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Correlation Between Steroid Therapy and Lipid Profile in Systemic Lupus Erythematosus Patients
Nur Atik1,2, Rira Uji Hayati3, Laniyati Hamijoyo2,4
1Department of Biomedical Sciences, Faculty of Medicine, Padjadjaran University, Bandung, West Java, Indonesia.
Insights
Steroid therapy in Systemic Lupus Erythematosus (SLE) patients correlates with increased total cholesterol and triglyceride levels. This finding highlights potential cardiovascular risks associated with steroid treatment in SLE management.
Area of Science:
- Rheumatology
- Cardiovascular Medicine
- Endocrinology
Background:
- Systemic lupus erythematosus (SLE) is a severe autoimmune disease.
- Cardiovascular events are a major cause of mortality in SLE patients.
- Dyslipidemia, a risk factor for cardiovascular disorders, can be induced by steroid therapy used in SLE treatment.
Purpose of the Study:
- To investigate the correlation between steroid dosage and lipid profiles in patients with SLE.
- To determine if steroid use impacts total cholesterol, LDL, HDL, and triglyceride levels in SLE patients.
Main Methods:
- Correlative analytic study with a cross-sectional design.
- Data collected from the Hasan Sadikin Lupus Registry and medical records (2008-2019).
- Included SLE patients on steroid therapy, excluding those on cyclosporine A, statins, or treated for less than a year; Pearson's correlation test used.
Main Results:
- A statistically significant correlation was found between steroid dose and increased total cholesterol (r = 0.375; p = 0.016) and triglyceride levels (r = 0.416; p = 0.007).
- No significant correlation was observed between steroid dose and HDL (r = 0.206; p = 0.196) or LDL levels (r = 0.308; p = 0.05).
- The study included 41 female SLE patients with an average age of 30.88 years and an average steroid dose of 5.63 mg/day.
Conclusions:
- Steroid dosage in SLE patients is significantly correlated with total cholesterol and triglyceride levels.
- The applied steroid dose did not show a significant correlation with HDL or LDL levels in this SLE cohort.
- Findings suggest monitoring lipid profiles in SLE patients undergoing steroid therapy is crucial for cardiovascular risk management.
Purpose:
Systemic lupus erythematosus (SLE) is an autoimmune disease with high mortality and morbidity rates, one of the causes of which is cardiovascular events. Dyslipidaemia is known to be one of the main risk factors for cardiovascular disorders and can be induced by steroid therapy, which is commonly administered to SLE patients. This study aimed to determine whether there is a correlation between steroid dose and lipid profile in SLE patients.
Methods:
The study was a correlative analytic study with a cross-sectional design. Data were obtained from the Hasan Sadikin Lupus Registry (HSLR) and the medical records of patients registered in the Rheumatology Division, Dr Hasan Sadikin Hospital, Bandung, from 2008 to 2019. Inclusion criteria were SLE patients who had undergone lipid profile examination and received steroid therapy. We excluded patients taking cyclosporine A or statins, and patients treated with steroids for less than a year. A simple random sampling method was performed and Pearson's correlation test was used for the analysis.
Results:
We recruited 41 female patients with an average age of 30.88 ± 9.29 years old. The average dose of steroid in this study was 5.63 mg/day, while the average lipid profile was 177.51 mg/dL, 105.22 mg/dL, 61 mg/dL and 92.98 mg/dL for total cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL) and triglycerides, respectively. Correlations between steroid dose and total cholesterol (r = 0.375; p = 0.016), and between steroid dose and triglyceride level (r = 0.416; p = 0.007) were statistically significant in SLE patients. However, this study showed no correlation between steroid and HDL level (r = 0.206; p = 0.196) or LDL level (r = 0.308; p = 0.05).
Conclusion:
This study showed that the applied steroid dose in SLE patients correlated with total cholesterol and triglyceride levels, but not with HDL or LDL.
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