As Alzheimer’s disease (AD) pathology presents decades before dementia manifests, unbiased biomarker cut-points may more closely reflect presence of pathology than clinically defined cut-points. Currently, unbiased cerebrospinal fluid (CSF) tau cut-points are lacking.
We investigated CSF t-tau and p-tau cut-points across the clinical spectrum using Gaussian mixture modelling, in two independent cohorts (Amsterdam Dementia Cohort and ADNI).
Individuals with normal cognition (NC) (total n = 1111), mild cognitive impairment (MCI) (total n = 1213) and Alzheimer’s disease dementia (AD) (total n = 1524) were included. In both cohorts, four CSF t- and p-tau distributions and three corresponding cut-points were identified. Increasingly high tau subgroups were characterized by steeper MMSE decline and higher progression risk to AD (cohort/platform-dependent HR, t-tau 1.9–21.3; p-tau 2.2–9.5).
The number of subjects in some subgroups and subanalyses was small, especially in the highest tau subgroup and in tau PET analyses.
In two independent cohorts, t-tau and p-tau levels showed four subgroups. Increasingly high tau subgroups were associated with faster clinical decline, suggesting our approach may aid in more precise prognoses.
Abnormal levels of amyloid-β 1-42 (Aβ42), total tau (t-tau) and tau phosphorylated at threonine 181 (p-tau-181) are biomarkers for the presence of Alzheimer’s disease (AD) pathology in the brain , and part of established research criteria for AD across the cognitive continuum [2, 3]. Classification schemes based on biomarkers depend on cut-points, and different approaches exist to determine such cut-points. The most often used traditional approach determines cut-points by optimizing the sensitivity and specificity to detect clinical AD-type dementia compared to controls [4,5,6]. However, approaches that use clinical labels as outcomes may not be optimal, because clinical labels do not optimally reflect the absence or presence of AD pathology: For example, almost 30% of cognitively intact individuals in their seventies have AD pathology , and up to 20% of clinical AD dementia cases do not show AD pathology at neuropathological examination [8,9,10,11]. As such, cut-point based on clinical labels can be biased.
Gaussian mixture modelling provides an approach to determine cut-points independent of clinical information . This approach is based on the notion that the distribution of biomarker values in a population is a mixture of values belonging to subpopulations, i.e. normal and affected individuals. Previous studies using this approach have found a bimodal distribution of Aβ42 levels, of which the cut-point (i.e. the intersection of these distributions) was higher than clinically based cut-points, resulting in more sensitive detection of predementia AD [13,14,15,16]. As of yet, however, it remains unclear whether it is also possible to detect unbiased cut-points in t-tau and p-tau levels.
High t-tau levels in the cerebrospinal fluid (CSF) are thought to reflect neuronal degeneration or injury, and elevated t-tau levels can be found in the CSF in various conditions involving neuronal death, for example after an acute stroke. In contrast, p-tau-181 is presumed to reflect the formation of phosphorylated tau in the brain and to represent more specifically the formation of neurofibrillary tangles, one of the neuropathological hallmarks of AD [17, 18]. As tau pathology is a hallmark of AD, it can be hypothesized that similarly to amyloid, t- and p-tau levels may be a mixture of values belonging to normal and affected individuals, from which unbiased cut-points might be determined.
The objective of this study was to investigate whether subgroups can be identified in CSF t- and p-tau levels using Gaussian mixture modelling and to determine cut-points. We characterized tau subgroups in terms of clinical and biological characteristics and longitudinal trajectories of cognitive decline. We repeated analyses in the independent ADNI cohort to determine the robustness of the identified subgroups and tested stability of group membership by studying longitudinal changes in t-tau and p-tau levels. Finally, we compared subgroups on tau PET uptake that was available for a subset of individuals in ADNI.
We investigated the existence of CSF t- and p-tau subgroups in data from two independent clinical cohorts. The memory clinic-based Amsterdam Dementia Cohort (ADC) was used for testing our hypothesis , and the Alzheimer’s Disease Neuroimaging Initiative (ADNI; www.adni-info.org) was used for validation of the results. ADNI started in 2003 as a public-private collaboration under the supervision of Principal Investigator Michael W. Weiner, MD. The primary goal of ADNI is to study whether serial magnetic resonance imaging (MRI), positron emission tomography (PET), other biological markers and clinical and neuropsychological measures can be combined to measure the progression of mild cognitive impairment (MCI) and early Alzheimer’s disease (AD). Please see www.adni-info.org for the latest information. The institutional review boards of all participating institutions approved the procedures for this study. Written informed consent was obtained from all participants or surrogates. Participant selection and CSF analyses are summarized below; for more detailed methods and information on Apolipoprotein E (APOE) genotyping and PET imaging, see Additional file 1.
In short, patients from the ADC who visited our memory clinic between November 2000 and December 2016 were selected (n = 2724) if they had baseline CSF tau measurements available and had subjective cognitive decline (considered as normal cognition (NC)), mild cognitive impairment (MCI) or AD dementia. Participants from ADNI who had baseline CSF biomarkers available were selected (n = 1221) for the replication analyses if they met the study-specific criteria of NC, MCI or dementia. A subset of 619 individuals in ADNI (51%; 183 NC, 345 MCI and 91 with AD dementia) with available follow-up CSF measures were selected for longitudinal analyses.
In ADC, CSF biomarkers (β-amyloid(1-42), hTAU-Ag, and phospo-tau 181P) were assessed with INNOTEST (Fujirebio, Ghent, Belgium) on a routine basis as described before . In ADNI, CSF biomarkers were analysed using a multiplex xMAP Luminex platform (Luminex Corp) with immunoassay kit-based reagents (INNO-BIA Alzbio3; Innogenetics)  (n = 1213 participants), and on Elecsys (Roche, Basel, Switserland)  (n = 1193 participants, overlap with Luminex 98%).
Gaussian mixture modelling was used to identify cut-points in the distribution of t-tau and p-tau values. First, the number of distributions that best described the data was determined with the R boot.comp function. This function sequentially tests increasing number of components in the data using parametric bootstrapping of the likelihood ratio (i.e. likelihood of x components vs. likelihood of having one more component, i.e. x + 1), until the null hypothesis cannot be rejected anymore (p > 0.05, i.e. no improvement of additional component for model fit). Then, we identified data-driven cut-points as the points where the lines of two fitted Gaussian distributions intersected. Using these cut-points, we labelled subjects according to tau subgroups. Next, within each cohort, we compared subgroups based on demographical, clinical and biological characteristics with ANOVA or chi-square tests, when appropriate. For a subset of individuals with available repeated mini-mental state examination (MMSE) and/or clinical follow-up, we further assessed whether subgroups showed differences in cognitive decline, stratifying subjects based on their baseline cognitive state (defined as NC, MCI or dementia). First, decline in MMSE (outcome) was assessed with linear mixed models using the R package “lmer4”, including the main terms time and tau subgroup, and interaction terms time*tau subgroup. For individuals without dementia at baseline, Cox proportional hazards models were used to compare the rate of progression from NC to MCI or AD dementia and from MCI to AD dementia between tau subgroups. We ran 5 models: (1) without covariates; (2) including age, sex and educational level; (3) model 2 + amyloid status; (4) model 3 + baseline cognitive state; and (5) model 4 + APOE-e4 carriership (dichotomous). For the Cox proportional hazards models, data from 945 subjects was available (357 normal and 588 MCI subjects). Subsets of individuals in ADNI also had repeated CSF tau measures available, for which we tested changes over time in tau subgroups, or had TAU PET available, for which we compared tau uptake according to Braak stages between subgroups. All analyses except for Cox proportional hazard analyses were stratified for baseline cognitive state, and adjusted for age and sex, and cognitive outcomes additionally for level of education . In Cox proportional hazard analyses, no stratification for baseline cognitive state was performed due to small size of the resulting groups; instead, baseline cognitive state was added as additional covariate. All statistical analyses were performed in R version 3.6.1 “Action of the Toes”, mixture modelling was performed with the mixtools package (version 1.1.0), estimated marginal means and trends were computed with the R package “emmeans” v1.4, and sensitivity and specificity analyses with epiR v.1.0-15.
Table 1 shows baseline characteristics of the ADC and ADNI cohorts. Compared to the ADC, subjects in the ADNI cohort were approximately 10 years older and had a lower prevalence of AD dementia and a higher prevalence of MCI. In ADC, subjects with NC were about 7 years younger compared to MCI and AD patients, and the NC and the MCI subjects were more often male than AD dementia subjects. In ADNI, MCI subjects were youngest, and MCI and AD dementia subjects were more often male than NC. In both cohorts, AD dementia subjects had lowest baseline MMSE scores, highest proportion of APOE e4 carriers, lowest levels of Aβ42, and highest levels of tau. MCI subjects had values in between NC subjects and AD dementia patients.
Gaussian mixture modelling reveals four subgroups
Mixture modeling showed that four distributions (i.e. a tetramodel distribution) best fitted the data for both t-tau and p-tau levels, with an optimal fit for four distributions (log-likelihood ratio for 3 vs. 4 distributions, for t-tau: 97.2, and p-tau: 28.3, both p < 0.001, no further improvement for 5 distributions: log-likelihood ratio for 5 vs 4 distributions, for t-tau: 3.9, and p-tau 15, both p > 0.05; see Additional file 2 for fit statistics of all fitted models, and Fig. 1a for a visualisation of the four distributions). In the ADC (using Innotest), this yielded three cutoffs (95% confidence interval (CI)), for t-tau—349 (304–382), 671 (582–834) and 1380 (1260–1505) pg/mL, and for p-tau—56 (46–60), 96 (71–121) and 159 (138–240) (for n per subgroup defined by cut-points, see Tables 2 and 3). The first cut-points for t-tau (349 pg/mL) and p-tau (56 pg/mL) were comparable to the t-tau and p-tau cut-points of 375 pg/ml and 52 pg/ml we previously reported , and showed similar sensitivity and specificity performance to distinguish between clinical AD dementia and controls (see Table 4 for sensitivity and specificity comparisons). Sensitivity and specificity for distinguishing NC vs MCI were also comparable to those resulting from the clinical cut-point (Table 4).
T-tau and p-tau strongly correlated across the total group (r = .92, p < .001); however, when comparing classification of individuals based on t-tau and p-tau, concordance was somewhat lower (79%; Table 2). Applying mixture modelling in ADNI showed that similar to the ADC, a tetramodal distribution best fitted the CSF t-tau and p-tau data (log-likelihood ratio for 3 vs 4 distributions, for t-tau: 25.2 and for p-tau: 54.3, both with p < 0.05, no further improvement for 5 distributions: log-likelihood ratio for 5 vs 4 distributions, for t-tau: 11.2, and p-tau: 20.3, with p = 0.08 and p = 0.05, respectively). The tetramodal distribution yielded three different cut-points for t-tau measured with Luminex (95%CI)—54 (42–68), 95 (68–125) and 171 (146–263) pg/mL respectively (Fig. 1b), and for p-tau levels (95%CI)—23 (20–28), 46 (38–57) and 99 (74–124). Comparing the first cut-point of t-tau (54 pg/mL) with the cut-point of 93 pg/mL previously determined for ADNI , our new cut-point for t-tau resulted in higher sensitivity to detect clinical AD dementia versus controls, at the cost of lower specificity (Table 4). The first p-tau cut-point (23 pg/mL) was identical to the cut-point reported in the literature .
In ADNI, we further repeated analyses on the novel Elecsys data as an analytical validation, and again observed a tetramodal distribution for t-tau (log-likelihood ratio for 3 vs 4 distributions, for t-tau: 12.4, and p-tau: 19.6, both with p < 0.05, no further improvement for 5 distributions: log-likelihood ratio for 5 vs 4 distributions, for t-tau: 7.1, and p-tau 10.6, both p > 0.05). The tetramodal distribution yielded for t-tau the cut-points (95%CI)—192 (129–235), 312 (239–405) and 515 (417–679), and for p-tau (95%CI)—21 (17–23), 36 (28–43) and 55 (47–68) (Fig. 1c). For the first t-tau cut-point measured with Elecsys (192 pg/mL) compared to the cut-point of 300 pg/mL previously reported for ADNI , our new cut-point also yielded higher sensitivity but lower specificity for Elecsys t-tau (Table 4). For Elecsys p-tau, the first cut-point of 21 pg/mL was comparable to a previously reported cut-point of 24 pg/mL  and yielded similar sensitivity and lower specificity estimates (Table 4). In ADNI, 81% of the subjects were labelled identically using t-tau labels for Luminex and Elecsys, whereas between-platform correspondence for p-tau labelling was 60% (Table 2). For Luminex, the correlation between t-tau and p-tau was .67 (p < .001) and the correspondence of t-tau and p-tau labelling was 52%. For Elecsys, the correlation between t-tau and p-tau was .98 (p < .001), and the correspondence of subgroup labelling was 71%.
Clinical and biological characteristics of tau subgroups
Gradually higher t- and p-tau subgroups in ADC were characterized by increasingly high prevalence of abnormal amyloid, with the highest two t-tau and p-tau groups consisting for more than 94% of amyloid abnormal participants. This relationship also held for lower t-tau values, with a higher prevalence of abnormal amyloid in the second subgroup than the lowest tau subgroup. T- and p-tau subgroups were also associated with cognitive state, with lower subgroups containing the highest proportion of cognitively normal participants, while highest subgroups contained more demented participants (Table 3). Therefore, we stratified subsequent comparisons between tau subgroups for cognitive state. Average MMSE was lower for higher tau subgroups, with the strongest effects observed in AD-type dementia (Fig. 2; Table 3). Tau subgroups also differed in demographic factors, including age (on average lower in the lowest tau subgroup in NC and MCI), sex (higher proportion of women in higher t-tau and p-tau subgroups), and APOE e4 carriership (higher prevalence in higher t-tau and p-tau subgroups) (Fig. 2; Table 3). The associations of higher t- and p-tau subgroups with amyloid, cognitive state, and demographic factors were mostly reproduced in ADNI.
Rates of cognitive decline over time depend on tau subgroups
We further studied whether subjects across tau subgroups differed in rates of cognitive decline, as measured with the MMSE stratified for cognitive state. In ADC, tau subgroups were not associated with cognitive decline in MCI or NC; however, in the dementia phase, higher tau subgroups were characterized by faster cognitive decline on MMSE (Fig. 3; Table 4). In ADNI, faster MMSE decline with higher tau subgroups in dementia was reproduced. While in ADC no association between tau subgroups and MMSE decline was found for participants with MCI, in ADNI, higher tau subgroups in MCI were associated with MMSE decline (Table 5).
Next, we tested for individuals without dementia (i.e. NC and MCI) whether tau-subgroups differed in terms of progression to MCI or AD-type dementia. In the ADC, 46/381 (12%) of NC patients showed clinical progression either to MCI (n = 39) within 2.3 ± 1.6 years or to AD-type dementia (n = 16) in 4.5 ± 4.0 years, and 178/591 (30%) of MCI patients progressed to AD-type dementia in 2.4 ± 1.6 years. Across the total group of non-demented subjects, hazard ratios (HRs) increased with increasing tau or p-tau subgroups compared to the lowest tau or p-tau subgroups (Fig. 4; Table 6). Repeating analyses including covariates sex, age and education level (model 2), amyloid status (model 3), baseline cognitive state (model 4) and APOE-e4 carriership (model 5) generated largely similar results for t-tau subgroups, although HRs were somewhat attenuated. Results were largely consistent for ADNI albeit with somewhat lower HR values (Table 6), where 65/371 (17.5%) NC showed clinical progression either to MCI (n = 47) within 3 ± 9 years or to AD-type dementia (n = 18) in 8 ± 3 years, and 212/622 (34%) MCI individuals to AD-type dementia in 4.1 ± 2.3 years. Of note is that in ADNI, individuals in the second Luminex t-tau subgroup had levels below the official cut-point defined by ADNI (i.e. 93 pg/ml ) and still showed higher HRs for progression to AD-type dementia compared to the first tau subgroup (HR (95%CI) = 2.1 (1.4, 3.0), p < .001).
Longitudinal changes in tau concentrations in ADNI
Examining transitions over time to higher tau groups in ADNI, we observed that the majority of individuals for both Luminex and Elecsys t-tau subgroups remained in the same subgroup as first measured (Luminex: 472 (76% of 619); Elecsys: 443 (76% of 586); Table 7; see Table 8 and Fig. 5 for continuous results). Of individuals who changed, the majority shifted to one tau group higher (Table 8).
Comparison with tau PET in ADNI
Finally, we compared CSF tau subgroups on tau PET uptake values available for 345 individuals (235 NC; 93 MCI; 28 dementia; of note, these included n = 232 new CSF observations not included in mixture analyses). Figure 6 shows that tau PET uptake increased with higher t-tau and p-tau subgroups. For all Braak regions, the uptake of the highest two tau subgroups was significantly higher than the lowest two (or three) subgroups (Table 9). The second lowest t-tau subgroup also showed higher average tau uptake in Braak I/II brain areas compared to subgroup 1, and the second lowest p-tau subgroup in addition also to Braak III/IV and V/VI compared to subgroup 1.
In this study, we used Gaussian mixture modelling to determine unbiased cut-points for CSF tau levels. We identified three cut-points resulting in four different distributions, and the cut-point between the lowest two subgroups corresponded closely to an existing clinically defined cut-point . Furthermore, two additional tau groups with highest t- and p-tau levels were discovered in the data. We similarly observed four distributions in the independent ADNI cohort, and despite differences between ADC and ADNI in cohort composition, tau subgroups showed similar clinical and biological characteristics in both study cohorts. These findings suggest that t-tau and p-tau levels may not necessarily reflect disease stage, but possibly different biological subtypes of AD.
Tau is an intracellular protein playing an important role in microtubule assembly and stabilization in axons . Hyperphosphorylation disturbs its function, resulting in the formation of aggregates or neurofibrillary tangles, which is one of the hallmarks of AD pathology. Still, the precise factors influencing t- and p-tau CSF levels remain unclear. Measures correlated highly, and even though subgroup labelling showed moderate concordance, t-tau and p-tau subgroups showed similar differences in tau PET uptake. Previous studies comparing CSF tau measures with tau PET have been inconsistent [25,26,27]. Together with our results, it remains unclear whether CSF t-tau and p-tau reflect similar or different aspects of neuronal injury. Higher levels of t- and p-tau might result from passive release into extracellular space due to neuronal death which increases with worse disease severity. However, tau is also actively secreted by neurons as part of normal physiology  and can increase in the presence of amyloid pathology . The majority of individuals remained in their t-tau subgroup over time, suggesting that at least part of their levels do not depend on disease stage, but perhaps reflect other biological aspects. The relative lack of change over time in tau levels within individuals seems at odds with the idea that tau increases with worsening cognition. Previous longitudinal CSF studies have reported conflicting results, observing increases in middle-age individuals with normal cognition during a follow-up period of 6 years , but also a lack of change in individuals with normal cognition, MCI and AD over a median follow-up of 2 years [31, 32]. This literature together with our observations suggests that increases over time in t-tau levels in CSF are slow, and follow-up times longer than 2–3 years might be necessary for participants to change subgroups.
One of the challenges in biomarkers research is how to define the cut-point between normal and abnormal levels. Pathology is the gold standard, but is also the end stage of the disease and difficult to obtain for large sample sizes. The cut-point for Luminex p-tau in ADNI was originally based on pathology , and we observed the same cut-off for the lowest p-tau subgroup (23 pg/ml). However, for t-tau, we observed a lower cut-off that was still related to increased risk for disease progression. A recent study defined cut-points for t- and p-tau measured with Elecsys (t-tau 300 pg/ml and p-tau 27 pg/ml) in ADNI based on their association with clinical progression in MCI patients . We expand upon previous studies [6, 11, 33, 34] by identifying additional cut-points that may have practical use for more specific prognoses to individual patients or in trial design: we identified lower cut-points than defined in the literature (resp. 193 and 22 pg/ml for t- and p-tau, respectively) that were already associated with increased risk for clinical progression, and also showed for the higher cut-points, that the corresponding subgroups were associated with gradually increasing hazard ratios and steeper decline on the MMSE.
The notion that higher tau subgroups also included non-demented individuals, and that higher tau levels were associated with faster cognitive decline, regardless of disease stage, suggests that tau subgroups may reflect differences in underlying biological processes, rather than disease severity per se. This is supported by the observation that higher tau subgroups showed increasing proportions of APOE e4 carriers, the strongest genetic risk factor for AD . Previous studies have also reported higher levels of tau in APOE-e4 carriers, also in predementia stages ; however, also see  where tau levels were similar between carriers and non-carriers. Other genetic risk factors may contribute to differences in tau levels as well, as another study reported that a polygenic risk score, including SNPs with moderate strength to detect AD, was strongly related to t-tau and p-tau levels, also after correcting for APOE . This suggests that multiple genetic risk factors may explain variability between individual tau levels. More studies with large sample sizes are needed to further investigate these biological factors associated with tau levels in CSF. Also, future studies should further investigate the longitudinal relationship of these tau subtypes with concurrent other biological measures that deteriorate during the AD process, such as synaptic markers in CSF or on PET, and cognitive data, to better understand differences in clinical progression amongst tau subtypes.
A potential limitation of our study is that although we used large clinical cohorts, the number of subjects in some subgroups and subanalyses was small: this was especially the case in the highest tau subgroup, as well as in tau PET analyses. The small size of the highest tau subgroup means that there is more uncertainty in the association of this subgroup with clinical characteristics. Therefore, the results regarding the highest tau subgroup and the tau PET analyses should be interpreted with caution, and if possible repeated in future studies in even larger cohorts. Furthermore, we used Gaussian mixtures as a data-driven approach to study potential subgroups in tau levels as a first step, it is possible that more complex models may improve the fit of tau levels distributions, which should be addressed in future studies. Also, we determined cut-points here as the intersections of the probability distributions of the normal mixtures, which may not be ideal in all settings. For example, in studies where minimizing misclassification costs is desired, e.g. in clinical trial design, it may be useful to choose cut-points so that misclassification is minimized of individuals with high tau as falling in the lowest tau group, to ensure that as many individuals with potentially fast progression are included in the trial. Future studies could test the efficacy of the data-driven cut-points in those settings. Strengths of the study are that we used a large cohort, and we validated the mixture modelling results in another independent cohort with two different analysis platforms for CSF tau, and both cohorts had detailed information of the characteristics of the study populations, including cognitive measures, follow-up data on clinical progression and information on APOE genotype available.
In conclusion, our studies suggest that abnormal levels of CSF t-tau and p-tau may convey different biological aspects in AD, which might be in part driven by genetic factors such as different APOE genotypes. The data-driven cut-points we found may aid daily practice in prognosis of patients and may aid trial design by allowing stratification of individuals according to their risk of clinical progression.
Availability of data and materials
The ADNI dataset analysed during the current study is available in the ADNI repository, www.adni-info.org. For ADC, the data that support the findings of this study are available from the corresponding author upon reasonable request.
Amsterdam Dementia Cohort
Alzheimer’s disease Neuroimaging Initiative
Mild cognitive impairment
Mini-Mental State Examination
Magnetic resonance imaging
Positron emission tomography
Tau phosphorylated at threonine 181
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Data was used for this project of which collection and sharing was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hoffmann-La Roche Ltd. and its affiliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfizer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.
This work has been supported by ZonMW Memorabel grant programme #733050824 (KW, BMT and PJV), Alzheimer Nederland grant #NL18003P (FD) and the Sigrid Juselius Foundation (LE). Funding was used in the analysis, interpretation and writing of the manuscript. Statistical analyses were performed at the VUmc Alzheimer Center that is part of the neurodegeneration research programme of the Neuroscience Campus Amsterdam. The VUmc Alzheimer Center is supported by Stichting Alzheimer Nederland and Stichting VUmc fonds.
Flora H. Duits and Kirsten E. J. Wesenhagen contributed equally to this work.
Authors and Affiliations
Department of Neurology, Alzheimer Center Amsterdam, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands
Flora H. Duits, Kirsten E. J. Wesenhagen, Laura Ekblad, Emma Wolters, Philip Scheltens, Wiesje M. van der Flier, Pieter Jelle Visser & Betty M. Tijms
Turku PET Centre, University of Turku and Turku University Hospital, Turku, Finland
Department of Radiology & Nuclear Medicine, Amsterdam Neuroscience, Amsterdam UMC, Amsterdam Neuroscience, Amsterdam, Netherlands
Department of Clinical Chemistry, Neurochemistry Laboratory, Amsterdam UMC, Amsterdam Neuroscience, Amsterdam, Netherlands
Eline A. J. Willemse & Charlotte E. Teunissen
Department of Epidemiology and Biostatistics, Amsterdam UMC, Amsterdam, The Netherlands
Wiesje M. van der Flier
Alzheimer Center Limburg, Department of Psychiatry & Neuropsychology, School of Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands
Pieter Jelle Visser
Division of Neurogeriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden
FD wrote the first drafts of the manuscript; KW and BT contributed further revisions. FD and BT performed the statistical analyses. LE contributed to the writing of the discussion. EWo contributed to methods and discussion related to PET imaging. PS and WF led the design and set-up of the ADC, from which data were used in this article. LE, EWo, EWi, WF, BT, CT and PV made suggestions on improvement of the manuscript. All authors read and approved the manuscript for submission.
The institutional review boards of all institutions participating in ADNI approved the procedures that were part of the study. For ADC, all procedures were approved by the local medical ethics committee. In both ADNI and ADC, written informed consent was obtained from all participants or surrogates.
Consent for publication
Prof. dr. Scheltens has acquired grants for the institution from GE Healthcare and Piramal and received consultancy/speaker fees paid to the institution from Novartis, Probiodrug, Biogen, Roche, and EIP Pharma, LLC in the past 2 years. Research programmes of Prof. dr. Wiesje van der Flier received funding by ZonMW, NWO, EU-JPND, Alzheimer Nederland, CardioVascular Onderzoek Nederland, Health~Holland, Topsector Life Sciences & Health, stichting Dioraphte, Gieskes-Strijbis fonds, stichting Equilibrio, Biogen MA Inc., Life-MI, AVID, Combinostics. WF holds the Pasman chair. WF has performed contract research for Biogen MA Inc. All funding is paid to her institution. Prof. dr. Teunissen received grants from the European Commission, the Dutch Research Council (ZonMW), Association of Frontotemporal Dementia/Alzheimer’s Drug Discovery Foundation, The Weston Brain Institute, Alzheimer Netherlands. Prof. Dr. Teunissen has functioned in advisory boards of Roche, received non-financial support in the form of research consumables from ADxNeurosciences and Euroimmun, performed contract research or received grants from Probiodrug, Biogen, Esai, Toyama, Janssen Prevention Center, Boehringer, AxonNeurosciences, EIP farma, PeopleBio, Roche. The other authors reported no conflicts of interest.
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Part of the data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: https://adni.loni.usc.edu/wpcontent/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf.
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Duits, F.H., Wesenhagen, K.E.J., Ekblad, L. et al. Four subgroups based on tau levels in Alzheimer’s disease observed in two independent cohorts.
Alz Res Therapy13, 2 (2021). https://doi.org/10.1186/s13195-020-00713-3