Mortality risk factors in primary Sjögren syndrome: a real-world, retrospective, cohort study.

Background

What baseline predictors would be involved in mortality in people with primary Sjögren syndrome (SjS) remains uncertain. This study aimed to investigate the baseline characteristics collected at the time of diagnosis of SjS associated with mortality and to identify mortality risk factors for all-cause death and deaths related to systemic SjS activity measured by the ESSDAI score.

Methods

In this international, real-world, retrospective, cohort study, we retrospectively collected data from 27 countries on mortality and causes of death from the Big Data Sjögren Registry. Inclusion criteria consisted of fulfilling 2002/2016 SjS classification criteria, and exclusion criteria included chronic HCV/HIV infections and associated systemic autoimmune diseases. A statistical approach based on a directed acyclic graph was used, with all-cause and Sjögren-related mortality as primary endpoints. The key determinants that defined the disease phenotype at diagnosis (glandular, systemic, and immunological) were analysed as independent variables.

Findings

Between January 1st, 2014 and December 31, 2023, data from 11,372 patients with primary SjS (93.5% women, 78.4% classified as White, mean age at diagnosis of 51.1 years) included in the Registry were analysed. 876 (7.7%) deaths were recorded after a mean follow-up of 8.6 years (SD 7.12). Univariate analysis of prognostic factors for all-cause death identified eight Sjögren-related variables (ocular and oral tests, salivary biopsy, ESSDAI, ANA, anti-Ro, anti-La, and cryoglobulins). The multivariate CPH model adjusted for these variables and the epidemiological features showed that DAS-ESSDAI (high vs no high: HR = 1.68; 95% CI, 1.27-2.22) and cryoglobulins (positive vs negative: HR = 1.72; 95% CI, 1.22-2.42) were independent predictors of all-cause death. Of the 640 deaths with available information detailing the specific cause of death, 14% were due to systemic SjS. Univariate analysis of prognostic factors for Sjögren-cause death identified five Sjögren-related variables (oral tests, clinESSDAI, DAS-ESSDAI, ANA, and cryoglobulins). The multivariate competing risks CPH model adjusted for these variables and the epidemiological features showed that oral tests (abnormal vs normal results: HR = 1.38; 95% CI, 1.01-1.87), DAS-ESSDAI (high vs no high: HR = 1.55; 95% CI, 1.22-1.96) and cryoglobulins (positive vs negative: HR = 1.52; 95% CI, 1.16-2) were independent predictors of SjS-related death.

Interpretation

The key mortality risk factors at the time of SjS diagnosis were positive cryoglobulins and a high systemic activity scored using the ESSDAI, conferring a 2-times increased risk of all-cause and SjS-related death. ESSDAI measurement and cryoglobulin testing should be considered mandatory when an individual is diagnosed with SjS.

Funding

Novartis.

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

AR and ADF received the following Grant sor Contracts: R01 DE018209/DE/NIDCR NIH HHS/United States; U54 GM104938/GM/NIGMS NIH HHS/United States; P30 AR053483/AR/NIAMS NIH HHS/United States; P50 AR060804/AR/NIAMS NIH HHS/United States; R01 AR065953/AR/NIAMS NIH HHS/United States. ADF received the following Grants: R01 AR074310/NIAMS NIH HHS/United States; Janssen Research and Development, LLC. ADF reported the following patent: Antibody Tests for Identifying Ro Negative Sjögren's Syndrome and Use as Biomarkers for Dysregulated B Cell Responses, B Cell Lymphoma, Tissue Fibrosis and Salivary Gland Dysfunction. U.S. Patent application 17/797,619, filed August 4, 2022, European Patent application 21750408.3, filed September 14, 2022 and Canadian Patent application, filed September 14, 2022. FA received Grants from Pfizer & Novartis, payments or honoraria from Abbvie, Pfizer, Galapagos, Novartis, BMS, Boeringher, Janssen, and participated on Safety/Advisory Boards of Janssen and Boeringher. MR participated on Safety/Advisory Boards by Janssen and in clinical trials (BMS, Novartis, Servier). PO participated on Safety/Advisory Boards by Fresenius Kabi, Novartis & Boehringer Ingelheim. RG received Grants from Pfizer and Abbvie, payments/honoraria from Abbvie, Pfizer, MSD, Novartis, BMS and Boeringher, and participated on Safety/Advisory Boards by Abbvie, Pfizer, and Boeringher. SR participated on Safety/Advisory Boards by Janssen. TM declared that is working as medical advisor for UCB Pharma Sweden. VCR declared that is working as medical advisor for UCB Pharma Sweden. All other authors declare no competing interests.