Sauvée Mathilde, DidierLaurent Guerric, Latarche Clotilde, Escanyé Marie-Christine, Olivier Jean-Luc, Malaplate-Armand Catherine
Service de Neurologie, Centre Hospitalier Universitaire, Nancy, France.
Laboratoire de Biochimie et Biologie Moléculaire, UF Oncologie - Endocrinologie - Neurobiologie, Hôpital Central, Centre Hospitalier Universitaire, Nancy, France.
J Alzheimers Dis. 2014;41(2):377-86. doi: 10.3233/JAD-131838.
Cerebrospinal fluid (CSF) biomarkers have recently been included in the criteria for the diagnosis of Alzheimer's disease (AD). Since interpretation of CSF profile requires the combination of three parameters, biological data are not always conclusive and isolated elevation of phosphorylated tau (P-tau) or reduction of amyloid-β (Aβ)42 alone can be observed. In these cases, Aβ42/Aβ40 ratio could be more relevant than Aβ42 absolute values by considering inter-individual variations in the total amyloid load.
The objective of this study was to assess the use of Aβ42/Aβ40 ratio to improve the accuracy of biological conclusions in the diagnosis of patients with ambiguous CSF Aβ42 or tau results.
Among 386 lumbar punctures analyzed in the lab in 2 years, 122 showed ambiguous biological data that were completed by CSF Aβ40 quantification and Aβ42/Aβ40 ratio calculation. A biological conclusion was then made using 0.05 as the Aβ42/Aβ40 ratio cut-off.
Our results showed that one-third of the biological profiles of patients with atypical dementia were ambiguous. The addition of Aβ42/Aβ40 ratio increased the proportion of interpretable biological profiles from 69% to 87%, without changing the conclusion when usual biomarkers (Aβ42 and P-tau) were concordant.
Our results support the use of the Aβ42/Aβ40 ratio in addition to the usual CSF AD biomarkers for patients with ambiguous biological profiles. This method could be specifically directed to this population in order to improve the level of certainty for clinical routine practice.
脑脊液(CSF)生物标志物最近已被纳入阿尔茨海默病(AD)的诊断标准。由于脑脊液分析结果的解读需要综合三个参数,生物学数据并不总是具有决定性,单独观察到磷酸化tau蛋白(P-tau)升高或淀粉样β蛋白(Aβ)42降低的情况也可能出现。在这些情况下,考虑到个体间总淀粉样蛋白负荷的差异,Aβ42/Aβ40比值可能比Aβ42绝对值更具相关性。
本研究的目的是评估Aβ42/Aβ40比值在脑脊液Aβ42或tau结果不明确的患者诊断中提高生物学结论准确性的应用。
在两年内在实验室分析的386次腰椎穿刺中,122次显示生物学数据不明确,通过脑脊液Aβ40定量和Aβ42/Aβ40比值计算对其进行补充。然后以0.
05作为Aβ42/Aβ40比值的临界值得出生物学结论。
我们的结果表明,非典型痴呆患者三分之一的生物学特征不明确。增加Aβ42/Aβ40比值后,可解释生物学特征的比例从69%提高到87%,当常规生物标志物(Aβ42和P-tau)一致时结论不变。
我们的结果支持在生物学特征不明确的患者中,除常规脑脊液AD生物标志物外使用Aβ42/Aβ40比值。该方法可专门针对这一人群,以提高临床常规实践的确定性水平。