The role of pentraxin 3 and oxidative status in the prognosis of multiple myeloma
dc.authorid | oguzman, hamdi/0000-0003-1412-7689 | |
dc.authorid | Kacmaz, Murat/0000-0003-1111-8605 | |
dc.contributor.author | Oguzman, Hamdi | |
dc.contributor.author | Kacmaz, Murat | |
dc.date.accessioned | 2024-09-18T20:55:33Z | |
dc.date.available | 2024-09-18T20:55:33Z | |
dc.date.issued | 2024 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Multiple myeloma (MM) is a bone marrow malignancy characterized by plasma cell proliferation. It was aimed to investigate pentraxin 3 (PTX3) levels, oxidative/antioxidative status, and their correlation in MM. In the study, four groups were established, including newly diagnosed MM (NDMM), MM in remission (Rem-MM), relapsed/refractory MM (RRMM) patients, and a healthy control group. PTX3 levels were measured using enzyme-linked immunosorbent assay, and the total antioxidant status (TAS) and total oxidant status (TOS) were assessed with an autoanalyzer. The oxidative stress index (OSI) was calculated using the formula: OSI (arbitrary unit) = TOS (mu mol H2O2 Eq/L)/TAS (mmol Trolox Eq/L) x 100. The study involved comparing PTX3, TAS, TOS, and OSI levels among these four groups. PTX3 levels were significantly elevated in NDMM and RRMM groups compared to controls and the Rem-MM group (NDMM vs control; p < 0.001, NDMM vs Rem-MM; p < 0.001, RRMM vs control; p < 0.001, and RRMM vs Rem-MM; p = 0.006). TAS was higher in NDMM and RRMM groups versus controls (p = 0.009 and p < 0.001, respectively), and TOS was higher in rem-MM group versus NDMM and control groups (p < 0.001 and p = 0.016, respectively). OSI was higher in the Rem-MM group than in NDMM and RRMM groups (p < 0.001 and p = 0.009, respectively). Multivariate analysis confirmed associations between MM groups and PTX3 levels. Receiver operating characteristic analysis revealed high specificity (90%) and sensitivity (79%) for PTX3 in NDMM at a >0.56 ng/mL cut-off value. This study suggests that PTX3 levels may have diagnostic and prognostic potential in MM and its relationship with oxidative stress requires further exploration. | en_US |
dc.identifier.doi | 10.1177/10815589241235662 | |
dc.identifier.endpage | 340 | en_US |
dc.identifier.issn | 1081-5589 | |
dc.identifier.issn | 1708-8267 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.pmid | 38373952 | en_US |
dc.identifier.scopus | 2-s2.0-85189770826 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 333 | en_US |
dc.identifier.uri | https://doi.org/10.1177/10815589241235662 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/11909 | |
dc.identifier.volume | 72 | en_US |
dc.identifier.wos | WOS:001196750300006 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Sage Publications Ltd | en_US |
dc.relation.ispartof | Journal of Investigative Medicine | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | PTX3 protein | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | bone marrow neoplasms | en_US |
dc.subject | hematology | en_US |
dc.subject | biomarkers | en_US |
dc.subject | myeloproliferative disorders | en_US |
dc.title | The role of pentraxin 3 and oxidative status in the prognosis of multiple myeloma | en_US |
dc.type | Article | en_US |