Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13654
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dc.contributor.authorKamanamool N.
dc.contributor.authorIngsathit A.
dc.contributor.authorRattanasiri S.
dc.contributor.authorNgamjanyaporn P.
dc.contributor.authorKasitanont N.
dc.contributor.authorChawanasuntorapoj R.
dc.contributor.authorPichaiwong W.
dc.contributor.authorAnutrakulchai S.
dc.contributor.authorSangthawan P.
dc.contributor.authorOphascharoensuk V.
dc.contributor.authorAvihingsanon Y.
dc.contributor.authorSumethkul V.
dc.date.accessioned2021-04-05T03:25:26Z-
dc.date.available2021-04-05T03:25:26Z-
dc.date.issued2018
dc.identifier.issn9612033
dc.identifier.other2-s2.0-85044406119
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13654-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85044406119&doi=10.1177%2f0961203317739131&partnerID=40&md5=f59b4a94a60bf5ac82e7b58c94ff0c22
dc.description.abstractWe conducted a prospective multicenter, opened-label, parallel, randomized, controlled trial to compare tacrolimus (TAC) and mycophenolate mofetil (MMF) for induction and maintenance therapy in lupus nephritis (LN). Adult patients with biopsy-proven LN International Society of Nephrology/Renal Pathology Society classes III–V and active nephritis were to receive prednisolone (0.7–1.0 mg/kg/day for four weeks of run-in period and tapered) and randomly assigned to receive TAC (0.1 mg/kg/day) or MMF (1.5–2 g/day) as induction therapy for six months. All patients who had remission received azathioprine (AZA) 1–2 mg/kg/day as standard treatment in the maintenance phase. The primary outcome was Systemic Lupus Erythematosus Disease Activity Index-2000 (SLEDAI-2K) at six and 12 months, and the secondary outcomes included renal SLEDAI, non-renal SLEDAI, modified SLEDAI-2K, immunity SLEDAI, and disease activity remission. Eighty-four patients were randomized. One patient who was randomized to the TAC group withdrew from the study immediately after randomization. Therefore, 42 patients received MMF and 41 patients received TAC. Disease activity remission rate and time to disease activity remission were similar in both groups. Twelve patients (28.57%) in the MMF group and 10 patients (24.39%) in the TAC group achieved disease activity remission. For disease activity scores, both regimens significantly improved SLEDAI-2K during induction and maintenance therapy. Overall, SLEDAI-2K score in the MMF group decreased more compared with the TAC group. In the MMF group, mean SLEDAI-2K decreased from 11.6 ± 4.8 to 6.3 ± 3.9 after induction therapy and to 5.4 ± 4.4 after maintenance therapy. In the TAC group, mean SLEDAI-2K decreased from 9.0 ± 3.7 to 6.3 ± 5.1 after induction therapy and to 7.1 ± 5.4 after maintenance therapy. Renal SLEDAI and modified SLEDAI-2K showed a similar pattern with SLEDAI-2K. In non-renal SLEDAI and immunity SLEDAI, both regimens also resulted in decreased disease activity scores during the first two months. After that the scores were slightly increased. In the MMF group, the scores were still lower than baseline but in the TAC group were not. In conclusion, disease activity remission rate was similar in the MMF and TAC groups. For disease activity score as measured by SLEDAI-2K, TAC was comparable with MMF during induction but MMF was more effective on disease activity of active LN classes III and IV at 12 months, especially in the renal system. © 2017, © The Author(s) 2017.
dc.subjectantinuclear antibody
dc.subjectazathioprine
dc.subjectcreatinine
dc.subjectdouble stranded DNA antibody
dc.subjectmycophenolate mofetil
dc.subjectprednisolone
dc.subjectprednisone
dc.subjecttacrolimus
dc.subjectimmunosuppressive agent
dc.subjectmycophenolic acid
dc.subjecttacrolimus
dc.subjectadult
dc.subjectArticle
dc.subjectclinical outcome
dc.subjectcontrolled study
dc.subjectcreatinine blood level
dc.subjectdisease activity
dc.subjectdisease activity score
dc.subjectdisease severity
dc.subjectdrug blood level
dc.subjectdrug dose reduction
dc.subjectfemale
dc.subjecthematuria
dc.subjecthistopathology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectlarge intestine perforation
dc.subjectlupus erythematosus nephritis
dc.subjectmaintenance therapy
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmulticenter study
dc.subjectnocardiosis
dc.subjectopen study
dc.subjectplasmablastic lymphoma
dc.subjectPneumocystis pneumonia
dc.subjectpriority journal
dc.subjectprospective study
dc.subjectproteinuria
dc.subjectrandomized controlled trial
dc.subjectremission
dc.subjectseptic shock
dc.subjectSLEDAI
dc.subjecttreatment outcome
dc.subjectbiopsy
dc.subjectclinical trial
dc.subjectcomparative study
dc.subjectimmunology
dc.subjectKaplan Meier method
dc.subjectlupus erythematosus nephritis
dc.subjectmiddle aged
dc.subjectseverity of illness index
dc.subjectThailand
dc.subjecttime factor
dc.subjectyoung adult
dc.subjectAdult
dc.subjectBiopsy
dc.subjectFemale
dc.subjectHumans
dc.subjectImmunosuppressive Agents
dc.subjectKaplan-Meier Estimate
dc.subjectLupus Nephritis
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectMycophenolic Acid
dc.subjectProspective Studies
dc.subjectRemission Induction
dc.subjectSeverity of Illness Index
dc.subjectTacrolimus
dc.subjectThailand
dc.subjectTime Factors
dc.subjectTreatment Outcome
dc.subjectYoung Adult
dc.titleComparison of disease activity between tacrolimus and mycophenolate mofetil in lupus nephritis: a randomized controlled trial
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationLupus. Vol 27, No.4 (2018), p.647-656
dc.identifier.doi10.1177/0961203317739131
Appears in Collections:Scopus 1983-2021

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