated groups, the study suggests a potential reduction in complications.

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我们能否改善妊娠头三个月血清 PAPP-A 偏低的孕妇的预后?
研究目的本研究旨在评估补充微粒化黄体酮(VMP4)对初孕期筛查中血清妊娠相关血浆蛋白-A(PAPP-A)值为中位数(MoM)倍值偏低的孕妇的影响:在接受评估的 8933 名患者中,有 116 名孕妇的血液中 PAPP-A 浓度较低,但未发现胎儿染色体异常(CA)。分为三组:第一组在 11-16 周接受 VMP4(29 名妇女,占 25%),第二组在 11-36 周接受 VMP4(25 名妇女,占 21.5%),第三组(62 名妇女,占 53.5%)作为对照组,不接受黄体酮:结果显示,第 3 组的并发症发生率较高,包括流产(16.37%)、早产(17.8%)和胎儿发育异常(19.4%)。未使用黄体酮的孕妇出生体重变化较大,而使用 VMP4 的孕妇出生体重变化较小。接受 VMP4 治疗至 36 周的第 2 组流产和早产(PB)发生率最低,平均出生体重最高:结论表明,每天补充 200 毫克 VMP4 至 36 周,可减少初产筛查时 PAPP-A 值极低(0.399 MoM)妇女的胎盘相关并发症。该研究报告称,经微粒化黄体酮治疗组的流产率、胎盘早剥率和胎儿发育异常率较低,这表明并发症有可能减少。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
217
审稿时长
2-3 weeks
期刊介绍: The official journal of The European Association of Perinatal Medicine, The Federation of Asia and Oceania Perinatal Societies and The International Society of Perinatal Obstetricians. The journal publishes a wide range of peer-reviewed research on the obstetric, medical, genetic, mental health and surgical complications of pregnancy and their effects on the mother, fetus and neonate. Research on audit, evaluation and clinical care in maternal-fetal and perinatal medicine is also featured.
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