Marcantonio Edward R, Rudolph James L, Culley Deborah, Crosby Gregory, Alsop David, Inouye Sharon K
Division of General Medicine and Primary Care, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02446, USA.
J Gerontol A Biol Sci Med Sci. 2006 Dec;61(12):1281-6. doi: 10.1093/gerona/61.12.1281.
This narrative review examines serum biomarkers for the diagnosis and monitoring of delirium. Serum biomarkers for delirium fall into three major groups: 1) those that are present or elevated prior to disease onset-risk markers, 2) those that rise with onset and fall with recovery-disease markers, and 3) those that rise in proportion to the consequences of disease-end products. As risk markers, we examine serum chemistries and genetic risk markers. As disease markers, we examine serum anticholinergic activity, amino acids, melatonin, cytokines, cortisol, and gene expression. As end products of delirium, we examine markers of neuronal injury. Finally, we discuss methodological and biostatistical considerations for future biomarker studies. Identifying accurate biomarkers for delirium may shed further light into its pathophysiology and on the interrelationship between delirium and dementia.
这篇叙述性综述探讨了用于谵妄诊断和监测的血清生物标志物。用于谵妄的血清生物标志物主要分为三大类:1)在疾病发作前就已存在或升高的标志物——风险标志物;2)随着发作而升高、随着恢复而下降的标志物——疾病标志物;3)与疾病后果成比例升高的标志物——终产物。作为风险标志物,我们研究了血清化学指标和遗传风险标志物。作为疾病标志物,我们研究了血清抗胆碱能活性、氨基酸、褪黑素、细胞因子、皮质醇和基因表达。作为谵妄的终产物,我们研究了神经元损伤的标志物。最后,我们讨论了未来生物标志物研究的方法学和生物统计学考量。确定准确的谵妄生物标志物可能会进一步揭示其病理生理学以及谵妄与痴呆之间的相互关系。