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        <identifier>oai:figshare.com:article/34012497</identifier>
        <datestamp>2026-09-28T08:57:33Z</datestamp>
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          <dc:title>Table 2_Pilot clinical study of Taxifolin Aqua effect in patients with amnestic mild cognitive impairment.docx</dc:title>
          <dc:creator>Elena V. Ponomareva (25121274)</dc:creator>
          <dc:creator>Natalya D. Selezneva (25121277)</dc:creator>
          <dc:creator>Irina S. Boksha (25121280)</dc:creator>
          <dc:creator>Olga K. Savushkina (25121283)</dc:creator>
          <dc:creator>Tatyana A. Prokhorova (25121286)</dc:creator>
          <dc:creator>Elena B. Tereshkina (25121289)</dc:creator>
          <dc:creator>Svetlana A. Zozulya (25121292)</dc:creator>
          <dc:creator>Svetlana I. Gavrilova (25121295)</dc:creator>
          <dc:creator>Igor V. Kolykhalov (25121298)</dc:creator>
          <dc:subject>Psychiatry (incl. Psychotherapy)</dc:subject>
          <dc:subject>antio×idant</dc:subject>
          <dc:subject>biochemical blood analysis</dc:subject>
          <dc:subject>mild cognitive impairment</dc:subject>
          <dc:subject>Taxifolin</dc:subject>
          <dc:subject>treatment response</dc:subject>
          <dc:description>&lt;p&gt;Taxifolin (dihydroquercetin), a potent antioxidant flavonoid, shows promise for neurodegenerative conditions. Our pilot study aimed at evaluation the efficacy and safety of Taxifolin in patients with amnestic mild cognitive impairment (aMCI) and monitored a set of blood measures. Twenty-three patients (18 female; aged 53-87) received dihydroquercetin oral solution for 8 weeks with a 4-week follow-up period in an open-label study design. Thirteen patients with aMCI were monitored as controls. Outcomes were assessed using cognitive status (MMSE, MoCA, FCSRT-IR), neuropsychiatric symptoms’ (NPI-Q, HDRS), and rater's impression (CGI) scales, along with blood measures monitoring (glutathione reductase (GR), glutamate dehydrogenase (GDH), and superoxide dismutase (SOD); plasma neutrophil elastase (NE), alpha-1-proteinase inhibitor (alpha-1PI)). Responder classification using composite Z-score changes was based on all clinical scales. Results: Eleven patients were classified as responders, showing significant MMSE and MoCA improvement (mean +2.73 points, p=0.001) sustained through 4-week follow-up. Non-responders and control group showed slight cognitive decline. Composite Z-score changes at the 4-week follow-up revealed differences between responders/non-responders (ANOVA F(2,20)=17.38, p=0.001); biomarker analysis revealed difference in NE/alpha-1PI ratio (p=0.034), SOD (p=0.023), and GR dynamics (p=0.022), which correlated negatively with clinical response (R=-0.547, p=0.007), and baseline GDH (p=0.049). Conclusion: Taxifolin treatment resulted in significant cognitive benefits in ~half of aMCI patients, with effects sustained for one month post-treatment. Biomarker changes reveal possible mechanisms involving oxidative stress modulation and inflammatory pathways. These findings support further controlled trials of Taxifolin in populations at risk of Alzheimer's disease.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T08:57:33Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fpsyt.2026.1814042.s002</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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