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A pilot trial of deferiprone in pantothenate kinase-associated neurodegeneration patients

机译:去铁酮在泛酸激酶相关的神经变性患者中的初步试验

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Pantothenate kinase-associated neurodegeneration (PKAN) is the most common form of neurodegeneration with brain iron accumulation, it is an autosomal recessive disease due to mutation in PANK 2 on chromosome 20, which causes the accumulation of iron in basal ganglia and production of free radicals that cause degeneration of the cells. Deferiprone is an iron chelator that was used in treatment of thalassemia patients, it can cross the blood-brain barrier and reverse the iron deposition in the brain. Five patients with genetically confirmed PKAN received 15 mg/kg deferiprone twice daily. All patients were examined at baseline, 12 and 18 months and magnetic resonance imaging (MRI) was done at the baseline and after 18 months. In our study qualitative evaluation of MRI showed that deferiprone was able to reduce the iron load in globus pallidus of all the patients and the results of clinical rating scales show that in four patients, there is an improvement in the first 12 months. The results of our paper show that deferiprone can prevent the progression of the disease.
机译:泛酸激酶相关的神经变性(PKAN)是最常见的神经变性形式,伴有脑铁积聚。由于20号染色体上PANK 2的突变,它是一种常染色体隐性遗传疾病,可导致铁在基底神经节中积聚并产生自由基。导致细胞变性。去铁酮是一种铁螯合剂,用于治疗地中海贫血患者,它可以穿过血脑屏障并逆转大脑中的铁沉积。 5名经遗传学证实为PKAN的患者每天两次接受15 mg / kg去铁酮。在基线,12和18个月时检查所有患者,并在基线和18个月后进行磁共振成像(MRI)。在我们的研究中,MRI的定性评估表明,去铁酮能够减轻所有患者的苍白球铁负荷,临床评分量表的结果显示,四名患者的头12个月有改善。我们的研究结果表明,去铁酮可以预防疾病的进展。

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