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Int J Alzheimers Dis. 2010; 2010: 959257.
Published online Aug 18, 2010. doi:  10.4061/2010/959257
PMCID: PMC2933894

CSF Biomarkers Profile in CADASIL—A Model of Pure Vascular Dementia: Usefulness in Differential Diagnosis in the Dementia Disorder

Abstract

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is considered a model of pure vascular dementia (VD) because it occurs in young adults unlikely to have concomitant age and Alzheimer's Disease-(AD-) related pathology. CSF levels of β-amyloid 1-42 (Aβ42), total tau protein (t-tau), and phosphorylated tau-protein (p-tau), well accepted biomarkers of AD, were evaluated in 10 CADASIL patients, 22 AD patients, and 17 healthy age-matched subjects. Innotest β-amyloid 1-42, Innotest hTAU-Ag, and Innotest Phospho-tau 181p sandwich enzyme-linked immunoassay were used to determine CSF biomarkers levels. A case-control statistical analysis was carried out. CSF Aβ42 levels were significantly lower in CADASIL patients and considerable overlap with AD whereas t-tau and p-tau levels were normal and significantly different with respect to AD. A significant altered CSF biomarkers profile in a pure VD supports the use of CSF Aβ42, t-tau, and p-tau levels in the differential diagnosis of VD and AD.

1. Introduction

Despite the increased use of widely accepted diagnostic criteria over the last 1-2 decades, the differential diagnosis between Alzheimer disease (AD) and vascular dementia (VD), the most common causes of dementia in the elderly, is not always easy in the clinical practice. Many cognitively impaired patients, with a progressive history of classical cortical dementia, show different degrees of concomitant vascular lesions [1]. Vascular comorbidity may be present in 30%–60% of AD patients [2], and, conversely, AD pathology may be present in 40%–80% of VD patients [3], thus hindering diagnosis accuracy. Further, because the prevalence of both AD and VD increases with age, the coexistence of AD and VD in the elderly patients would also be expected to occur.

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is an inherited microvascular disease associated with a wide range of symptoms including migraine, mood disorders, and recurrent subcortical TIA/strokes [4, 5]. Two thirds of CADASIL patients early develop subcortical dementia, usually in the fourth-fifth decades of life [6]. Due to its monogenic nature and occurrence in young adults, CADASIL is considered a useful model of VD, in whom age- and AD-related pathology unlikely to coexist [7].

Beta-amyloid1-42 (Aβ42), total tau (t-tau), and phospho-tau (p-tau) proteins, indices of amyloid deposition, axonal damage, or tangle formation respectively, have been suggested as biomarkers for the diagnosis in dementia disorders [8]. The CSF profile of these proteins in patients with AD is characterized by decreased Aβ42 and increased t-tau and p-tau levels [9, 10]. On the contrary in VD, studies on these CSF biomarkers showed conflicting results: t-tau levels have been reported to be increased [1113], normal [14, 15] or intermediate [16, 17], but in any case much lower than in AD; Aβ42 CSF levels in VD have been reported to be moderately decreased [18] or significantly overlapping with AD [19]. Few works deal with p-tau reporting either normal [20] or increased CSF levels [21] in VD.

Since previous studies showed contradictory results in VD, we evaluated CSF biomarkers in CADASIL, a young-onset monogenic disease which offers a unique opportunity to define CSF biomarkers profile in a pure VD. For this purpose we assessed CSF Aβ42, t-tau, and p-tau levels in ten CADASIL patients, comparing the results with those obtained for twenty-two AD patients and seventeen control subjects.

2. Patients and Methods

After obtaining informed consent, we measured CSF Aβ42, t-tau, and p-tau levels in CADASIL patients, AD patients, and control subjects.

CADASIL group included ten genetically confirmed patients (age range 49–66 years), followed in our department and already described in previous works by our group [22, 23]. Patients have been enrolled in a study on CSF biomarkers for the early diagnosis of dementia approved by local ethical committee. Detailed demographic data and molecular features of CADASIL patients are reported in Table 1.

Table 1
Clinical and molecular features of CADASIL patients.

The AD group consists of twenty-two patients with probable AD (age range 58–74 years) diagnosed in our department according to the NIN-CDS-ADRDA criteria [24]. AD patients with more than one cardiovascular risk factor and patient with even 1-2 white matter lacunes were excluded. None of the AD patients was under treatment for dementia at the time of lumbar puncture.

The control group included seventeen age-matched subjects with polyneuropathy and without signs of cognitive decline or central nervous system lesions.

Overall cognitive performance was evaluated in all three groups by Mini-Mental-State Examination (MMSE). MMSE scores below 26 indicate the presence of cognitive impairment.

CSF was obtained by standard procedures, collected in polypropylene tubes and immediately centrifuged. All blood contamination-free samples were stored at −80°C until assay, CSF levels of Aβ42, t-tau, and p-tau were determined by sensitive sandwich enzyme-linked immunoassay ELISA: Innotest β-amyloid 1-42, Innotest hTAU-Ag, and Innotest Phospho-tau 181p (specific for tau proteins phosphorylated at threonine 181) (Innogenetics, Ghent, Belgium). All determinations were done in duplicate.

3. Statistical Analysis

The nonparametric test of Kruskal-Wallis was used instead of the Analysis of Variance (ANOVA) because Levene's test rejected the hypothesis of equality of sample variances. Pairwise group comparisons were then made using the nonparametric test of Mann-Whitney with Bonferroni correction of type-I error probability.

A statistical significance level of 95% (type-I error probability, P, less than .05) was considered for all tests.

Statistical analysis was executed with the statistical package SPSS 10.

4. Results

Descriptive statistics of clinical features and CSF levels of Aβ42, t-tau, and p-tau, including median and interquartile distance (25th to 75th percentile), for CADASIL, Alzheimer patients, and controls are reported at the bottom of Table 1. Figures 1(a)1(c) supply a box plot representation of CSF grouped data.

Figure 1
Box plots of CADASIL and Alzheimer patients and control subjects. They include median (horizontal line within box), interquartile interval, that is, 25th to 75th percentile (grey box) and range of variation (whiskers): (a) t-tau data, (b) p-tau data, ...

Aβ42. CSF Aβ42 levels were significantly lower both in CADASIL and in Alzheimer patients than in controls (Kruskal-Wallis and Bonferroni-corrected Mann-Whitney tests, P < .05). However CSF Aβ42 levels in CADASIL did not significantly differ from those in Alzheimer (Bonferroni-corrected Mann-Whitney test, P > .05). Group differences are illustrated in Figure 1(a): grey boxes, which represent group interquartile intervals (25th to 75th percentiles), overlap only for CADASIL and Alzheimer data.

t-tau and p-tau. Statistically significant higher values were found in Alzheimer with respect to both control and CADASIL subjects (Kruskal-Wallis and Bonferroni-corrected Mann-Whitney tests, P < .05), while these last two groups are not result statistically different (Bonferroni-corrected Mann-Whitney test, P > .05). Figures 1(b) and 1(c) show clear differences.

5. Discussion

Many studies evaluated changes in CSF Aβ42 and tau protein in prodromal stages of AD or in other types of dementia. Tau is an axonal protein that binds to tubulin in microtubules, promoting their assembly and stability [25]. Elevated CSF levels of t-tau and p-tau have been interpreted as indicators of ongoing neuronal and axonal degeneration and/or the presence of neurofibrillary tangles in the brain [26]. β-amyloid (Aβ) peptides are a major component of amyloid plaques deposited in the brain of patients with different neurodegenerative diseases. Decreased CSF Aβ42 levels have been ascribed to accumulation in senile plaques [27]. However alternative mechanisms, such as formation of a CSF chaperon complex with high-affinity binding and epitope masking of Aβ42, have also been reported [28].

Low CSF Aβ42, high t-tau, and p-tau levels are the typical pattern in AD, whereas in VD, until now, results on CSF biomarkers are conflicting [17, 18].

Ethnic and methodological differences may account for this discrepancy, as high assay variability is present amongst laboratories using the same ELISA test [29]. However VD is a heterogeneous entity and different authors may study different subpopulations of patients, and it is difficult to assess the specificity of CSF biomarkers profile. Furthermore, as many patients with VD also show cholinergic lesions of aging and AD, possible overlaps of vascular pathology and AD cannot be ruled out [3032].

In a previous study we reported significantly lower CSF Aβ42 levels in CADASIL patients than in controls whereas CSF t-tau and p-tau did not differ between the two groups [33].

In the present study the CSF biomarkers levels of the same CADASIL patients have been compared with those of AD patients showing an altered profile in CADASIL patients: Aβ42 levels were markedly decreased and considerably overlapped with AD, whereas t-tau and p-tau levels were normal and significantly different with respect to AD.

Recent studies on CSF biomarkers profile in sporadic VD showed a clear decrease of Aβ42 levels [19]. The mechanism of decreased CSF Aβ42 levels in cerebrovascular disease is unclear however the presence of these features in sporadic VD and in patients with a young-onset vascular disorder like CADASIL suggests that altered CSF Aβ42 levels may be related to subcortical vascular lesions and independent from an age- and AD-related pathology. Recently, a link between white matter lesions and low CSF Aβ42 has also been reported [34]. Moreover, the significant overlap of CSF Aβ42 levels in a pure VD and AD suggests to rule out any possible correlation between decreased CSF Aβ42 levels and accumulation in senile plaques and strengthens the most recent hypotheses about alternative mechanisms of Aβ42 reduction [28].

Normal t-tau and p-tau CSF levels we found in CADASIL contrast with the majority of the results of other groups on t-tau and p-tau values in sporadic VD. However, in the latter group of patients the possible presence of additional neuropathological changes associated with age and AD cannot be ruled out. Since CADASIL represents a model of pure VD, we can argue that t-tau and p-tau CSF levels in CADASIL patients closely reflect a pathological condition almost exclusively due to cerebrovascular features. We can thus suggest that CSF neurochemical phenotypes, especially t-tau and p-tau levels, sufficiently discriminate between AD and VD.

In conclusion, although our little sample size can reduce the statistical power of our results, significant differences in CSF biomarkers profile between pure VD, AD, and controls were found. These data support the use of CSF Aβ42, t-tau, and p-tau levels in the differential diagnosis of VD and AD.

In any case, this study represents a preliminary investigation whose statistical results should be confirmed by further examinations on larger data samples.

Acknowledgments

The research is partly financed by a grant from Regione Toscana and Ministero della Salute to A. Federico and from Fondazione Monte dei Paschi di Siena to M. T. Dotti.

References

1. Jellinger KA. Diagnostic accuracy of Alzheimer’s disease: a clinicopathological study. Acta Neuropathologica. 1996;91(2):219–220. [PubMed]
2. Jellinger KA. The enigma of vascular cognitive disorder and vascular dementia. Acta Neuropathologica. 2007;113(4):349–388. [PubMed]
3. Kalaria RN, Ballard C. Overlap between pathology of Alzheimer disease and vascular dementia. Alzheimer Disease and Associated Disorders. 1999;13(3):S115–S123. [PubMed]
4. Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genetics. 1993;3(3):256–259. [PubMed]
5. Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser M-G. CADASIL. The Lancet Neurology. 2009;8(7):643–653. [PubMed]
6. Chabriat H, Tournier-Lasserve E, Vahedi K, et al. Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Neurology. 1995;45(6):1086–1091. [PubMed]
7. Charlton RA, Morris RG, Nitkunan A, Markus HS. The cognitive profiles of CADASIL and sporadic small vessel disease. Neurology. 2006;66(10):1523–1526. [PubMed]
8. Waldemar G, Dubois B, Emre M, et al. Recommendations for the diagnosis and management of Alzheimer’s disease and other disorders associated with dementia: EFNS guideline. European Journal of Neurology. 2007;14(1):e1–e26. [PubMed]
9. Blennow K. Cerebrospinal fluid protein biomarkers for Alzheimer’s disease. NeuroRx. 2004;1(2):213–225. [PMC free article] [PubMed]
10. Formichi P, Battisti C, Radi E, Federico A. Cerebrospinal fluid tau, Aβ, and phosphorylated tau protein for the diagnosis of Alzheimer’s disease. Journal of Cellular Physiology. 2006;208(1):39–46. [PubMed]
11. Skoog I, Vanmechelen E, Andreasson LA, et al. A population-based study of tau protein and ubiquitin in cerebrospinal fluid in 85-year-olds: relation to severity of dementia and cerebral atrophy, but not to the apolipoprotein E4 allele. Neurodegeneration. 1995;4(4):433–442. [PubMed]
12. Andreasen N, Vanmechelen E, Van De Voorde A, et al. Cerebrospinal fluid tau protein as a biochemical marker for Alzheimer’s disease: a community based follow up study. Journal of Neurology Neurosurgery and Psychiatry. 1998;64(3):298–305. [PMC free article] [PubMed]
13. Jia JP, Meng R, Sun YX, Sun WJ, Ji XM, Jia LF. Cerebrospinal fluid tau, Aβ1-42 and inflammatory cytokines in patients with Alzheimer’s disease and vascular dementia. Neuroscience Letters. 2005;383(1-2):12–16. [PubMed]
14. Arai H, Satoh-Nakagawa T, Higuchi M, et al. No increase in cerebrospinal fluid tau protein levels in patients with vascular dementia. Neuroscience Letters. 1998;256(3):174–176. [PubMed]
15. Paraskevas GP, Kapaki E, Liappas I, et al. The diagnostic value of cerebrospinal fluid tau protein in dementing and nondementing neuropsychiatric disorders. Journal of Geriatric Psychiatry and Neurology. 2005;18(3):163–173. [PubMed]
16. Leszek J, Małyszczak K, Janicka B, Kiejna A, Wiak A. Total tau in cerebrospinal fluid differentiates Alzheimer’s disease from vascular dementia. Medical Science Monitor. 2003;9(11):CR484–CR488. [PubMed]
17. Paraskevas GP, Kapaki E, Papageorgiou SG, et al. CSF biomarker profile and diagnostic value in vascular dementia. European Journal of Neurology. 2009;16(2):205–211. [PubMed]
18. Stefani A, Bernardini S, Panella M, et al. AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis. Journal of the Neurological Sciences. 2005;237(1-2):83–88. [PubMed]
19. Nägga K, Gottfries J, Blennow K, Marcusson J. Cerebrospinal fluid phospho-tau, total tau and β-amyloid1-42 in the differentiation between Alzheimer’s disease and vascular dementia. Dementia and Geriatric Cognitive Disorders. 2002;14(3-4):183–190. [PubMed]
20. Schönknecht P, Pantel J, Hunt A, et al. Levels of total tau and tau protein phosphorylated at threonine 181 in patients with incipient and manifest Alzheimer’s disease. Neuroscience Letters. 2003;339(2):172–174. [PubMed]
21. Ravaglia S, Bini P, Sinforiani E, et al. Cerebrospinal fluid levels of tau phosphorylated at threonine 181 in patients with Alzheimer’s disease and vascular dementia. Neurological Sciences. 2008;29(6):417–423. [PubMed]
22. Dotti MT, Federico A, Mazzei R, et al. The spectrum of Notch3 mutations in 28 Italian CADASIL families. Journal of Neurology, Neurosurgery and Psychiatry. 2005;76(5):736–738. [PMC free article] [PubMed]
23. Stromillo ML, Dotti MT, Battaglini M, et al. Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Journal of Neurology, Neurosurgery and Psychiatry. 2009;80(1):41–47. [PubMed]
24. McKhann G, Drachman D, Folstein M, et al. Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s disease. Neurology. 1984;34(7):939–944. [PubMed]
25. Goedert M. Tau protein and the neurofibrillary pathology of Alzheimer’s disease. Trends in Neurosciences. 1993;16(11):460–465. [PubMed]
26. Hansson O, Zetterberg H, Buchhave P, Londos E, Blennow K, Minthon L. Association between CSF biomarkers and incipient Alzheimer’s disease in patients with mild cognitive impairment: a follow-up study. Lancet Neurology. 2006;5(3):228–234. [PubMed]
27. Andreasen N, Hesse C, Davidsson P, et al. Cerebrospinal fluid β-amyloid((1-42)) in Alzheimer disease: differences between early- and late-onset Alzheimer disease and stability during the course of disease. Archives of Neurology. 1999;56(6):673–680. [PubMed]
28. Wiltfang J, Esselmann H, Smirnov A, et al. β-amyloid peptides in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Annals of Neurology. 2003;54(2):263–267. [PubMed]
29. Verwey NA, Van Der Flier WM, Blennow K, et al. A worldwide multicentre comparison of assays for cerebrospinal fluid biomarkers in Alzheimer’s disease. Annals of Clinical Biochemistry. 2009;46(3):235–240. [PubMed]
30. Vagnucci AH, Jr., Li WW. Alzheimer’s disease and angiogenesis. Lancet. 2003;361(9357):605–608. [PubMed]
31. Román GC, Royall DR. A diagnostic dilemma: is “Alzheimer’s dementia” Alzheimer’s disease, vascular dementia, or both? Lancet Neurology. 2004;3(3):p. 141. [PubMed]
32. De La Torre JC. Is Alzheimer’s disease a neurodegenerative or a vascular disorder? Data, dogma, and dialectics. Lancet Neurology. 2004;3(3):184–190. [PubMed]
33. Formichi P, Parnetti L, Radi E, Cevenini G, Dotti MT, Federico A. CSF levels of β-amyloid 1-42, tau and phosphorylated tau protein in CADASIL. European Journal of Neurology. 2008;15(11):1252–1255. [PubMed]
34. Stenset V, Johnsen L, Kocot D, et al. Associations between white matter lesions, cerebrovascular risk factors, and low CSF Aβ42. Neurology. 2006;67(5):830–833. [PubMed]

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