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Age, vascular disease, and Alzheimer’s disease pathologies in amyloid negative elderly adults



We recently reported that CSF phosphorylated tau (p-Tau181) relative to Aβ40 (CSF p-Tau/Aβ40 ratio) was less noisy and increased associations with Alzheimer’s disease (AD) biomarkers compared to CSF p-Tau181 alone. While elevations of CSF p-Tau/Aβ40 can occur in amyloid-β (Aβ) negative (Aβ-) individuals, the factors associated with these elevations and their role in neurodegeneration and cognitive decline are unknown. We aim to explore factors associated with elevated tau in CSF, and how these elevated tau are related to neurodegeneration and cognitive decline in the absence of Aβ positivity.


We examined relationships between CSF p-Tau/Aβ40, and CSF Aβ42/Aβ40, Aβ PET, and white matter hyperintensities (WMH) as well as vascular risk factors in 149 cognitively unimpaired and 52 impaired individuals who were presumably not on the Alzheimer’s disease (AD) pathway due to negative Aβ status on both CSF and PET. Subgroups had 18F-fluorodeoxyglucose (FDG) PET and adjusted hippocampal volume (aHCV), and longitudinal measures of CSF, aHCV, FDG PET, and cognition data, so we examined CSF p-Tau/Aβ40 associations with these measures as well.


Elevated CSF p-Tau/Aβ40 was associated with older age, male sex, greater WMH, and hypertension as well as a pattern of hippocampal atrophy and temporoparietal hypometabolism characteristic of AD. Lower CSF Aβ42/Aβ40, higher WMH, and hypertension but not age, sex, Aβ PET, APOE-ε4 status, body mass index, smoking, and hyperlipidemia at baseline predicted CSF p-Tau/Aβ40 increases over approximately 5 years of follow-up. The relationship between CSF p-Tau/Aβ40 and subsequent cognitive decline was partially or fully explained by neurodegenerative measurements.


These data provide surprising clues as to the etiology and significance of tau pathology in the absence of Aβ. It seems likely that, in addition to age, both cerebrovascular disease and subthreshold levels of Aβ are related to this tau accumulation. Crucially, this phenotype of CSF tau elevation in amyloid-negative individuals share features with AD such as a pattern of metabolic decline and regional brain atrophy.


Amyloid-β (Aβ) plaques and tau neurofibrillary tangles are the core features of Alzheimer’s disease (AD) [1]. According to the NIA-AA research framework [2], individuals with evidence of Aβ pathology are on the Alzheimer’s disease continuum, while Aβ-negative (Aβ−) individuals who have abnormal tau and/or neurodegeneration have been regarded as harboring non-Alzheimer’s pathologic change (also known as suspected non-Alzheimer’s pathophysiology or SNAP). Neuropathologically, Aβ- individuals with mild/moderate tau pathology have been characterized as having Primary-Age Related Pathology (PART) [3]. Previous studies [4,5,6,7,8] suggest that medial temporal lobe (MTL) tau aggregation may occur in the absence of abnormal Aβ pathology while Aβ pathology may be involved in driving the spread of tau out of MTL regions, producing neocortical neurodegeneration, and global cognitive decline. On the AD continuum, it is likely that elevated Aβ pathology alone may be insufficient to result in global brain atrophy, cortical hypometabolism, and generalized cognitive decline, requiring this spread of tau to induce these global and neocortical abnormalities [9,10,11,12,13]. This series of events raises the question of whether Aβ is necessary for these downstream events. Recent work has suggested that while elevated MTL tau may be related to local atrophy and cognitive decline regardless of Aβ status [14,15,16], evidence of cortical hypometabolism appears to require elevated Aβ [17, 18].

While PET provides spatial information on where tau deposits, CSF measurement of phosphorylated tau (p-Tau) provides complementary, although not interchangeable [19,20,21], information. Our laboratory [21] and other groups [19, 20] very recently observed evidence that CSF p-Tau may be superior to tau PET for detection of early tau increase. Recent data suggests that CSF p-Tau may start to increase even in those who are Aβ- by PET [20, 22]. However, the significance of elevated CSF p-Tau in the absence of Aβ, and how it relates to neurodegeneration, cognitive decline, and other factors, remains unclear. Previous studies in Aβ- individuals have reported inconsistent relationships between CSF p-Tau, neurodegeneration [23,24,25], and cognition [26,27,28].

Recently, we reported that using a CSF p-Tau/Aβ40 ratio reduced measurement error likely related to individual differences in CSF production rather than pathology and improved associations with AD biomarkers compared to using CSF p-Tau alone [21]. Specifically, we found that normalizing CSF p-Tau by Aβ40 eliminated a linear positive relationship otherwise observed between CSF p-Tau and Aβ42 among individuals with high (normal) Aβ42. This positive association (increasingly abnormal tau as Aβ42 becomes elevated or less abnormal within the high Aβ42 range) appears to reflect variability in CSF production and not a physiologically meaningful relationship. CSF p-Tau/Aβ40 therefore appears to increase sensitivity to detect tau-related neurodegeneration and cognitive decline compared to CSF p-Tau alone, particularly within the low, relatively restricted range of tau measurements observed in Aβ- individuals.

Relationships between tau and a number of other variables have been reported, including age [29,30,31,32,33], sex [33, 34], apolipoprotein E (APOE) genotype [31, 35, 36], and vascular risk factors including white matter hyperintensities (WMH) [25, 37, 38] and blood pressure [39,40,41]. The question of how these factors relate to tau among Aβ- individuals who are not (yet) on the AD pathway is not fully understood. Exploration of relationships between CSF p-Tau and non-AD-specific risk factors such as WMH, neurodegeneration, and cognitive decline in individuals who are not yet on the AD pathway provide insight into the heterogeneity of AD and other neurodegenerative diseases. In this study, we examined Alzheimer’s disease neuroimaging initiative (ADNI) participants who were unambiguously Aβ- based on both CSF Aβ42/Aβ40 and Aβ PET biomarkers in order to investigate how age, sex, APOE-ε4, and vascular risk factors associate with the earliest detectable CSF tau cross-sectionally and longitudinally, and whether elevation of CSF p-Tau can predict longitudinal hippocampal atrophy, hypometabolism, and cognitive decline.



Data used in this study were obtained from the ADNI database ( The ADNI study was approved by institutional review boards of all participating centers, and written informed consent was obtained from all participants or their authorized representatives. We identified 150 cognitively unimpaired (CU) participants, and 53 cognitively impaired (CI) participants (51 mild cognitive impairment (MCI) and 2 AD patients) who were Aβ- at baseline on both CSF Aβ42/Aβ40 and Aβ PET using CSF and PET thresholds described below, and had concurrent (acquisition intervals within 1 year) Aβ PET (18F-florbetapir (FBP) or 18F-florbetaben (FBB)), CSF Aβ40, Aβ42, and p-Tau181, WMH measurements, vascular risk factor data, and the ADNI cognitive test battery. Notably, one CU and one MCI individual whose WMHs were 3 and 4 standard deviations (SD) below the mean of the sample were excluded from the analysis. In addition, 81 individuals had concurrent 18F-fluorodeoxyglucose (FDG) PET and hippocampal volume.

Vascular risk factors

Based on the vascular risk factor data that is available in ADNI [42], we selected body mass index (BMI), smoking history, diabetes, hyperlipidemia (HLD), and hypertension (HTN). BMI was calculated according to the formula: BMI = (body weight in kg)/(body height in meters2). To define smoking, diabetes, HLD, and HTN as present (+) or absent (−), we searched text fields within the participants’ self-reported medical history (RECMHIST.csv and INITHEALTH.csv files downloaded from LONI website at September 12, 2020) using the following criteria to define the presence of these risk factors: smoking: “smok,” diabetes: “diabete,” HLD: “hyperlipidemia” or “'cholesterol,” and HTN: “hypertension” or “HTN” or “high blood pressure.” Cases where “w/o HTN” was noted were designated HTN-.

CSF Aβ40, Aβ42, and p-Tau

CSF Aβ40, Aβ42, and p-Tau181 were analyzed by the University of Pennsylvania ADNI Biomarker core laboratory using the fully automated Roche Elecsys and cobas e 601 immunoassay analyzer system [43]. The CSF Aβ42/Aβ40 and CSF p-Tau/Aβ40 ratios were calculated by dividing each CSF measurement by CSF Aβ40. We used a Gaussian-mixture model to estimate 2 Gaussian distributions of high CSF Aβ42/Aβ40 and low CSF Aβ42/Aβ40 among all 474 (251 CU, 184 MCI, and 39 AD) ADNI participants with CSF Aβ42/Aβ40 ratio (203 of them were included in this study) and defined an unsupervised threshold of ≤ 0.051 for abnormal CSF Aβ42/Aβ40, which corresponds to a 90% probability of belonging to the low CSF Aβ42/Aβ40 distribution (Supplemental fig. 1).

Slopes of CSF Aβ42/Aβ40 (ΔCSF Aβ42/Aβ40), CSF Aβ40 (ΔCSF Aβ40), and CSF p-Tau/Aβ40 (ΔCSF p-Tau/Aβ40) were calculated based on longitudinal CSF data among 28% of 201 participants (mean of 5.2±2.7 years of follow-up; 2.8±0.7 visits) using a linear mixed-effect (LME) model that included time and a random slope and intercept as independent variables for each participant. We did not adjust for age and sex when we calculated slopes of CSF biomarkers, because we treated them as potential risk factors of CSF biomarkers changes.

PET imaging and analysis

Details on FBP, FBB, and FDG PET image acquisition and analysis are given elsewhere ( Briefly, PET data were acquired in 5-min frames from 50–70 min (FBP), 90–110 min (FBB), and 30–60 min (FDG) post-injection ( Pre-processed FBP, FBB, FDG, PET, and structural MRI scans were downloaded from the LONI website ( Aβ PET scans were coregistered to the structural MRI scan that was closest in time to the baseline PET. Freesurfer-defined regions of interest (v5.3.0) on structural MRIs were used to extract regional FBP and FBB measurements from the co-registered PET images as described previously [9]. Cross-sectional (at the baseline timepoint) FBP or FBB standardized uptake value ratios (SUVRs) were calculated by dividing uptake across frontal, cingulate, parietal, and temporal regions by that in the whole cerebellum to generate cortical summary SUVRs [44]. Cortical summary SUVR thresholds were defined as FBP ≥1.11 or FBB ≥1.08 as described on the ADNI website ( FBP and FBB SUVRs were converted to Centiloids as described previously [9].

FDG PET images for voxel-wise analyses were spatially normalized to the PET template and intensity normalized at the voxel-wise level using the upper 50% of voxels in a pons/vermis reference region [45] using SPM12 (Welcome Department of Imaging Neuroscience, London, UK). These spatially normalized and intensity normalized images were also used to extract FDG SUVRs from a set of predefined and previously validated “metaROIs” (left angular gyrus, right angular gyrus, bilateral posterior cingulate, left inferior temporal gyrus, right inferior temporal gyrus) [46]. FDG SUVR slope (ΔFDG SUVR) was calculated for each participant based on longitudinal FDG data which was available in 19.5% of 201 participants with a mean of 2.9±1.8 years of follow-up (2.2±0.4 visits) using LME model that included time, age, and sex, and a random slope and intercept as independent variables.

Hippocampal volume and white matter hyperintensities

Hippocampal volume (HCV) (mm3) was calculated with Freesurfer and adjusted (aHCV) for intracranial volume (ICV) using the regression approach [47] as described previously [21]. aHCV slope (ΔaHCV) data was available for 30.5% of 201 participants (mean of 5.0±2.6 years of follow-up; 5.8±2.1 visits) using the structural MRI scan that was closest in time to, and after, the baseline CSF p-Tau/Aβ40. These slopes were estimated using LME model, including the following independent variables: time, age, and sex, and a random slope and intercept.

WMH measurement was calculated at the University of California, Davis, based on a Bayesian approach to segmentation of high-resolution T1-weighted and FLAIR images as described previously [48] and also on the ADNI website. In order to compensate for individual variance in brain size and non-normal distribution, WMH was normalized to ICV (WMH/ICV) and log10 transformed prior to analysis.


Preclinical Alzheimer’s Cognitive Composite (PACC) scores [49] were calculated as described by combing the standard z scores (using the mean values of all the ADNI CU participants regardless of amyloid positivity) of the Delayed Recall portion of the Alzheimer’s Disease Assessment Scale, the delayed recall score on the logical memory IIa subtest from the Wechsler Memory Scale, the digit symbol substitution test score from the Wechsler Adult Intelligence Scale–Revised and the MMSE total score. PACC slope (ΔPACC) was calculated based on longitudinal cognitive scores in 37% of 201 participants (mean follow-up=4.8±2.8 years, 5.4±2.4 visits) using LME model, including the following independent variables: time, age, sex, and education and a random slope and intercept.

Statistical analysis

The normality of distributions was tested using the Shapiro-Wilk test and visual inspection of data. Data are presented as median (interquartile range (IQR)) or number (%) unless otherwise noted. Baseline characteristics were compared between Aβ- CU and CI groups by using a two-tailed Mann-Whitney test or Fisher’s exact test.

In order to determine the factors related to CSF p-Tau/Aβ40 increase, we examined the associations of CSF p-Tau/Aβ40 and ΔCSF p-Tau/Aβ40 with CSF Aβ42/Aβ40, Aβ PET, age, sex, APOE-ε4 status, WMH, BMI, Smoking, Diabetes, HLD, and HTN using Pearson’s correlation or Mann-Whitney tests. Diabetes was excluded from some following analyses due to limited sample size (Fig. 1). Because CSF p-Tau/Aβ40 has been recently validated in Aβ- individuals [21] but is still a relatively novel measurement, we also examined baseline non-ratio CSF p-Tau and ΔCSF p-Tau in the significant associations identified using the ratio CSF p-Tau/Aβ40 measurement. We also investigated the prediction of ΔCSF Aβ42/Aβ40 and ΔCSF Aβ40 by baseline CSF p-Tau/Aβ40, and its significantly associated risk factors (CSF Aβ42/Aβ40, WMH, and HTN, see Fig. 1 in the “Results” section). Besides, we used generalized linear models (GLM) models to investigate the associations of CSF p-Tau/Aβ40 and ΔCSF p-Tau/Aβ40 with their significant risk factors (see Fig. 1 in the “Results” section) together in the same model, respectively.

Fig. 1
figure 1

Risk factors related to elevated tau in Aβ- individuals. The associations of risk factors with baseline CSF p-Tau/Aβ40 (A-F) and longitudinal CSF p-Tau/Aβ40 annualized change (G-L). Abbreviations: Aβ amyloid-β, CSF cerebrospinal fluid, CU cognitively unimpaired, CI cognitively impaired, p-Tau phosphorylated tau, WMH white matter hyperintensities

Associations of voxel-wise FDG PET images with CSF p-Tau/Aβ40 and its significant risk factors were analyzed using regression models implemented in SPM12 (Welcome Department of Imaging Neuroscience, London, UK), controlling for age, sex, and diagnosis. Voxel-wise results between CSF p-Tau/Aβ40 and FDG PET were presented using an uncorrected voxel threshold of p < 0.001. T-maps were converted to R-maps using CAT12 toolbox ( and displayed at both without and with family-wise error (FWE) corrected p < 0.05 at the cluster level.

We included as covariates in the multivariate analyses only risk factors of CSF p-Tau/Aβ40 that had significant associations with FDG SUVR, aHCV, and PACC. We used GLM models to investigate the associations between CSF p-Tau/Aβ40, FDG SUVR (metaROIs), and ΔFDG SUVR, controlling for age, sex, and diagnosis. We also investigated the predictive effect of baseline CSF p-Tau/Aβ40 on aHCV and ΔaHCV, controlling for HTN, age, sex, and diagnosis. In order to understand the association between aHCV and FDG SUVR, we investigated the predictive effect of baseline FDG SUVR on ΔaHCV controlling for HTN, age, sex, and diagnosis, and baseline aHCV on ΔFDG SUVR controlling for age, sex, and diagnosis.

Finally, we investigated the prediction of ΔPACC with baseline CSF p-Tau/Aβ40, FDG SUVR, and aHCV as the predictors, controlling for HTN, age, sex, education, and diagnosis. We also examined the sequential mediation associations between baseline CSF p-Tau/Aβ40, aHCV, FDG SUVR, and ΔPACC using latent variable modeling (R; Lavaan package) [50]. CSF p-Tau/Aβ40, aHCV, FDG SUVR, and ΔPACC were converted to standard z scores. Total, direct, and indirect associations were calculated via a 5000-iteration bootstrapping procedure.

We selected two-sided p < 0.05 as the significance level unless otherwise noted. Longitudinal data of biomarkers were defined as the data that was closest in time to, and after, the baseline CSF p-Tau/Aβ40. Statistical analyses were performed in the statistical program R (v3.6.2, The R Foundation for Statistical Computing) unless otherwise noted.



Measurements were acquired between July 2010 and August 2020. Demographics of 201 Aβ- participants and the comparisons between CU individuals and CI individuals can be found in Table 1. Longitudinally, 56, 61, 39, and 74 participants had > 2 CSF, aHCV, FDG PET, and PACC cognitive data respectively.

Table 1 Demographics of amyloid-negative participants

Risk factors related to elevated tau in Aβ- individuals

At baseline, elevated CSF p-Tau/Aβ40 was unrelated to CSF Aβ42/Aβ40 but was associated with older age (R = 0.28 [95% ci, 0.15, 0.41]), male sex (estimate = 4.2×10-5 [95% ci, 6.4×10-7, 6.8×10-5]), higher WMH (R = 0.19 [95% ci, 0.06, 0.32]), and HTN (estimate = 4.1×10-5 [95% ci, 2.9×10-5, 1.0×10-4]) but not diabetes (Fig. 1A–F). When all significant risk factors were entered into a single model, only age was significantly related to CSF p-Tau/Aβ40 (Supplemental fig. 2A, standardized β (βstd) = 0.22 [95% ci, 0.08, 0.37], p = 0.003). None of these significant risk factors (age, sex, WMH, HTN) were related to CSF Aβ42/Aβ40 or CSF Aβ40, and only age was related (R = 0.25 [95% ci, 0.11, 0.37], p < 0.001) to the non-ratio CSF p-Tau measurement (Supplemental fig. 3). In addition, older age was related to higher WMH (R = 0.29 [95% ci, 0.16, 0.42], p < 0.001) and HTN (estimate = 3.3 [95% ci, 1.2, 5.3], p = 0.001); HTN and WMH were also positively associated (estimate = 0.24 [95% ci, 0.08, 0.39], p = 0.005).

CSF Aβ42/Aβ40 predicted (R = −0.43 [95% ci, −0.62, −0.19]) subsequent ΔCSF p-Tau/Aβ40 (Fig. 1G), whereas CSF p-Tau/Aβ40 was unrelated to ΔCSF Aβ42/Aβ40 or ΔCSF Aβ40 (Supplemental fig. 4). In addition, higher WMH (R = 0.32 [95% ci, 0.06, 0.54]) and HTN (estimate = 4.7×10-6 [95% ci, 6.2×10-7, 8.7×10-6]) were associated with subsequent ΔCSF p-Tau/Aβ40 (Fig. 1J, K) (but not ΔCSF Aβ42/Aβ40 or ΔCSF Aβ40, Supplemental fig. 4). Individuals with diabetes had faster ΔCSF p-Tau/Aβ40 (Fig. 1L), but the small number (n=6) of individuals with diabetes limits interpretation. When all the significant risk factors (age, sex, CSF Aβ42/Aβ40, WMH, and HTN) were entered into a single model, CSF Aβ42/Aβ40 (βstd = −0.40 [95%ci, −0.65, −0.14], p = 0.003) and HTN (βstd = 0.51 [95%ci, 0.02, 0.99], p = 0.04) were related to ΔCSF p-Tau/Aβ40 (Supplemental fig. 2B). Among these significant risk factors related to ΔCSF p-Tau/Aβ40, only CSF Aβ42/Aβ40 was associated (R = −0.28 [95% ci, −0.50, −0.02], p = 0.038) with the non-ratio ΔCSF p-Tau measurement (Supplemental fig. 4I).

The associations of Aβ PET, APOE-ε4 status, BMI, smoking, diabetes, HLD with either baseline CSF p-Tau/Aβ40, or ΔCSF p-Tau/Aβ40 were not significant (Supplemental fig. 5).

Elevated tau and neurodegeneration in Aβ− individuals

Voxel-wise multiple regression analysis showed that elevated CSF p-Tau/Aβ40 was associated with hypometabolism predominantly in inferior temporal, middle temporal, angular gyrus, posterior cingulate/precuneus, inferior parietal, middle frontal, and middle occipital regions (Fig. 2A, p<0.001 uncorrected). After FWE correction (p<0.05), significant negative associations remained in bilateral posterior cingulate/precuneus, right inferior temporal, middle temporal, and inferior parietal regions (Supplemental fig. 6). Overlap between these results with temporoparietal metaROIs that are characteristic of AD (Supplemental fig. 7) suggests that the metaROI SUVRs are a reasonable measurement of hypometabolism in these Aβ- individuals.

Fig. 2
figure 2

Associations of elevated tau, hypometabolism, and hippocampal atrophy in Aβ- individuals. A Voxel-wise correlation between CSF p-Tau/Aβ40 and FDG PET. Cross-sectional associations between CSF p-Tau/Aβ40, and B FDG SUVR (metaROIs) and C aHCV. Prediction of ΔFDG SUVR by baseline D CSF p-Tau/Aβ40 and F aHCV. Prediction of ΔaHCV by baseline E CSF p-Tau/Aβ40 and G FDG SUVR (metaROIs). Abbreviations: Aβ amyloid-β, aHCV adjusted hippocampal volume, CSF cerebrospinal fluid, CU cognitively unimpaired, CI cognitively impaired, FDG 18F-fluorodeoxyglucose, p-Tau phosphorylated tau, SUVR standardized uptake value ratio

Among these significant risk factors related to CSF p-Tau/Aβ40, we found HTN was related to aHCV (βstd = −0.52 [95% ci, −0.90, −0.14], p = 0.009) and ΔPACC (βstd = −0.46 [95% ci, −0.88, −0.04], p = 0.037) (Supplemental fig. 8). Cross-sectionally, CSF p-Tau/Aβ40 was related to both FDG SUVR in the metaROIs (Fig. 2B, βstd = −0.40 [95% ci, −0.62, −0.18]) and aHCV (Fig. 2C, βstd = −0.25 [95% ci, −0.45, −0.04]). aHCV was correlated with FDG SUVR (βstd = 0.22 [95% ci, 0.02, 0.42], R = 0.38 [95% ci, 0.17, 0.55], p = 0.032). Elevated CSF p-Tau/Aβ40 predicted subsequent FDG SUVR decrease (Fig. 2D, βstd = −0.43[95% ci, −0.72, −0.14]), but did not predict change in aHCV (Fig. 2E). Lower aHCV predicted subsequent FDG SUVR decrease (Fig. 2F, βstd = 0.16 [95% ci, 0.22, 0.85]). Conversely, FDG SUVR also predicted subsequent aHCV decrease (Fig. 2G, βstd = 0.13 [95% ci, 0.05, 0.54]).

In order to control for the possible influence from longitudinal Aβ changes on our analyses, we also investigated the associations of CSF p-Tau/Aβ40, FDG SUVR (metaROIs), aHCV, ΔFDG SUVR, and ΔaHCV after excluding 5 individuals who developed to Aβ+ at follow-up (one MCI changed at CSF Aβ42/Aβ40 and Aβ PET, 2 CU changed Aβ PET, and 2 CU changed CSF Aβ42/Aβ40). The results were substantially the same (Supplemental fig. 9).

The baseline non-ratio CSF p-Tau and CSF Aβ40 measures were not associated with FDG SUVR (metaROIs), aHCV, ΔFDG SUVR, and ΔaHCV (Supplemental fig. 10).

Prediction of longitudinal cognitive decline in Aβ- individuals

The median (IQR) annual ΔPACC of CI individuals (−0.56 (1.47)) was faster (estimate = −0.54 [95% ci, −0.97, 0.18], p<0.001) than CU individuals (0.09 (0.46)). CSF p-Tau/Aβ40 (Fig. 3A, βstd = −0.29 [95% ci, −0.50, −0.09]), FDG SUVR (metaROIs) (Fig. 3B, βstd = 0.28 [95% ci, 0.07, 0.50]), and aHCV (Fig. 3C, βstd = 0.52 [95% ci, 0.33, 0.72]) all predicted subsequent cognitive decline (ΔPACC). The baseline non-ratio CSF p-Tau and CSF Aβ40 measures were not associated with ΔPACC (Supplemental fig. 10).

Fig. 3
figure 3

Associations of elevated tau, hypometabolism, hippocampal atrophy, and longitudinal cognitive decline in Aβ- individuals. Prediction of ΔPACC by baseline A CSF p-Tau/Aβ40, B FDG SUVR, and C aHCV. D Pathways between CSF p-Tau/Aβ40, FDG SUVR, and ΔPACC. E Pathways between CSF p-Tau/Aβ40, aHCV, and ΔPACC. Abbreviations: Aβ amyloid-β, aHCV adjusted hippocampal volume, CSF cerebrospinal fluid, CU cognitively unimpaired, CI cognitively impaired, FDG 18F-fluorodeoxyglucose, PACC Preclinical Alzheimer Cognitive Composite, p-Tau phosphorylated tau, SUVR standardized uptake value ratio

In the mediation analysis, FDG SUVR (Fig. 3D) partially and aHCV (Fig. 3E) fully mediated the association between CSF p-Tau/Aβ40 and ΔPACC. Furthermore, only aHCV was significantly (β = 0.0003[95% ci: 0.0002, 0.0004]) related to longitudinal PACC decline when all the predictors were entered into one model (Fig. 4).

Fig. 4
figure 4

Prediction of longitudinal cognitive decline (ΔPACC) by baseline CSF p-Tau/Aβ40, FDG SUVR, and aHCV in one multivariate model. Abbreviations: Aβ amyloid-β, aHCV adjusted hippocampal volume, CSF cerebrospinal fluid, CU cognitively unimpaired, CI cognitively impaired, FDG 18F-fluorodeoxyglucose, PACC Preclinical Alzheimer Cognitive Composite, p-Tau phosphorylated tau, SUVR standardized uptake value ratio


In this study, we investigated a broad range of biomarker, cerebrovascular, and cognitive associations with tau in elderly adults who were unambiguously Aβ- on the basis of both CSF and PET measurements at baseline and therefore seemingly unlikely to be on the pathway to AD. In these individuals, elevated tau measured with CSF was associated with several risk factors (older age, male sex, greater WMH burden, and hypertension), as well as a pattern of neurodegeneration that is characteristic of AD (temporoparietal hypometabolism, and hippocampal atrophy). In longitudinal analyses, lower CSF Aβ42/Aβ40, higher WMH, and hypertension at baseline predicted tau increases over about 5 years of follow-up. Elevated baseline tau was also associated with subsequent cognitive decline, which was partially mediated by temporoparietal hypometabolism but fully mediated by hippocampal atrophy. These relationships between tau, cerebrovascular disease, and neurodegeneration biomarkers that are typical of AD raise interesting questions about non-amyloid pathways that may be important in the etiology of cognitive decline.

Although there was no relationship between CSF Aβ42/Aβ40 and CSF p-Tau/Aβ40 at baseline, lower CSF Aβ42/Aβ40 predicted subsequent longitudinal CSF p-Tau/Aβ40 increase but not vice versa. There was thus no countervailing evidence that tau deposition drives changes in Aβ in these data or in a previous report from our laboratory [9]. These findings seem most compatible with the hypothesis that, at least in part, Aβ pathology can drive changes in tau even when Aβ is in a “normal” range. Other data have shown significant CSF p-Tau increases in Aβ PET negative individuals [20, 22], and our data extend these results by indicating that Aβ and tau are positively associated with one another prior to reaching the positivity thresholds of both CSF Aβ and Aβ PET. Together with other studies reporting significant Aβ-related tau deposition and cognitive decline in Aβ PET negative cognitively healthy individuals [51,52,53,54,55], these data indicate that tau can begin depositing in nominally “Aβ- individuals.”

One of the key findings in this study was that white matter lesions and hypertension were related to both baseline and longitudinal CSF p-Tau/Aβ40 increases in the absence of abnormal Aβ pathology whereas they had no association with CSF Aβ42/Aβ40 or Aβ40 alone, suggesting vascular risk factors may be closely linked to CSF p-Tau/Aβ40 independent of Aβ pathology. ADNI data have previously been explored to examine some of the relationships between tau and the variables we measured, though usually not in Aβ- individuals. For example, a few studies based on the ADNI cohort reported significant associations of CSF p-Tau or plasma p-Tau with WMH [25, 37, 56] and hypertension [41]. In addition, some non-ADNI studies reported similar findings although without specifically examining relationships in Aβ- individuals. For instance, a few studies found CSF p-Tau was associated with WMH [38], global mean diffusivity in white matter [57], and hypertension [40]; two PET studies found PET measures of brain tau [58, 59] were related to vascular health variables. In addition, neuropathological studies also found that higher WMH were related to greater neurofibrillary tangles [60] or both tangles and plaques [61], and higher blood pressure was related to higher number of neurofibrillary tangles [62] or both plaques and tangles [63].

Age is a well-known risk factor for tau accumulation, and it was also related to these vascular factors in our data. In a multivariable model, age was the only variable associated with tau. However, both WMH and HTN, but not age, were related to longitudinal tau increases. Together, these findings suggest that both age and cerebrovascular risk factors may be related to tau increases in the absence of abnormal Aβ pathology.

A surprising result of this study was the association between tau and regional cerebral hypometabolism in a pattern typically associated with AD despite the absence of measurable Aβ. In patients with clinical and biomarker evidence of AD, patterns of tau deposition are highly correlated with glucose metabolism while Aβ deposition is not [64]. Although we do not know the level of cortical tau deposition in our subjects because CSF measurements of tau cannot provide regional information, these results are suggestive of tau deposition affecting regional metabolism in a topography that recapitulates AD, suggesting that tau-related, AD-like neurodegeneration can occur in a setting of low Aβ.

Further evidence that elevated tau is related to neurodegeneration is found in its relationship with hippocampal volume. In fact, all three variables–tau, glucose metabolism in typically affected AD regions, and hippocampal volume–were related to one another at baseline and to a large extent in longitudinal relationships (although baseline p-Tau/Aβ40 predicted metabolic decline but not progressive atrophy). Previous work is inconsistent, with some studies of Aβ- ADNI participants failing to find associations between CSF p-Tau and hippocampal or cortical atrophy [24, 25], while others find significant relationships between CSF p-Tau and reduced cortical thickness independent of Aβ pathology [23]. It is difficult to understand how opposite findings can arise from the same study, although differences in the sample (such as the sample size and/or the proportion with cognitive impairment), CSF assays, and our use of the normalizing Aβ40 ratio [21] may play a role. Regardless of these discrepancies, our data seem to provide strong evidence for an Alzheimer’s-type neurodegeneration that is progressive and related to tau even in amyloid negative individuals.

In addition to its relationship with neurodegeneration, tau was also related to cognitive decline, providing further evidence that it is not benign when Aβ is low. These “downstream” pathways appear to be related as tau affects cognition through both glucose metabolism and hippocampal atrophy. Previous studies have not been in agreement that elevated CSF p-Tau in Aβ- individuals is linked to significant cognitive decline [26, 65], although our sample was older and included those with cognitive impairment.


This study has several limitations. Our findings were based on tau measured using CSF p-Tau181/Aβ40, but it would be helpful to validate the findings in other samples and with other phosphorylation sites [66]. Furthermore, it is possible that the use of the p-Tau181/Aβ40 ratio introduces a confounder that could account for these associations, we think that this is unlikely since CSF Aβ40 alone was not associated with any of the factors we investigated. Therefore, we believe that these findings reinforce earlier evidence [21] that there is considerable noise among Aβ-negative individuals in CSF p-Tau181 measurements due to individual variability in CSF production and due to the limited dynamic range in this group, and this variability can be attenuated by adjusting for Aβ40. This noise reduction appears to facilitate the observation of subtle associations between tau and other risk factors at early stages of abnormality. An additional limitation of this study was that some Aβ- subgroups we examined were very small, such as APOE-ε4 carriers, which limited our ability to examine covariates and other risk factors. Finally, tau PET is a relatively late addition to ADNI, so we did not include this because of minimal longitudinal tau data. Nevertheless, CSF p-Tau may have been an advantageous measure for the scientific questions in this study because it probably reflects earlier tau pathology than PET [20, 21].


The elevation of p-Tau in CSF in our Aβ- subjects is consistent, at least nosologically, with the disorder that has been described as PART; however, in the absence of neuropathology we cannot confirm this diagnosis. These data provide surprising clues as to the etiology and significance of tau pathology in aging. It seems likely that, in addition to age, both cerebrovascular disease and subthreshold levels of Aβ are related to this tau accumulation. Whether cerebrovascular factors alone or in concert with low levels of Aβ can drive tau pathology is uncertain, but the literature is replete with evidence for a relationship between tau and cerebrovascular disease. Crucially, evidence of this tau pathology occurs early, as CSF probably reflects tau abnormalities before PET scans do, and shares features with AD such as a pattern of metabolic decline and regional brain atrophy. Further longitudinal follow-up of these individuals will be critical for determining whether these processes are Alzheimer’s-independent. However, our data indicate that this phenotype of Aβ- CSF tau elevation is similar to AD, which implies that it may represent an amyloid-independent pathway to AD, a pathophysiology that mimics AD, or an important, and very early, interaction between Aβ and vascular disease that underlies neurodegeneration and cognitive decline.

Availability of data and materials

The dataset supporting the conclusions of this article is available in the ADNI repository ( Derived data is available from the corresponding author on request by any qualified investigator subject to a data use agreement.





Alzheimer’s disease


Alzheimer’s Disease Neuroimaging Initiative


Adjusted hippocampal volume


Body mass index

βstd :

Standardized β coefficient


Confidence interval


Cerebrospinal fluid


Cognitively unimpaired








Generalized linear model




Hippocampal volume




Intracranial volume


Linear mixed-effect


Mild cognitive impairment


Preclinical Alzheimer Cognitive Composite


Primary-Age Related Tauopathy


phosphorylated tau


Regions of interest


Standardized uptake value ratio


White matter hyperintensities


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The data collection and sharing for this project 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.; 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 ( The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Disease Cooperative Study at the University of California, San Diego. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.


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T.G contributed to the study design, drafting and editing the manuscript, data and statistical analysis, and interpretation of the results; W.J.J and S.M.L contributed to the study design, acquiring the data, interpretation of the results, and editing the manuscript. The authors read and approved the final manuscript.

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Correspondence to Tengfei Guo.

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Guo, T., Landau, S.M., Jagust, W.J. et al. Age, vascular disease, and Alzheimer’s disease pathologies in amyloid negative elderly adults. Alz Res Therapy 13, 174 (2021).

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  • Alzheimer’s disease
  • Amyloid negative
  • CSF p-Tau
  • Hippocampal atrophy
  • Hypometabolism
  • Vascular disease