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Mortality in systemic lupus erythematosusopen access

Authors
Bernatsky, Sasha R.Boivin, Jean Franc̃oisJoseph, LawrenceManzi, SusanGinzler, Ellen M.Gladman, Dafna D.Urowitz, Murray B.Fortin, Paul R.Pétri, Michelle A.Barr, Susan G.Gordon, CarolineBae, Sang-cheolIsenberg, David A.Zoma, Asad A.Aranow, Cynthia B.Dooley, Mary AnneNived, OlaSturfelt, Gunnar K.Steinsson, KristjánAlarcón, Graciela S.Sénécal, Jean LucZummer, MichelHanly, John G.Ensworth, StephaniePope, Janet ElizabethEnsworth, StephanieRahman, A. T.M.AnishurSibley, John T.El-Gabalawy, Hani S.McCarthy, TimothyPierre, YvanStClarke, Ann ElaineRamsey-Goldman, R.
Issue Date
Aug-2006
Publisher
WILEY-BLACKWELL
Citation
ARTHRITIS AND RHEUMATISM, v.54, no.8, pp.2550 - 2557
Indexed
SCIE
SCOPUS
Journal Title
ARTHRITIS AND RHEUMATISM
Volume
54
Number
8
Start Page
2550
End Page
2557
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181164
DOI
10.1002/art.21955
ISSN
0004-3591
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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