کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6265453 1614081 2010 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Research Report1H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Research Report1H MR spectroscopy in Friedreich's ataxia and ataxia with oculomotor apraxia type 2
چکیده انگلیسی

Background and aimFriedreich's ataxia (FRDA) and ataxia with oculomotor apraxia type 2 (AOA2) are the two most frequent forms of autosomal recessive cerebellar ataxias. However, brain metabolism in these disorders is poorly characterized and biomarkers of the disease progression are lacking. We aimed at assessing the neurochemical profile of the pons, the cerebellar hemisphere and the vermis in patients with FRDA and AOA2 to identify potential biomarkers of these diseases.MethodsShort-echo, single-voxel proton (1H) magnetic resonance spectroscopy data were acquired from 8 volunteers with FRDA, 9 volunteers with AOA2, and 38 control volunteers at 4T. Disease severity was assessed by the Friedreich's Ataxia Rating Scale (FARS).ResultsNeuronal loss/dysfunction was indicated in the cerebellar vermis and hemispheres in both diseases by lower total N-acetylaspartate levels than controls. The putative gliosis marker myo-inositol was higher than controls in the vermis and pons in AOA2 and in the vermis in FRDA. Total creatine, another potential gliosis marker, was higher in the cerebellar hemispheres in FRDA relative to controls. Higher glutamine in FRDA and lower glutamate in AOA2 than controls were observed in the vermis, indicating different mechanisms possibly leading to altered glutamatergic neurotransmission. In AOA2, total N-acetylaspartate levels in the cerebellum strongly correlated with the FARS score (p < 0.01).ConclusionDistinct neurochemical patterns were observed in the two patient populations, warranting further studies with larger patient populations to determine if the alterations in metabolite levels observed here may be utilized to monitor disease progression and treatment.

Research highlights► Friedreich's ataxia (FRDA) and ataxia with oculomotor apraxia type 2 (AOA2) are the two most frequent forms of autosomal recessive cerebellar ataxias. ► Biomarkers of the disease progression are lacking. ► (1H) magnetic resonance spectroscopy (MRS) was used to assess the neurochemical profile of the pons, the cerebellar hemisphere and the vermis in patients with FRDA and AOA2 to identify potential biomarkers of these diseases.► Distinct neurochemical patterns were observed in the two patient populations.► In AOA2, total N-acetylaspartate levels in the cerebellum strongly correlated with the FARS score (p  <  0.01). ► Studies with larger patient populations will determine if the alterations in metabolite levels observed here may be utilized to monitor disease progression and treatment.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research - Volume 1358, 28 October 2010, Pages 200-210
نویسندگان
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