Ferreira Gillene Santos, Frota Melissa Lopes, Gonzaga Maria José Dias, Vattimo Maria de Fátima Fernandes, Lima Camila
Department of Medical-Surgical Nursing, School of Nursing, University of São Paulo, São Paulo 05403-000, Brazil.
Biomedicines. 2024 Apr 23;12(5):931. doi: 10.3390/biomedicines12050931.
Sepsis and acute kidney injury (AKI) are two major public health concerns that contribute significantly to illness and death worldwide. Early diagnosis and prompt treatment are essential for achieving the best possible outcomes. To date, there are no specific clinical, imaging, or biochemical indicators available to diagnose sepsis, and diagnosis of AKI based on the KDIGO criterion has limitations. To improve the diagnostic process for sepsis and AKI, it is essential to continually evolve our understanding of these conditions. Delays in diagnosis and appropriate treatment can have serious consequences. Sepsis and AKI often occur together, and patients with kidney dysfunction are more prone to developing sepsis. Therefore, identifying potential biomarkers for both conditions is crucial. In this review, we talk about the main biomarkers that evolve the diagnostic of sepsis and AKI, namely neutrophil gelatinase-associated lipocalin (NGAL), proenkephalin (PENK), and cell-free DNA.
脓毒症和急性肾损伤(AKI)是两大主要的公共卫生问题,在全球范围内对疾病和死亡有重大影响。早期诊断和及时治疗对于取得最佳治疗效果至关重要。迄今为止,尚无用于诊断脓毒症的特异性临床、影像学或生化指标,且基于KDIGO标准诊断AKI存在局限性。为改善脓毒症和AKI的诊断流程,不断深化对这些病症的认识至关重要。诊断和适当治疗的延迟可能会产生严重后果。脓毒症和AKI常同时发生,肾功能不全患者更易发生脓毒症。因此,识别这两种病症的潜在生物标志物至关重要。在本综述中,我们探讨了用于改进脓毒症和AKI诊断的主要生物标志物,即中性粒细胞明胶酶相关脂质运载蛋白(NGAL)、前脑啡肽原(PENK)和游离DNA。