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Decreasing Serum Adropin Levels in Patients With Systemic Lupus Erythematosus: A Case-Control Study.
Mehrzad Hajialilo1, Amir Ghorbanihaghjo2, Kamran Javidi-Aghdam3
1Connective Tissue Diseases Research Center Tabriz University of Medical Sciences Tabriz Iran.
Serum adropin levels are significantly lower in patients with systemic lupus erythematosus (SLE), indicating a potential link to disease activity and cardiovascular risk. Lower adropin may predict hypertension and anti-phospholipid antibodies in SLE patients.
Area of Science:
- Endocrinology
- Immunology
- Cardiovascular Research
Background:
- Systemic lupus erythematosus (SLE) is a complex autoimmune disease affecting many women, often co-occurring with obesity.
- Adropin, a peptide hormone, regulates metabolism and possesses anti-inflammatory and immune-modulating properties.
- Understanding adropin's role in SLE is crucial for managing associated metabolic and cardiovascular complications.
Purpose of the Study:
- To investigate serum adropin levels in patients diagnosed with SLE.
- To explore the association between adropin levels and coronary risk factors in SLE.
- To examine the relationship between adropin and clinical manifestations of SLE.
Main Methods:
- A cross-sectional study involving 59 SLE patients and 30 healthy controls.
- Serum adropin levels were quantified using high-sensitivity human ELISA kits.
Main Results:
- SLE patients exhibited significantly lower serum adropin levels compared to controls (0.41 vs. 0.69 ng/mL, p=0.001).
- Lower adropin levels were associated with hyperlipidemia, hypertension, nephritis, serositis, hypocomplementemia, and positive anti-phospholipid antibodies (APLAs).
- Serum adropin levels negatively correlated with disease duration and were independently associated with hypertension and APLAs.
Conclusions:
- Serum adropin levels are significantly decreased in SLE patients.
- Adropin may serve as a potential biomarker for cardiovascular risk, particularly hypertension, in SLE.
- These findings highlight adropin's clinical relevance in assessing cardiovascular risk within the SLE population.
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