- Research article
- Open Access
Saliva levels of Abeta1-42 as potential biomarker of Alzheimer's disease: a pilot study
BMC Neurology volume 10, Article number: 108 (2010)
Simple, non-invasive tests for early detection of degenerative dementia by use of biomarkers are urgently required. However, up to the present, no validated extracerebral diagnostic markers for the early diagnosis of Alzheimer disease (AD) are available. The clinical diagnosis of probable AD is made with around 90% accuracy using modern clinical, neuropsychological and imaging methods. A biochemical marker that would support the clinical diagnosis and distinguish AD from other causes of dementia would therefore be of great value as a screening test. A total of 126 samples were obtained from subjects with AD, and age-sex-matched controls. Additionally, 51 Parkinson's disease (PD) patients were used as an example of another neurodegenerative disorder. We analyzed saliva and plasma levels of β amyloid (Aβ) using a highly sensitive ELISA kit.
We found a small but statistically significant increase in saliva Aβ42 levels in mild AD patients. In addition, there were not differences in saliva concentration of Aβ42 between patients with PD and healthy controls. Saliva Aβ40 expression was unchanged within all the studied sample. The association between saliva Aβ42 levels and AD was independent of established risk factors, including age or Apo E, but was dependent on sex and functional capacity.
We suggest that saliva Aβ42 levels could be considered a potential peripheral marker of AD and help discrimination from other types of neurodegenerative disorders. We propose a new and promising biomarker for early AD.
With increasing life expectancy across the world, Alzheimer's disease (AD), the most common cause of dementia, is a rapidly growing socioeconomic and medical problem. AD diagnosis is time consuming and requires a combination of clinical assessment, psychological testing, imaging and exclusion of other neurological disorders. In light of these facts, a molecular biomarker that could identify and classify AD would be particularly useful in order to confirm the diagnosis, to perform epidemiological screening, to identify distinct groups of patients, to predict the outcome of the disease, and to monitor its progression and its sensitivity to treatment. In fact, lack of tools to detect preclinical AD has been suggested to be one of the main obstacles for the development of new treatments . The ideal biomarker for AD should detect a fundamental feature of neuropathology: it should be as sensitive and specific as the clinical diagnosis, reliable, reproducible, simple to perform, inexpensive and non-invasive (studies on blood, urine, saliva, or buccal scrapings). Moderately invasive tests (skin, rectal biopsies, bone marrow samples, or cerebrospinal fluid -CSF-) or cerebral biopsy, are inconvenient for routine clinical practice.
In humans, in addition to the classical accumulation in the brain, amyloid-beta protein (Aβ) deposits are found in peripheral regions, including skin , nasal mucosa , and the lacrimal , and lingual glands . The use of human salivary gland biopsies has been recently described as a tool for research on familial amyloidotic polyneuropathy (FAD) , and on AD  because both amyloid precursor protein (APP) and Aβ are expressed in human salivary epithelial cells . Saliva is produced from salivary glands and mucous membranes and, as a biological fluid, is simple to obtain. Additionally, salivary levels may reflect changes in CSF . Recent studies showed association of activity and levels of salivary acetylcholinesterase (AChE) with AD . These findings may prove to be a useful marker of central cholinergic activity which is a key event in the biochemistry of AD.
The majority of the studies of accepted AD biomarkers to date have been carried out using samples of CSF obtained by lumbar puncture . This is an invasive procedure that is particularly unpleasant for the subject and for which explicit consent is required. Recently, it has been shown that identification of blood biomarkers may allow the development of tests for AD [11, 12]. In this study, we report that significant and reproducible levels of salivary Aβ42 can be detected in subjects and there is a specific correlation with development of AD pathology.
The study included three groups: (1) 70 Alzheimer's disease (AD); (2) 56 elderly nondemented controls without neurological disease or cognitive impairment; and (3) 51 Parkinson's disease (PD) patients. All AD cases included in these series were diagnosed with dementia according to the Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV criteria , and NINCDS-ADRDA criteria , and diagnosis required evidence of cognitive decline, (neuropsychological test battery, clinical mental examination) as well as evidence of impairment in social or occupational function. The mini-mental state examination (MMSE) was used to assess cognitive function . The mean value of MMSE score for the AD patients was 17. All cases had an extensive biochemical measurement including levels of vitamin B12 and folate and thyroid hormones and neuroimaging techniques (brain MRI and/or CT scan). Classification of mild, moderate and severe degrees of AD was performed, and the diagnosis of vascular dementia was excluded in all cases, using DSM-III-R criteria. The control group was formed of family members or caregivers of the AD patients, who all had a clinical interview with a senior neurologist that showed a completely normal cognitive and functional level. No formal neuropsychological battery was performed in this group. PD group was formed of patients who had been diagnosed under the criteria of probable PD [16, 17]. Demographic and health characteristics of the final sample (n = 136) are presented (table 1).
Saliva and blood collection
This study was approved by the Ethic Committee of Clinical Investigation of the Hospital '12 de Octubre'. Informed consent from all subjects was obtained prior to their participation Saliva samples were obtained from both healthy volunteers and patients with AD and PD and the study was carried out with full ethical permission. Saliva samples were collected in sterile plastic containers previously treated with 2% sodium azide solution, a concentration which has been shown to be sufficient to prevent microbial decomposition of saliva . Participants were asked to wait at least 4 hours after eating or drinking (initiated at approximately the same time for each participant (13:00 hours), before providing saliva samples of approximately 1 ml into the containers, and these were centrifuged at 1500 rpm for 5 minutes to remove debris, in a similar manner to that previously described . Then, the samples were immediately frozen at -80°C until used. Blood samples were obtained through antecubital vein puncture. Blood was centrifuged at 2500 rpm for 10 minutes, and plasma was collected, aliquoted and immediately frozen at -80°C. Cellular fraction was used for DNA extraction and genotyping assays.
Apo E genotyping
Apo E genotypes of AD and control subjects were determined by established methods as described previously . Genomic DNA was extracted from peripheral blood using Illustra™ blood genomicPrep Mini Spin Kit (GE Healthcare). Apo E genotyping (ε2/ε3/ε4 isoforms) was performed using FRET probes.
30 μl of saliva sample was mixed with an equal volume of 2× SDS sample buffer and denatured by heating at 95°C for 5 minutes. All samples were resolved by 10% SDS-polyacrylamide gel electrophoresis and transferred to nitrocellulose membranes (Bio-Rad) by electroblotting as previously described . The following antibodies were used: mouse monoclonal anti-gelsolin (Sigma-Aldrich), rabbit polyclonal anti-TTR (Santa Cruz Biotechnology), goat anti-mouse HRP-conjugated (Bio-Rad), and goat anti-rabbit HRP-conjugated (Bio-Rad). Peroxidase-labeled lectin (Sigma) was used as gel loading control. Densitometric analysis was performed using ImageJ software (NIH Image).
Levels of human endogenous Aβ40 and Aβ42 in saliva and human plasma samples were determined with human specific enzyme-linked immunosorbent assay (ELISA) (Biosource International, Invitrogen), according to the manufacturer's instructions and as previously described . 50 μl of saliva and plasma samples were added in duplicate to the microtiter wells. Detection limit of the assay was 6 pg/ml for Aβ40 and 1 pg/ml for Aβ42.
Previous to the immunoassays, protein concentration was assessed using a Spectrophotometer NanoDrop ND-1000, to normalize sample protein levels.
Data were analysed with SPSS for Windows (version 15.0). To compare demographic, clinical, and saliva and plasma data between groups, we used ANOVA followed by a Tuckey-Kramer test, and Mann-Whitney U-test analysis when appropriate. The differences were considered to be significant at p < 0.05. The Spearman rank correlation was used for correlation analyses.
177 patients with AD, PD and aged controls were assessed, and Aβ40 and Aβ42 levels were measured in saliva from these patients using a sensitive and specific Aβ ELISA. It is particularly relevant that we were able to detect Aβ40 and Aβ42 in human saliva by a simple and reproducible method. The groups did not differ significantly by age or sex. Our findings show that saliva concentration of Aβ42 has a tendency to increase in AD patients compared with PD and control groups, but this effect was not statistically significant. Interestingly, when we analyzed the three categories of AD patients, we found that saliva Aβ42 levels were significantly increased in the first category of AD patients [in mild AD stage (p = 0.043, and table 2)], whereas saliva Aβ42 levels in moderate AD stage are also increased but with a high standard deviation (SD). Interestingly, the third category of AD, the severe AD stage, has similar than those observed in control group (table 2). Age range was similar between all AD stages and the control group. A 2 × 2 contingency table analysis, with a cut-off = 7.85 pg/ml, allowed the calculation of sensitivity and specificity (defined as the proportion of true positive and the portion of true negative that are correctly identified by the test, respectively). The results were 16% and 93%, respectively. In addition, we performed ROC curve analysis, with 0.547 (area under the curve) AUC (95% CI 0.4-0.68). On the other hand, Aβ40 was unchanged between AD patients and healthy subjects (table 2). We also analyzed the ratio between saliva Aβ42 and Aβ40 and we found that this ratio was higher, but not statistically significant (p = 0.2), in mild and moderate AD patients (0.35 and 0.54, respectively) in compared with control subject (0.13), whereas it was unchanged in severe AD patients (0.12).
Overall, saliva Aβ42levels were not significantly higher with age
However, comparison of AD patients aged 60-65 with those aged 66-70 showed highly significant elevation in saliva Aβ42 levels (1.64 ± 0.44 pg/ml versus 6.46 ± 3.43 pg/ml, p = 0.016).
In addition, plasma levels of Aβ40 and Aβ42 did not differ significantly between patients with AD and control subjects (259 ± 91.9 pg/ml versus 225.1 ± 77.3 pg/ml, and 42.4 ± 92.7 pg/ml versus 52.4 ± 68.9 pg/ml, respectively), in accordance with recent studies . Spearman rank analysis of plasma and saliva levels was not significant for either Aβ40 or Aβ42 levels.
To determine whether the elevated saliva Aβ42 was associated with the Apo E ε4 allele, all subjects were genotyped for ApoE and their Aβ42 levels were analyzed according to the ApoE genotypes. The Apo E ε4 allele frequencies were 45% (15 with Apo E ε3/4 genotype and 3 with Apo E ε4/4 genotype) in the AD group and 12% (3 with Apo E ε3/4 genotype and 1 with Apo E ε2/4 genotype) in the control group. Firstly, we found that ApoE genotype correlates with AD onset (Spearman rank correlation R = 0.428, p = 0.001). Levels of Aβ42 were higher, but not statistically significantly, in patients with AD and without the Apo E ε4 allele than in those with the allele (table 3). Levels of Aβ42 were similar in controls with and without Apo E ε4 allele (table 3).
To test that protein changes are specific to Aβ42 levels, we measured protein concentration in saliva samples from all experimental groups. We did not find significant differences between groups (6.39 ± 3.68 ng/μl in aged subjects, 6.49 ± 4.79 ng/μl in AD patients, and 6.67 ± 5.71 ng/μl in PD patients, data are expressed as mean ± SEM). Additionally, we tested others protein concentrations in these saliva samples. We choose two proteins with Aβ-carrier function, gelsolin, and transthyretin. Using Western-blot assays, we did not observe an alteration in gelsolin (figure 1a) and transthyretin (figure 1b) expression in AD patients compared with control subjects. These results support our finding in human saliva that Aβ42 levels are closely associated with AD diagnosis.
Demographic risk factors could modify the association between pathological saliva Aβ42 and progression to AD. One of the studied variables was MMSE score. Mean MMSE score of AD patients was 17 (range 4-28) (table 1), and correlates with the three categories of AD (Spearman rank correlation R = -0.763, p = 0.001). The relationship between these variables was similar for males or females. Other studied risk factors in the AD group were: hypertension (with a prevalence of 47.1%), hypercholesterol (10%), arthritis (20%), depression (20%), diabetes (12.9%), and heart disease (15.7%). We analyzed whether there was an association between these risk factors and saliva Aβ42 levels. With Mann-Whitney U-test analysis, we found that the concentration of saliva Aβ42 correlates with sex (95% CI 0.71-2.29, p = 0.002) in the AD group.
Early diagnosis of AD represents a primary goal, and the role of biomarkers seems to be crucial in a routine clinical setting. The main findings of this study are that saliva Aβ42 levels are significantly elevated in early stage AD patients in comparison to control subjects, and we suggest that this effect is specific to AD and not to other neurodegenerative disorders, including PD. These data result in a slightly higher specificity, and suggest that measuring saliva Aβ42 may be used as biomarker to identify and confirm early AD diagnosis.
Biomarkers are required to improve the diagnostic sensitivity and specificity and to monitor the biological activity of AD in terms of the burden of neuronal involvement and the rate of disease progression. They must initially supplement our more traditional neuropsychological and imaging markers and may progress to provide useful tool to test the pharmacological action of anti-dementia compounds [24, 25]. The currently best validated CSF biomarkers, pTau and Aβ42, with a reported sensitivity and specificity of around 90-95% for the diagnosis of AD, show generally a good correlation with cerebral tau and Aβ pathology [26–28]. As biomarkers in plasma several substances have been examined, but none of these markers had enough sensitivity or specificity to diagnose AD .
Saliva is frequently used to test for the levels of a number of hormones, and is considered as a non-invasive technique . Therefore, the identification of robust and reproducible Aβ42 expression in saliva is of particular importance as it may serve as a potential indicator of AD neuropathology that can be measured with the minimum of stress for the subject. The mechanism by which Aβ42 accumulates in saliva is unclear. This localization could result from release of this peptide from salivary glands by APP processing as a consequence of secretase enzymes action in salivary epithelial cells . Our data could reflect a similar situation to brain Aβ generation. The vast majority of studies performed so far have reported an increased accumulation of Aβ42 in cerebral parenchyma, mainly as senile plaques , whereas Aβ42 levels were reduced in CSF of patients with AD [31, 32]. The significance of saliva Aβ levels in relation to Aβ accumulation in the brain is unknown; however, their concentrations are comparable with those observed from tissues other than brain, including lens . Lower levels of CSF Aβ42 in the AD group may be explained due to loss of neurons that produce the APP, brain Aβ accumulation, and/or decreased Aβ clearance, as a consequence of impaired blood-brain barrier. As, the latter is not present in salivary glands, Aβ produced from APP glands may be delivered and accumulated in the saliva, mainly in mild AD patients, whereas, in severe AD stage, saliva Aβ42 levels return to control values. This pattern may reflect a parallelism with CSF Aβ42 levels. The association of different combinations of saliva Aβ levels with AD was independent of established risk factors such as age or Apo E genotype, major risk factors for sporadic AD. However, we found a significant correlation between sex and saliva Aβ42 levels in patients with AD. With several discrepancies, our data are consistent with previous studies using CSF and plasma samples [27, 34]. Several studies had described no correlation between CSF Aβ levels and dementia severity [27, 34–36]. However, others showed weak , or strong  correlation between these variables. In our study, we showed no significant relationship between saliva Aβ42 levels and MMSE scores, however when we analyzed the three categories of AD patients, accordingly with the functional capacity, we found a significant correlation. Thus, large and longitudinal studies with a greater number of samples will be necessary to determine conclusively whether there is a relationship between saliva Aβ42 levels and progression of AD.
Decreased saliva production is common amongst elderly people, and in patients with AD, salivary flow from the submandibular gland has been found to be significantly impaired . However, the protein concentration of the saliva samples obtained from the elderly control subjects was similar to those of the subjects either with AD or PD. Additionally, we decided to investigate whether the concentration of other proteins may be changed in saliva samples from AD patients. Aβ forms complexes with protein carriers, including transthyretin or gelsolin, to prevent peptide polymerization and aggregation [40–42]. Since these proteins are present in body fluids [32, 43], and are significantly reduced in CSF from AD patients [32, 44, 45], we chose them to test our hypothesis. Since total protein concentration was similar in AD patients and healthy subjects, and these secreted proteins was unchanged in both groups, we may suggest that elevated Aβ42 levels represent a specific change for AD, and can not be attributed to a general increase in salivary protein concentration.
As usual, there were various difficulties in the measurement of Aβ levels in body fluids. Additionally, Aβ values decreased over time, even if the samples were frozen . Although range of saliva Aβ42 levels was high, we consider that is not in discrepancy with those reported in plasma or CSF samples from AD patients, with range seen from 100 pg/ml to 770 pg/ml, and 25 pg/ml to 325 pg/ml, respectively . In this study, we demonstrate the remarkable reproducibility of the saliva Aβ ELISA in different series of repetitive measurements. It is particularly significant that saliva analyses of Aβ42 are increased in mild AD patients, whereas in the severe stage, associated with a greater neurodegeneration, the levels are unchanged. Our data was supported by the ratio Aβ42 /Aβ40 in saliva that was higher in mild and moderate AD patients in compared with control subject, whereas it was unchanged in severe AD patients. This fact is consistent with the main objective of AD biomarkers: the early diagnosis. Indeed, further studies will be performed to determine saliva Aβ42 levels in mild cognitive impairment (MCI), an intermediate stage to dementia, how these levels change across the transition from normal to MCI, and the interactions with age and Apo E genotype. If validated in other consecutive studies with long follow-up and large number of patients, these results may have an effect on diagnosis and on the design of clinical trials of patients with mild AD.
There were no significant differences in Aβ42 levels between AD, PD and controls subjects. However, our findings show that saliva concentration of Aβ42 differs between mild AD and non-demented control subjects, and that this is a specific characteristic of AD, being absent in PD. To our knowledge, no study to date has investigated the possibility of overlapping AD-associated Aβ levels in saliva and brain of subjects with this disorder. Our results show that saliva analyses of Aβ42 are powerful risk markers for development of clinical AD in patients.
Lansbury PT: Back to the future: the old-fashioned way to new medications for neurodegeneration. Nat Med. 2004, 10: 51-57. 10.1038/nrn1435.
Gasparini L, Racchi M, Binetti G, Trabucchi M, Solerte SB, Alkon D, Etcheberrigaray R, Gibson G, Blass J, Paoletti R, Govoni S: Peripheral markers in testing pathophysiological hypotheses and diagnosing Alzheimer's disease. FASEB J. 1998, 12: 17-34.
Attems J, Lintner F, Jellinger KA: Olfactory involvement in aging and Alzheimer's disease: an autopsy study. J Alzheimers Dis. 2005, 7: 149-157.
Frederikse PH, Garland D, Zigler JS, Piatigorsky J: Oxidative stress increases production of beta-amyloid precursor protein and beta-amyloid (Abeta) in mammalian lenses, and Abeta has toxic effects on lens epithelial cells. J Biol Chem. 1996, 271: 10169-10174. 10.1074/jbc.271.17.10169.
Fukuchi K, Li L, Hart M, Lindsey JR: Accumulation of amyloid-beta protein in exocrine glands of transgenic mice overexpressing a carboxyl terminal portion of amyloid protein precursor. Int J Exp Pathol. 2000, 81: 231-239. 10.1046/j.1365-2613.2000.00156.x.
Sousa MM, do Amaral JB, Guimarães A, Saraiva MJ: Up-regulation of the extracellular matrix remodeling genes, biglycan, neutrophil gelatinase-associated lipocalin, and matrix metalloproteinase-9 in familial amyloid polyneuropathy. FASEB J. 2005, 19: 124-126.
Oh YS, Turner RJ: Effect of gamma-secretase inhibitors on muscarinic receptor-mediated calcium signaling in human salivary epithelial cells. Am J Physiol Cell Physiol. 2006, 291: 76-82. 10.1152/ajpcell.00508.2005.
Scherber A, Richter K, Schaps P: Distribution of antiepileptic drugs between plasma, plasma water, cerebrospinal fluid, saliva and brain. Monogr Neural Sci. 1980, 5: 208-212.
Sayer R, Law E, Connelly PJ, Breen KC: Association of a salivary acetylcholinesterase with Alzheimer's disease and response to cholinesterase inhibitors. Clin Biochem. 2004, 37: 98-104. 10.1016/j.clinbiochem.2003.10.007.
Blennow K, Hampel H: CSF markers for incipient Alzheimer's disease. Lancet Neurol. 2003, 2: 605-613. 10.1016/S1474-4422(03)00530-1.
Ray S, Britschgi M, Herbert C, Takeda-Uchimura Y, Boxer A, Blennow K, Friedman LF, Galasko DR, Jutel M, Karydas A, Kaye JA, Leszek J, Miller BL, Minthon L, Quinn JF, Rabinovici GD, Robinson WH, Sabbagh MN, So YT, Sparks DL, Tabaton M, Tinklenberg J, Yesavage JA, Tibshirani R, Wyss-Coray T: Classification and prediction of clinical Alzheimer's diagnosis based on plasma signaling proteins. Nat Med. 2007, 13: 1359-1362. 10.1038/nm1653.
German DC, Gurnani P, Nandi A, Garner HR, Fisher W, Diaz-Arrastia R, O'Suilleabhain P, Rosenblatt KP: Serum biomarkers for Alzheimer's disease: proteomic discovery. Biomed Pharmacother. 2007, 61: 383-389. 10.1016/j.biopha.2007.05.009.
American Psychiatric Association: DSM-IV. Diagnostic and Statistical Manual of Mental Disorders. 1994, Washington DC: American Psychiatric Association
McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM: 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: 939-944.
Folstein MF, Folstein SE, McHugh PR: "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975, 12: 189-198. 10.1016/0022-3956(75)90026-6.
Calne DB, Snow BJ, Lee C: Criteria for diagnosing Parkinson's disease. Ann Neurol. 1992, 32: 125-127. 10.1002/ana.410320721.
Gelb DJ, Oliver E, Gilman S: Diagnostic criteria for Parkinson disease. Arch Neurol. 1999, 56: 33-39. 10.1001/archneur.56.1.33.
Decker SA: Low salivary cortisol and elevated depressive affect among rural men in Botswana: reliability and validity of laboratory results. J Physiol Anthropol. 2006, 25: 91-101. 10.2114/jpa2.25.91.
Boston PF, Gopalkaje K, Manning L, Middleton L, Loxley M: Developing a simple laboratory test for Alzheimer's disease: measuring acetylcholinesterase in saliva - a pilot study. Int J Geriatr Psychiatry. 2008, 23: 439-440. 10.1002/gps.1882.
Aslanidis C, Schmitz G: High-speed apolipoprotein E genotyping and apolipoprotein B3500 mutation detection using real-time fluorescence PCR and melting curves. Clin Chem. 1999, 45: 1094-1097.
Yao C, Karabasil MR, Purwanti N, Li X, Akamatsu T, Kanamori N, Hosoi K: Tissue kallikrein mK13 is a candidate processing enzyme for the precursor of interleukin-1beta in the submandibular gland of mice. J Biol Chem. 2006, 281: 7968-7976. 10.1074/jbc.M507705200.
Lehman EJ, Kulnane LS, Gao Y, Petriello MC, Pimpis KM, Younkin L, Dolios G, Wang R, Younkin SG, Lamb BT: Genetic background regulates beta-amyloid precursor protein processing and beta-amyloid deposition in the mouse. Hum Mol Genet. 2003, 12: 2949-2956. 10.1093/hmg/ddg322.
Xia W, Yang T, Shankar G, Smith IM, Shen Y, Walsh DM, Selkoe DJ: A specific enzyme-linked immunosorbent assay for measuring beta-amyloid protein oligomers in human plasma and brain tissue of patients with Alzheimer disease. Arch Neurol. 2009, 66: 190-199. 10.1001/archneurol.2008.565.
Irizarry MC: Biomarkers of Alzheimer disease in plasma. NeuroRx. 2004, 1: 226-234. 10.1602/neurorx.1.2.226.
Blennow K: CSF biomarkers for Alzheimer's disease: use in early diagnosis and evaluation of drug treatment. Expert Rev Mol Diagn. 2005, 5: 661-672. 10.1586/1473718.104.22.1681.
Buerger K, Ewers M, Pirttila T, Zinkowski R, Alafuzoff I, Teipel SJ, DeBernardis J, Kerkman D, McCulloch C, Soininen H, Hampel H: CSF phosphorylated tau protein correlates with neocortical neurofibrillary pathology in Alzheimer's disease. Brain. 2006, 129: 3035-3041. 10.1093/brain/awl269.
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 Neurol. 2006, 5: 228-234. 10.1016/S1474-4422(06)70355-6.
Buerger K, Alafuzoff I, Ewers M, Pirttila T, Zinkowski R, Hampel H: No correlation between CSF tau protein phosphorylated at threonine 181 with neocortical neurofibrillary pathology in Alzheimer's disease. Brain. 2007, 130: e82-10.1093/brain/awm140.
Cook CJ: Rapid noninvasive measurement of hormones in transdermal exudate and saliva. Physiol Behav. 2002, 75: 169-181. 10.1016/S0031-9384(01)00658-8.
Hardy J, Selkoe DJ: The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics. Science. 2002, 297: 353-356. 10.1126/science.1072994.
Sunderland T, Linker G, Mirza N, Putnam KT, Friedman DL, Kimmel LH, Bergeson J, Manetti GJ, Zimmermann M, Tang B, Bartko JJ, Cohen RM: Decreased beta-amyloid1-42 and increased tau levels in cerebrospinal fluid of patients with Alzheimer disease. JAMA. 2003, 289: 2094-2103. 10.1001/jama.289.16.2094.
Dietrich MO, Spuch C, Antequera D, Rodal I, de Yébenes JG, Molina JA, Bermejo F, Carro E: Megalin mediates the transport of leptin across the blood-CSF barrier. Neurobiol Aging. 2008, 29: 902-912. 10.1016/j.neurobiolaging.2007.01.008.
Goldstein LE, Muffat JA, Cherny RA, Moir RD, Ericsson MH, Huang X, Mavros C, Coccia JA, Faget KY, Fitch KA, Masters CL, Tanzi RE, Chylack LT, Bush AI: Cytosolic beta-amyloid deposition and supranuclear cataracts in lenses from people with Alzheimer's disease. Lancet. 2003, 361: 1258-1265. 10.1016/S0140-6736(03)12981-9.
Mehta PD, Pirttilä T, Mehta SP, Sersen EA, Aisen PS, Wisniewski HM: Plasma and cerebrospinal fluid levels of amyloid beta proteins 1-40 and 1-42 in Alzheimer disease. Arch Neurol. 2000, 57: 100-105. 10.1001/archneur.57.1.100.
Motter R, Vigo-Pelfrey C, Kholodenko D, Barbour R, Johnson-Wood K, Galasko D, Chang L, Miller B, Clark C, Green R: Reduction of beta-amyloid peptide42 in the cerebrospinal fluid of patients with Alzheimer's disease. Ann Neurol. 1995, 38: 643-648. 10.1002/ana.410380413.
Tamaoka A, Sawamura N, Fukushima T, Shoji S, Matsubara E, Shoji M, Hirai S, Furiya Y, Endoh R, Mori H: Amyloid beta protein 42(43) in cerebrospinal fluid of patients with Alzheimer's disease. J Neurol Sci. 1997, 148: 41-45. 10.1016/S0022-510X(96)00314-0.
Galasko D, Chang L, Motter R, Clark CM, Kaye J, Knopman D, Thomas R, Kholodenko D, Schenk D, Lieberburg I, Miller B, Green R, Basherad R, Kertiles L, Boss MA, Seubert P: High cerebrospinal fluid tau and low amyloid beta42 levels in the clinical diagnosis of Alzheimer disease and relation to apolipoprotein E genotype. Arch Neurol. 1998, 55: 937-945. 10.1001/archneur.55.7.937.
Samuels SC, Silverman JM, Marin DB, Peskind ER, Younki SG, Greenberg DA, Schnur E, Santoro J, Davis KL: CSF beta-amyloid, cognition, and APOE genotype in Alzheimer's disease. Neurology. 1999, 52: 547-551.
Ship JA, DeCarli C, Friedland RP, Baum BJ: Diminished submandibular salivary flow in dementia of the Alzheimer type. J Gerontol. 1990, 45: 61-66.
Chodobski A, Szmydynger-Chodobska J: Choroid plexus: target for polypeptides and site of their synthesis. Microsc Res Tech. 2001, 52: 65-82. 10.1002/1097-0029(20010101)52:1<65::AID-JEMT9>3.0.CO;2-4.
Carro E, Trejo JL, Gomez-Isla T, LeRoith D, Torres-Aleman I: Serum insulin-like growth factor I regulates brain amyloid-beta levels. Nat Med. 2002, 8: 1390-1397. 10.1038/nm793.
Ray I, Chauhan A, Wegiel J, Chauhan VP: Gelsolin inhibits the fibrillization of amyloid beta-protein, and also defibrillizes its preformed fibrils. Brain Res. 2000, 853: 344-351. 10.1016/S0006-8993(99)02315-X.
Kwiatkowski DJ, Stossel TP, Orkin SH, Mole JE, Colten HR, Yin HL: Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain. Nature. 1986, 323: 455-458. 10.1038/323455a0.
Gloeckner SF, Meyne F, Wagner F, Heinemann U, Krasnianski A, Meissner B, Zerr I: Quantitative analysis of transthyretin, tau and amyloid-beta in patients with dementia. J Alzheimers Dis. 2008, 14: 17-25.
Antequera D, Vargas T, Ugalde C, Spuch C, Molina JA, Ferrer I, Bermejo-Pareja F, Carro E: Cytoplasmic gelsolin increases mitochondrial activity and reduces Aβ burden in a mouse model of Alzheimer's disease. Neurobiol Dis. 2009, 36: 42-50. 10.1016/j.nbd.2009.06.018.
Southwick PC, Yamagata SK, Echols CL, Higson GJ, Neynaber SA, Parson RE, Munroe WA: Assessment of amyloid beta protein in cerebrospinal fluid as an aid in the diagnosis of Alzheimer's disease. J Neurochem. 1996, 66: 259-265. 10.1046/j.1471-4159.1996.66010259.x.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2377/10/108/prepub
This work was supported by grants from Fondo de Investigación Sanitaria (FIS) (PI060155, PI0901636), Fundación Investigación Médica Mutua Madrileña (2006.125), CIBERNED. This work was made possible by the generous participation of the patients, the control subjects, and their families. We thank Joe Healey for editorial revision, and Dr J Manzanares, who suggested the possible utility of the saliva study in the neurodegenerative disorders.
FB-P: conceived of the study, provide clinical samples and diagnostic data, and participated in its design and coordination.
DA: carried out the immunoassays and performed the statistical analysis.
TV: carried out the molecular genetic studies.
JAM: provide clinical samples and diagnostic data.
EC: conceived of the study, participated in its design and coordination, and wrote the manuscript.
All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Bermejo-Pareja, F., Antequera, D., Vargas, T. et al. Saliva levels of Abeta1-42 as potential biomarker of Alzheimer's disease: a pilot study. BMC Neurol 10, 108 (2010). https://doi.org/10.1186/1471-2377-10-108
- Saliva Sample
- Saliva Concentration
- Salivary Epithelial Cell