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Inactive matrix Gla protein in relation to diabetic retinopathy in type 2 diabetes
Hend Adel1, Olfat Fawzy1, Eman Mahmoud1
1Department of Endocrinology and Metabolism, Faculty of Medicine for Girls, Al-Azhar University, Cairo, Egypt.
Background And Aims:
The contribution of inactive Matrix Gla protein (MGP) to ectopic vascular calcification associated with type 2 diabetes mellitus (T2DM) is well recognized. However, its role in diabetic microvascular complications remains unknown. The study aim was to identify any association between inactive MGP and diabetic retinopathy (DR). Its relation to insulin resistance was also explored.
Methods:
The study included 90 participants, 65 Type 2 diabetic patients (25 without DR and 40 with DR) and 25 healthy controls. Serum inactive MGP was measured using ELISA. HOMA-IR was also assessed.
Results:
Inactive MGP was significantly higher in both diabetic groups compared to controls (P < 0.001), as well as in Type 2 diabetic patients with retinopathy compared to Type 2 diabetes without retinopathy (P = 0.002). Inactive MGP was positively correlated with HbA1c, HOMA-IR, LDL-C and triglycerides (P < 0.001), and negatively correlated with HDL-C (P = 0.008) and eGFR (P < 0.001). Logistic Regression Analysis showed that inactive MGP was one of the most associated factors with DR.
Conclusions:
Inactive MGP was found to be related to DR, insulin resistance and other dysmetabolic risk factors. These findings highlight that inactive MGP may be a significant contributor to the pathogenesis, evolution, and progression of DR.
Insights
Inactive Matrix Gla protein (MGP) is elevated in type 2 diabetes and linked to diabetic retinopathy (DR). This protein may play a role in DR development and progression.
Area of Science:
- Endocrinology
- Ophthalmology
- Vascular Biology
Background:
- Inactive Matrix Gla protein (MGP) is implicated in vascular calcification in type 2 diabetes mellitus (T2DM).
- The role of inactive MGP in diabetic microvascular complications, specifically diabetic retinopathy (DR), is not well understood.
Purpose of the Study:
- To investigate the association between inactive MGP and DR in patients with T2DM.
- To explore the relationship between inactive MGP and insulin resistance.
Main Methods:
- Study included 90 participants: 65 with T2DM (25 without DR, 40 with DR) and 25 healthy controls.
- Serum inactive MGP levels were quantified using ELISA.
- Insulin resistance was assessed using the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR).
Main Results:
- Inactive MGP levels were significantly higher in diabetic patients (with and without DR) compared to controls.
- Patients with DR exhibited higher inactive MGP levels than those without DR.
- Inactive MGP showed positive correlations with HbA1c, HOMA-IR, LDL-C, and triglycerides, and negative correlations with HDL-C and eGFR.
- Logistic regression identified inactive MGP as a key factor associated with DR.
Conclusions:
- Inactive MGP is associated with DR and insulin resistance in T2DM patients.
- Findings suggest inactive MGP may contribute to the pathogenesis and progression of DR.
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