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Influence of Metabolic Parameters and Treatment Method on OCT Angiography Results in Children with Type 1 Diabetes
Marta Wysocka-Mincewicz1, Marta Baszyńska-Wilk1, Joanna Gołębiewska2,3
1Department of Endocrinology and Diabetology, The Children's Memorial Health Institute, Warsaw, Poland.
Insights
Metabolic factors and treatment methods impact optical coherence tomography angiography (OCTA) findings in children with type 1 diabetes (T1D). These OCTA results may serve as early indicators for diabetic retinopathy (DR).
Area of Science:
- Ophthalmology
- Endocrinology
- Medical Imaging
Background:
- Diabetic retinopathy (DR) is a significant complication of type 1 diabetes (T1D).
- Early detection of microvascular changes in T1D is crucial for preventing vision loss.
- Optical coherence tomography angiography (OCTA) offers a non-invasive method to visualize retinal vasculature.
Purpose of the Study:
- To investigate the influence of metabolic parameters and treatment modalities on OCTA findings in children with T1D.
- To assess OCTA results as potential early biomarkers for DR in pediatric T1D patients.
Main Methods:
- A prospective study involving 175 children with T1D.
- OCTA imaging was performed using AngioVue to analyze superficial and deep capillary vessel density, foveal thickness, and foveal avascular zone (FAZ).
- Data were analyzed in relation to metabolic factors (HbA1c), age at onset, diabetes duration, and treatment type (MDI vs. CSII).
Main Results:
- No DR was detected by fundus ophthalmoscopy.
- Higher HbA1c levels correlated with decreased whole superficial vessel density (wsVD).
- Children treated with continuous subcutaneous insulin infusion (CSII) showed significantly lower fsVD, wdVD, pdVD, and larger FAZ compared to those on multiple daily injections (MDI).
Conclusions:
- Metabolic status, age of diabetes onset, and insulin delivery method influence OCTA parameters in children with T1D.
- These OCTA findings may have implications for the early detection and prediction of DR severity in young T1D patients.
- Further longitudinal studies are warranted to validate the predictive value of these OCTA markers.
Aim:
To evaluate the influence of metabolic parameters and the treatment method in children with type 1 diabetes (T1D) on the optical coherence tomography angiography (OCTA) results as early markers of diabetic retinopathy (DR). Material and Methods. This prospective study enrolled 175 consecutive children with T1D. OCTA was performed using AngioVue (Avanti, Optovue). Whole superficial capillary vessel density (wsVD), fovea superficial vessel density (fsVD), parafovea superficial vessel density (psVD), whole deep vessel density (wdVD), fovea deep vessel density (fdVD), parafovea deep vessel density (pdVD), foveal thickness (FT), parafoveal thickness (PFT), and foveal avascular zone (FAZ) in superficial plexus were evaluated and analyzed in relation to individual characteristics, i.e., sex, weight, height, body mass index (BMI), and metabolic factors: current and mean value of glycated hemoglobin A1c (HbA1c). Furthermore, the analysis concerned the diabetes duration, age at the T1D onset, and type of treatment-multiple daily insulin injections (MDI) or continuous subcutaneous insulin infusion (CSII).
Results:
In the study group, we did not identify any patient with DR in fundus ophthalmoscopy. Age at the onset of diabetes correlated negatively with FAZ (r = -0.17, p < 0.05). The higher level of HbA1c corresponded to a decrease of wsVD (r = -0.13, p < 0.05). We found significantly lower fsVD (32.25 ± .1 vs. 33.98 ± .1, p < 0.01), wdVD (57.87 ± .1 vs. 58.64 ± .9, p < 0.01), and pdVD (60.60 ± .2 vs. 61.49 ± .1, p < 0.01) and larger FAZ area (0.25 ± .1 vs. 0.23 ± .1, p < 0.05) in the CSII vs. MDI group.
Conclusion:
The metabolic parameters, age of the onset of diabetes, and treatment method affected the OCTA results in children with T1D. Further studies and observation of these young patients are needed to determine if these findings are important for early detection of DR or predictive of future DR severity.
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