Author:
Chen Tao,Sui Chaofan,Lin Suna,Guo Bin,Wang Yuanyuan,Yang Linfeng
Abstract
PurposeThe purpose of this study was to investigate whether baseline cerebral magnetic resonance imaging (MRI) characteristics could predict therapeutic responsiveness in patients with cobalamin C (cblC) defects.Materials and methodsThe cerebral MRI results of 40 patients with cblC defects were evaluated by a neuroradiologist. Neuropsychological scores and imaging data were collected. Neuropsychological tests were performed before and after standardized treatment.ResultsThirty-eight patients initially underwent neuropsychological testing [developmental quotient (DQ)]. CblC defects with cerebellar atrophy, corpus callosum thinning and ventricular dilation had significantly lower DQs than those without (P < 0.05). Through a multivariate linear stepwise regression equation after univariate analysis, ventricular dilation was the most valuable predictor of lower DQs. Thirty-six patients (94.7%) underwent follow-up neuropsychological testing. The pre- and post-treatment DQ values were not significantly different (Z = −1.611, P = 0.107). The post-treatment DQ classification (normal, moderately low, or extremely low) showed nearly no change compared to the pretreatment DQ classification (k = 0.790, P < 0.001).ConclusionVentricular dilation, cerebral atrophy and corpus callosum thinning are the main MRI abnormalities of cblC defects, and these manifestations are significantly correlated with delayed development in children. MRI findings can be considered an important tool for determining the severity of cblC defects.
Reference39 articles.
1. Long-term follow-up of 77 patients with isolated methylmalonic acidaemia.;Baumgarter;J. Inherit. Metab. Dis.,1995
2. Cobalamin (Cbl) C/D deficiency: Clinical, neurophysiological and neuroradiologic findings in 14 cases.;Biancheri;Neuropediatrics,2001
3. CT and NR of the brain in disorders of the propionate and methylmalonate metabolism.;Brismar;Am. J. Neuroradiol.,1994
4. Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management.;Carrillo-Carrasco;J. Inherit. Metab. Dis.,2012
5. Late-onset cblC deficiency around puberty: A retrospective study of the clinical characteristics, diagnosis, and treatment.;Chen;Orphanet J. Rare Dis.,2022
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