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Abstract Number: 2290

Patterns and Predictors of Clinical Improvement in Patients with Sjögren’s Disease: A Longitudinal Analysis of ESSDAI and ESSPRI Improvements

Alejandro Gómez Gómez1, Sergio H. Martínez Mateu2, Jose Luis Tandaipan3, Monica Fernandez Castro4, Guillermo gonzalez5, Sheila Melchor-Díaz6, Miren Uriarte Ecenarro7, Raúl Menor Almagro8, Paloma Vela Casasempere9, Beatriz Paredes-Romero10, Judit Font-Urgelles11, Paula Estrada-Alarcón12, Sara Manrique-Arija13, Mª Angeles Blazquez Cañamero14, Clara Moriano15, Juan José Alegre-Sancho16, Marina Rodríguez López17, Marta López18, Gema Bonilla19, Rafaela Ortega-Castro20, Sara Maria Rojas Herrera21, Ignacio Braña22, Lilian López-Núñez23, Javier Narváez24, Jose Rosas Gómez de Salazar25, Ruben D. López-Sánchez26, Carles Galisteo Veiga27, Javier Martínez-Ferrin28, Jose Javier Pérez Venegas29, Guadalupe Manzano-Canabal30, Cilia Peralta-Ginés31, Lara Sánchez Bilbao32, José Andrés Román Ivorra33, Rafael Cáliz-Cáliz34, Belén Serrano-Benavente35, Sabela Fernández-Aguado36, Natalia Boix- Martí37, Eric Kirkegaard-Biosca38, Iago Alvarez Saez39, Ares Selles-Rius40, Maribel Pérez41, Juan Cañete42, Sara Marsal1 and Jose Luis Andreu43, 1Vall d'Hebron Hospital Research Institute, Rheumatology Research Group, Barcelona, Spain, 2IMIDomics, Barcelona, Spain, 3Rheumatology. Hospital Universitario de la Santa Creu i Sant Pau, Barcelona, Spain, 4PUERTA DE HIERRO HOSPITAL, Madrid, Spain, 5Hospital Universitario de A Coruña, A Coruña, Spain, 6Hospital Universitario 12 de Octubre, Rheumatology, Madrid, Madrid, 7Hospital Universitario La Princesa, Madrid, Spain, 8Department of Rheumatology, Hospital de Jerez, Spain, Puerto De Santa María, Spain, 9Hospital General Universitario Alicante, Alicante, Comunidad Valenciana, Spain, 10Hospital Universitario Infanta Sofía;Universidad Europea de Madrid. Faculty of Medicine, Health and Sports. Department of Medicine; FIIB HUIS-HUHEN, San Sebastian de los Reyes, Spain, 11Hospital Universitari Germans Trias i Pujol, Badalona, Spain, 12Hospital de San Juan Despí Moisès Broggi, Barcelona, Spain, 13Hospital Regional Universitario Málaga, Malaga, Spain, 14Hospital Ramon y Cajal, Madrid, Spain, 15Hospital León, LEON, Castilla y Leon, Spain, 16Hospital Universitario Doctor Peset, Valencia, Spain, 17Complejo Hospitalario Universitario de Santiago, Rheumatology, Santiago de Compostela., Santiago de Compostela, Spain, 18Complex Hospitalari Universitari Moisés Broggi, Barcelona, Spain, 19Hospital Universitario La Paz, Rheumatology, Madrid, Madrid, Spain, 20Rheumatology service/Maimonides Institute for Research in Biomedicine of Cordoba (IMIBIC)/ Reina Sofia University Hospital/ University of Cordoba, Spain, Cordoba, Andalucia, Spain, 21Hospital de Mérida, Rheumatology, Badajoz, Badajoz, Spain, 22Hospital Universitario Central de Asturias, Oviedo, Spain, 23Hospital Son Llatzer, Rheumatology, Palma de Mallorca, Palma de Mallorca, Spain, 24Hospital Universitario de Bellvitge, Barcelona, Spain, 25Hospital Marina Baixa, PALMA DE MALLORCA, Spain, 26Hospital Universitario de Gran Canaria Dr. Negrín, Gran Canaria, Spain, 27Hospital Parc Taulí, Rheumatology, Sabadell, Sabadell, Spain, 28Hospital Universitario Virgen de la Arrixaca, Rheumatology, Murcia, Murcia, Spain, 29Virgen Macarena University Hospital, Sevilla, Spain, Sevilla, Spain, 30Hospital Virgen de la Concha (Zamora), Zamora, Spain, 31Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain, 32Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Immunopathology Group, Santander, Spain, Santander, Cantabria, Spain, 33Hospital Universitari i Politècnic La Fe, Valencia, Spain, 34Hospital Universitario Virgen de las Nieves, Rheumatology, Granada, Granada, Spain, 35Hospital Gregorio Marañon, Madrid, Spain, 36Hospital Universitario de Pontevedra, Pontevedra, Spain, 37Hospital Univetsitari Vall d'Hebron, Rheumatology Department, Barcelona, Spain, 38Hospital Univetsitari Vall d'Hebron, Ophthalmology Department, Barcelona, Spain, 39Hospital Univetsitari Vall d'Hebron, Maxilofacial Surgery Department, Barcelona, Spain, 40Rheumatology Research Group, Vall d'Hebron University Hospital, Barcelona, Spain, 41IMIDomics, Barcelona, Barcelona, Spain, 42Rheumatology Department, Hospital Clínic and IDIBAPS, Barcelona, Spain, Barcelona, Spain, 43Hospital Universitario Puerta de Hierro, Majadahonda, Spain

Meeting: ACR Convergence 2025

Keywords: Disease Activity, Disease-Modifying Antirheumatic Drugs (Dmards), Sjögren's syndrome

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Session Information

Date: Tuesday, October 28, 2025

Title: (2290–2304) Sjögren’s Disease – Basic & Clinical Science Poster III: Treatment and Trial Outcome Measures

Session Type: Poster Session C

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

Background/Purpose: Assessing clinical improvements in Sjögren’s Disease (SjD) is challenging. Our objective was to describe patterns of improvement in SjD using ESSDAI and ESSPRI indices and identify factors associated with these improvements.

Methods: Patients from the prospective SSAD cohort, which collects biological and clinical data from SjD cases, were included. ESSDAI improvement (ESSDAI-I) was defined by improvement in ≥1 ESSDAI domain (transition from high (H) or moderate (M) to low (L) or no activity (NA) in most domains; from M to L or NA in the glandular domain; and from H to M or NA in the CNS domain) without worsening in any other. ESSPRI improvement (ESSPRI-I) was defined as a reduction ≥2 points or ≥30% from baseline.Patients were classified as improvers if improvement between two visits (3 months apart) was maintained at a subsequent visit 3 months later; the visit preceding improvement was considered baseline. Non-improvers (NI) were defined as patients with baseline ESSDAI or ESSPRI >0 but without observed improvement.Among ESSDAI-I patients, clinical (ClinESSDAI) and isolated biological improvements were analyzed separately. As not all patients received therapeutic interventions at baseline, analyses were conducted for the entire cohort and separately for a subgroup initiating rituximab (RTX) at baseline.Logistic regression models assessed the association of clinical variables with improvement status, adjusting for sex, age, disease duration, and baseline ESSDAI and ESSPRI scores. Fisher’s exact test and Kruskal–Wallis tests were used for categorical and continuous variables, respectively. Unadjusted p-values < 0.05 were considered statistically significant. Analyses were performed using R v4.4.

Results: A total of 363 patients susceptible to improvement were analyzed. Improvement was observed in 30 patients (8.3%): 15 (4.1%) showed ESSDAI-I, 14 (3.86%) ESSPRI-I, and 1 patient (0.27%) showed simultaneous improvement in ESSDAI and ESSPRI. Four of the 16 ESSDAI-I cases improved only in the biological domain.Overall improvement (ESSDAI or ESSPRI) was positively associated with higher baseline biological domain scores, initiation of RTX at baseline, and improvements in hypergammaglobulinemia and Schirmer’s test, but negatively with elevated β2-microglobulin (B2M).ESSDAI-I patients showed higher baseline scores in articular, biological, and glandular domains and more frequent RTX or MTX initiation than NI patients. Negative associations were noted with low C3 levels and cryoglobulinemia.ESSPRI-I was positively associated with RTX initiation, higher peripheral nervous system domain and lower articular domain scores. ESSDAI-I patients had significantly higher baseline articular domain scores compared to ESSPRI-I patients.In patients initiating RTX therapy, higher baseline biological scores predicted improvement, and Ro52 positivity trended toward significance.

Conclusion: ESSDAI and ESSPRI improvements rarely coincided in our cohort. Higher baseline biological and articular domain scores predicted ESSDAI improvement. Initiation of RTX strongly correlated with improvement, whereas elevated B2M, low C3 levels, and cryoglobulinemia negatively predicted improvement.

Supporting image 1Table 1

Supporting image 2Table 2

Supporting image 3Table 3


Disclosures: A. Gómez Gómez: None; S. Martínez Mateu: None; J. Tandaipan: None; M. Fernandez Castro: None; G. gonzalez: None; S. Melchor-Díaz: None; M. Uriarte Ecenarro: None; R. Menor Almagro: None; P. Vela Casasempere: None; B. Paredes-Romero: None; J. Font-Urgelles: None; P. Estrada-Alarcón: None; S. Manrique-Arija: None; M. Blazquez Cañamero: Astrazeneca, 12, conference registrations, Gsk, 6, Novartis, 12, conference registrations, Rubio, 12, conference registrations; C. Moriano: None; J. Alegre-Sancho: None; M. Rodríguez López: None; M. López: None; G. Bonilla: None; R. Ortega-Castro: None; S. Rojas Herrera: None; I. Braña: None; L. López-Núñez: None; J. Narváez: None; J. Rosas Gómez de Salazar: None; R. López-Sánchez: None; C. Galisteo Veiga: None; J. Martínez-Ferrin: None; J. Pérez Venegas: AstraZeneca, 6, Janssen, 4, 6, UCB, 6; G. Manzano-Canabal: None; C. Peralta-Ginés: None; L. Sánchez Bilbao: AbbVie/Abbott, 6, Eli Lilly, 6, Janssen, 6, UCB, 6; J. Andrés Román Ivorra: AstraZeneca, 6, GSK, 6, UCB, 6; R. Cáliz-Cáliz: None; B. Serrano-Benavente: None; S. Fernández-Aguado: None; N. Boix- Martí: None; E. Kirkegaard-Biosca: None; I. Alvarez Saez: None; A. Selles-Rius: None; M. Pérez: None; J. Cañete: None; S. Marsal: AbbVie/Abbott, 5, Bristol-Myers Squibb(BMS), 5, Eli Lilly, 1, 5, IMIDomics, 4, 8, Janssen, 5, Merck/MSD, 5, Novartis, 5, Roche, 5, UCB, 5; J. Andreu: None.

To cite this abstract in AMA style:

Gómez Gómez A, Martínez Mateu S, Tandaipan J, Fernandez Castro M, gonzalez G, Melchor-Díaz S, Uriarte Ecenarro M, Menor Almagro R, Vela Casasempere P, Paredes-Romero B, Font-Urgelles J, Estrada-Alarcón P, Manrique-Arija S, Blazquez Cañamero M, Moriano C, Alegre-Sancho J, Rodríguez López M, López M, Bonilla G, Ortega-Castro R, Rojas Herrera S, Braña I, López-Núñez L, Narváez J, Rosas Gómez de Salazar J, López-Sánchez R, Galisteo Veiga C, Martínez-Ferrin J, Pérez Venegas J, Manzano-Canabal G, Peralta-Ginés C, Sánchez Bilbao L, Andrés Román Ivorra J, Cáliz-Cáliz R, Serrano-Benavente B, Fernández-Aguado S, Boix- Martí N, Kirkegaard-Biosca E, Alvarez Saez I, Selles-Rius A, Pérez M, Cañete J, Marsal S, Andreu J. Patterns and Predictors of Clinical Improvement in Patients with Sjögren’s Disease: A Longitudinal Analysis of ESSDAI and ESSPRI Improvements [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/patterns-and-predictors-of-clinical-improvement-in-patients-with-sjogrens-disease-a-longitudinal-analysis-of-essdai-and-esspri-improvements/. Accessed .
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