Plasma cytokines as potential biomarkers of kidney damage in patients with systemic lupus erythematosus

dc.contributor.authorPacheco-Lugo, L
dc.contributor.authorSáenz-García, J
dc.contributor.authorNavarro Quiroz, E
dc.contributor.authorGonzález Torres, H
dc.contributor.authorFang, L
dc.contributor.authorDíaz-Olmos, Y
dc.contributor.authorGaravito de Egea, G
dc.contributor.authorEgea Bermejo, E
dc.contributor.authorAroca Martínez, G
dc.date.accessioned2018-11-22T14:33:12Z
dc.date.available2018-11-22T14:33:12Z
dc.date.issued2018-11
dc.description.abstractBackground: Systemic lupus erythematosus is a heterogeneous chronic inflammatory autoimmune disorder characterized by an exacerbated expression of cytokines and chemokines in different tissues and organs. Renal involvement is a significant contributor to the morbidity and mortality of systemic lupus erythematosus, and its diagnosis is based on renal biopsy, an invasive procedure with a high risk of complications. Therefore, the development of alternative, non-invasive diagnostic tests for kidney disease in patients with systemic lupus erythematosus is a priority. Aim: To evaluate the plasma levels of a panel of cytokines and chemokines using multiplex xMAP technology in a cohort of Colombian patients with active and inactive systemic lupus erythematosus, and to evaluate their potential as biomarkers of renal involvement. Results: Plasma from 40 systemic lupus erythematosus non-nephritis patients and 80 lupus nephritis patients with different levels of renal involvement were analyzed for 39 cytokines using Luminex xMAP technology. Lupus nephritis patients had significantly increased plasma eotaxin, TNF-a, interleukin-17-a, interleukin-10, and interleukin-15 as compared to the systemic lupus erythematosus non-nephritis group. Macrophage-derived chemokine, growth regulated oncogene alpha, and epidermal growth factor were significantly elevated in systemic lupus erythematosus non-nephritis patients when compared to lupus nephritis individuals. Plasma eotaxin levels allowed a discrimination between systemic lupus erythematosus non-nephritis and lupus nephritis patients, for which we performed a receiver operating characteristic curve to confirm. We observed a correlation of eotaxin levels with active nephritis (Systemic Lupus Erythematosus Disease Activity Index). Our data indicate that circulating cytokines and chemokines could be considered good predictors of renal involvement in individuals with systemic lupus erythematosus.eng
dc.identifier.issn09612033
dc.identifier.urihttp://hdl.handle.net/20.500.12442/2356
dc.language.isoengeng
dc.publisherSage Publisingeng
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.licenseLicencia de Creative Commons Reconocimiento-NoComercial-CompartirIgual 4.0 Internacionaleng
dc.sourceRevista Lupusspa
dc.source.urihttps://journals.sagepub.com/doi/full/10.1177/0961203318812679eng
dc.subjectBiomarkerseng
dc.subjectCytokineseng
dc.subjectEotaxineng
dc.subjectLupus nephritiseng
dc.subjectSystemic lupus erythematosuseng
dc.titlePlasma cytokines as potential biomarkers of kidney damage in patients with systemic lupus erythematosuseng
dc.typearticleeng
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