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De-regulation of diabetic regulatory genes in psoriasis: Deciphering the unsolved riddle
Suad AlFadhli1, Alaa A M Al-Zufairi1, Rasheeba Nizam1
1Department of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Kuwait University, Kuwait.
Abstract:
The purpose of our study was to identify the currently lacking molecular mechanism that accounts for the co-occurrence of two seemingly disparate diseases: psoriasis and type II diabetes. We aimed to investigate a panel of 84 genes related to the diabetic regulatory network in psoriasis (Ps), psoriasis type II diabetes (Ps-T2D), type II diabetes (T2D) and healthy control (HC). We hypothesize that such attempts would provide novel diagnostic markers and/or insights into pathogenesis of the disease. A quantitative Real Time-PCR Human Diabetes RT(2) Profiler PCR Array was chosen to explore the expression profile 84 diabetic genes in study subjects. Statistical analysis was carried out using appropriate software. The analysis revealed three candidate genes GSK3B, PTPN1, STX4 that are differentially expressed in study subjects. GSK3B was highly significant in Ps-T2D (P=0.00018, FR=-26.6), followed by Ps (P=0.0028, FR=-14.5) and T2D groups (P=0.032, FR=-5.9). PTPN1 showed significant association only with PS-T2D (P=0.00027, FR=-8.5). STX4 showed significant association with both Ps (P=0.0002, FR=-20) and Ps-T2D (P=0.0016, FR=-11.2). ACE represents an additional marker that showed suggestive association with Ps (P=0.0079, FR=-9.37). Our study highlights the complex genetics of Ps-T2D and present biomarkers for the development of T2D in Ps cases.
Insights
This study identifies key genes like GSK3B, PTPN1, and STX4 involved in the molecular link between psoriasis and type II diabetes, offering potential biomarkers for disease development.
Area of Science:
- Genetics and Molecular Biology
- Endocrinology
- Dermatology
Background:
- Psoriasis and type II diabetes are distinct conditions with a poorly understood molecular connection.
- Investigating shared genetic factors may reveal underlying pathogenic mechanisms and diagnostic markers.
Purpose of the Study:
- To identify the molecular mechanisms linking psoriasis and type II diabetes.
- To explore the expression of 84 diabetes-related genes in individuals with psoriasis, type II diabetes, and co-occurring conditions.
- To discover novel biomarkers for the development of type II diabetes in psoriasis patients.
Main Methods:
- Quantitative Real-Time PCR using a Human Diabetes RT(2) Profiler PCR Array.
- Analysis of gene expression profiles in psoriasis, type II diabetes, psoriasis with type II diabetes, and healthy control groups.
- Statistical analysis to identify differentially expressed genes.
Main Results:
- Three candidate genes (GSK3B, PTPN1, STX4) were found to be differentially expressed.
- GSK3B showed high significance in psoriasis with type II diabetes, psoriasis, and type II diabetes groups.
- PTPN1 was significantly associated with psoriasis and type II diabetes, while STX4 was associated with both psoriasis and psoriasis with type II diabetes.
Conclusions:
- The study highlights the complex genetic basis of co-occurring psoriasis and type II diabetes.
- GSK3B, PTPN1, and STX4 are identified as potential biomarkers for type II diabetes development in psoriasis patients.
- These findings offer insights into the pathogenesis and potential diagnostic strategies for these conditions.
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