
Archives of Medical Research, Journal Year: 2024, Volume and Issue: 56(2), P. 103114 - 103114
Published: Nov. 2, 2024
Language: Английский
Archives of Medical Research, Journal Year: 2024, Volume and Issue: 56(2), P. 103114 - 103114
Published: Nov. 2, 2024
Language: Английский
Clinical and Experimental Hypertension, Journal Year: 2024, Volume and Issue: 46(1)
Published: Aug. 12, 2024
Background Complex interconnections are evident among gut microbiota, circulating metabolites, inflammatory cytokines, and the pathogenesis of abdominal aortic aneurysms (AAA), with causal dynamics yet to be comprehensively elucidated. The primary objective this study was elucidate potential relationships involving microbiota-mediated plasma AAA.
Language: Английский
Citations
3Heliyon, Journal Year: 2024, Volume and Issue: 10(12), P. e32831 - e32831
Published: June 1, 2024
The gut microbiome has come to prominence across research disciplines, due its influence on major biological systems within humans. Recently, a relationship between the and hematopoietic system been identified coined gut-bone marrow axis. It is well established that separately alter with age; however, these changes how each other demands investigation. Since produces immune cells help govern commensal bacteria, it important identify interacts stem (HSCs). microbiota shown development outcomes of hematologic disorders, suggesting dysbiosis may maintenance HSCs age. Short chain fatty acids (SCFAs), lactate, iron availability, tryptophan metabolites, bacterial extracellular vesicles, microbe associated molecular patterns (MAMPs), toll-like receptor (TLR) signalling have proposed as key mediators communication axis will be reviewed in this article context aging.
Language: Английский
Citations
1Journal of Cellular and Molecular Medicine, Journal Year: 2024, Volume and Issue: 28(12)
Published: June 1, 2024
Despite remarkable advancements in the treatment of multiple myeloma (MM), relapse remains a challenge. However, mechanisms underlying this disease remain unclear. This study aimed to identify potential biomarkers that could open new avenues for MM treatment. Microarray data and clinical characteristics patients with were obtained from Gene Expression Omnibus database. Differential expression analysis protein-protein interaction (PPI) network construction used hub genes associated MM. Predictive performance was further assessed using receiver operating characteristic curves nomogram construction. Functional enrichment conducted investigate possible mechanisms. Mendelian randomization (MR) evaluate causal relationship between crucial gene risk. Topological PPI revealed five MM, myeloperoxidase (MPO) being key owing its highest degree area under curve values. MPO showed significant differences controls across all datasets. strong association immune-related pathways MR confirmed risk By integrating microarray MR, we successfully identified validated as promising biomarker is potentially implicated pathogenesis progression through pathways.
Language: Английский
Citations
0Archives of Medical Research, Journal Year: 2024, Volume and Issue: 56(2), P. 103114 - 103114
Published: Nov. 2, 2024
Language: Английский
Citations
0