Clinic and Polyclinic for Pediatric and Adolescent Medicine, University Hospital Cologne, Faculty of Medicine, University of Cologne, 50937 Cologne, Germany.
Department of Obstetrics and Gynecology, University Hospital Leipzig, 04103 Leipzig, Germany.
Cells. 2024 Mar 13;13(6):501. doi: 10.3390/cells13060501.
Intrauterine growth restriction (IUGR) and being small for gestational age (SGA) are two distinct conditions with different implications for short- and long-term child development. SGA is present if the estimated fetal or birth weight is below the tenth percentile. IUGR can be identified by additional abnormalities (pathological Doppler sonography, oligohydramnion, lack of growth in the interval, estimated weight below the third percentile) and can also be present in fetuses and neonates with weights above the tenth percentile. There is a need to differentiate between IUGR and SGA whenever possible, as IUGR in particular is associated with greater perinatal morbidity, prematurity and mortality, as well as an increased risk for diseases in later life. Recognizing fetuses and newborns being "at risk" in order to monitor them accordingly and deliver them in good time, as well as to provide adequate follow up care to ameliorate adverse sequelae is still challenging. This review article discusses approaches to differentiate IUGR from SGA and further increase diagnostic accuracy. Since adverse prenatal influences increase but individually optimized further child development decreases the risk of later diseases, we also discuss the need for interdisciplinary follow-up strategies during childhood. Moreover, we present current concepts of pathophysiology, with a focus on oxidative stress and consecutive inflammatory and metabolic changes as key molecular mechanisms of adverse sequelae, and look at future scientific opportunities and challenges. Most importantly, awareness needs to be raised that pre- and postnatal care of IUGR neonates should be regarded as a continuum.
胎儿宫内生长受限(IUGR)和小于胎龄儿(SGA)是两种不同的情况,对儿童短期和长期发育有着不同的影响。如果估计的胎儿或出生体重低于第 10 百分位,则存在 SGA。IUGR 可以通过其他异常(病理性多普勒超声、羊水过少、间隔期生长不良、估计体重低于第 3 百分位)来识别,也可能存在于体重高于第 10 百分位的胎儿和新生儿中。无论何时都需要区分 IUGR 和 SGA,因为 IUGR 特别是与围产期发病率、早产和死亡率增加,以及以后生活中患病风险增加有关。识别处于“风险中”的胎儿和新生儿,以便对其进行相应的监测并及时分娩,并提供足够的后续护理以改善不良后果仍然具有挑战性。这篇综述文章讨论了区分 IUGR 和 SGA 并进一步提高诊断准确性的方法。由于不良产前影响增加,但个体优化的进一步儿童发育降低了以后患病的风险,我们还讨论了在儿童期需要采用跨学科的随访策略的必要性。此外,我们介绍了目前关于病理生理学的概念,重点是氧化应激和随后的炎症和代谢变化作为不良后果的关键分子机制,并探讨了未来的科学机会和挑战。最重要的是,需要提高认识,即 IUGR 新生儿的产前和产后护理应被视为一个连续的过程。