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1.
Int J Mol Sci ; 17(10)2016 Sep 30.
Artigo em Inglês | MEDLINE | ID: mdl-27706045

RESUMO

Changes in cerebral lesion load by magnetic resonance imaging (MRI) in patients from a double-blind, placebo-controlled, phase II study on erythropoietin in clinically isolated optic neuritis (ClinicalTrials.gov, NCT00355095) were analyzed. Therefore, patients with acute optic neuritis were assigned to receive either 33,000 IU of recombinant human erythropoietin (IV) daily for three days, or a placebo, as an add-on to methylprednisolone. Of 35 patients, we investigated changes in cerebral lesion load in MRIs obtained at baseline and at weeks 4, 8, and 16. In 5 of the 35 patients, we found conversion into multiple sclerosis (MS) based on MRI progression only. These five patients had received the placebo. Another five patients showed MRI progression together with relapses. Three of these patients had received erythropoietin, and two the placebo. Yet, analyzing the change in absolute numbers of periventricular, juxtacortical, and infratentorial lesions including gadolinium-enhancing lesions, there were no significant differences between the groups. Although effective in terms of retinal nerve fiber layer protection, erythropoietin treatment of acute isolated optic neuritis did not influence further evolution of MRI lesions in the brain when comparing absolute numbers. However, early conversion from clinically isolated syndrome to MS assessed by MRI activity seemed to occur more frequently in the placebo-treated group.


Assuntos
Epoetina alfa/uso terapêutico , Hematínicos/uso terapêutico , Esclerose Múltipla/diagnóstico , Neurite Óptica/tratamento farmacológico , Adolescente , Adulto , Progressão da Doença , Método Duplo-Cego , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Metilprednisolona/uso terapêutico , Pessoa de Meia-Idade , Esclerose Múltipla/etiologia , Fármacos Neuroprotetores/uso terapêutico , Neurite Óptica/complicações , Efeito Placebo , Acuidade Visual , Adulto Jovem
2.
Ann Neurol ; 72(2): 199-210, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22926853

RESUMO

OBJECTIVE: Based on findings in animal models of autoimmune optic nerve inflammation, we have assessed the safety and efficacy of erythropoietin in patients presenting with a first episode of optic neuritis. METHODS: Patients with optic neuritis who attended the University Hospitals of Homburg/Saar, Göttingen, or Hamburg (Germany) were included in this double-blind, placebo-controlled, phase 2 study (ClinicalTrials.gov, NCT00355095). They were randomly assigned to groups receiving either 33,000IU recombinant human erythropoietin intravenously daily for 3 days or placebo as an add-on therapy to methylprednisolone. The primary outcome parameter was change in retinal nerve fiber layer (RNFL) thickness after 16 weeks. Secondary outcome parameters included optic nerve atrophy as assessed by magnetic resonance imaging, and changes in visual acuity, visual field, and visual evoked potentials (VEPs). RESULTS: Forty patients were assigned to the treatment groups (21/19 erythropoietin/placebo). Safety monitoring revealed no relevant issues. Thirty-seven patients (20/17 erythropoietin/placebo) were analyzed for the primary endpoint according to the intention-to-treat protocol. RNFL thinning was less apparent after erythropoietin treatment. Thickness of the RNFL decreased by a median of 7.5µm by week 16 (mean ± standard deviation, 10.55 ± 17.54µm) compared to a median of 16.0µm (22.65 ± 29.18µm) in the placebo group (p = 0.0357). Decrease in retrobulbar diameter of the optic nerve was smaller in the erythropoietin group (p = 0.0112). VEP latencies at week 16 were shorter in erythropoietin-treated patients than in the placebo group (p = 0.0011). Testing of visual functions revealed trends toward an improved outcome after erythropoietin treatment. INTERPRETATION: These results give the first indications that erythropoietin might be neuroprotective in optic neuritis.


Assuntos
Anti-Inflamatórios/uso terapêutico , Eritropoetina/uso terapêutico , Neurite Óptica/tratamento farmacológico , Adulto , Método Duplo-Cego , Potenciais Evocados Visuais/efeitos dos fármacos , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Metilprednisolona/uso terapêutico , Pessoa de Meia-Idade , Nervo Óptico/efeitos dos fármacos , Nervo Óptico/patologia , Neurite Óptica/patologia , Retina/efeitos dos fármacos , Retina/patologia , Tomografia de Coerência Óptica , Resultado do Tratamento , Acuidade Visual/efeitos dos fármacos , Testes de Campo Visual , Campos Visuais/efeitos dos fármacos , Adulto Jovem
3.
J Phys Chem A ; 114(29): 7733-41, 2010 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-20597535

RESUMO

An in situ infrared spectroscopic analysis of the thermal dehydration of zirconyl chloride octahydrate was carried out to identify bending mode vibrations of distinctive water molecules in this well-defined zirconium(IV) cluster cation. TG-MS analysis revealed the particular temperatures where one water molecule at a time was removed from the solid hydrate. In situ IR data unveiled remarkable spectral changes featuring isosbestic behavior. We were able to experimentally distinguish between delta(H(2)O) modes from coordinatively bound water molecules (Zr-(OH(2))(3), 1595 cm(-1)), tetrahedrally coordinated lattice water (H(2)O dimer, 1620 cm(-1)), as well as strongly H-bonded lattice waters accommodating hydrated protons (1705 and 1666 cm(-1)). Spectral changes in the range from 1050 and 900 cm(-1) during dehydration are discussed.

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