Remission and low disease activity (LDA) prevent damage accrual in patients with systemic lupus erythematosus: results from the Systemic Lupus International Collaborating Clinics (SLICC) inception cohort

被引:41
作者
Francisco Ugarte-Gil, Manuel [1 ,2 ]
Hanly, John [3 ,4 ,5 ]
Urowitz, Murray [6 ]
Gordon, Caroline [7 ]
Bae, Sang-Cheol [8 ,9 ,10 ]
Romero-Diaz, Juanita [11 ]
Sanchez-Guerrero, Jorge [11 ,12 ,13 ]
Bernatsky, Sasha [14 ,15 ]
Clarke, Ann Elaine [16 ]
Wallace, Daniel J. [17 ]
Isenberg, David Alan [18 ]
Rahman, Anisur [18 ]
Merrill, Joan T. [19 ]
Fortin, Paul R. [20 ]
Gladman, Dafna D. [6 ]
Bruce, Ian N. [21 ]
Petri, Michelle [22 ]
Ginzler, Ellen M. [23 ]
Dooley, Mary Anne [24 ]
Ramsey-Goldman, Rosalind [25 ,26 ]
Manzi, Susan [27 ]
Jonsen, Andreas [28 ]
van Vollenhoven, Ronald F. [29 ]
Aranow, Cynthia [30 ]
Mackay, Meggan [30 ]
Ruiz-Irastorza, Guillermo [31 ]
Lim, Sam [32 ]
Inanc, Murat [33 ]
Kalunian, Ken [34 ]
Jacobsen, Soren [35 ]
Peschken, Christine [36 ,37 ]
Kamen, Diane L. [38 ]
Askanase, Anca [39 ]
Pons-Estel, Bernardo A. [40 ]
Alarcon, Graciela S. [41 ,42 ]
机构
[1] Univ Cient Sur, Grp Peruano Estudio Enfermedades Autoinmunes Sist, Lima, Peru
[2] Hosp Nacl Guillermo Almenara Irigoyen, EsSalud, Rheumatol, Lima, Peru
[3] Queen Elizabeth 2 Hlth Sci Ctr, Dept Med, Div Rheumatol, Halifax, NS, Canada
[4] Queen Elizabeth 2 Hlth Sci Ctr, Dept Pathol, Halifax, NS, Canada
[5] Dalhousie Univ, Halifax, NS, Canada
[6] Univ Toronto, Toronto Western Hosp, Schroeder Arthrit Inst, Krembil Res Inst, Toronto, ON, Canada
[7] Univ Birmingham, Coll Med & Dent Sci, Inst Inflammat & Ageing, Rheumatol Res Grp, Birmingham, W Midlands, England
[8] Hanyang Univ Hosp Rheumat Dis, Seoul, South Korea
[9] Hanyang Univ, Inst Rheumatol Res, Seoul, South Korea
[10] Hanyang Univ, Inst Biosci & Biotechnol, Seoul, South Korea
[11] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Inmunol & Reumatol, Mexico City, DF, Mexico
[12] Univ Toronto, Sinai Hlth Syst, Toronto, ON, Canada
[13] Univ Toronto, Univ Hlth Network, Div Rheumatol, Toronto, ON, Canada
[14] McGill Univ, Div Rheumatol, Montreal, PQ, Canada
[15] McGill Univ, Div Clin Epidemiol, Montreal, PQ, Canada
[16] Univ Calgary, Cumming Sch Med, Div Rheumatol, Calgary, AB, Canada
[17] Univ Calif Los Angeles, David Geffen Sch Med, Cedars Sinai, Los Angeles, CA 90095 USA
[18] UCL, Med, London, England
[19] Oklahoma Med Res Fdn, Dept Clin Pathol, 825 NE 13th St, Oklahoma City, OK 73104 USA
[20] CHU Quebec Univ Laval, Ctr ARThrite, Rheumatol, Quebec City, PQ, Canada
[21] Univ Manchester, Manchester Acad Hlth Sci Ctr, Fac Biol Med & Hlth, Manchester, Lancs, England
[22] Johns Hopkins Univ, Sch Med, Div Rheumatol, Baltimore, MD USA
[23] Suny Downstate Med Ctr, Dept Med, Brooklyn, NY 11203 USA
[24] Univ N Carolina, Thurston Arthrit Res Ctr, Chapel Hill, NC 27515 USA
[25] Northwestern Univ, Dept Med, Div Rheumatol, Chicago, IL 60611 USA
[26] Feinberg Sch Med, Chicago, IL 60611 USA
[27] Allegheny Hlth Network, Lupus Ctr Excellence, Pittsburgh, PA USA
[28] Lund Univ, Dept Clin Sci Lund, Rheumatol, Lund, Sweden
[29] Amsterdam Univ Med Ctr, Dept Rheumatol, Amsterdam, Netherlands
[30] Feinstein Inst Med Res, Northwell Hlth Manhasset, Manhasset, NY USA
[31] Univ Basque Country, BioCruces Bizkaia Hlth Res Inst, Autoimmune Dis Res Unit, Balakaldo, Spain
[32] Emory Univ, Sch Med, Div Rheumatol, Atlanta, GA USA
[33] Istanbul Univ, Istanbul Med Fac, Dept Internal Med, Div Rheumatol, Istanbul, Turkey
[34] Univ Calif San Diego, Sch Med, La Jolla, CA 92093 USA
[35] Univ Copenhagen, Rigshosp, Copenhagen Res Ctr Autoimmune Connect Tissue Dis, Copenhagen, Denmark
[36] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[37] Univ Manitoba, Dept Community Hlth Sci, Winnipeg, MB, Canada
[38] Med Univ South Carolina, Div Rheumatol, Charleston, SC 29425 USA
[39] Columbia Univ, Irving Med Ctr, New York, NY USA
[40] Ctr Reg Enfermedades Autoinmunes & Reumat GO CREA, Rosario, Argentina
[41] Univ Alabama Birmingham, Heersink Sch Med, Birmingham, AL USA
[42] Univ Peruana Cayetano Heredia, Fac Med, Lima, Peru
基金
新加坡国家研究基金会; 英国惠康基金;
关键词
systemic lupus erythematosus; outcome assessment; health care; epidemiology; PHYSICIAN GLOBAL ASSESSMENT; ACTIVITY STATE; PROLONGED REMISSION; INITIAL VALIDATION; CAUCASIAN PATIENTS; PREVALENCE; LUMINA; SLE; DEFINITIONS; PREDNISONE;
D O I
10.1136/ard-2022-222487
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To determine the independent impact of different definitions of remission and low disease activity (LDA) on damage accrual. Methods Patients with >= 2 annual assessments from a longitudinal multinational inception lupus cohort were studied. Five mutually exclusive disease activity states were defined: remission off-treatment: clinical Systemic Lupus Erythematosus Disease Activity Index (cSLEDAI)-2K=0, without prednisone or immunosuppressants; remission on-treatment: cSLEDAI-2K score=0, prednisone <= 5 mg/day and/or maintenance immunosuppressants; low disease activity Toronto cohort (LDA-TC): cSLEDAI-2K score of <= 2, without prednisone or immunosuppressants; modified lupus low disease activity (mLLDAS): Systemic Lupus Erythematosus Disease Activity Index-2K score of 4 with no activity in major organ/systems, no new disease activity, prednisone <= 7.5 mg/day and/or maintenance immunosuppressants; active: all remaining visits. Only the most stringent definition was used per visit. Antimalarials were allowed in all. The proportion of time that patients were in a specific state at each visit since cohort entry was determined. Damage accrual was ascertained with the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI). Univariable and multivariable generalised estimated equation negative binomial regression models were used. Time-dependent covariates were determined at the same annual visit as the disease activity state but the SDI at the subsequent visit. Results There were 1652 patients, 1464 (88.6%) female, mean age at diagnosis 34.2 (SD 13.4) years and mean follow-up time of 7.7 (SD 4.8) years. Being in remission off-treatment, remission on-treatment, LDA-TC and mLLDAS (per 25% increase) were each associated with a lower probability of damage accrual (remission off-treatment: incidence rate ratio (IRR)=0.75, 95% CI 0.70 to 0.81; remission on-treatment: IRR=0.68, 95% CI 0.62 to 0.75; LDA: IRR=0.79, 95% CI 0.68 to 0.92; and mLLDAS: IRR=0.76, 95% CI 0.65 to 0.89)). Conclusions Remission on-treatment and off-treatment, LDA-TC and mLLDAS were associated with less damage accrual, even adjusting for possible confounders and effect modifiers.
引用
收藏
页码:1541 / 1548
页数:8
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