ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1491

Feasibility of Extrarenal Systemic Lupus Erythematosus Disease Modification in GLADEL 2.0, a Latin American Cohort

julián Barahona-correa1, Santiago Bernal-Macías2, Daniel Fernandez3, Óscar Muñoz2, Lucia Hernández4, Erika Susana Palacios Santillan5, Laura Maurelli6, Paula Alba7, Veronica Saurit8, Lucila Garcia9, María Emilia Sattler10, Maria Constanza Bertolaccini11, Marina Laura Micelli12, Graciela Gomez13, Micaela A. Cosatti14, Ana Carolina Ralle15, Joaquín Martinez Serventi16, Ana Silva17, ODIRLEI MONTICIELO18, Ángela Luzia Branco Pinto Duarte19, Laíssa Cristina Alves Alvino20, Eduardo Borba21, Eloisa Bonfa21, Edgard dos Reis-Neto22, Iris Guerra Herrera23, Milena Mimica24, Gustavo Aroca Martínez25, Lorena Gómez Escorcia26, Carlos Alberto Cañas27, Gerardo Quintana-Lopez28, Carlos Toro-Gutierrez29, José Maximiliano Martínez Pérez30, Reyna Elizabeth Sánchez-Briones31, Mario Pérez Cristóbal32, Eduardo Martin-Nares33, Yaneli Juarez-Vicuña34, Ignacio García-Valladares35, Rodrigo Ortiz Hernández36, Jorge Antonio Esquivel Valerio37, Maria Isabel Acosta38, Astrid Paats39, Jorge Cieza Calderón40, Manuel Ugarte-Gil41, Armando Calvo42, Rodamin Ambiorix Alvarez Santana43, Analía Cánepa44, Carina Pizzarossa44, Federico Zazzetti45, Ashley Orillion46 and Cristina Drenkard47, 1Colombian Association of Rheumatology (ASOREUMA), Bogotá, Colombia; Hospital Universitario San Ignacio, Bogotá, Colombia, Bogotá, Colombia, 2Hospital Universitario San Ignacio, Bogotá, Colombia, Bogotá, Colombia, 3Facultad de Medicina, Pontificia Universidad Javeriana, Bogotá, Colombia; Departamento de Medicina Interna, Unidad de Reumatología, Hospital Universitario San Ignacio, Bogotá, Colombia, BOGOTA, Colombia, 4Centro Regional de Enfermedades Autoinmunes y Reumáticas (GO-CREAR), Rosario, Argentina, Rosario, Argentina, 5Hospital Italiano de Buenos Aires, Buenos Aires, Argentina, Buenos Aires, Argentina, 6Hospital Italiano de Córdoba, Córdoba, Argentina, Córdoba, Argentina, 7Hospital Córdoba y Sanatorio Allende, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Córdoba, Argentina, Cordoba, Argentina, 8Hospital Privado Universitario de Cordoba, Córdoba, Argentina, Córdoba, Argentina, 9Hospital San Martin de La Plata, La Plata, Argentina, La Plata, Argentina, 10Sanatorio Británico, Rosario, Argentina, Rosario, Argentina, 11Hospital Ángel C. Padilla, Tucumán, Argentina, Tucumán, Argentina, 12Hospital J.M Ramos Mejía, Buenos Aires, Argentina, Buenos Aires, 13Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Buenos Aires, Argentina, Buenos Aires, Argentina, 14CEMIC Centro de Educación Médica e Investigaciones Clínicas ‘‘Norberto Quirno,’’ Buenos Aires, Argentina, Buenos Aires, Argentina, 15Hospital Señor del Milagro Salta, Salta, Argentina, Salta, Argentina, 16Hospital General de Agudos Dr. Juan A. Fernández, Buenos Aires, Argentina, Buenos Aires, Argentina, 17Hospital das Clinicas da Universidade Federal de Goias, Goiania, Brazil, Goiania, Brazil, 18Hospital de Clínicas de Porto Alegre, Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brazil, PORTO ALEGRE, Rio Grande do Sul, Brazil, 19Universidad Federal de Pernambuco, Recife, Brazil, Recife, Brazil, 20Hospital Universitário Pedro Ernesto - Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil, Rio de Janeiro, Brazil, 21Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, São Paulo, Brazil, 22Escola Paulista de Medicina / Universidade federal de São Paulo (EPM / Unifesp), São Paulo, Brazil, São Paulo, Brazil, 23Hospital del Salvador Santiago de Chile, Santiago, Chile, Santiago, Chile, 24Facultad de Medicina y Ciencia, Universidad San Sebastián, Santiago, Chile, Santiago, Chile, 25Universidad Simón Bolívar, Barranquilla, Colombia y Clínica de la Costa, Barranquilla, Colombia, 26Clínica de la Costa y Universidad Simón Bolívar Barranquilla, Barranquilla, Colombia, Barranquilla, Colombia, 27Fundación Valle del Lili, Universidad Icesi, Cali, Colombia, Cali, Colombia, 28Facultad de Medicina, Universidad Nacional de Colombia; Hospital Universitario Fundación Santa Fe de Bogotá; Hospital Universitario Nacional de Colombia, Bogotá, Colombia, Bogotá, Colombia, 29Pontificia Universidad Javeriana de Cali, Cali, Colombia, Cali, Colombia, 30Universidad de Especialidades Espíritu Santo, Guayaquil, Ecuador, Guayaquil, Ecuador, 31Hospital de Especialidades Dr. Antonio Fraga Mouret, Centro Médico Nacional La Raza, Instituto Mexicano del Seguro Social, Mexico City, Mexico, Mexico City, Mexico, 32Hospital de Especialidades del Centro Médico Nacional SXXI, Instituto Mexicano del Seguro Social (IMSS), Mexico City, Mexico, Mexico City, Mexico, 33Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, Mexico City, Mexico, 34Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico, Mexico City, Mexico, 35Centro de Estudios de Investigación Básica y Clínica, S.C., Guadalajara, Mexico, Guadalajara, Mexico, 36Facultad de Medicina de la Universidad Autónoma de San Luis Potosí y Hospital Central "Dr. Ignacio Morones Prieto," San Luis Potosi, Mexico, San Luis Potosi, Mexico, 37Universidad Autónoma de Nuevo León, Rheumatology Service, Hospital Universitario "Dr. José Eleuterio González", Monterrey, Nuevo León, México., MONTERREY, Mexico, 38Facultad de Ciencias Medicas, Universidad Nacional de Asunción, San Lorenzo, Paraguay, Asuncion, Paraguay, 39Facultad de Ciencias Medicas, Universidad Nacional de Asunción, San Lorenzo, Paraguay, Asunción, Paraguay, 40Hospital Nacional Edgardo Rebagliati Martins-EsSalud, Lima, Peru, Lima, Peru, 41Grupo Peruano de Estudio de Enfermedades Autoinmunes Sistémicas, Universidad Científica del Sur, Lima, Peru; Hospital Guillermo Almenara Irigoyen, EsSalud, Lima, Peru, Lima, Peru, 42Hospital Nacional Cayetano Heredia Universidad Peruana Cayetano Heredia, Lima, Peru, Jesús María, Peru, 43Hospital Docente Padre Billini, Santo Domingo, Distrito Nacional, Dominican Republic, 44Hospital de Clínicas, Facultad de Medicina, UDELAR, Montevideo, Uruguay, Montevideo, Uruguay, 45Johnson & Johnson, Horsham, PA, USA, Ambler, PA, 46Johnson & Johnson, Spring House, PA, USA, Spring House, PA, 47Rollins School of Public Health, Emory University, Atlanta, Georgia, USA, Acworth, GA

Meeting: ACR Convergence 2025

Keywords: Cohort Study, Disease Activity, socioeconomic factors, Systemic lupus erythematosus (SLE)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Monday, October 27, 2025

Title: (1467–1516) Systemic Lupus Erythematosus – Diagnosis, Manifestations, & Outcomes Poster II

Session Type: Poster Session B

Session Time: 10:30AM-12:30PM

Background/Purpose: The concept of disease modification (DM) has been recently introduced to improve the long-term care of patients (pts) with SLE. DM is defined as ‘the minimization of disease activity with the fewest treatment (tx)-associated toxicities and slowing/preventing organ damage progression.’ To claim DM ultimately requires delayed or prevented progression of organ damage beyond 5 years. The concept of DM is valuable for assessing ‘whether an intervention is on track for achieving DM at the 5-year mark,’ based on interim evaluations during the first 5 years. Latin American pts with SLE are prone to poorer outcomes, which are associated with both disease severity and social determinants of health (SDH). This preliminary study evaluates the prevalence of extrarenal DM in Latin American pts with SLE and examines differences in SDH and tx between those who did and did not achieve extrarenal DM.

Methods: GLADEL 2.0 is a longitudinal cohort assessing the incidence and prevalence of SLE. Forty-three centers from 10 Latin-American countries enrolled pts ≥18 years of age who fulfilled the 1982/1997 ACR and/or the 2012 Systemic Lupus International Collaborating Clinics (SLICC) classification criteria for SLE. The composite definition of DM for extrarenal SLE included: (i) a significant reduction in SLE Disease Activity Index (SLEDAI; >3 points), (ii) no severe flares, and (iii) ≤10 mg/day of prednisone for months 0–12 and ≤5 mg/day prednisone-equivalent for years 2–5. Pts with complete data at baseline, 12, 24, 36, 48, and 60 months were analyzed. We compared baseline SDH and exposure to medications between pts who did and did not achieve DM criteria over time.

Results: Among 1083 pts who entered the GLADEL 2.0 cohort, 709 had the baseline data needed to fulfill DM criteria. Table 1 shows differences in demographic and SDH data by extrarenal DM achievement groups over time. Data from month 60 were not analyzed as data were available for only 64 pts. Although educational attainment varied between groups and genders at each time point, a higher proportion of pts achieved DM among men compared to women at the 36 and 48-month marks. Overall, the proportion of pts achieving DM criteria ranged between 16%–20% across time points (Fig 1a). Figure 1b shows DM trajectories during follow-up. Medication exposure is depicted in Fig 2. A higher number of pts achieving extrarenal DM at months 36 and 48 received cyclophosphamide.

Conclusion: In this preliminary investigation, up to 20% of Latin American pts with SLE achieved extrarenal DM. The study highlights critical disparities, indicating that pts with lower educational attainment and women were less likely to achieve DM. Our findings suggest that specific medication exposure plays a significant role in extrarenal DM achievement, particularly with medications like cyclophosphamide. These results underscore the importance of addressing SDH and tailoring tx strategies to improve outcomes for marginalized groups within this population. Continued research is essential to discern the independent contributions of SDH and different tx modalities on achieving extrarenal DM, ultimately aiming to enhance long-term care and pt quality of life.

Supporting image 1Table 1. Baseline sociodemographics and their differences among patients with SLE who did and did not achieve extrarenal disease modification over time

Supporting image 2Figure 1. Percentage of patients achieving potential for extrarenal SLE disease modification (A) and disease modification trajectory (B)

Supporting image 3Figure 2. Medication exposure in patients who did (A) and (B) did not achieve DM


Disclosures: j. Barahona-correa: Colombian Association of Rheumatology (ASOREUMA), 12, Supported by the Colombian Association of Rheumatology (ASOREUMA); S. Bernal-Macías: None; D. Fernandez: None; Ó. Muñoz: None; L. Hernández: None; E. Palacios Santillan: None; L. Maurelli: None; P. Alba: None; V. Saurit: None; L. Garcia: None; M. Sattler: None; M. Bertolaccini: None; M. Micelli: None; G. Gomez: None; M. Cosatti: None; A. Ralle: None; J. Serventi: None; A. Silva: AstraZeneca, 6, GSK, 6; O. MONTICIELO: None; Á. Duarte: None; L. Alves Alvino: None; E. Borba: Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (303378/2022-0), 5, GlaxoSmithKlein(GSK), 5; E. Bonfa: Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) #305242/2019-9, 5, Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) (2022/12925-8), 5, GlaxoSmithKlein(GSK), 5; E. dos Reis-Neto: None; I. Guerra Herrera: None; M. Mimica: None; G. Aroca Martínez: None; L. Gómez Escorcia: None; C. Cañas: None; G. Quintana-Lopez: None; C. Toro-Gutierrez: None; J. Martínez Pérez: None; R. Sánchez-Briones: None; M. Pérez Cristóbal: None; E. Martin-Nares: None; Y. Juarez-Vicuña: None; I. García-Valladares: None; R. Hernández: None; J. Esquivel Valerio: None; M. Acosta: None; A. Paats: None; J. Calderón: None; M. Ugarte-Gil: AstraZeneca, 2, 6, Ferrer, 2, 6, GSK, 2, 6, Johnson & Johnson, 5, Novartis, 2, 6, Tecnofarma, 2, 6; A. Calvo: None; R. Alvarez Santana: None; A. Cánepa: None; C. Pizzarossa: None; F. Zazzetti: Johnson & Johnson, 3, 11; A. Orillion: Johnson & Johnson, 3, 11; C. Drenkard: None.

To cite this abstract in AMA style:

Barahona-correa j, Bernal-Macías S, Fernandez D, Muñoz Ó, Hernández L, Palacios Santillan E, Maurelli L, Alba P, Saurit V, Garcia L, Sattler M, Bertolaccini M, Micelli M, Gomez G, Cosatti M, Ralle A, Serventi J, Silva A, MONTICIELO O, Duarte Á, Alves Alvino L, Borba E, Bonfa E, dos Reis-Neto E, Guerra Herrera I, Mimica M, Aroca Martínez G, Gómez Escorcia L, Cañas C, Quintana-Lopez G, Toro-Gutierrez C, Martínez Pérez J, Sánchez-Briones R, Pérez Cristóbal M, Martin-Nares E, Juarez-Vicuña Y, García-Valladares I, Hernández R, Esquivel Valerio J, Acosta M, Paats A, Calderón J, Ugarte-Gil M, Calvo A, Alvarez Santana R, Cánepa A, Pizzarossa C, Zazzetti F, Orillion A, Drenkard C. Feasibility of Extrarenal Systemic Lupus Erythematosus Disease Modification in GLADEL 2.0, a Latin American Cohort [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/feasibility-of-extrarenal-systemic-lupus-erythematosus-disease-modification-in-gladel-2-0-a-latin-american-cohort/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2025

ACR Meeting Abstracts - https://acrabstracts.org/abstract/feasibility-of-extrarenal-systemic-lupus-erythematosus-disease-modification-in-gladel-2-0-a-latin-american-cohort/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology