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Homocysteic Acid in Blood Can Detect Mild Cognitive Impairment: A Preliminary Study.
Tohru Hasegawa1, Yoshinori Kosoku2, Yuka Sano2
1Saga Women's Junior College, Saga, Japan.
Plasma homocysteic acid (HCA) shows promise as an early diagnostic marker for mild cognitive impairment (MCI), a precursor to Alzheimer's disease (AD). This minimally invasive biomarker can help identify MCI patients with high sensitivity and specificity.
Area of Science:
- Neurology
- Biochemistry
- Biomarker Discovery
Background:
- Early intervention is crucial for Alzheimer's disease (AD) treatment effectiveness.
- Minimally invasive, cost-effective biomarkers are needed for early AD diagnosis.
- Plasma amyloid-beta (Aβ) shows potential but its direct link to AD development is unproven.
Purpose of the Study:
- To evaluate homocysteic acid (HCA) as an early diagnostic marker for mild cognitive impairment (MCI).
- To assess the diagnostic performance of plasma HCA in distinguishing MCI from healthy controls.
Main Methods:
- Plasma concentrations of HCA, TNF-α, cortisol, tau, and p-tau were measured.
- Analysis included patients with AD, MCI, and negative controls (NC).
- Receiver operating characteristic (ROC) curves were used to evaluate HCA's diagnostic accuracy.
Main Results:
- Plasma HCA levels were significantly elevated in MCI patients compared to NC.
- HCA demonstrated high diagnostic accuracy, with an Area Under the Curve (AUC) distinguishing MCI from NC.
- A cut-off concentration of 0.116μM for HCA yielded 95.7% sensitivity and 70% specificity.
Conclusions:
- Plasma HCA is a potential early diagnostic marker for MCI.
- HCA may precede neurodegeneration in AD pathology, potentially via NMDA receptor overactivation.
- Further research into HCA's role in AD pathogenesis is warranted.
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