Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/26862
Title: Associations of metabolic syndrome in SLE.
Authors: Morand E. ;Vincent F.;Hoi A. ;Apostolopoulos D. 
Monash Health Department(s): Rheumatology
Institution: (Apostolopoulos, Hoi, Morand) Department of Rheumatology, Monash Health, Melbourne, VIC, Australia (Vincent) Centre for Inflammatory Diseases, Monash University, Clayton, VIC, Australia (Hoi) Department of Medicine, Monash University, Faculty of Medicine Nursing and Health Sciences, Clayton, VIC, Australia
Issue Date: 27-Mar-2021
Copyright year: 2020
Publisher: BMJ Publishing Group
Place of publication: United Kingdom
Publication information: Lupus Science and Medicine. 7 (1) (no pagination), 2020. Article Number: e000436. Date of Publication: 13 Nov 2020.
Journal: Lupus Science and Medicine
Abstract: Objectives To characterise the prevalence and associations of metabolic syndrome (MetS) in a multiethnic cohort of patients with SLE. Methods Using a standardised protocol, baseline demographics, per visit disease activity (Systemic Lupus Erythematosus Disease Activity Index-2K) and treatment data, and annual recording of organ damage accrual (Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC-ACR) Damage Index) were captured on patients with SLE from a single tertiary centre. The presence of MetS, defined using modified updated joint consensus criteria, was assessed at the final visit from patient records. Serum concentrations of adipocytokines were measured by Quantibody. Results 116 patients, with median (Q1, Q3) age at enrolment of 39.5 (31.4-51.1) years and disease duration of 6.1 (1.4-12) years, were followed for a median of 6.7 (4.1-8.1) years. The prevalence of MetS was 29% (34/116), while the prevalence of MetS components varied: hypertension (59%), low high-density lipoproteins (HDLs) (51%), hypertriglyceridaemia (32%), obesity (16%) and hyperglycaemia (22%). In univariable analysis, MetS was associated with baseline organ damage (OR 4.34; 95% CI 1.80 to 10.48; p<0.01) and organ damage accrual (OR 2.34; 95% CI 1.02 to 5.36; p=0.04) but not with disease activity. In multivariable analysis, baseline organ damage remained significantly associated with MetS (adjusted OR 3.36; 95% CI 1.32 to 8.59; p=0.01). Glucocorticoid use was not associated with MetS or any of its five components. High serum concentrations of resistin were significantly negatively associated with MetS (OR 0.17; 95% CI 0.04 to 0.70; p=0.014). Conclusion MetS was common in a multiethnic cohort of patients with SLE, with the most frequent components being hypertension and low HDL. An independent association was found between MetS and organ damage but not glucocorticoid exposure or disease activity.Copyright ©
DOI: http://monash.idm.oclc.org/login?url=
http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/lupus-2020-000436
ISSN: 2053-8790 (electronic)
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/26862
Type: Article
Subjects: middle aged
multivariate analysis
obesity
odds ratio
organ injury
prevalence
priority journal
protein blood level
*systemic lupus erythematosus
univariate analysis
young adult
adipocytokine/ec [Endogenous Compound]
glucocorticoid
high density lipoprotein/ec [Endogenous Compound]
hydroxychloroquine
immunosuppressive agent
prednisolone
resistin/ec [Endogenous Compound]
female
adult
article
cohort analysis
confidence interval
demography
*disease association
disease duration
human
human tissue
hyperglycemia
hypertension
hypertriglyceridemia
major clinical study
male
*metabolic syndrome X
human tissue
hyperglycemia
hypertension
hypertriglyceridemia
major clinical study
male
*metabolic syndrome X
middle aged
multivariate analysis
obesity
odds ratio
organ injury
Article
priority journal
protein blood level
*systemic lupus erythematosus
univariate analysis
young adult
adult
prevalence
cohort analysis
confidence interval
demography
*disease association
disease duration
female
human
Type of Clinical Study or Trial: Observational study (cohort, case-control, cross sectional or survey)
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