Copyright: © 2024 by the authors. Licensee: Pirogov University.
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ORIGINAL RESEARCH

Role of oxidative stress in pathogenesis of bone destruction syndrome in patients with chronic lymphocytic leukemia

Osikov MV1,2, Korobkin EA1,2
About authors

1 South Ural State Medical University, Chelyabinsk, Russia

2 Chelyabinsk Regional Clinical Hospital, Chelyabinsk, Russia

Correspondence should be addressed: Mikhail V. Osikov
Vorovsky, 64, Chelyabinsk, 454092, Russia; ur.xednay@vokiso.forp

About paper

Author contribution: Osikov MV — developing the study idea, concept, and design, editing and approval of the final version of the manuscript; Korobkin EA — experimental phase of the study, statistical data processing, data interpretation, manuscript writing and editing.

Compliance with ethical standards: the study was approved by the Ethics Committee of the South Ural State Medical University (protocol No. 3 dated 10 April 2023). All subjects submitted the informed consent to participation in the study.

Received: 2024-10-11 Accepted: 2024-11-13 Published online: 2024-11-30
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Table 1. Bone mineral density indicators (Ме [Q1; Q3])
Note: * — significant (p < 0.05) differences from group 1 based on the Kruskal–Wallis test, # — from group 2; $ — differences in group 2; & — differences in group 3.
Table 2. Bone tissue oxidative stress indicators in patients with CLL (Ме [Q1; Q3])
Note: # — significant (p < 0.05) differences from group 2 based on the Mann–Whitney U test; (h) — heptane phase of the bone tissue lipid extract; (i) — isopropanol phase.
Table 3. Serum oxidative stress inficators (Ме [Q1; Q3])
Note: * — significant (p < 0.05) differences from group 1 based on the Kruskal–Wallis test, # — from group 2; $ — differences in group 2; & — differences in group 3; (h) — heptane phase of the bone tissue lipid extract; (i) — isopropanol phase.
Table 4. Regression models
Note: * — significant (p < 0.05) differences.