Karampas Grigorios, Tzelepis Athanasios, Koulouraki Sevasti, Lykou Despoina, Metallinou Dimitra, Erlandsson Lena, Panoulis Konstantinos, Vlahos Nikolaos, Hansson Stefan Rocco, Eleftheriades Makarios
Second Department of Obstetrics and Gynaecology, Aretaieio University Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece.
Division of Obstetrics and Gynecology, Institute of Clinical Sciences Lund, Lund University, 22185 Lund, Sweden.
Biomolecules. 2025 Jun 8;15(6):840. doi: 10.3390/biom15060840.
Preeclampsia is a serious pregnancy complication without curative treatment. The central nervous system (CNS) is affected in severe cases of preeclampsia. Until now, no biomarker or other predictive method has been established for predicting severe CNS injury, including the development of eclampsia and/or long-term complications. In this systematic review, we aimed to investigate the association between maternal blood (serum or plasma) S100B levels and preeclampsia, focusing on its predictive value and correlation with the severity of the disease, with a particular focus on neurological symptoms.
A search of online databases, including Medline via PubMed, Scopus databases, and Web of Science, was performed based on the PRISMA guidelines for systematic reviews.
Ten case-control studies that met the inclusion criteria were identified and further evaluated according to the Newcastle-Ottawa Scale (NOS). All of the studies revealed that S100B blood levels were higher in preeclampsia compared to uncomplicated pregnancies before onset, after its diagnosis, and one year postpartum. Its predictive value seems to be adequate long before the onset of preeclampsia, especially in the early third trimester. Furthermore, its levels seem to correlate with severe complications during pregnancy, such as eclampsia and HELLP syndrome, as well as neurological dysfunction postpartum.
S100B is a promising biomarker for the prediction of acute and long-term CNS injury in preeclampsia. Still, additional studies should be conducted in order to establish a standard method of measurement and solidify its clinical use in preeclampsia management, providing individualized care in order to improve perinatal outcomes and provide personalized follow-up postpartum.
子痫前期是一种严重的妊娠并发症,尚无治愈性治疗方法。重度子痫前期会影响中枢神经系统(CNS)。到目前为止,尚未建立用于预测严重中枢神经系统损伤(包括子痫的发生和/或长期并发症)的生物标志物或其他预测方法。在本系统评价中,我们旨在研究母体血液(血清或血浆)S100B水平与子痫前期之间的关联,重点关注其预测价值以及与疾病严重程度的相关性,尤其关注神经症状。
根据系统评价的PRISMA指南,对包括通过PubMed检索的Medline、Scopus数据库和Web of Science在内的在线数据库进行了检索。
确定了10项符合纳入标准的病例对照研究,并根据纽卡斯尔-渥太华量表(NOS)进行了进一步评估。所有研究均显示,与未合并子痫前期的妊娠相比,子痫前期患者在发病前、诊断后及产后一年的血液S100B水平更高。其预测价值在子痫前期发病前很长时间似乎就足够了,尤其是在妊娠晚期。此外,其水平似乎与妊娠期间的严重并发症(如子痫和HELLP综合征)以及产后神经功能障碍相关。
S100B是预测子痫前期急性和长期中枢神经系统损伤的一种有前景的生物标志物。尽管如此,仍需进行更多研究,以建立标准的测量方法并巩固其在子痫前期管理中的临床应用,提供个性化护理以改善围产期结局并提供产后个性化随访。