Mortality in systemic lupus erythematosus

Sasha Bernatsky(Montreal General Hospital), J.‐F. Boivin(McGill University), L. Joseph(Montreal General Hospital), S Manzi(University of Pittsburgh), Ellen M. Ginzler(SUNY Downstate Health Sciences University), Dafna D. Gladman(Toronto Western Hospital), Murray B. Urowitz(Toronto Western Hospital), Paul R. Fortin(Toronto Western Hospital), Michelle Petri(Johns Hopkins University), Susan G. Barr(University of Calgary), Caroline Gordon(University of Birmingham), Sang‐Cheol Bae(Hanyang University Seoul Hospital), David Isenberg(UCL Australia), Asad Zoma(NHS Lanarkshire), Cynthia Aranow(Yeshiva University), Mary Anne Dooley(University of North Carolina at Chapel Hill), Ola Nived(Lund University), Gunnar Sturfelt(Lund University), K Steinsson(National University Hospital of Iceland), Graciela S. Alarcón(University of Alabama at Birmingham), Jean‐Luc Senécal(Université de Montréal), Michel Zummer(Hôpital Maisonneuve-Rosemont), JG Hanly(Dalhousie University), Stephanie Ensworth(University of British Columbia), Janet Pope(Western University), Steven M. Edworthy(University of Calgary), Anisur Rahman(UCL Australia), John Sibley(Royal University Hospital), Hani El‐Gabalawy(University of Manitoba), T McCarthy(University of Manitoba), Y. St. Pierre(McGill University), Ann E. Clarke(McGill University), Rosalind Ramsey‐Goldman(Northwestern University)
Arthritis & Rheumatism
July 25, 2006
Cited by 1,181Open Access
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Abstract

OBJECTIVE: To examine mortality rates in the largest systemic lupus erythematosus (SLE) cohort ever assembled. METHODS: Our sample was a multisite international SLE cohort (23 centers, 9,547 patients). Deaths were ascertained by vital statistics registry linkage. Standardized mortality ratio (SMR; ratio of deaths observed to deaths expected) estimates were calculated for all deaths and by cause. The effects of sex, age, SLE duration, race, and calendar-year periods were determined. RESULTS: The overall SMR was 2.4 (95% confidence interval 2.3-2.5). Particularly high mortality was seen for circulatory disease, infections, renal disease, non-Hodgkin's lymphoma, and lung cancer. The highest SMR estimates were seen in patient groups characterized by female sex, younger age, SLE duration <1 year, or black/African American race. There was a dramatic decrease in total SMR estimates across calendar-year periods, which was demonstrable for specific causes including death due to infections and death due to renal disorders. However, the SMR due to circulatory diseases tended to increase slightly from the 1970s to the year 2001. CONCLUSION: Our data from a very large multicenter international cohort emphasize what has been demonstrated previously in smaller samples. These results highlight the increased mortality rate in SLE patients compared with the general population, and they suggest particular risk associated with female sex, younger age, shorter SLE duration, and black/African American race. The risk for certain types of deaths, primarily related to lupus activity (such as renal disease), has decreased over time, while the risk for deaths due to circulatory disease does not appear to have diminished.


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