Gleerup Helena Sophia, Sanna Federica, Høgh Peter, Simrén Joel, Blennow Kaj, Zetterberg Henrik, Hasselbalch Steen Gregers, Ashton Nicholas J, Simonsen Anja Hviid
Department of Neurology, Danish Dementia Research Centre, Copenhagen University Hospital, Copenhagen, Denmark.
Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
Front Aging Neurosci. 2021 May 10;13:659898. doi: 10.3389/fnagi.2021.659898. eCollection 2021.
Neurodegeneration and axonal injury result in an increasing release of neurofilament light chain (NfL) into bodily fluids, including cerebrospinal fluid (CSF) and blood. Numerous studies have shown that NfL levels in CSF and blood are increased in neurodegenerative disorders and monitor neurodegeneration. Saliva is an easily accessible biofluid that could be utilized as a biofluid measurement of Alzheimer's disease (AD) biomarkers. In this study, for the first time, salivary NfL was measured and compared to plasma NfL in a consecutive cohort of patients referred to cognitive assessments. In two mixed memory clinic cohorts, saliva samples were taken from 152 patients, AD ( = 49), mild cognitive impairment (MCI) ( = 47), non-AD ( = 56), and also 17 healthy controls. In addition, 135 also had a matching plasma sample. All saliva and plasma samples were analyzed for NfL, and the association between saliva and plasma NfL and CSF levels of total tau (t-tau), phosphorylated tau (p-tau), and beta amyloid 1-42 (Aβ42) were investigated. In total, 162/169 had quantifiable levels of salivary NfL by single molecule array (Simoa). No statistically significant differences were found in salivary NfL concentration across the diagnostic groups, but as expected, significant increases were found for plasma NfL in dementia cases ( < 0.0001). There was no association between saliva and plasma NfL levels. Furthermore, saliva NfL did not correlate with CSF Aβ42, p-tau, or tau concentrations. In conclusion, NfL is detectable in saliva but does not reflect neurodegeneration in the brain.
神经退行性变和轴突损伤导致神经丝轻链(NfL)越来越多地释放到包括脑脊液(CSF)和血液在内的体液中。大量研究表明,神经退行性疾病中脑脊液和血液中的NfL水平会升高,并可监测神经退行性变。唾液是一种易于获取的生物流体,可用于测量阿尔茨海默病(AD)生物标志物。在本研究中,首次在接受认知评估的连续队列患者中测量唾液NfL并与血浆NfL进行比较。在两个混合记忆门诊队列中,从152例患者中采集唾液样本,其中AD患者49例、轻度认知障碍(MCI)患者47例、非AD患者56例,还有17名健康对照者。此外,135例患者还采集了匹配的血浆样本。对所有唾液和血浆样本进行NfL分析,并研究唾液和血浆NfL与脑脊液中总tau(t-tau)、磷酸化tau(p-tau)和β淀粉样蛋白1-4(Aβ42)水平之间的关联。通过单分子阵列(Simoa)总共检测到162/169例唾液NfL水平可量化。各诊断组之间唾液NfL浓度未发现统计学显著差异,但正如预期的那样,痴呆病例的血浆NfL显著升高(<0.0001)。唾液和血浆NfL水平之间没有关联。此外,唾液NfL与脑脊液Aβ42、p-tau或tau浓度无关。总之,NfL在唾液中可检测到,但不能反映大脑中的神经退行性变。