Wierzchowska-Opoka Magdalena, Domańska Aleksandra, Masiarz Angelika, Olbrot Natalia, Oleszczuk Anna
Chair and Department of Obstetrics and Perinatology, Medical University of Lublin, Lublin, Poland.
Student's Scientific Association at the Chair and Department of Obstetrics and Perinatology, Medical University of Lublin, Lublin, Poland.
Med Sci Monit. 2025 Jun 30;31:e947679. doi: 10.12659/MSM.947679.
The global obesity epidemic has seen a dramatic rise, with maternal obesity increasing from 20.9% to a projected 23.3% by 2030. In pregnancy, metabolic dysregulation linked to obesity and gestational diabetes mellitus (GDM) elevates risks for both mother and child, contributing to complications such as macrosomia, fetal growth restriction (FGR), preterm labor, and higher cesarean rates. Central to these processes is fatty acid-binding protein 4 (FABP4), a key regulator of lipid metabolism, vascular inflammation, and insulin sensitivity. FABP4, primarily expressed in adipose tissue and macrophages, plays a pivotal role in placental lipid transport and intracellular fatty acid handling, with elevated serum levels correlating with higher body mass index (BMI) and inflammatory states in obese individuals. Emerging evidence highlights FABP4 as a potential biomarker for predicting metabolic complications, including GDM and pregnancy-induced hypertension, offering opportunities for early intervention. This review underscores the critical role of FABP4 in obesity-related pregnancy complications, emphasizing its potential as both a biomarker and therapeutic target. Advancing research into FABP4's mechanisms and therapeutic applications could significantly improve outcomes for pregnant women with obesity, fostering healthier pregnancies and reducing long-term metabolic risks for mother and child. This article reviews the metabolic roles of fatty acid binding protein 4 (FABP4) in fetal and maternal health and maintenance of pregnancy in women with obesity.
全球肥胖流行率急剧上升,孕妇肥胖率从20.9%上升,预计到2030年将达到23.3%。在孕期,与肥胖和妊娠期糖尿病(GDM)相关的代谢失调会增加母婴风险,导致巨大儿、胎儿生长受限(FGR)、早产和剖宫产率升高等并发症。这些过程的核心是脂肪酸结合蛋白4(FABP4),它是脂质代谢、血管炎症和胰岛素敏感性的关键调节因子。FABP4主要在脂肪组织和巨噬细胞中表达,在胎盘脂质转运和细胞内脂肪酸处理中起关键作用,肥胖个体血清水平升高与更高的体重指数(BMI)和炎症状态相关。新出现的证据表明,FABP4是预测包括GDM和妊娠高血压在内的代谢并发症的潜在生物标志物,为早期干预提供了机会。本综述强调了FABP4在肥胖相关妊娠并发症中的关键作用,强调了其作为生物标志物和治疗靶点的潜力。推进对FABP4机制和治疗应用的研究,可显著改善肥胖孕妇的结局,促进更健康的妊娠,降低母婴长期代谢风险。本文综述了脂肪酸结合蛋白4(FABP4)在肥胖女性胎儿和母亲健康及维持妊娠中的代谢作用。