BACKGROUND AND PURPOSE: Our work evaluates visual function before and after treatment with cytidine-5-diphosphocholine (Citicoline) in patients with non-arteritic ischaemic optic neuropathy (NION). METHODS: Twenty-six patients in which at least 6 months elapsed from NION, were randomly divided into two age-similar groups: 14 patients had Citicoline (Cebrolux-Tubilux, Italy, 1600 mg/diem for 60 days, followed by a 120-day period of wash out, days 60-180) (T-NION); 12 patients had no treatment during the same period (NT-NION). At day 180, in T-NION a second period of treatment (days 181-240) followed by a wash-out (days 241-360) was performed. Fourteen age-matched healthy subjects provided normative data. In all patients, pattern-electroretinogram (PERG), visual evoked potentials (VEPs) and visual acuity (VA) measurements were performed at baseline and at days 60 and 180. In T-NION, further measurements were achieved at days 240 and 360. RESULTS: At baseline, NT-NION and T-NION patients showed abnormal PERGs and VEPs, and reduced VA, compared to controls. At the end of treatment (days 60 and 240), T-NION patients showed improvement (P < 0.01) of PERGs, VEPs parameters and VA, compared to pre-treatment values. After wash out, functional improvements persisted compared to baseline. No changes in NT-NION patients were observed. CONCLUSIONS: Our results suggest a beneficial effect of oral Citicoline in NION.

Parisi, V., Coppola, G., Ziccardi, L., Gallinaro, G., Falsini, B., Cytodine-5 diphosphocholine (citicoline): a pilot study in patients with non-arteritic ischaemic optic neuropathy, <<EUROPEAN JOURNAL OF NEUROLOGY>>, 2008; (15): 465-474 [http://hdl.handle.net/10807/70248]

Cytodine-5 diphosphocholine (citicoline): a pilot study in patients with non-arteritic ischaemic optic neuropathy

G; Ziccardi;G; Falsini
2008

Abstract

BACKGROUND AND PURPOSE: Our work evaluates visual function before and after treatment with cytidine-5-diphosphocholine (Citicoline) in patients with non-arteritic ischaemic optic neuropathy (NION). METHODS: Twenty-six patients in which at least 6 months elapsed from NION, were randomly divided into two age-similar groups: 14 patients had Citicoline (Cebrolux-Tubilux, Italy, 1600 mg/diem for 60 days, followed by a 120-day period of wash out, days 60-180) (T-NION); 12 patients had no treatment during the same period (NT-NION). At day 180, in T-NION a second period of treatment (days 181-240) followed by a wash-out (days 241-360) was performed. Fourteen age-matched healthy subjects provided normative data. In all patients, pattern-electroretinogram (PERG), visual evoked potentials (VEPs) and visual acuity (VA) measurements were performed at baseline and at days 60 and 180. In T-NION, further measurements were achieved at days 240 and 360. RESULTS: At baseline, NT-NION and T-NION patients showed abnormal PERGs and VEPs, and reduced VA, compared to controls. At the end of treatment (days 60 and 240), T-NION patients showed improvement (P < 0.01) of PERGs, VEPs parameters and VA, compared to pre-treatment values. After wash out, functional improvements persisted compared to baseline. No changes in NT-NION patients were observed. CONCLUSIONS: Our results suggest a beneficial effect of oral Citicoline in NION.
Inglese
Parisi, V., Coppola, G., Ziccardi, L., Gallinaro, G., Falsini, B., Cytodine-5 diphosphocholine (citicoline): a pilot study in patients with non-arteritic ischaemic optic neuropathy, <<EUROPEAN JOURNAL OF NEUROLOGY>>, 2008; (15): 465-474 [http://hdl.handle.net/10807/70248]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/70248
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