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Updated: Apr 25, 2026

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study
Published on: April 11, 2018
Cystic fibrosis and new trends by ophthalmological evaluation: a pilot study
Marcella Nebbioso1, Serena Quattrucci2, Emanuela Leggieri2
1Department of Sense Organs, Ocular Electrophysiology Center, Policlinico Umberto I, Viale del Policlinico 155, 00161 Rome, Italy ; Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.
Background:
Cystic fibrosis (CF) is characterized by hypoxia that affects several organic tissues. Retinal ganglion cells may suffer from the hypoxic status, and this may lead to alterations of retinal nerve fiber.
Methods:
Twenty-two eyes in CF patients were analyzed. A complete ocular evaluation and visual field exams of the 30 central degrees were performed using the frequency doubling technology (FDT). Forced expiratory volume in one second (FEV1%), forced vital capacity (FVC%), oxyhaemoglobin saturation (SpO2%), and hematocrit (Ht%) have been calculated. FDT analyzed parameters were mean deviation (MD) and pattern standard deviation (PSD). Pearson's correlation was chosen as statistical analysis.
Results:
Data showed statistically significant relationship between MD and Ht% (r value -0.18; P = 0.04), MD and FEV1% (r value -0.68; P = 0.001), and MD and FVC% (r value -0.45; P = 0.005). Moreover, there were correlations between PSD and Ht% (r value 0.29; P = 0.03), PSD and SpO2% (r value -0.31; P = 0.01), PSD and FEV1% (r value 0.71; P = 0.0005), and PSD and FVC% (r value 0.63; P = 0.003).
Conclusions:
The oxygen supply alterations might determine hypoxia of the ganglion cells causing a decrease of receptive optic nerve fiber activity. This method could be also useful to evaluate indirectly pulmonary activity of the CF disease.
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