Risk factors for symptomatic Avascular Necrosis (AVN) in a multi-ethnic Systemic Lupus Erythematosus (SLE) cohort
Adult
Male
Pathogenesis and Treatment of Osteonecrosis
RC31-1245 Internal medicine
Science
610
Logistic regression
Rheumatoid Arthritis
Infectious disease (medical specialty)
Cohort Studies
Young Adult
03 medical and health sciences
Systemic lupus erythematosus
0302 clinical medicine
Rheumatology
Risk Factors
Health Sciences
Ethnicity
Prevalence
Humans
Lupus Erythematosus, Systemic
Orthopedics and Sports Medicine
Disease
Internal medicine
Femoral head
Univariate analysis
Q
R
Osteonecrosis
Cohort
Middle Aged
3. Good health
Coronavirus disease 2019 (COVID-19)
Logistic Models
Avascular necrosis
Systemic Lupus Erythematosus and Antiphospholipid Syndrome
Multivariate analysis
Multivariate Analysis
Medicine
Female
Surgery
Avascular Necrosis
Research Article
Hydroxychloroquine
DOI:
10.1371/journal.pone.0248845
Publication Date:
2021-03-19T17:29:46Z
AUTHORS (8)
ABSTRACT
Avascular necrosis of bone (AVN) is increasingly being recognized as a complication of SLE and causes significant disability due to pain and mobility limitations. We studied the prevalence and factors associated with avascular necrosis (AVN) in a multiethnic SLE cohort. SLE patients who visited the outpatient clinic from October 2017 to April 2019 were considered eligible. Their medical records were reviewed to identify patients who developed symptomatic AVN, as confirmed by either magnetic resonance imaging or plain radiography. Subsequently, their SLE disease characteristics and treatment were compared with the characteristics of patients who did not have AVN. Multivariable logistic regression analyses were performed to determine the independent factors associated with AVN among the multiethnic SLE cohort. A total of 390 patients were recruited, and the majority of them were females (92.6%); the patients were predominantly of Malay ethnicity (59.5%), followed by Chinese (35.9%) and Indian (4.6%). The prevalence of symptomatic AVN was 14.1%, and the mean age of AVN diagnosis was 37.6 ± 14.4 years. Both univariate and multivariable logistic regression analyses revealed that a longer disease duration, high LDL-C (low density lipoprotein cholesterol), positive anti-cardiolipin (aCL) IgG and anti-dsDNA results, a history of an oral prednisolone dose of more than 30 mg daily for at least 4 weeks and osteoporotic fractures were significantly associated with AVN. On the other hand, hydroxychloroquin (HCQ), mycophenolate mofetil (MMF) and bisphosphonate use were associated with a lower risk of AVN. No associations with ethnicity were found. In conclusion, several modifiable risk factors were found to be associated with AVN, and these factors may be used to identify patients who are at high risk of developing such complications. The potential protective effects of HCQ, MMF and bisphosphonates warrant additional studies.
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