Circulating anti-citrullinated peptide antibodies, cytokines and genotype as biomarkers of response to disease-modifying antirheumatic drug therapy in early rheumatoid arthritis

dc.contributor.authorAlly, Mahmood Moosa Tar Mahomed
dc.contributor.authorHodkinson, Bridget
dc.contributor.authorMeyer, Pieter Willem Adriaan
dc.contributor.authorMusenge, Eustasius
dc.contributor.authorTintinger, Gregory Ronald
dc.contributor.authorTikly, Mohammed
dc.contributor.authorAnderson, Ronald
dc.date.accessioned2015-09-02T05:12:21Z
dc.date.available2015-09-02T05:12:21Z
dc.date.issued2015-05-29
dc.descriptionAdditional file 1: Table S1. SDAI (Simplified disease activity index) base line disease activity. Table S2. changes in SDAI and circulating biomarker concentrations following 6 months of synthetic DMARD therapy. Table S3. SDAI (Simplified disease activity index) response at 6 months. Table S4. SDAI (Simplified disease activity index) response at 6 months treatment sub-groups. Table S5. SDAI (Simplified disease activity index) response at 6 months risk allele sub-groups.en_ZA
dc.description.abstractBACKGROUND : To measure circulating anti-citrullinated peptide antibodies (ACPA) and cytokines pre- and 6 months post-therapy as a strategy to predict and optimize responses to traditional disease-modifying antirheumatic drugs (DMARDs) in early RA, which is an unmet need in developing countries. PATIENTS AND METHODS : A cohort of 140 predominantly (88.5 %) black female South African patients with early RA was treated with synthetic DMARDs, mostly methotrexate (MTX) alone, or in combination with low-dose oral corticosteroids (CS). Circulating ACPA and a panel of circulating cytokines/chemokines/growth factors were measured at baseline and after 6 months of therapy in relation to disease activity and Shared Epitope (SE). RESULTS : Following 6 months of therapy, the median simplified disease activity index (SDAI) declined from a baseline of 41.4 to 16.0 (p = 0.0001) for the entire cohort, which was paralleled by significant falls in median serum ACPA levels (516.6 vs. 255.7 units/ml, p = <0.0001) and several of the circulating cytokines (IL-4, IL-7, IL-8, G-CSF, VEGF; p < 0.0010 – p < 0.0001) which were most evident in the subgroup of patients treated with a combination of MTX and CS. Although biomarker concentrations decreased most notably in the low-disease activity group post-therapy, no significant correlations between these biomarkers and disease activity were observed, Baseline ACPA levels, but not SDAI or cytokines, were significantly higher in the subgroup of risk allele-positive patients (561.1 vs. 331.9 units/ml, p < 0.05), while no associations with ACPA and a smoking history were evident. CONCLUSIONS : The use of DMARDs in RA is associated with significant decreases in ACPA and cytokines which did not correlate with changes in SDAI, precluding the utility of serial measurement of these biomarkers to monitor early responses to therapy, but may have prognostic value.en_ZA
dc.description.librarianam2015en_ZA
dc.description.sponsorshipThe South African Medical Research Council and the National Health Laboratory Service Research Trust of South Africa.en_ZA
dc.description.urihttp://www.biomedcentral.com/bmcmusculoskeletdisorden_ZA
dc.identifier.citationAlly, MMTM, Hodkinson, B, Meyer, PWA, Musenge, E, Tintinger, GR, Tikly, M & Anderson, R 2015, 'Circulating anti-citrullinated peptide antibodies, cytokines and genotype as biomarkers of response to disease-modifying antirheumatic drug therapy in early rheumatoid arthritis', BMC Musculoskeletal Disorders, vol. 16, art. no. 130, pp. 1-9.en_ZA
dc.identifier.issn1471-2474
dc.identifier.other10.1186/s12891-015-0587-1
dc.identifier.urihttp://hdl.handle.net/2263/49685
dc.language.isoenen_ZA
dc.publisherBioMed Centralen_ZA
dc.rights© 2015 Ally et al.; licensee BioMed Central. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.en_ZA
dc.subjectAnticyclic citrullinated peptide antibodiesen_ZA
dc.subjectCytokinesen_ZA
dc.subjectShared epitopeen_ZA
dc.subjectDisease modifying antirheumatic drugsen_ZA
dc.subjectRheumatoid arthritisen_ZA
dc.titleCirculating anti-citrullinated peptide antibodies, cytokines and genotype as biomarkers of response to disease-modifying antirheumatic drug therapy in early rheumatoid arthritisen_ZA
dc.typeArticleen_ZA

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