Polat Murat, Sapmaz Mehmet Alican, Erbey Sait, Kindan Aziz, Ruzgar Muhammed Said, Kahyaoglu İnci
Department of Obstetrics and Gynecology, Ankara Etlik City Hospital, Ankara, Turkey.
Department of Perinatalogy, Ankara Etlik City Hospital, Ankara, Turkey.
Medicine (Baltimore). 2025 Jul 25;104(30):e43423. doi: 10.1097/MD.0000000000043423.
Pre-eclampsia (PE) is a severe pregnancy complication associated with increased maternal and fetal morbidity and mortality. In this retrospective study, we aimed to evaluate the predictive value of hemoglobin-albumin-lymphocyte-platelet score and fibrinogen/albumin ratio (FAR) for early diagnosis of PE. Medical records of 252 pregnant women categorized as severe pre-eclampsia, non-severe pre-eclampsia and control groups were analyzed. Biomarker levels including hemoglobin, albumin, lymphocytes, fibrinogen, creatinine, alanine transaminase, aspartate aminotransferase, and platelets were analyzed throughout the first trimester. The results showed that FAR was significantly higher in PE groups compared to controls and correlated with disease severity (area under curve = 0.65, sensitivity = 59%, specificity = 66%, P < .001). Albumin levels were moderately predictive for PE (area under curve = 0.70, sensitivity = 66%, specificity = 71%, P < .001). In contrast, the hemoglobin-albumin-lymphocyte-platelet score did not differ significantly between groups, indicating limited utility for early prediction. Elevated FAR is thought to result from increased fibrinogen levels due to inflammatory and procoagulant mechanisms, whereas decreased albumin levels reflect systemic inflammation associated with PE. Although FAR and albumin show potential as early biomarkers for PE, their diagnostic power alone is moderate. The findings suggest that these parameters may be more effective when combined with established markers such as placental growth factor and soluble fms-like tyrosine kinase-1. The study underlines the need for larger prospective studies to confirm these findings and explore additional biomarkers for improved PE prediction.
子痫前期(PE)是一种严重的妊娠并发症,与孕产妇和胎儿的发病率及死亡率增加相关。在这项回顾性研究中,我们旨在评估血红蛋白-白蛋白-淋巴细胞-血小板评分及纤维蛋白原/白蛋白比值(FAR)对PE早期诊断的预测价值。分析了252名孕妇的病历,这些孕妇被分为重度子痫前期、非重度子痫前期和对照组。在整个孕早期分析了包括血红蛋白、白蛋白、淋巴细胞、纤维蛋白原、肌酐、丙氨酸转氨酶、天冬氨酸转氨酶和血小板在内的生物标志物水平。结果显示,与对照组相比,PE组的FAR显著更高,且与疾病严重程度相关(曲线下面积=0.65,敏感性=59%,特异性=66%,P<0.001)。白蛋白水平对PE有中度预测价值(曲线下面积=0.70,敏感性=66%,特异性=71%,P<0.001)。相比之下,血红蛋白-白蛋白-淋巴细胞-血小板评分在各组之间无显著差异,表明其早期预测效用有限。FAR升高被认为是由于炎症和促凝机制导致纤维蛋白原水平升高所致,而白蛋白水平降低反映了与PE相关的全身炎症。尽管FAR和白蛋白显示出作为PE早期生物标志物的潜力,但其单独的诊断能力中等。研究结果表明,这些参数与胎盘生长因子和可溶性fms样酪氨酸激酶-1等既定标志物联合使用时可能更有效。该研究强调需要进行更大规模的前瞻性研究来证实这些发现,并探索其他生物标志物以改善PE预测。