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Population-Specific Biomarker Signatures in Alcohol Use Disorder: Ethnic and Viral Influences in a Central Asian Cohort

Natalya TseomashkoRepublican Specialized Scientific and Practical Medical Center for Mental Health, TashkentTimur SyunyakovInternational Centre for Education and Research in Neuropsychiatry (ICERN), Samara State Medical University,, Russia, SamaraI. I. KhayredinovaDepartment of Psychiatry and Narcology of, Tashkent Medical Academy, TashkentUktam TadjibaevRepublican Specialized Scientific and Practical Medical Center for Mental Health, TashkentFurkat BahramovDepartment of Narcology and Adolescent Psychopathology, of the Center for the Develop-ment of Professional Qualifications of Medical Workers, TashkentZarifjon AshurovDepartment of Psychiatry and Narcology of, Tashkent Medical Academy, Tashkent
F1000Researchjournal2025en
ABI

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<ns3:p>Background This study examined biomarker signatures in men with alcohol use disorder (AUD) in Uzbekistan, with and without viral infections. Methods A cross-sectional study included 292 males with stage II AUD (virus-negative: n = 251; virus-positive: n = 41) and 49 alcohol-free controls. Clinical, hematological, and biochemical parameters were measured, and ROC analysis evaluated diagnostic performance. Results Virus-negative patients showed the clearest biomarker profile of alcohol dependence, with reduced glucose, creatinine, and urea, and elevated total protein, α-amylase, De Ritis ratio, and direct bilirubin. ROC analysis confirmed strong diagnostic value for AST (AUC = 0.951), FIB-4 (0.877), MAP (0.817), and creatinine (0.711). Leukocytes (AUC = 0.790) and lymphocytes (0.735) best differentiated viral status. Fibrosis risk in virus-positive patients was 1.5-fold higher, with splenomegaly in 7.3%. Mild thrombocytopenia, absence of granulocytopenia, and rare delirium (&lt;5.5%) distinguished this cohort from European groups, resembling East Asian patterns. Conclusions Liver enzymes, α-amylase, bilirubin, MCV, FIB-4, and MAP provide strong diagnostic value for AUD. Multimarker panels including leukocyte, lymphocyte, and creatinine levels support viral status differentiation. Findings emphasize population-specific biomarker signatures in Central Asians and the utility of multimarker strategies for personalized AUD management.</ns3:p>

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Показатели — AkademScholar · Скоро