Matches in SemOpenAlex for { <https://semopenalex.org/work/W2891349445> ?p ?o ?g. }
Showing items 1 to 99 of
99
with 100 items per page.
- W2891349445 abstract "Accumulated damage is an important prognostic factor in systemic lupus erythematous. However, the pattern of disease damage and its risk factors have not been well studied in childhood-onset systemic lupus erythematosus (cSLE) in Asia. The objectives are to evaluate the pattern of damage and to identify the risk factors for accumulated damage in an Asian group of cSLE. A retrospective chart review was conducted on a group of 59 patients with cSLE. Patient demographics and clinical variables were first collected at diagnosis. Over the course of their disease, clinical variables considered as risk factors for damage were also collected. Damage was measured using the Systemic Lupus International Collaborating Clinics/ American College of Rheumatology Damage Index (SDI) for each patient at their last encounter. Based on their SDI scores, patients were then dichotomized to two groups: a group with presence of disease damage (SDI ≥1) and a group with absence of disease damage (SDI score = 0). Clinical variables including age at diagnosis, gender, ethnicity, disease duration, disease manifestations, laboratory values at diagnosis, disease activity at diagnosis and last encounter, major organ involvement, number of lupus flares, major infection, and intensity of immunosuppressive medications were compared between the two groups. Growth failure and estimated glomerular filtration rate (eGFR) were also analysed as secondary outcomes. After a median disease duration and follow up of 7.8 years, 39 patients (66.1%) had no disease damage while 20 patients (33.9%) had acquired disease damage. Disease damage most frequently occurred in the ocular (15.3%), neuropsychiatric (11.9%) and musculoskeletal (11.9%) domains. The most frequent forms of damage were cataracts (11.9%), and avascular necrosis (unilateral and bilateral combined 10.2%). After controlling for other variables, presence of neuropsychiatric manifestations remained the only statistically significant risk factor for damage. The rate of growth failure in our group of patients was 16%. Patients who experienced growth failure were significantly younger at disease diagnosis. The median age of diagnosis was 10 for those who experienced growth failure, whereas the median age of diagnosis was 13 for those who did not experience growth failure. Despite a high rate of renal involvement in the group (79.7%), renal damage was only seen in 3.2% of the patients. 91.5% of the studied group had normal eGFR of ≥90 ml/min/1.73m2 at their last follow up. This group of patients had a low rate of damage accrual, with one of the lowest rates in renal damage when compared to other cohorts reported. The presence of neuropsychiatric manifestations was identified as the most significant risk factor for disease damage, while the most frequent forms of damage were cataracts and avascular necrosis, which were both related to prolonged steroid use. Despite the limitations of this study, it highlights the need for larger prospective studies to understand the relationship between childhood-onset SLE and its resulting damage." @default.
- W2891349445 created "2018-09-27" @default.
- W2891349445 creator A5048061679 @default.
- W2891349445 creator A5058632651 @default.
- W2891349445 date "2018-09-10" @default.
- W2891349445 modified "2023-10-01" @default.
- W2891349445 title "Risk factors for damage in childhood-onset systemic lupus erythematosus in Asians: a case control study" @default.
- W2891349445 cites W1483165618 @default.
- W2891349445 cites W1583773754 @default.
- W2891349445 cites W1851080694 @default.
- W2891349445 cites W1922829029 @default.
- W2891349445 cites W1965883352 @default.
- W2891349445 cites W1978259933 @default.
- W2891349445 cites W1993773061 @default.
- W2891349445 cites W1996722581 @default.
- W2891349445 cites W2010623154 @default.
- W2891349445 cites W2018455360 @default.
- W2891349445 cites W2027537346 @default.
- W2891349445 cites W2039883294 @default.
- W2891349445 cites W2040149302 @default.
- W2891349445 cites W2051573899 @default.
- W2891349445 cites W2064999867 @default.
- W2891349445 cites W2070527591 @default.
- W2891349445 cites W2077817813 @default.
- W2891349445 cites W2077900363 @default.
- W2891349445 cites W2078835744 @default.
- W2891349445 cites W2079344468 @default.
- W2891349445 cites W2097454153 @default.
- W2891349445 cites W2108905161 @default.
- W2891349445 cites W2120562059 @default.
- W2891349445 cites W2124951499 @default.
- W2891349445 cites W2131637475 @default.
- W2891349445 cites W2146203649 @default.
- W2891349445 cites W2152073293 @default.
- W2891349445 cites W2153550592 @default.
- W2891349445 cites W2155965977 @default.
- W2891349445 cites W2156821245 @default.
- W2891349445 cites W2159860161 @default.
- W2891349445 cites W2171080480 @default.
- W2891349445 cites W2284370684 @default.
- W2891349445 cites W2303658165 @default.
- W2891349445 cites W2410477589 @default.
- W2891349445 cites W2551262309 @default.
- W2891349445 cites W2561536790 @default.
- W2891349445 cites W2607031541 @default.
- W2891349445 doi "https://doi.org/10.1186/s12969-018-0271-8" @default.
- W2891349445 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6131800" @default.
- W2891349445 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30201026" @default.
- W2891349445 hasPublicationYear "2018" @default.
- W2891349445 type Work @default.
- W2891349445 sameAs 2891349445 @default.
- W2891349445 citedByCount "18" @default.
- W2891349445 countsByYear W28913494452020 @default.
- W2891349445 countsByYear W28913494452021 @default.
- W2891349445 countsByYear W28913494452022 @default.
- W2891349445 countsByYear W28913494452023 @default.
- W2891349445 crossrefType "journal-article" @default.
- W2891349445 hasAuthorship W2891349445A5048061679 @default.
- W2891349445 hasAuthorship W2891349445A5058632651 @default.
- W2891349445 hasBestOaLocation W28913494451 @default.
- W2891349445 hasConcept C126322002 @default.
- W2891349445 hasConcept C167135981 @default.
- W2891349445 hasConcept C198451711 @default.
- W2891349445 hasConcept C2776912625 @default.
- W2891349445 hasConcept C2777767895 @default.
- W2891349445 hasConcept C2779134260 @default.
- W2891349445 hasConcept C50440223 @default.
- W2891349445 hasConcept C71924100 @default.
- W2891349445 hasConceptScore W2891349445C126322002 @default.
- W2891349445 hasConceptScore W2891349445C167135981 @default.
- W2891349445 hasConceptScore W2891349445C198451711 @default.
- W2891349445 hasConceptScore W2891349445C2776912625 @default.
- W2891349445 hasConceptScore W2891349445C2777767895 @default.
- W2891349445 hasConceptScore W2891349445C2779134260 @default.
- W2891349445 hasConceptScore W2891349445C50440223 @default.
- W2891349445 hasConceptScore W2891349445C71924100 @default.
- W2891349445 hasIssue "1" @default.
- W2891349445 hasLocation W28913494451 @default.
- W2891349445 hasLocation W28913494452 @default.
- W2891349445 hasLocation W28913494453 @default.
- W2891349445 hasLocation W28913494454 @default.
- W2891349445 hasLocation W28913494455 @default.
- W2891349445 hasOpenAccess W2891349445 @default.
- W2891349445 hasPrimaryLocation W28913494451 @default.
- W2891349445 hasRelatedWork W2011903210 @default.
- W2891349445 hasRelatedWork W2024591865 @default.
- W2891349445 hasRelatedWork W2069343534 @default.
- W2891349445 hasRelatedWork W2070527027 @default.
- W2891349445 hasRelatedWork W2312991170 @default.
- W2891349445 hasRelatedWork W2323899267 @default.
- W2891349445 hasRelatedWork W2410065254 @default.
- W2891349445 hasRelatedWork W2622204852 @default.
- W2891349445 hasRelatedWork W2891349445 @default.
- W2891349445 hasRelatedWork W3210359220 @default.
- W2891349445 hasVolume "16" @default.
- W2891349445 isParatext "false" @default.
- W2891349445 isRetracted "false" @default.
- W2891349445 magId "2891349445" @default.
- W2891349445 workType "article" @default.