Overall and Sex-specific Mortality in Psoriatic Arthritis and Ankylosing Spondylitis: A Meta-analysis

Objective. This study examined the all-cause and sex-specific standardized mortality ratios (SMRs) in patients with spondyloarthropathy. Methods. Studies examining the all-cause and/or cause-specific SMRs in patients with psoriatic arthritis (PsA) and ankylosing spondylitis (AS) compared to the gene...

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Veröffentlicht in:Journal of rheumatic diseases 2018, 25(3), , pp.197-202
Hauptverfasser: Lee, Young Ho, Song, Gwan Gyu
Format: Artikel
Sprache:eng
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Zusammenfassung:Objective. This study examined the all-cause and sex-specific standardized mortality ratios (SMRs) in patients with spondyloarthropathy. Methods. Studies examining the all-cause and/or cause-specific SMRs in patients with psoriatic arthritis (PsA) and ankylosing spondylitis (AS) compared to the general population were surveyed using MEDLINE, EMBASE, and Cochrane databases and manual searches. A meta-analysis of the all-cause and sex-specific SMRs in patients with rheumatic diseases was then performed. Results. In total, 7 comparisons (5 PsA and 2 AS) from 6 reports met the inclusion criteria. Disease-specific meta-analysis showed that the pooled SMR was 1.299 (95% confidence interval [CI] 1.092∼1.605, p=0.015) for PsA and 1.784 (95% CI 1.576∼2.020, p<0.001) for AS. Meta-analysis showed that the SMRs of PsA and AS were significantly higher (1.299 to 1.784 times) than those in the general population. The age- and sex-adjusted SMR was highest for AS (1.784), followed by PsA (1.299). Moreover, sex-specific meta-analysis showed that the all-cause SMRs were increased in female and male patients with PsA. On the other hand, mortality increased in male patients with AS (SMR 1.834), whereas there was no significant increase in female patients with AS. Conclusion. All-cause mortality is higher in patients with PsA and AS compared to the general population. On the other hand, the mortality was higher in males with AS but not in females. KCI Citation Count: 0
ISSN:2093-940X
2233-4718
DOI:10.4078/jrd.2018.25.3.197