Description of Malignancy Rates in Childhood- and Adult-Onset Systemic Lupus Erythematous by Proportional Meta-analysis
Autor: | Regina El Dib, Clovis A. Silva, Priscila Rodrigues da Silva Aoki, Claudia Saad Magalhães |
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Rok vydání: | 2017 |
Předmět: |
Adult
medicine.medical_specialty Malignancy Gastroenterology Risk Assessment 03 medical and health sciences 0302 clinical medicine Rheumatology Risk Factors Internal medicine Neoplasms medicine Humans Lupus Erythematosus Systemic Age of Onset Child 030203 arthritis & rheumatology Lupus erythematosus Systemic lupus business.industry Incidence (epidemiology) Incidence medicine.disease Confidence interval 030220 oncology & carcinogenesis Meta-analysis Age of onset business Cohort study |
Zdroj: | Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 23(4) |
ISSN: | 1536-7355 |
Popis: | OBJECTIVE Describe malignancy rates in childhood onset and adult onset systemic lupus erythematous (SLE) by proportional meta-analysis. METHODS Two reviewers screened data from PubMed (1966-2015), EMBASE (1980-2015), and LILACS (1982-2015) for SLE-associated malignancy. Proportional meta-analysis with a random-effects model and 95% confidence intervals (CIs) were calculated according to SLE onset age and mean follow-up time. Statistical difference was defined by 95% CI overlap. RESULTS Overall the malignancy rate reported in 30 case series with 96,578 subjects was 3.4% (95% CI, 0.0260-0.0442; I = 97.6%; P < 0.0001). The malignancy rate was 4.2% (95% CI, 0.0318-0.0531; I = 98%; P < 0.0001) in 25 adult-onset SLE series, compared with 0.5% (95% CI, 0.0003-0.0154; I = 62.6%; P = 0.03) in 5 childhood-onset SLE series. Overall, in those with less than 5 years' follow-up, the malignancy rate was 2.8% (95% CI, 0.013-0.047; I = 91%; P < 0.0001) compared with 3.6% (95% CI, 0.0226-0.0531; I = 98.3%; P < 0.0001) in those with more than 5 years' follow-up, which was not significant, with 95% CI overlap. CONCLUSIONS The meta-analysis indicated lower malignancy rates in pediatric-onset SLE compared with adult-onset SLE, but accrued data from childhood-onset SLE are still needed. |
Databáze: | OpenAIRE |
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