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Genetic Polymorphisms of miR-146a and miR-155 in Psoriasis and Psoriatic Arthritis: Evidence from a Turkish
Fadime Mutlu Icduygu1, Isil Deniz Oguz2, Egemen Akgun3
1Department of Medical Genetics, Faculty of Medicine, Giresun University, Giresun, Turkey.
Introduction:
Psoriasis, a widespread inflammatory cutaneous disease, is driven by an interplay of genetic and environmental risk factors. miR-155 and miR-146a have been implicated in the regulation of inflammatory pathways.
Objectives:
In the current study, we examined the association between miR-155 rs767649 and miR-146a rs2910164 variants and the predisposition to psoriasis and psoriatic arthritis.
Methods:
A total of 544 individuals, including 284 psoriasis cases (68 with psoriatic arthritis) and 260 controls, were enrolled in the present study. Real-time polymerase chain reaction (qPCR) method was used to detect the genotypes of study groups.
Results:
The frequencies of the rs2910164 C allele, CC, and GC genotypes were significantly higher in the patient group (P<0.001), while the frequencies of the rs767649 A allele and AA genotype were higher in the control group (P=0.005 and P=0.002, respectively). No statistically significant difference in genotype or allele frequency was observed between patients with and without psoriatic arthritis (P>0.05). Rs2910164 CC and GC genotypes were found to be associated with a younger age at disease onset (P=0.006), and CC genotype was associated with higher PASI score (P=0.024).
Conclusion:
The present data suggest an association between the presence of the miR-155 rs767649 and miR-146a rs2910164 variants and susceptibility to psoriasis in the Turkish population. However, although the number of patients with psoriatic arthritis in our study was relatively small, no association was found between these variants and the development of psoriatic arthritis. Furthermore, the rs2910164 polymorphism was found to be associated with both early-onset disease and PASI score.
Insights
Genetic variants in miR-155 and miR-146a are associated with psoriasis susceptibility in the Turkish population. These microRNA variants may influence disease onset and severity but not psoriatic arthritis development.
Area of Science:
- Genetics
- Immunology
- Dermatology
Background:
- Psoriasis is a common inflammatory skin condition influenced by genetic and environmental factors.
- MicroRNAs (miRNAs), specifically miR-155 and miR-146a, play roles in regulating inflammatory processes.
- Understanding the genetic basis of psoriasis susceptibility is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the association between specific genetic variants (rs767649 in miR-155 and rs2910164 in miR-146a) and the risk of developing psoriasis and psoriatic arthritis.
- To explore the potential correlation of these variants with disease severity and age of onset in psoriasis patients.
Main Methods:
- A case-control study involving 544 participants (284 psoriasis cases, 260 controls).
- Genotyping of miR-155 rs767649 and miR-146a rs2910164 variants using real-time polymerase chain reaction (qPCR).
- Statistical analysis to compare allele and genotype frequencies between patient and control groups, and to assess associations with clinical parameters.
Main Results:
- The miR-146a rs2910164 C allele and associated genotypes (CC, GC) were more frequent in psoriasis patients (P<0.001).
- The miR-155 rs767649 A allele and AA genotype were more prevalent in controls (P=0.005, P=0.002).
- Rs2910164 polymorphism correlated with earlier disease onset (P=0.006) and higher Psoriasis Area and Severity Index (PASI) scores (P=0.024).
Conclusions:
- The study suggests that miR-155 rs767649 and miR-146a rs2910164 variants are linked to psoriasis susceptibility in the Turkish population.
- No significant association was found between these variants and the development of psoriatic arthritis.
- The miR-146a rs2910164 variant is associated with earlier psoriasis onset and increased disease severity.
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