All-cause and Cause-specific Mortality in Systemic Lupus Erythematosus: A Population-based Study

Rheumatology ◽  
2021 ◽  
Author(s):  
Bahar Moghaddam ◽  
Shelby Marozoff ◽  
Lingyi Li ◽  
Eric C Sayre ◽  
J Antonio Aviña Zubieta

Abstract Objective To investigate all-cause and cause-specific mortality in SLE patients between two time periods, 1997-2005 and 2006-2014. Methods We used an administrative health database from the province of British Columbia, Canada to match all incident SLE patients to 10 non-SLE individuals on sex, age and index date. Cohorts were divided into two sub-groups, according to diagnosis year: early cohort 1997-2005 and late cohort 2006-2014. The outcome was death (all-cause, renal disease, cancer, infection, cardiovascular disease (CVD), and other). Hazard ratios (HR and 95% confidence intervals) were estimated using univariate and multivariable Cox models. Results Among 6,092 SLE patients and 60,920 non-SLE individuals, there were 451 and 1,910 deaths, respectively. The fully-adjusted all-cause mortality HR (95% CI) in the overall SLE cohort was 1.85 (1.66-2.06), with no statistically significant improvement between early and late cohorts (1.95 (1.69-2.26) versus 1.74 (1.49-2.04). There was excess mortality from renal disease (3.04 (2.29-4.05)), infections (2.74 (2.19-3.43)) and CVD (2.05 (1.77-2.38)), but not cancer (1.18 (0.96-1.46)), in the overall SLE cohort. There was no statistically significant improvement in cause-specific mortality between early and late cohorts for renal disease (3.57 (2.37-5.36) versus 2.65 (1.78-3.93)), infection (2.94 (2.17-3.98) versus 2.54 (1.84-3.51)), and CVD (1.95 (1.60-2.38) versus 2.18 (1.76-2.71)). There was no increase in cancer-related mortality in either cohort (1.27 (0.96-1.69) versus 1.10 (0.82-1.48)). Conclusion This population-based study demonstrates a persisting mortality gap in all-cause and cause-specific deaths in SLE patients, compared to the general population.

2021 ◽  
Author(s):  
Johan Björklund ◽  
Pär Stattin ◽  
Erik Rönmark ◽  
Markus Aly ◽  
Olof Akre

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Pierluca Piselli ◽  
Diego Serraino ◽  
Mario Fusco ◽  
Enrico Girardi ◽  
Angelo Pirozzi ◽  
...  

Abstract Background Hepatitis C virus (HCV) infection represents a global health issue with severe implications on morbidity and mortality. This study aimed to evaluate the impact of HCV infection on all-cause, liver-related, and non-liver-related mortality in a population living in an area with a high prevalence of HCV infection before the advent of Direct-Acting Antiviral (DAA) therapies, and to identify factors associated with cause-specific mortality among HCV-infected individuals. Methods We conducted a cohort study on 4492 individuals enrolled between 2003 and 2006 in a population-based seroprevalence survey on viral hepatitis infections in the province of Naples, southern Italy. Study participants provided serum for antibodies to HCV (anti-HCV) and HCV RNA testing. Information on vital status to December 2017 and cause of death were retrieved through record-linkage with the mortality database. Hazard ratios (HRs) for cause-specific mortality and 95% confidence intervals (CIs) were estimated using Fine-Grey regression models. Results Out of 626 deceased people, 20 (3.2%) died from non-natural causes, 56 (8.9%) from liver-related conditions, 550 (87.9%) from non-liver-related causes. Anti-HCV positive people were at higher risk of death from all causes (HR = 1.38, 95% CI: 1.12–1.70) and liver-related causes (HR = 5.90, 95% CI: 3.00–11.59) than anti-HCV negative ones. Individuals with chronic HCV infection reported an elevated risk of death due to liver-related conditions (HR = 6.61, 95% CI: 3.29–13.27) and to any cause (HR = 1.51, 95% CI: 1.18–1.94). The death risk of anti-HCV seropositive people with negative HCV RNA was similar to that of anti-HCV seronegative ones. Among anti-HCV positive people, liver-related mortality was associated with a high FIB-4 index score (HR = 39.96, 95% CI: 4.73–337.54). Conclusions These findings show the detrimental impact of HCV infection on all-cause mortality and, particularly, liver-related mortality. This effect emerged among individuals with chronic infection while those with cleared infection had the same risk of uninfected ones. These results underline the need to identify through screening all people with chronic HCV infection notably in areas with a high prevalence of HCV infection, and promptly provide them with DAAs treatment to achieve progressive HCV elimination and reduce HCV-related mortality.


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