Lewczuk Piotr, Matzen Anja, Blennow Kaj, Parnetti Lucilla, Molinuevo Jose Luis, Eusebi Paolo, Kornhuber Johannes, Morris John C, Fagan Anne M
Department of Psychiatry and Psychotherapy, Universitätsklinikum Erlangen, and Friedrich-Alexander-Universität, Erlangen-Nürnberg, Erlangen, Germany.
Department of Neurodegeneration Diagnostics, Medical University of Białystok, and Department of Biochemical Diagnostics, University Hospital of Bialystok, Bialystok, Poland.
J Alzheimers Dis. 2017;55(2):813-822. doi: 10.3233/JAD-160722.
Decreased concentrations of amyloid-β 1-42 (Aβ42) in cerebrospinal fluid (CSF) and increased retention of Aβ tracers in the brain on positron emission tomography (PET) are considered the earliest biomarkers of Alzheimer's disease (AD). However, a proportion of cases show discrepancies between the results of the two biomarker modalities which may reflect inter-individual differences in Aβ metabolism. The CSF Aβ42/40 ratio seems to be a more accurate biomarker of clinical AD than CSF Aβ42 alone.
We tested whether CSF Aβ42 alone or the Aβ42/40 ratio corresponds better with amyloid PET status and analyzed the distribution of cases with discordant CSF-PET results.
CSF obtained from a mixed cohort (n = 200) of cognitively normal and abnormal research participants who had undergone amyloid PET within 12 months (n = 150 PET-negative, n = 50 PET-positive according to a previously published cut-off) was assayed for Aβ42 and Aβ40 using two recently developed immunoassays. Optimal CSF cut-offs for amyloid positivity were calculated, and concordance was tested by comparison of the areas under receiver operating characteristic (ROC) curves (AUC) and McNemar's test for paired proportions.
CSF Aβ42/40 corresponded better than Aβ42 with PET results, with a larger proportion of concordant cases (89.4% versus 74.9%, respectively, p < 0.0001) and a larger AUC (0.936 versus 0.814, respectively, p < 0.0001) associated with the ratio. For both CSF biomarkers, the percentage of CSF-abnormal/PET-normal cases was larger than that of CSF-normal/PET-abnormal cases.
The CSF Aβ42/40 ratio is superior to Aβ42 alone as a marker of amyloid-positivity by PET. We hypothesize that this increase in performance reflects the ratio compensating for general between-individual variations in CSF total Aβ.
脑脊液(CSF)中β淀粉样蛋白1-42(Aβ42)浓度降低以及正电子发射断层扫描(PET)显示大脑中Aβ示踪剂滞留增加被认为是阿尔茨海默病(AD)最早的生物标志物。然而,一部分病例在这两种生物标志物检测结果之间存在差异,这可能反映了个体间Aβ代谢的差异。脑脊液Aβ42/40比值似乎比单独的脑脊液Aβ42更能准确地作为临床AD的生物标志物。
我们测试单独的脑脊液Aβ42或Aβ42/40比值是否与淀粉样蛋白PET状态更相符,并分析脑脊液-PET结果不一致的病例分布情况。
从认知正常和异常的研究参与者混合队列(n = 200)中获取脑脊液,这些参与者在12个月内进行了淀粉样蛋白PET检查(根据先前公布的临界值,n = 150 PET阴性,n = 50 PET阳性),使用两种最新开发的免疫测定法检测Aβ42和Aβ40。计算淀粉样蛋白阳性的最佳脑脊液临界值,并通过比较受试者操作特征(ROC)曲线下面积(AUC)和配对比例的McNemar检验来测试一致性。
脑脊液Aβ42/40与PET结果的相符性优于Aβ42,相符病例比例更高(分别为89.4%和74.9%,p < 0.0001),且该比值的AUC更大(分别为0.936和0.814,p < 0.0001)。对于两种脑脊液生物标志物,脑脊液异常/PET正常病例的百分比高于脑脊液正常/PET异常病例。
脑脊液Aβ42/40比值作为PET淀粉样蛋白阳性的标志物优于单独的Aβ42。我们推测这种性能的提高反映了该比值补偿了脑脊液总Aβ个体间的一般差异。