Bile acid quantification of 20 plasma metabolites identifies lithocholic acid as a putative biomarker in Alzheimer's disease
- PMID: 29249916
- PMCID: PMC5725507
- DOI: 10.1007/s11306-017-1297-5
Bile acid quantification of 20 plasma metabolites identifies lithocholic acid as a putative biomarker in Alzheimer's disease
Abstract
Introduction: There is still a clear need for a widely available, inexpensive and reliable method to diagnose Alzheimer's disease (AD) and monitor disease progression. Liquid chromatography-mass spectrometry (LC-MS) is a powerful analytic technique with a very high sensitivity and specificity.
Objectives: The aim of the present study is to measure concentrations of 20 bile acids using the novel Kit from Biocrates Life Sciences based on LC-MS technique.
Methods: Twenty bile acid metabolites were quantitatively measured in plasma of 30 cognitively healthy subjects, 20 patients with mild cognitive impairment (MCI) and 30 patients suffering from AD.
Results: Levels of lithocholic acid were significantly enhanced in plasma of AD patients (50 ± 6 nM, p = 0.004) compared to healthy controls (32 ± 3 nM). Lithocholic acid plasma levels of MCI patients (41 ± 4 nM) were not significantly different from healthy subjects or AD patients. Levels of glycochenodeoxycholic acid, glycodeoxycholic acid and glycolithocholic acid were significantly higher in AD patients compared to MCI patients (p < 0.05). All other cholic acid metabolites were not significantly different between healthy subjects, MCI patients and AD patients. ROC analysis shows an overall accuracy of about 66%. Discriminant analysis was used to classify patients and we found that 15/23 were correctly diagnosed. We further showed that LCA levels increased by about 3.2 fold when healthy subjects converted to AD patients within a 8-9 year follow up period. Pathway analysis linked these changes to a putative toxic cholesterol pathway.
Conclusion: In conclusion, 4 bile acids may be useful to diagnose AD in plasma samples despite limitations in diagnostic accuracy.
Keywords: Alzheimer; Bile acid; Biomarkers; Diagnosis; Lithocholic acid; Plasma.
Conflict of interest statement
Compliance with ethical standardsThe authors declare that they have no conflict of interest. TK is employed by Biocrates.The study was approved by the Ethics Committee of the Medical University of Innsbruck and was performed in accordance with the Helsinki Declaration. All subjects gave written informed consent. Data and material are available on request.
Figures


Similar articles
-
Alteration of Metabolic Profile and Potential Biomarkers in the Plasma of Alzheimer's Disease.Aging Dis. 2020 Dec 1;11(6):1459-1470. doi: 10.14336/AD.2020.0217. eCollection 2020 Dec. Aging Dis. 2020. PMID: 33269100 Free PMC article.
-
Electrochemical impedance-based biosensor for label-free determination of plasma P-tau181 levels for clinically accurate diagnosis of mild cognitive impairment and Alzheimer's disease.Anal Chim Acta. 2023 Sep 8;1273:341535. doi: 10.1016/j.aca.2023.341535. Epub 2023 Jun 15. Anal Chim Acta. 2023. PMID: 37423666
-
A Community-Based Study Identifying Metabolic Biomarkers of Mild Cognitive Impairment and Alzheimer's Disease Using Artificial Intelligence and Machine Learning.J Alzheimers Dis. 2020;78(4):1381-1392. doi: 10.3233/JAD-200305. J Alzheimers Dis. 2020. PMID: 33164929
-
Neurofilament Light Chain as a Potential Biomarker in Plasma for Alzheimer's Disease and Mild Cognitive Impairment: A Systematic Review and a Meta-Analysis.J Integr Neurosci. 2023 Jun 30;22(4):85. doi: 10.31083/j.jin2204085. J Integr Neurosci. 2023. PMID: 37519166
-
Structural magnetic resonance imaging for the early diagnosis of dementia due to Alzheimer's disease in people with mild cognitive impairment.Cochrane Database Syst Rev. 2020 Mar 2;3(3):CD009628. doi: 10.1002/14651858.CD009628.pub2. Cochrane Database Syst Rev. 2020. PMID: 32119112 Free PMC article.
Cited by
-
Dysbiosis of Gut Microbiota from the Perspective of the Gut-Brain Axis: Role in the Provocation of Neurological Disorders.Metabolites. 2022 Nov 3;12(11):1064. doi: 10.3390/metabo12111064. Metabolites. 2022. PMID: 36355147 Free PMC article. Review.
-
The Differences of Serum Metabolites Between Patients With Early-Stage Alzheimer's Disease and Mild Cognitive Impairment.Front Neurol. 2019 Nov 22;10:1223. doi: 10.3389/fneur.2019.01223. eCollection 2019. Front Neurol. 2019. PMID: 31824405 Free PMC article.
-
Bile acid profile associated with CSF and PET biomarkers in Alzheimer's disease.Aging Clin Exp Res. 2024 Mar 7;36(1):62. doi: 10.1007/s40520-024-02729-3. Aging Clin Exp Res. 2024. PMID: 38451317 Free PMC article.
-
Bile acid receptors and signaling crosstalk in the liver, gut and brain.Liver Res. 2021 Jul 18;5(3):105-118. doi: 10.1016/j.livres.2021.07.002. eCollection 2021 Sep. Liver Res. 2021. PMID: 39957847 Free PMC article. Review.
-
The Food Contaminants Pyrrolizidine Alkaloids Disturb Bile Acid Homeostasis Structure-Dependently in the Human Hepatoma Cell Line HepaRG.Foods. 2021 May 18;10(5):1114. doi: 10.3390/foods10051114. Foods. 2021. PMID: 34069968 Free PMC article.
References
-
- Anstey KJ, Lipnicki DM, Low LF. Cholesterol as a risk factor for dementia and cognitive decline: A systematic review of prospective studies with meta-analysis. The American Journal of Geriatric Psychiatry. 2008;16(5):343–354. doi: 10.1097/01.JGP.0000310778.20870.ae. - DOI - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials