Majida Ali , Madiha Ahmed , Mehwish Memon , Fozia Chandio , Quratulain Shaikh , Amna Parveen , Abdul-Rehman Phull
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The present study was designed and executed to review the existing scientific literature, specifically focusing on the etiology (gestational diabetes mellitus and maternal obesity, insulin resistance, metabolic syndrome, maternal infection, periodontal disease, altered microbiome, and genetics), clinical presentations (hypertension, blood disorders, proteinuria, hepatic dysfunction, renal dysfunction, pulmonary edema, cardiac dysfunction, fetal growth restrictions, and eclampsia), therapeutic clinical biomarkers (creatinine, albuminuria, and cystatin C) along with their associations and mechanisms in PE. In addition, this study provides insights into the potential of nanomedicines for targeting these mechanisms for PE management and treatment. Inflammation, OS, proteinuria, and an altered microbiome are prominent biomarkers associated with progression and PE-related pathogenesis. 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引用次数: 0
摘要
子痫前期(PE)是一种危及生命的妊娠疾病,也是导致新生儿和孕产妇死亡和发病的主要原因。全世界约有 5-10% 的妊娠会受到子痫前期的影响,对围产期和孕产妇的健康构成重大风险。PE 的特点是各种相互关联的病理级联反应刺激血管内炎症、氧化应激(OS)、内皮细胞活化和合胞滋养细胞应激,这些反应汇聚在一个共同的途径上,最终导致疾病进展。本研究旨在回顾现有的科学文献,尤其侧重于病因(妊娠糖尿病和孕产妇肥胖、胰岛素抵抗、代谢综合征、孕产妇感染、牙周病、微生物组改变和遗传学)、临床表现(高血压、血液紊乱、蛋白尿、肝功能异常、肾功能异常、肺水肿、心功能异常、胎儿生长受限和子痫)、治疗性临床生物标志物(肌酐、白蛋白尿和胱抑素 C)及其在 PE 中的关联和机制。此外,本研究还深入探讨了纳米药物针对这些机制进行 PE 管理和治疗的潜力。炎症、OS、蛋白尿和微生物组改变是与 PE 进展和相关发病机制有关的重要生物标志物。了解分子机制、探索合适的标记物、有针对性的干预措施、全面筛查和综合策略对于降低 PE 的发病率和促进母胎健康至关重要。本研究全面回顾了纳米药物在治疗和管理 PE 方面的病因、临床表现、治疗生物标志物和预防潜力。
Preeclampsia (PE) is a life-threatening disease of pregnancy and a prominent cause of neonatal and maternal mortality and morbidity. PE affects approximately 5–10% of pregnancies worldwide, posing significant risks to perinatal and maternal health. It is characterized by a variety of interconnected pathological cascades contributing to the stimulation of intravascular inflammation, oxidative stress (OS), endothelial cell activation, and syncytiotrophoblast stress that converge on a common pathway, ultimately resulting in disease progression. The present study was designed and executed to review the existing scientific literature, specifically focusing on the etiology (gestational diabetes mellitus and maternal obesity, insulin resistance, metabolic syndrome, maternal infection, periodontal disease, altered microbiome, and genetics), clinical presentations (hypertension, blood disorders, proteinuria, hepatic dysfunction, renal dysfunction, pulmonary edema, cardiac dysfunction, fetal growth restrictions, and eclampsia), therapeutic clinical biomarkers (creatinine, albuminuria, and cystatin C) along with their associations and mechanisms in PE. In addition, this study provides insights into the potential of nanomedicines for targeting these mechanisms for PE management and treatment. Inflammation, OS, proteinuria, and an altered microbiome are prominent biomarkers associated with progression and PE-related pathogenesis. Understanding the molecular mechanisms, exploring suitable markers, targeted interventions, comprehensive screening, and holistic strategies are critical to decreasing the incidence of PE and promoting maternal-fetal well-being. The present study comprehensively reviewed the etiology, clinical presentations, therapeutic biomarkers, and preventive potential of nanomedicines in the treatment and management of PE.
期刊介绍:
The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells.
The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.