CSF-Targeted Proteomics Indicate Amyloid-Beta Ratios in Patients with Alzheimer's Dementia Spectrum. (6th February 2023)

• Record Type: Journal Article
• Authors: Behzad, Maryam; Zirak, Negin; Madani, Ghazal Hamidi; Baidoo, Linda; Rezaei, Ali; Karbasi, Shima; Sadeghi, Mohammad; Shafie, Mahan; Mayeli, Mahsa; Alzheimer's Disease Neuroimaging Initiative,
• Other Names: Abate Giulia Academic Editor.
• Is Part Of: International journal of alzheimer's disease. Volume 2023(2023)
• Publication Date: 2023-02-06
• Subjects: Alzheimer's disease -- Periodicals; 616.831005
• DOI: 10.1155/2023/5336273
• Languages: English
• ISSNs: 2090-8024

Abstract

Abstract : Background . According to recent studies, amyloid- β (A β ) isoforms as cerebrospinal fluid (CSF) biomarkers have remarkable predictive value for cognitive decline in the early stages of Alzheimer's disease (AD). Herein, we aimed to investigate the correlations between several targeted proteomics in CSF samples with A β ratios and cognitive scores in patients in AD spectrum to search for potential early diagnostic utility. Methods . A total of 719 participants were found eligible for inclusion. Patients were then categorized into cognitively normal (CN), mild cognitive impairment (MCI), and AD and underwent an assessment of A β and proteomics. Clinical Dementia Rating (CDR), Alzheimer's Disease Assessment Scale (ADAS), and Mini Mental State Exam (MMSE) were used for further cognitive assessment. The A β 42, A β 42/A β 40, and A β 42/38 ratios were considered as means of comparison to identify those peptides corresponding significantly to these established biomarkers and cognitive scores. The diagnostic utility of the IASNTQSR, VAELEDEK, VVSSIEQK, GDSVVYGLR, EPVAGDAVPGPK, and QETLPSK was assessed. Results . All investigated peptides corresponded significantly to A β 42 in controls. In those with MCI, VAELEDEK and EPVAGDAVPGPK were significantly correlated with A β 42 (p value < 0.001). Additionally, IASNTQSR, VVSSIEQK, GDSVVYGLR, and QETLPSK were significantly correlated with A β 42/A β 40 and A β 42/38 (p value < 0.001) in this group. This group of peptides similarly corresponded to A β ratios in those with AD. Eventually, IASNTQSR, VAELEDEK, and VVSSIEQK were significantly associated with CDR, ADAS-11, and ADAS-13, particularly in MCI group. Conclusion . Our research suggests potential early diagnostic and prognostic utilities for certain peptides extracted from CSF-targeted proteomics research. The ethical approval of ADNI is available at ClinicalTrials.gov with Identifier: NCT00106899 .