Sim Ming Ann, Wilding Helen, Atkins Kelly J, Silbert Brendan, Scott David A, Evered Lisbeth Anne
From the Department of Anesthesia and Acute Pain Medicine, St Vincent's Hospital, Melbourne, Victoria, Australia.
Department of Anesthesia, Yong Loo Lin School of Medicine, National University of Singapore, and National University Health System, Singapore.
Anesth Analg. 2025 Sep 1;141(3):570-587. doi: 10.1213/ANE.0000000000007316. Epub 2024 Nov 21.
Preoperative biofluid biomarkers reflecting pathophysiological, neuronal injury, and inflammation as well as those for Alzheimer's disease (AD) may be valuable tools for the risk stratification of perioperative neurocognitive disorders (PNDs) in older adults. We summarized current evidence relating these preoperative biomarkers to PND beyond 7 days, in older surgical participants aged ≥60 years. Studies that evaluated the association of preoperative biomarkers with cognitive decline as an outcome, beyond 7 days, were identified through searches of 6 databases and 3 trial registries to 17 January 2024. Preclinical studies, intracranial surgical, or studies with participants aged <60 years were excluded. Studies varied widely in the assessment of PND, so a wide range of cognitive outcomes was accepted, including those using the term postoperative cognitive dysfunction (POCD) to define cognitive decline. The pooled incidence of POCD utilizing a binary cognitive outcome was summarized. Fifteen studies involving 2103 participants were included. Marked heterogeneity was evident in the cognitive outcome metrics, assessment timeframes, limiting a quantitative synthesis. Of the 9 studies using binarized cognitive outcomes, the incidence of POCD was 23.4% (95% confidence interval [CI], 6.6-46.2) at <3 months, 11.4% (95% CI, 8.1-15.0) at 3 to <12 months, and 6.9% (95% CI, 1.9-14.5) at ≥12 months postoperatively. Of the 15 studies, 9 described blood-based biomarkers, 4 described cerebrospinal fluid (CSF) biomarkers, and 2 measured both blood and CSF markers. The biomarkers evaluated reflected the pathogenic indicators neuronal injury (9 studies), inflammation (5 studies) and of amyloid (5 studies), and Tau (1 study). The studies included were of medium to high quality. Evidence was the most promising for amyloid biomarkers, with 4 of 5 included studies demonstrating associations of lower preoperative biofluid amyloid biomarker levels with increased risk of POCD. In conclusion, preoperative biofluid amyloid biomarkers may hold potential utility for the prediction of POCD, although current evidence remains limited. Other potential preoperative biomarkers for POCD included p-Tau181 and Neurofilament Light, however small sample sizes, study heterogeneity, and conflicting results limited conclusions drawn. Standardized cognitive outcome metrics and common assessment timeframes are additionally required in future studies to ascertain the prognostic utility of these biomarkers for POCD.
反映病理生理、神经元损伤、炎症以及阿尔茨海默病(AD)的术前生物流体生物标志物,可能是老年患者围手术期神经认知障碍(PND)风险分层的重要工具。我们总结了截至2024年1月17日,关于这些术前生物标志物与60岁及以上老年手术参与者术后7天以上PND相关性的现有证据。通过检索6个数据库和3个试验注册库,确定了评估术前生物标志物与7天以上认知功能下降之间关联的研究。排除临床前研究、颅内手术研究或参与者年龄小于60岁的研究。PND评估方法差异很大,因此接受了广泛的认知结果,包括那些使用术后认知功能障碍(POCD)来定义认知功能下降的研究。汇总了使用二元认知结果的POCD合并发病率。纳入了15项涉及2103名参与者的研究。认知结果指标、评估时间框架存在明显异质性,限制了定量综合分析。在9项使用二元认知结果的研究中,术后<3个月时POCD发病率为23.4%(95%置信区间[CI],6.6 - 46.2),3至<12个月时为11.4%(95%CI,8.1 - 15.0),≥12个月时为6.9%(95%CI,1.9 - 14.5)。在15项研究中,9项描述了基于血液的生物标志物,4项描述了脑脊液(CSF)生物标志物,2项同时检测了血液和CSF标志物。评估的生物标志物反映了神经元损伤(9项研究)、炎症(5项研究)以及淀粉样蛋白(5项研究)和Tau(1项研究)的致病指标。纳入的研究质量为中到高。淀粉样蛋白生物标志物的证据最有前景,5项纳入研究中有4项表明术前生物流体淀粉样蛋白生物标志物水平较低与POCD风险增加相关。总之,术前生物流体淀粉样蛋白生物标志物可能对POCD具有预测作用,尽管目前证据仍然有限。其他潜在的POCD术前生物标志物包括p - Tau181和神经丝轻链,但样本量小、研究异质性和结果相互矛盾限制了得出的结论。未来研究还需要标准化的认知结果指标和共同的评估时间框架,以确定这些生物标志物对POCD的预后价值。