4.4 Article

Ocular changes in nephrotic syndrome patients with preserved renal functions

Journal

PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY
Volume 39, Issue -, Pages -

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ELSEVIER
DOI: 10.1016/j.pdpdt.2022.103024

Keywords

Nephrotic syndrome; Inflammation; Choroidal thickness; Hypoalbuminemia; Ocular changes; Optical Coherence tomography

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This study evaluated ocular changes in primary NS patients with preserved renal functions. The results suggest that measurements of CCT, CFT, and RAC with OCT may serve as markers of inflammation in NS patients.
Background: Optical coherence tomography (OCT) measurements of central choroidal thickness (CCT) and retinal thickness have been proposed as inflammatory indicators for a variety of systemic disorders, particularly those with a vascular component. The relationship between nephrotic syndrome (NS) and visual impairment is not clear. The aim of this study was to evaluate the ocular changes in primary NS patients with preserved renal functions. Methods: A total of 60 participants (30 NS patients, 30 healthy control subjects) was recruited in this cross-sectional and comparative study. Retinal and choroidal examinations were performed via the spectral domain OCT. Enhanced depth imaging (EDI) mode of the OCT was used for choroidal analysis. Results: Although not statistically significant, CCT was found to be higher in the NS group compared to the control group (p = 0.07). Central foveal thickness (CFT) and retinal arteriolar caliber (RAC) values were sta-tistically significantly lower in the patients with nephrotic syndrome, whereas retinal venular caliber (RVC) and choroidal vascularity index (CVI) values were similar in both groups. RAC and RVC were not statistically significantly correlated with CCT or CFT in both groups (p > 0.05). Conclusion: The results of the current study showed a significant difference between the NS group and the control group in terms of some ocular changes (i.e., CFT and RAC). As a result, CCT, CFT and RAC measurements with OCT may be used as a marker of inflammation in NS patients.

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