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. 2016 Feb 9;6:20709. doi: 10.1038/srep20709

Cerebral white matter lesions – associations with Aβ isoforms and amyloid PET

Danielle van Westen 1,2,a, Daniel Lindqvist 3,4, Kaj Blennow 5, Lennart Minthon 6,7, Katarina Nägga 6,7, Erik Stomrud 6,7, Henrik Zetterberg 5,8, Oskar Hansson 6,7
PMCID: PMC4746584  PMID: 26856756

Abstract

Small vessel disease (SVD) and amyloid deposition may promote each other, with a potential association between SVD and altered production or clearance of β-amyloid (Aβ) affecting its cleavage products. We investigated the relationship between SVD, multiple isoforms of Aβ in cerebrospinal fluid (CSF) and cortical Aβ in 831 subjects with cognitive performance ranging from normal to Alzheimer’s disease (AD) (the Swedish BioFINDER study). SVD was estimated as white matter lesions (WML) and lacunes. 18F-flutemetamol PET was performed in 321 subjects. Lower CSF levels of Aβ38 and Aβ40 were consistently associated with increased WML in all subgroups, while lower levels of CSF Aβ42 were associated with WML mainly in AD. CSF Aβ38 and Aβ40 were associated with regional WML in all regions, while CSF Aβ42 was associated with temporal WML only. A composite measure of 18F-flutemetamol uptake was not associated with WML, and regional 18F-flutemetamol uptake only with temporal WML. Lacunes were not associated with Aβ isoforms nor 18F-flutemetamol uptake. Our results suggest that WML may be associated with alterations in the production or clearance of Aβ species, particularly of Aβ38 and Aβ40. However, in AD cases, Aβ42 pathology might be associated with WML, especially in the temporal lobe.

While cerebral small vessel disease (SVD) affects perforating cerebral arterioles, capillaries and venules, the term SVD is also used to describe the resulting brain damage, comprising mainly subcortical lesions such as small infarcts, lacunes, white matter lesions (WML), enlarged perivascular spaces and microbleeds1. WML are the most common manifestation of SVD and especially abundant in elderly, but the suggested prevalence has varied substantially between different studies2,3,4. Cerebral microbleeds (MB) are markers of vascular pathology including cerebral amyloid angiopathy (CAA) and potentially have direct effects on brain function5. SVD will lead to a number of downstream effects including fibrosis impairing drainage of fluid and proteins from the extravascular space along the blood vessels6, with accumulation of proteins, including amyloid beta (Aβ)7,8.

Cleavage of the amyloid precursor protein (APP) by β- and γ-secretases yields Aβ peptides with Aβ38, Aβ40 and Aβ42 as the most common variants9. In most cells, Aβ38 and Aβ42 are produced at relatively low levels, typically 5–20% of the total Aβ detected, and the major species generated is Aβ40 that typically constitutes over 50% of total Aβ10,11. Aβ38, Aβ40 and Aβ42 differ in aggregation propensity: Aβ38 is soluble, present in the vasculature of in sporadic and familial AD patients and never found in senile plaques, Aβ40 is somewhat aggregation-prone, it is the main component for vascular amyloid and is often found in CAA, whereas Aβ42 is the most aggregation-prone, forming cortical fibrillar Aβ that will be deposited as amyloid plaques associated with Alzheimer’s disease12,13.

SVD and AD share common risk factors, such as hypertension during midlife, diabetes mellitus, smoking, the apolipoprotein E (APOE) ε4 allele and particularly age14,15. A two hit, potentially self-reinforcing mechanism has been proposed, suggesting that SVD may initiate amyloid deposition on the one hand, and amyloid deposition may increase the susceptibility to develop SVD on the other hand16,17. Increased knowledge about the role of Aβ species in SVD may improve treatment and prevention strategies for individuals with SVD, since accumulation of multiple vascular risk factors, especially in midlife, can substantially increase the risk for dementia18. This has been confirmed by the suggested declining trend in dementia risk, occurring in parallel with the decreasing incidence of cardiovascular events in high-income countries19,20. A recent study on the association between SVD and amyloid accumulation found higher WML to be associated with lower levels of CSF Aβ42 in vascular dementia and in subjective cognitive decline but not in AD, which was interpreted as a connection between SVD and AD pathology21. However, these findings may alternatively suggest that SVD is related to a general decrease in beta amyloid, reflecting a diminished secretion of amyloid precursor protein (APP), rather than the AD specific phenomenon of Aβ42 aggregation. If this were the case, WML would be associated with lower CSF levels of all amyloid species, including Aβ38 and Aβ40 in addition to Aβ42. Therefore, we readdressed the association between SVD and amyloid deposition including multiple markers of amyloidogenic APP-processing and Aβ deposition. Specifically, we studied the relationship between WML and lacunes assessed with neuroimaging and CSF levels of Aβ38, Aβ40 and Aβ42. In addition we measured amyloid uptake using 18F-flutemetamol PET, that reflects cortical levels of fibrillar Aβ associated with amyloid plaques. The study population consisted of 831 individuals from four diagnostic groups that differed in their cognitive performance, cognitively healthy elderly (CHE), and subjects with subjective cognitive decline (SCD), mild cognitive impairment (MCI) and AD; in order to confirm results in a separate cohort of subjects with a neurodegenerative disease, other than AD albeit associated with amyloid accumulation, a fifth diagnostic group, consisting of subjects with Parkinson’s disease (PD) without dementia, was also included.

Results

Demographics

Demographic data are given in Table 1. WML volume, total Fazekas score and total Age Related White Matter Changes (ARWMC) score were highly correlated, average partial correlation coefficient 0.806, p < 0.001, pooled data from the CHE, SCD, MCI and PD cohorts. CSF levels of Aβ38 and Aβ40 did not correlate with the composite SUVR for amyloid PET, partial correlation coefficient 0.027 and 0.088, respectively, p > 0.05. In contrast, the CSF level of Aβ42 showed a high inverse correlation with the composite SUVR for amyloid PET, partial correlation coefficient −0.668, p < 0.001, pooled data from the CHE, SCD and MCI cohorts. All correlation analyses were corrected for age, sex and hippocampal volume.

Table 1. Baseline characteristics by clinical diagnosis.

  Cognitively healthy elderly (n = 267) Subjective cognitive deficit (n = 165) Mild cognitive impairment (n = 195) PD patients (n = 89) AD patients (n = 110)
Age (mean + SD) 72.9 + 5.0 70.0 + 5.8a*** 71.2 + 5.6a*** 65.4 + 11.2a,b, c*** 74.5 + 7.3a*,b, c, d***
Proportion female (%) 61.4 57.6 44.6a***, b* 38.2a,b*** 62.7c, d***
APOE ε4 carriers (%) 30.7 38.5 47.9a*** N/A 67.3a,b*** c***
WML volume          
(median, IQR) 5.3, 2.0–14.2 6.5, 1.7–18.9 12.5, 4.5–34.0a,b*** 5.0, 1.5–16.4c*** N/A
Fazekas total score (median, IQR) 4.0, 2.0–6.0 5.0, 3.0–7.0 6.0, 3.0–10.0a,b*** 4.0, 1.0–7.5b*, c*** 4.0, 2.0–7.0c***
AWMRC total (median, IQR) 4.0, 1.0–8.0 5.0, 2.0–8.0 6.0, 2.0–10.0a***, b* 4.0, 0.0–7.50c* 3.5, 0.8–8.0c***
Lacunes (%) 5.7 8.1 11.3a* 2.2c* 3.6c*
CSF Aβ38 (median, IQR, pg/mL) 1727.5, 1492.3–2011.0 1797.0, 1432.3–2065.3 1646.5, 1357.0–1889.3a***, b* 1626.0, 1310.0–1841.0a,b*** 1649.0, 1360.8–1935.8a, b***
CSF Aβ40 (median, IQR, pg/mL) 4549.0, 3515.5–5483.5 4837.5, 3514.3–6298.8 4339.0, 3427.8–5546.0b* 3757.0, 2996.5–4784.0a, b, c*** 3826.5, 3120.5–5159.8a, b***, c**
CSF Aβ42 (median, IQR, pg/mL) 665.0, 509.8–778.0 657.0, 440.9–802.8 468.0, 351.0–711.0a,b*** 644.0, 481.5–766.5c*** 365.0, 297.8–428.8a, b, c, d***
Composite PET SUVR (median, IQR) 1.24, 1.12–1.34 (n = 122) 1.23,1.13–1.68 (n = 101)a* 1.55, 1.20–2.09 (n = 98)a, b*** N/A N/A
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avs cognitively healthy elderly.

bvs subjective cognitive deficit.

cvs mild cognitive impairment.

dvs PD. •p < 0.05, **p < 0.01, ***p < 0.005

Only p-values < 0.005. should be considered significant according to Bonferroni-adjustment.

Associations between total WML and CSF Aβ38, Aβ40 and Aβ42

In the CHE, SCD, MCI, and PD groups, lower CSF levels of Aβ38 and Aβ40 were significantly associated with increased WML volume (Table 2). However, there were no significant associations between CSF levels of Aβ42 and WML volume in any of the groups (Table 2). To confirm these results, visual assessment of WML using the Fazekas scale was performed, now including the AD group. Again, higher Fazekas scores (indicating more severe WML) was associated with lower CSF levels of Aβ38 and Aβ40 in the SCD and the MCI groups, and lower levels of Aβ38 in the PD group (Table 2). CSF Aβ42 was associated with WML only in the AD group, in addition to CSF Aβ38 and Aβ40 (Table 2).

Table 2. Associations between cerebrovascular disease, Aβ isoforms and amyloid PET per diagnostic group.

Group Parameter WML volume ± 95% CI Fazekas score ± 95% CI Lacunes ± 95% CI
Cognitively CSF Aβ38 −0.151** −0.260 −0.042 −0.071 −0.191 0.048 −0.254 −1.369 0.861
healthy CSF Aβ40 −0.118* −0.228 −0.008 −0.058 −0.178 0.061 −0.363 −1.940 1.213
elderly CSF Aβ42 −0.075 −0.185 0.036 0.017 −0.103 0.137 −0.795 −2.406 0.815
  Composite SUVR 0.037 −0.137 0.210 −0.057 −0.241 0.127 0.570 −2.911 4.052
                     
Subjective CSF Aβ38 −0.211** −0.341 −0.081 −0.170* −0.312 −0.028 2.306 −0.317 −0.030
cognitive CSF Aβ40 −0.243*** −0.371 −0.115 −0.197** −0.337 −0.057 1.144 −0.309 −0.020
deficit CSF Aβ42 −0.079 −0.213 0.055 −0.066 −0.211 0.079 0.976 −0.154 0.142
  Composite SUVR 0.099 −0.075 0.273 0.070 −0.118 0.257 −0.686 −0.187 0.231
                     
Mild CSF Aβ38 −0.264*** −0.396 −0.133 −0.174* −0.317 −0.030 −1.947* −3.655 −0.239
cognitive CSF Aβ40 −0.286*** −0.417 −0.155 −0.164* −0.309 −0.020 −1.018 −2.312 0.276
impairment CSF Aβ42 0.000 −0.138 0.138 −0.006 −0.154 0.142 0.715 −0.501 1.931
  Composite SUVR −0.028 −0.226 0.170 0.022 −0.187 0.231 0.149 −2.755 3.052
                     
PD−patients CSF Aβ38 −0.181** −0.310 −0.053 −0.188* −0.365 −0.011 NA    
  CSF Aβ40 −0.185** −0.314 −0.056 −0.175 −0.225 −0.125 NA    
  CSF Aβ42 −0.066 −0.204 0.072 0.010 0.386 −0.366 NA    
                     
AD−patients CSF Aβ38 NA     −0.258* −0.447 −0.070 NA    
  CSF Aβ40 NA     −0.299** −0.485 −0.113 NA    
  CSF Aβ42 NA     −0.225* −0.413 −0.038 NA    
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Values represent standardized beta (linear regression, WML volume and total Fazekas score) and Beta (logistic regression, lacunes) with 95% confidence intervals; prior to analysis, the natural logarithm of parameters was calculated where appropriate in order to ensure normal distribution. Values are corrected for age, gender and hippocampal volume; the latter was determined using Adaboost, the mean value of the left and right hippocampus was normalized using the scaling factor provided by this software to account for head size differences.

In the PD and AD groups, 2.3% and 3.6% of the subjects had lacunes and the association between CSF Aβ species and lacunes was not analyzed. Data on WML volume were not available for the AD group, where imaging mainly was performed using CT.

*p < 0.05, **p < 0.0125, ***p > 0.001.

Only p−values < 0.0125 should be considered significant according to Bonferroni−adjustment.

Next, the subjects where 18F-flutemetamol PET was performed, namely the CHE, SCD and MCI cases, were pooled to perform subgroup analyses. Lower CSF levels of Aβ38 and Aβ40 were significantly and consistently associated with increased WML volume in all participants (Table 3). The relationship between WML volume and CSF levels of Aβ42 was stronger in APOE ε4 negative than APOE ε4 positive participants (Table 3). Lower levels of CSF Aβ42 were also associated with increased WML volume, but at a lower magnitude than Aβ38 and Aβ40 (Table 3).

Table 3. Associations between SVD, estimated as the volume of white matter lesions (WML), the total score of WML according to Fazekas, and lacunes, and amyloid isoforms in CSF and amyloid PET, in the pooled CHE, SCD and MCI subgroups.

Group Parameter WML volume ± 95% CI Fazekas ± 95% CI Lacunes ± 95% CI
All CHE, SCD CSF Aβ38 −0.219*** −0.288 −0.15 −0.150*** −0.227 −0.073 −0.841 −1.966 0.284
and MCI CSF Aβ40 −0.205*** −0.274 −0.136 −0.128*** −0.205 −0.051 −0.418 −1.253 0.417
  CSF Aβ42 −0.086* −0.158 −0.014 −0.055 −0.135 0.025 0.298 −0.513 1.109
  Composite SUVR 0.074 −0.031 0.179 0.071 −0.044 0.186 −0.12 −1.723 1.483
                     
APOE ε4 − CSF Aβ38 −0.282*** −0.394 −0.17 −0.203** −0.328 −0.078 −2.354** −4.104 −0.604
positive CSF Aβ40 −0.266*** −0.381 −0.071 −0.154* −0.277 −0.031 −1.544* −2.879 −0.209
CHE, SCD CSF Aβ42 −0.127* −0.247 −0.007 −0.09 −0.221 0.041 0.971 −0.278 2.22
and MCI Composite SUVR 0.153 −0.031 0.337 0.103 −0.105 0.311 −1.128 −3.842 1.598
                     
APOE ε4 − CSF Aβ38 −0.187*** −0.276 −0.098 −0.125* −0.224 −0.026 0.229 −1.292 1.75
negative CSF Aβ40 −0.174*** −0.263 −0.085 −0.117* −0.216 −0.018 0.314 −0.776 1.404
CHE, SCD CSF Aβ42 −0.128** −0.22 −0.036 −0.086 −0.188 0.016 0.054 −1.275 1.383
and MCI Composite SUVR 0.08 −0.052 0.213 0.06 −0.084 0.204 0.432 −1.969 2.833
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Values represent standardized beta (linear regression, WML volume and total Fazekas score) and Beta (logistic regression, lacunes) with 95% confidence intervals; prior to analysis, the natural logarithm of parameters was calculated where appropriate in order to ensure normal distribution. Values are corrected for age, gender and hippocampal volume; the latter was determined using Adaboost, the mean value of the left and right hippocampus was normalized using the scaling factor provided by this software to account for head size differences.

*p < 0.05, **p < 0.0125, ***p > 0.001.

Only p-values < 0.0125 should be considered significant according to Bonferroni-adjustment.

Associations between total WML and amyloid PET

We also used amyloid PET imaging with the 18F-flutemetamol ligand to study the cortical levels of Aβ fibrils in CHE, SCD and MCI. The 18F-flutemetamol composite score was not significantly associated with WML volume or Fazekas score in any of the studied groups (Table 3).

Associations between regional distribution of WML and CSF Aβ species or amyloid PET

The potential regional impact of SVD was assessed from WML in various brain regions using the ARWMC scale. Lower levels of CSF Aβ38 and Aβ40 were significantly associated with increased WML in the frontal, parieto-occipital and temporal lobes, but not in infratentorial regions (Table 4). Lower levels of CSF Aβ42 and higher levels of the composite 18F-flutemetamol uptake were significantly associated with WML in the temporal lobe only (Table 4). Since regional ARWMC scores correlated significantly with the total ARWMC, analysis was redone with the total ARWMC included as a predictor. Again, only the association between CSF Aβ42 and temporal ARWMC was significant.

Table 4. Associations between regional cerebrovascular disease, Aβ isoforms and amyloid PET, pooled data from the CHE, SCD and MCI groups.

Group Parameter ARWMC total ARWMC frontal ARWMC parieto- occipital ARWMC temporal ARWMC infratententorial
CHE, SCD, MCI CSF Aβ38 −0.142*** −0.130*** −0.142*** −0.155*** −0.013
  CSF Aβ40 −0.121** −0.111** −0.122** −0.137** 0.019
  CSF Aβ42 −0.040 −0.026 −0.073 −0.088* 0.031
  Composite SUVR 0.094 0.088 0.084 0.136* 0.015
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SVD was estimated as the total and regional white matter lesion score according to the ARWMC scale. Values represent standardized beta (linear regression, ARWMC score) with 95% confidence intervals; prior to analysis, the natural logarithm of the CSF and PET parameters was calculated to ensure normal distribution. Values are corrected for age, sex and hippocampal volume; the latter was determined using Adaboost, the mean value of the left and right hippocampus was normalized using the scaling factor provided by this software to account for head size differences. *p < 0.05, **p < 0.0125, ***p > 0.001.

Only p-values < 0.0125 should be considered significant according to Bonferroni-adjustment.

When examining the relationship between regional WML and regional 18F-flutemetamol uptake, increased 18F-flutemetamol uptake in frontal, parietal, temporal, occipital regions were all associated with a higher temporal ARWMC score (Table 5).

Table 5. Associations between regional cerebrovascular disease and regional amyloid uptake measured as PET SUVR for CHE, SCD and MCI subjects.

Group Parameter ARWMC frontal ARWMC parito-occipital ARWMC temporal
CHE, SCD, MCI Frontal SUVR 0.088 −0.027 0.203 0.079 −0.036 0.194 0.140* 0.022 0.259
  Parietal SUVR 0.119 0.004 0.233 0.117 0.002 0.231 0.168** 0.050 0.285
  Occipital SUVR 0.097 −0.018 0.213 0.092 −0.023 0.207 0.148* 0.029 0.266
  Temporal SUVR 0.061 −0.053 0.175 0.055 −0.059 0.168 0.104 −0.014 0.221
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Values represent standardized beta from linear regression with regional ARWMC as dependent and regional amyloid uptake as independent variable as well as the confidence intervals, and are corrected for age, sex and hippocampal volume. Cerebrovascular disease was estimated as the total score of white matter lesion rating according to the ARWMC scale, total sum, and regional, mean of left and right. PET SUVR was estimated the regional uptake, mean of left and right; the natural logarithm of PET estimates was used.

*p < 0.05, **p < 0.0125, ***p > 0.001.

Only p-values < 0.0125 should be considered significant according to Bonferroni-adjustment.

Lack of association between lacunes and CSF Aβ species or amyloid PET

Neither CSF Aβ42 nor the composite 18F-flutemetamol uptake were associated with the presence of lacunes in any group (Table 3, results from CHE, SCD, MCI groups).

Discussion

Our main findings are firstly that more pronounced WML is strongly and consistently associated with lower levels of CSF Aβ38 and Aβ40, while the association with CSF Aβ42 levels is weak or absent. This pattern was found in all diagnostic groups, except for the AD group where WML were associated with all three Aβ isoforms. Secondly, the composite 18F-flutemetamol SUVR, that reflects cortical fibrillar Aβ deposition and strongly correlated with CSF Aβ42, was not associated with WML in any of the CHE, SCD and MCI groups (PET data unavailable for the PD and AD groups).

Two hypotheses might explain this consistent, negative relationship between WML and Aβ38 and Aβ40. Firstly, reduced clearance of Aβ38 and Aβ40 from the brain parenchyma may enhance deposition of these Aβ species in the cerebral vessel walls, as has been reported for Aβ4011,22. Evidence favors the hypothesis that amyloid fibrils deposited in the vessel wall and senile plaques differ from each other, as the major species in CAA is Aβ39 or Aβ40, and in senile plaque Aβ42, although Aβ40 may also be present23,24. Similarly, Aβ38 seems to be predominantly located within the vasculature in postmortem brains of sporadic and familial AD patients11,25. Impaired vascular clearance of Aβ across the BBB and increased Aβ brain capillary deposition has been reported in transgenic mice producing low levels of the poorly cleared Dutch/Iowa mutant forms of Aβ, which are vasculotropic and rich in β-sheets26. β-amyloid deposition, that is directly toxic to smooth muscle cells, leads to constriction of cerebral blood vessels, and thus to perturbation of cerebral perfusion, loss of homeostasis of the neuronal environment, ultimately leading to ischemia and consequently WML27,28. Also the previously reported positive association between the Aβ40 level in plasma and WMH in subjects with MCI, AD and CAA, suggests that circulating Aβ40 is a potential contributor to microvascular dysfunction29. Reduced clearance may play also a role in CAA that is associated with vascular deposition of Aβ40 and Aβ42 with Aβ40 as the major isoform. Decreased levels of CSF Aβ40 as well as Aβ42 have been reported in CAA patients, suggesting that Aβ40 and Aβ42 may be trapped in the cerebral vasculature and escape the drainage pathways that otherwise transport amyloid β proteins toward the cerebrospinal fluid30. It has been hypothesized that SVD may exacerbate CAA by promoting cerebral edema that needs to compete with Aβ for clearance via perivascular drainage pathways31. A larger prevalence of WML in CAA compared to AD and MCI has been reported with WMH correlating with plasma levels of Aβ4029.

Secondly, SVD, and especially WML, may be associated with reduced production of Aβ in the brain. An inverse relationship between the volume of WML and CSF APP metabolites (including Aβ38, Aβ40 and Aβ42) in both stroke patients and SCD/MCI patients has been reported32. In that study, lower levels of CSF APP metabolites in the stroke group compared to the SCD/MCI-group suggested that ischemia influences APP metabolism, probably through inhibition of fast axonal transport of APP. This is consistent with evidence from a combined animal and neuropathological study that acute ischemic lesions can trigger accelerated amyloid deposition, most likely through interference with amyloid clearance pathways33. White matter pathology underlying WML has been suggested to affect neuronal activity by a body of clinical work reporting a direct relationship between white matter integrity and cognitive performance34. In addition, a negative correlation has been reported between WML volume and connectivity strength in regions with decreased connectivity in MCI patients as compared to controls35. Notably, the production of Aβ and its secretion into the extracellular space are tightly regulated by neuronal activity in vitro and in vivo; increased neuronal activity enhances Aβ production, and blocking neuronal activity has the opposite effect36.

An inverse association between WML and AD specific CSF Aβ42 has recently been reported in subjects with MCI21. Even though we reproduced this association in the pooled CHE, SCD and MCI data (Table 3), our results showed that the association with WML was much stronger for Aβ38 and Aβ40, that were not investigated in the study by Kester et al.21 We confirm this by the lack of association between WML and 18F-flutemetamol PET imaging, that reflects fibrillar Aβ deposition. We found that only in cases with AD dementia, Aβ42 pathology might be associated with WML, especially in the temporal lobes. Previous smaller scale studies in subjects with cognitive status ranging from normal to mild dementia have reported a similar lack of association between WML and amyloid PET37,38,39,40. Thus, non-AD-specific subcortical changes may affect global levels of Aβ isoforms in the central nervous system32. It should be noted that amyloid ligands such as 18F-flutemetamol were developed to bind to aggregated Aβ. For example, the Pittsburgh compound B (PiB) ligand may bind to vascular amyloid41,42 Higher PIB uptake has been consistently reported in non-demented CAA patients, at a level intermediate between healthy controls and AD43,44.

Parenchymal deposition of Aβ protein and lower CSF levels of Aβ42 are associated with increased risk for AD development. In addition, vascular deposition of Aβ may also be a primary driver of AD and affect the production and clearance of APP. Thus increased WML burden among patients with AD might reflect accumulation of vascular Aβ to some degree. Interestingly, we found a significant association between WML and CSF Aβ42 in the AD dementia group, indicating that Aβ42-related plaque pathology might be associated with SVD in individuals with dementia due to AD.

Amyloid PET-uptake and WML volume have been shown to independently predict AD diagnosis and thus WML may be involved in the clinical manifestation of AD38. WML are more prevalent and severe in AD patients compared with nondemented adults matched for demographic characteristics and brain regions where WML are most severe in AD, reportedly occur in the same location as AD pathology and areas showing the greatest metabolic dysfunction in AD45. It cannot be ruled out that some of the subjects with clinically diagnosed AD may actually suffer from mixed dementia, with both AD and vascular (i.e. WML) contributions46. While this may affect the associations with amyloid species presently found in this group, the total Fazekas and ARWMC scores in the AD group were comparable to those in the CHE, SCD and PD groups and lower than in the MCI group.

Our main finding that the much stronger association between WML and CSF Aβ38 and Aβ40, than CSF Aβ42 was confirmed in the PD group. This strengthens previous evidence suggesting that also PD should be targeted by treatment for vascular risk factors since comorbid WML are common in PD and affect motor function and cognition47,48 We did not assess the impact of the interplay between amyloid and SVD on cognition. According to a recent study in non-demented elderly amyloid and vascular pathologies seemed to be at least partly independent processes that both affect longitudinal cognitive trajectories adversely and are major drivers of cognitive decline in the elderly49. This further stresses the need for treatment of risk factors for SVD in neurodegenerative disease.

We acknowledge limitations in the present study. Firstly, some data are lacking, as for example 18F-flutemetamol PET for the PD and AD cases and quantitative WML analysis for AD cases; in the CHE, SCD and MCI groups, 18F-flutemetamol PET was available for 321 subjects (Table 1). Also, there is some heterogeneity in the imaging data since mainly CT images were available for the AD group. Data on cerebral microbleeds as marker of cerebral amyloid angiopathy are not included, since susceptibility weighted images (SWI) to assess their presence were available for the PD group. Secondly, the use of linear regression for ordinal scales as the Fazekas and ARWMC scales, may be questioned since the number of categories is limited, and the underlying model assumptions (linear change with each unit change in category) may not be valid. Data from these scales were included since the WML volume could not be determined in the AD group; in addition, these scales have been used in other studies, for example the study by Kester et al.14 Instead, the WML volume provides a continuous variable and the lack of significant association between the Fazekas score and CSF Aβ species in the CHE and PD groups, where WML were less abundant, should be explained by the inherent differences in these two variables. Thirdly, lacunes, also markers of SVD, showed a significant association with CSF Aβ38 and CSF Aβ40 only in the MCI group. Lacunes and WML differ regarding their pathogenesis, with lacunes being due to sudden, total occlusion of an end artery, whereas white matter lesions are associated with longstanding, less severe general hypoperfusion of brain tissue. The consequences of lacunes and WML with regard to amyloid production and clearance are also likely to differ, with the former resulting in severe, but focal damage to the brain parenchyma in a smaller area, and the latter in less severe, but more widespread damage. In addition, the low prevalence of lacunes in the CHE and SCD groups may have reduced statistical power.

In conclusion, our findings suggest that WML are associated with lower CSF Aβ38 and Aβ40 levels, probably reflecting lower overall Aβ production due to either decreased expression or secretase processing of APP. This is confirmed by the lack of association between WML and 18F-flutemetamol PET, that reflects fibrillar Aβ deposition. However, in cases with AD dementia Aβ42 pathology might be associated with WML, especially in the temporal lobes.

Methods

Ethical approval and patient consent

The study protocol was designed in accordance with guidelines outlined in the Declaration of Helsinki and approved by the Research Ethics Committee at Lund University, Lund, Sweden. Written informed consent was obtained from all participants.

Study population

The first sample, including cognitively healthy elderly (CHE) subjects and subjects with mild cognitive symptoms (MCS), i.e. patients with either subjective cognitive decline (SCD) or objective impairment (MCI), was part of the prospective and longitudinal Swedish BioFINDER (Biomarkers For Identifying Neurodegenerative Disorders Early and Reliably) study (http://www.biofinder.se). The 267 CHE participants, recruited from the population-based Malmö Diet Cancer study50, were eligible for inclusion in the cognitively healthy elderly cohort of the Swedish BioFinder study if they 1) were aged ≥60 years old, 2) scored 28–30 points on Mini-Mental State Examination (MMSE), 3) did not suffer from any subjective cognitive impairment and 4) were fluent in Swedish51. Exclusion criteria included presence of significant neurologic disease, severe psychiatric disease, dementia or MCI. The 360 MCS cases complaints consisted of patients enrolled consecutively at three memory outpatient clinics in Sweden. They were thoroughly assessed by physicians with special interest in dementia disorders. The inclusion criteria were: 1) referred to the memory clinics because of cognitive impairment; 2) not fulfilling the criteria for dementia; 3) a MMSE score of 24–30 points; 4) age 60–80 years and; 5) fluent in Swedish. Exclusion criteria were: 1) cognitive impairment that without doubt could be explained by a condition other than prodromal dementia; 2) severe somatic disease, and; 3) refusing lumbar puncture or neuropsychological investigation. MCS patients were assessed based on a neuropsychological battery assessing four broad cognitive domains including verbal ability, visuospatial construction, episodic memory, and executive functions. A senior neuropsychologist then stratified all patients into those with SCD (no measurable cognitive deficits) or MCI according to the consensus criteria for MCI suggested by Petersen52. In total 165 patients (46%) were classified as SCD and 195 (54%) patients as MCI.

The second sample here referred to as the ‘AD cohort’, comprised 110 subjects with AD. Subjects were recruited from a retrospective study performed between 2008 and 2014. All patients met the dementia criteria and were diagnosed as probable AD according to NINCDS-ADRDA53 and to have CSF Aβ42 below 550 ng/L to confirm the presence of amyloid pathology.

The third sample, comprising 89 PD cases without dementia, here referred to as the “PD cohort”, is also part of the prospective Swedish BioFINDER study. PD diagnosis was set according to the NINDS Diagnostic Criteria54.

Demographic characteristics of the participants are presented in Table 1. More information is given in the Supplementary information online and at www.biofinder.se.

Image acquisition and assessment of cerebrovascular disease

In CHE, SCD, MCI and PD subjects, MR imaging was performed at 3 T systems and included trasnversal T2 FLAIR and high resolution isotropic MPRAGE. In AD subjects, imaging data included axial CT images in 96 cases and axial FLAIR images acquired at 1.5 T MR systems in 14 cases.

WML and lacunes assessed from MRI, and WML from CT were used as markers of SVD. For MR data in the CHE, SCD, MCI and PD subjects, automated segmentation of WML using the LST toolbox implemented in SPM8, generated a total lesion volume [mL], here named ‘WML volume’, for each individual55. Visual rating of WML on FLAIR images according to the Fazekas scale56, resulted in a total Fazekas score, and according to the ARWMC scale57, resulting in regional as well as total scores. CT images in the AD cohort were assessed for WML according to the Fazekas scale. Scores from the left and right hemispheres were summarized for statistical analysis. The presence of lacunes was assessed on FLAIR and MPRAGE images according to Wardlaw58. This variable was dichotomized as lacunes, present or absent. More information is given in the Supplementary Methods online.

CSF collection and analysis

The collection procedure and analysis of CSF followed the Alzheimer’s Association Flow Chart for CSF biomarkers59. Lumbar CSF samples were collected and stored in polypropylene tubes at −80 °C and analyzed in one batch. CSF levels of Aβ38 and Aβ40 were measured using EUROIMMUN ELISAs (EUROIMMUN AG, Lübeck, Germany), and CSF Aβ42 and CSF P-tau were measured using INNOTEST ELISAs (Fujirebio Europe, Gent, Belgium).

18F-Flutemetamol PET imaging and analysis

In 122 CHE, 101 SCD and 98 MCI subjects, the cerebral Aβ burden was measured using [18F]-flutemetamol PET. Subjects received a single dose of [18F]flutemetamol and its average uptake was estimated from sum images acquired 90–110 min post injection60. Image processing was performed as previously described61. The standardized uptake value ratio (SUVR) was determined as the regional and composite tracer uptake normalized for the mean uptake in the cerebellar cortex, which is free of fibrillar plaques. More information is given in the Supplementary Methods online.

Statistics

Statistics were computed using SPSS version 22 (IBM). Non-normally distributed variables were transformed into normality using log transformation. Group-wise comparisons of baseline characteristics were performed using the Pearson Chi-square test for categorical variables and ANOVA for continuous variables. Since WML rating in the AD group mainly was performed on CT images, WML scores were not compared between the AD group and the other groups.

Regression analyses were performed to test the associations between estimates of SVD and amyloid deposition, with WML volume, Fazekas and ARWMC scores and lacunes as dependent variables and CSF-biomarkers and PET composite scores as independent variables. Regressions were conducted separately for each independent variable. Linear regression was used for continuous (WML volume, Fazekas and ARWMC scores) and logistic regression for binary variables (lacunes). All regression analyses were adjusted for age, sex, and hippocampal volume. Hippocampal volume was included as a co-variate in the regression analyses to adjust for AD disease stage as suggested by Kester et al.21 The values in Table 2, 3, 4 and 5 represent standardized betas from linear regression in each group as specified in the first column. Since four markers of amyloid deposition were studied, only p-values < 0.0125 should be considered significant according to Bonferroni-adjustment. Comparison of the demographic data in Table 1 involved comparison of each diagnostic group to each of the other groups; application of Bonferroni correction would result in a significance level of p-values < 0.005 as indicated.

Additional Information

How to cite this article: van Westen, D. et al. Cerebral white matter lesions – associations with Aβ isoforms and amyloid PET. Sci. Rep. 6, 20709; doi: 10.1038/srep20709 (2016).

Supplementary Material

Supplementary Information
srep20709-s1.pdf (206.1KB, pdf)

Acknowledgments

The authors thank all collaborators in the BioFINDER Study group (www.biofinder.se). This work was supported by the European Research Council, the Swedish Research Council, the Strategic Research Area MultiPark (Multidisciplinary Research in Parkinson’s disease) at Lund University, the Crafoord Foundation, the Swedish Brain Foundation, the Skåne University Hospital Foundation, the Swedish Alzheimer Association, Stiftelsen för Gamla Tjänarinnor, the Knut and Alice Wallenberg Foundation and the Swedish federal government under the ALF agreement. Doses of 18F-flutemetamol injection were sponsored by GE Healthcare. The funding sources had no role in the design and conduct of the study; in the collection, analysis, interpretation of the data; nor in the preparation, review, or approval of the manuscript. The Torsten Söderberg Foundation at the Royal Swedish Academy of Sciences, Stockholm, Sweden.

Footnotes

Doses of 18F-flutemetamol injection were sponsored by GE Healthcare. Dr Blennow has served at advisory boards for Koyowa Kirin Pharma, Eli Lilly, Pfizer, and Roche. Dr Hansson has served at advisory boards for GE Healthcare. Drs van Westen, Lindqvist, Minthon, Nägga, Stomrud and Zetterberg report no disclosures.

Author Contributions D.V.W. co-designed the study, collected, analyzed and interpreted the data, conducted literature searches, prepared figures, cowrote the manuscript. D.L. co-designed the study, analyzed and interpreted the data, conducted literature searches, cowrote the manuscript. K.B., L.M., K.N., E.S. and H.Z. collected and analyzed the data and reviewed the manuscript for intellectual content. O.H. was the principal designer and coordinator of the study, overviewed collection, analysis and interpretation of the study data, cowrote the manuscript and obtained funding.

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Supplementary Materials

Supplementary Information
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