Effects silymarin and rosuvastatin on amyloid-carriers level in dyslipidemic Alzheimer’s patients: A double-blind placebo-controlled randomized clinical trial

The production/excretion rate of Amyloid-β (Aβ) is the basis of the plaque burden in alzheimer's disease (AD), which depends on both central and peripheral clearance. In this study, the effect of silymarin and rosuvastatin on serum markers and clinical outcomes in dyslipidemic AD patients was i...

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Veröffentlicht in:IBRO neuroscience reports 2024-12, Vol.17, p.108-121
Hauptverfasser: Rustamzadeh, Auob, Sadigh, Nader, Vahabi, Zahra, Khamseh, Fatemeh, Mohebi, Nafiseh, Ghobadi, Zahra, Moradi, Fatemeh
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Sprache:eng
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Zusammenfassung:The production/excretion rate of Amyloid-β (Aβ) is the basis of the plaque burden in alzheimer's disease (AD), which depends on both central and peripheral clearance. In this study, the effect of silymarin and rosuvastatin on serum markers and clinical outcomes in dyslipidemic AD patients was investigated. Participants (n=36) were randomized to silymarin (140 mg), placebo, and rosuvastatin 10 mg orally three times a day for 6 months. Serum collection and clinical outcome tests were performed at baseline and after completion of treatment. Lipid profile markers, oxidative stress markers, Aβ1–42/Aβ1–40 ratio, and Soluble Low-density lipoprotein receptor-Related Protein-1 (sLRP1)/Soluble Receptor for Advanced Glycation End Products (sRAGE) ratio were measured. There was a statistically significant increase in Δ-high density lipoprotein (ΔHDL) between silymarin and placebo (P
ISSN:2667-2421
2667-2421
DOI:10.1016/j.ibneur.2024.07.002