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Antiphospholipid antibodies, steroid dose, arterial hypertension, relapses, and late-onset predict organ damage in a population of Colombian patients with systemic lupus erythematosus
- Source :
- Clinical Rheumatology. 37:949-954
- Publication Year :
- 2017
- Publisher :
- Springer Science and Business Media LLC, 2017.
-
Abstract
- Organ damage predicts mortality, increased accrual of detriment, and poor quality of life in systemic lupus erythematosus patients. The objective of this study is to determine the damage-free survival and its predictive factors in a population of Colombian subjects. The method used in this study is the retrospective follow-up of a cohort; damage was measured with SLICC/ACR index. Predictors of impairment were assessed by logistic regression and survival analysis. One hundred sixty-one individuals were included; 28.9% suffered damage, primarily neuropsychiatric, renal, and vascular. Arterial hypertension, antiphospholipid antibodies, prednisone dose, and number of relapses were all predictors of detriment. Onset after age 50 and daily prednisone dose higher than 7.5 mg determined earlier occurrence of damage.
- Subjects :
- Adult
Male
medicine.medical_specialty
Adolescent
Population
Late onset
Colombia
030204 cardiovascular system & hematology
Kidney
Severity of Illness Index
Young Adult
03 medical and health sciences
0302 clinical medicine
Rheumatology
Recurrence
Prednisone
Internal medicine
Severity of illness
medicine
Humans
Lupus Erythematosus, Systemic
education
Survival analysis
Retrospective Studies
030203 arthritis & rheumatology
education.field_of_study
business.industry
Retrospective cohort study
General Medicine
Middle Aged
humanities
Hypertension
Cohort
Antibodies, Antiphospholipid
Disease Progression
Female
business
medicine.drug
Subjects
Details
- ISSN :
- 14349949 and 07703198
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- Clinical Rheumatology
- Accession number :
- edsair.doi.dedup.....b2492cf7b1cdb46b395749de0ce07057
- Full Text :
- https://doi.org/10.1007/s10067-017-3927-8