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Investigating Ganglion Cell Complex Thickness in Children with Chronic Heart Failure due to Dilated Cardiomyopathy
Klaudia Rakusiewicz1, Krystyna Kanigowska1, Wojciech Hautz1
1Department of Ophthalmology, Children's Memorial Health Institute, 04-730 Warsaw, Poland.
Insights
This study found no significant differences in ganglion cell complex thickness in children with chronic heart failure (CHF) due to dilated cardiomyopathy (DCM) compared to healthy children. Optical coherence tomography (OCT) revealed no changes in these key retinal measurements.
Area of Science:
- Ophthalmology
- Cardiology
- Pediatrics
Background:
- Chronic heart failure (CHF) in children, often due to dilated cardiomyopathy (DCM), can have systemic effects.
- Assessing ocular health in pediatric patients with CHF is crucial for comprehensive care.
Purpose of the Study:
- To evaluate ganglion cell complex (GCC) thickness in pediatric patients with CHF/DCM using optical coherence tomography (OCT).
- To compare GCC parameters between children with CHF/DCM and healthy controls.
Main Methods:
- Sixty eyes from 30 pediatric patients with CHF/DCM and 60 eyes from 30 healthy children were analyzed.
- Optical coherence tomography (OCT) was used to measure average GCC (avgGCC), superior GCC (supGCC), inferior GCC (infGCC), global loss of volume (GLV), and focal loss of volume (FLV).
- Statistical analysis compared parameters between the CHF/DCM group and the control group, and explored correlations with clinical factors.
Main Results:
- No significant differences were found in avgGCC, supGCC, infGCC, GLV, or FLV between children with CHF/DCM and healthy controls.
- No correlations were observed between GCC parameters and ocular biometry, refractive errors, age, NT-proBNP, or LVEF.
- No significant differences were noted based on sex or between the left and right eyes.
Conclusions:
- This study, the first of its kind, indicates no alterations in GCC thickness in pediatric patients with DCM-related CHF.
- The findings suggest that GCC thickness may not be a sensitive indicator of cardiac dysfunction in this specific pediatric population.
- Further research may explore other ocular parameters or different etiologies of pediatric heart failure.
Purpose:
To assess ganglion cell complex (GCC) thickness in children with chronic heart failure (CHF) due to dilated cardiomyopathy (DCM) using optical coherence tomography (OCT).
Methods:
Sixty eyes of 30 patients with chronic heart failure (CHF) due to dilated cardiomyopathy (DCM) and 60 eyes of 30 age- and sex-matched healthy volunteers (control group) were enrolled. The mean age of the patients and controls was 9.9 ± 3.57 (range 5-17) years and 10.08 ± 3.41 (range 4-16) years, respectively. All patients underwent a complete ophthalmic assessment and OCT imaging using RTVue XR Avanti (Optovue). The following OCT-based parameters were analysed: average ganglion cell complex thickness (avgGCC), superior ganglion cell complex thickness (supGCC), inferior ganglion cell complex thickness (infGCC), global loss of volume (GLV) and focal loss of volume (FLV).
Results:
There were no significant differences in avgGCC (98.13 μm vs. 99.96 μm, p = 0.21), supGCC (97.17 μm vs. 99.29 μm, p = 0.13), infGCC (99.03 μm vs. 100.71 μm, p = 0.25), FVL (0.49% vs. 0.4%, p = 0.25) and GVL (2.1% vs. 1.3%, p = 0.09) between patients with chronic heart failure due to dilated cardiomyopathy and healthy children. There was no correlation between avgGCC, supGCC, infGCC, FLV, GLV and ocular biometry, refractive errors or age. There was no correlation between avgGCC, supGCC, infGCC, FLV, GLV and NT-proBNP or LVEF. There were no significant differences in the studied parameters between the sexes. There were no significant differences in the studied parameters between the left and right eye.
Conclusion:
Our study seems to be the first to analyse ganglion cell complex in paediatric patients with dilated cardiomyopathy. We have demonstrated no changes in the ganglion cell complex thickness parameters in children with chronic heart failure due dilated cardiomyopathy, as compared to their healthy peers.
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