Alkhatabi Hind A, Alahmadi Alaa G, Alotibi Reem M, Alhashmi Mohammad H, Basabrain Ammar A, Pushparaj Peter Natesan
Department of Biochemistry, College of Science, University of Jeddah, Jeddah, 21959, Saudi Arabia.
Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Bioinformation. 2024 Jul 31;20(7):802-807. doi: 10.6026/973206300200802. eCollection 2024.
Dengue, caused by the dengue virus (DENV), a member of the flavivirus family, continues to pose a significant threat to populations worldwide, despite advances in technology. Nearly half of the global population is at risk of contracting the disease, ranging from mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF) and Dengue Shock Syndrome (DSS). The precise mechanisms underlying the progression of DF to DHF and DSS remain unclear and the presence of various DENV serotypes exacerbates this situation. Urbanization and climate change are expected to affect dengue epidemiology, potentially increasing the frequency and intensity of outbreaks. This review aims to consolidate the current knowledge on the biological characteristics, pathogenesis and application of "Omics" based strategies for biomarker discovery for precision medicine. Although the precise mechanisms behind the progression from DF to DHF/DSS are not fully understood, hypotheses include immune over-activation, cytokine storms and antibody-dependent enhancement. Studies of comorbid conditions have shown no significant association with the development of DHF/DSS in patients with diabetes, hypertension, or other chronic diseases. Despite the far-reaching and intricate nature of dengue, the inconsistencies found in clinical pathophysiological studies underscore the need for additional research aimed at elucidating the pathogenesis of DHF/DSS and devising effective preventive measures. Identifying the differentially expressed genes, proteins and metabolites in DF, DHF and DSS may enrich our understanding of the mechanisms underlying their pathogenesis. Moreover, these differentially regulated pathways may serve as novel therapeutic targets. These biomarkers may also be utilized for disease surveillance and the evaluation of the efficacy of therapeutic interventions for personalized treatment. Continuous research is essential to gain deeper insights into the mechanisms and progression of dengue fever and to formulate more effective prevention and control strategies. A multidisciplinary approach is vital for comprehending dengue virus pathogenesis, identifying risk factors and creating targeted interventions, particularly through biomarker discovery using "Omics" approaches.
登革热由黄病毒科的登革病毒(DENV)引起,尽管技术有所进步,但它仍然对全球人口构成重大威胁。全球近一半人口有感染该疾病的风险,症状从轻度登革热(DF)到严重登革出血热(DHF)和登革休克综合征(DSS)不等。DF发展为DHF和DSS的确切机制尚不清楚,而且多种DENV血清型的存在使情况更加复杂。城市化和气候变化预计会影响登革热流行病学,可能增加疫情爆发的频率和强度。本综述旨在整合当前关于生物学特性、发病机制以及基于“组学”策略发现精准医学生物标志物的应用等方面的知识。虽然从DF发展到DHF/DSS的确切机制尚未完全了解,但假说是免疫过度激活、细胞因子风暴和抗体依赖增强。对合并症的研究表明,糖尿病、高血压或其他慢性病患者发生DHF/DSS与这些疾病的发展没有显著关联。尽管登革热影响深远且错综复杂,但临床病理生理学研究中发现的不一致之处凸显了开展更多研究以阐明DHF/DSS发病机制并制定有效预防措施的必要性。确定DF、DHF和DSS中差异表达的基因、蛋白质和代谢物可能会加深我们对其发病机制的理解。此外,这些差异调节的途径可能成为新的治疗靶点。这些生物标志物还可用于疾病监测以及评估个性化治疗中治疗干预措施的疗效。持续研究对于更深入了解登革热的机制和病程以及制定更有效的预防和控制策略至关重要。多学科方法对于理解登革病毒发病机制、识别风险因素和制定针对性干预措施至关重要,特别是通过使用“组学”方法发现生物标志物。