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Abnormal levels of expression of plasma microRNA-33 in patients with psoriasis
S García-Rodríguez1, S Arias-Santiago2, J Orgaz-Molina3
1Departamento de Biología Celular e Inmunología, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, Consejo Superior de Investigaciones Científicas (CSIC), Parque Tecnológico Ciencias de la Salud, Armilla, Granada, España.
Introduction And Objectives:
Circulating microRNAs (miRNA) are involved in the posttranscriptional regulation of genes associated with lipid metabolism (miRNA-33) and vascular function and angiogenesis (miRNA-126). The objective of this exploratory study was to measure plasma levels of miRNA-33 and miRNA-126 in patients with plaque psoriasis and evaluate their association with clinical parameters.
Material And Methods:
We studied 11 patients with plaque psoriasis. The median Psoriasis Area Severity Index (PASI) was 13 (interquartile range [IQR], 9-14) and body surface area involvement was 12 (IQR, 11-15). Eleven healthy controls matched for age and sex were also included. We analyzed cardiovascular risk factors and subclinical carotid atheromatosis. Plasma miRNAs were evaluated using quantitative real-time polymerase chain reaction.
Results:
Carotid intima-media thickness was greater in patients (0.57mm; IQR, 0.54-0.61; n=11) than in controls (0.50mm; IQR, 0.48-0.54; data available for 9 controls) (P=.0055, Mann-Whitney). Expression of miRNA-33 in patients (5.34; IQR, 3.12-7.96; n=11) was significantly higher than in controls (2.33; IQR, 1.71-2.84; only detected in 7 of 11 controls) (P=.0049, Wilcoxon signed rank). No differences in miRNA-126 levels were observed between patients and controls. In patients (n=11), we observed a positive correlation between miRNA-33 and insulin levels (r=0.7289, P=.0109) and a negative correlation between miRNA-126 and carotid intima-media thickness (r=-0.6181, P=.0426).
Conclusion:
In psoriasis patients plasma levels of lipid and glucose metabolism-related miRNA-33 are increased and correlated with insulin. The study of circulating miRNA-33 in psoriasis may provide new insights about the associated systemic inflammatory abnormalities.
Insights
Plasma levels of microRNA-33 (miRNA-33), linked to lipid metabolism, are elevated in patients with plaque psoriasis and correlate with insulin. This finding may offer new insights into psoriasis-related systemic inflammation.
Area of Science:
- Biochemistry
- Genetics
- Dermatology
Background:
- Circulating microRNAs (miRNAs) regulate genes involved in lipid metabolism (miRNA-33) and vascular function (miRNA-126).
- Plaque psoriasis is associated with systemic inflammation and cardiovascular risk factors.
Purpose of the Study:
- To measure plasma levels of miRNA-33 and miRNA-126 in plaque psoriasis patients.
- To evaluate the association of these miRNAs with clinical parameters and cardiovascular risk.
Main Methods:
- Quantitative real-time polymerase chain reaction was used to analyze plasma miRNA levels in 11 plaque psoriasis patients and 11 healthy controls.
- Cardiovascular risk factors and subclinical carotid atheromatosis were assessed.
Main Results:
- Psoriasis patients exhibited significantly higher plasma miRNA-33 levels compared to controls (P=.0049).
- A positive correlation was found between miRNA-33 and insulin levels in patients (r=0.7289, P=.0109).
- No significant differences in miRNA-126 levels were observed between groups, though a negative correlation with carotid intima-media thickness was noted in patients (r=-0.6181, P=.0426).
Conclusions:
- Elevated plasma miRNA-33 levels in psoriasis patients suggest a role in lipid and glucose metabolism dysregulation.
- Circulating miRNA-33 may serve as a biomarker for systemic inflammatory abnormalities associated with psoriasis.
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