Large-scale mortality gap between SLE and control population is associated with increased infection-related mortality in lupus

Author:

Kedves Melinda1ORCID,Kósa Fruzsina2,Kunovszki Péter2,Takács Péter2,Szabó Melinda Zsuzsanna3,Karyekar Chetan4,Lofland Jennifer H4,Nagy György567

Affiliation:

1. Department of Rheumatology, Hospital of Bács-Kiskun County, Kecskemét

2. Janssen Global Commercial Strategy Organization, Budapest

3. New Saint John Hospital and Outpatient Clinic, Budapest, Hungary

4. Janssen R&D Services, Janssen Global Commercial Organization, Horsham, PA, USA

5. Department of Rheumatology, 3rd Department of Internal Medicine, Semmelweis University, Budapest

6. Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest

7. Department of Rheumatology, Buda Hospital of the Hospitaller Order of Saint John of God, Budapest, Hungary

Abstract

Abstract Objective The aim of the present study was to analyse the incidence, prevalence, mortality and cause of death data of adult SLE patients and matched controls in a full-populational, nationwide, retrospective study. Methods This non-interventional study was based on database research of the National Health Insurance Fund of Hungary. A total of 7888 patients were included in the analyses, within which two subgroups of incident patients were created: the ‘All incident SLE patients’ group consisted of all incident SLE patients (4503 patients), while the ‘Treated SLE patients’ group contained those who received relevant therapy in the first 6 months after diagnosis (2582 patients). Results The median age of the SLE population was found to be 46.5 years (women 85%). The incidence rate was 4.86 and 2.78 per 100 000 inhabitants in the ‘All incident SLE patients’ and ‘Treated SLE patients’ groups, respectively. The standardized mortality ratio was 1.63 and 2.09 in the ‘All incident SLE patients’ and ‘Treated SLE patients’ groups, respectively. Overall survival was significantly lower (P < 0.001) in both groups than in the general population, with hazard ratio = 2.17 in the ‘All incident SLE patients’ group and hazard ratio = 2.75 in the ‘Treated SLE patients’ group. There was no significant difference between SLE and control deaths regarding cerebrovascular conditions as the cause of death. Generally, cancer-related deaths were less common, while haematological cancer and infection-related deaths were more common in SLE patients. Conclusion Infections, especially sepsis, had the largest positive effect on top of the extra mortality of SLE. This highlights that SLE patients are at increased risk of infection-related death.

Funder

Pharmaceutical Companies of Johnson & Johnson

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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