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作 者:孙峰[1] 邢永红[2] 孔屏[1] 张本恕[3] 张云亭[4]
机构地区:[1]天津医科大学总医院干部保健部,天津300052 [2]天津市环湖医院神经内科,天津300060 [3]天津医科大学总医院神经内科,天津300052 [4]天津医科大学总医院放射科,天津300052
出 处:《临床荟萃》2010年第5期401-404,共4页Clinical Focus
摘 要:目的利用氢质子磁共振波谱(1H MRS)技术,研究认知障碍的帕金森病(PD)患者脑部代谢变化。进一步探索帕金森痴呆(PDD)患者发生痴呆的病因。方法早期PD患者(H&Y分级<Ⅲ级)38例(MMSE评分≥26分)、PDD患者(H&Y分级<Ⅲ级)33例和健康对照组(HC)25例行1H MRS检查,测定脑部壳核与额叶的N-乙酰天门冬氨酸/肌酸(NAA/Cr)和乙酰天门冬氨酸/胆碱复合物(NAA/Cho)比值。结果PDD组比HC组患肢同侧壳核NAA/Cr的比值明显降低,(1.365±0.127)vs(1.522±0.188)(P<0.01),PDD组与PD组比HC组患肢对侧壳核的NAA/Cr比值明显降低,(1.123±0.154)vs(1.393±0.195)vs(1.529±0.196)(均P<0.01),PDD组与PD组比HC组患肢对侧额叶的NAA/Cr的比值明显降低,(1.419±0.206)和(1.536±0.178)vs(1.633±0.198)(P<0.05)。3组的NAA/Cho比值差异无统计学意义(P>0.05)。结论1H MRS可以检测到PDD患者脑部的代谢改变,有助于PDD的病因诊断及风险预测。Objective To evaluate N-acetylaspartate/creatine (NAA/Cr) and NAA/choline (Cho) using hydrogen proton magnetic resonance spectroscopy(^1H MRS) in Parkinson disease with dementia(PDD) for the cause of cognitive impairment with PDD. Methods Seventy-one patients (PD = 38, PDD= 33) and 25 age-matched healthy controls(HC) underwent serial volumetric 1.5T ^1H MRS. All patients (H&Y〈Ⅲ )were assessed using unified Parkinson disease rating scale(UPDRS) and mini-mental state examination(MMSE),^1H MRS collection in the areas of the putamen and frontal lobe. Results There was a significant reduction in NAA/Cr ratio in contra-putamen to the worst clinically affected limbs of patients with PDD compared with PD, (1. 123± 0. 154) vs (1. 393±0, 195) (P〈 0.01),and PD was lower compared to HC ( 1. 393± 0. 195) vs ( 1. 529 ± 0. 196) ( P 〈0.01). There were significant reductions in NAA/Cr ratio in ipsil-putamen to the worst clinically affected limbs of the patients with PDD compared to HC, (1. 365 ± 0.127 ) vs ( 1. 522 ±0. 188) ( P 〈0.01). Compared to HC, NAA/Cr ratio of contra-frontal lobe was significantly decreased in PD and PDD (1. 536±0. 178), (1. 419±0. 206) vs (1. 633±0. 198) ( P 〈0.01). There were no significant differences in other compared groups of NAA/Cr ratio. No abnormalities were observed in NAA/Cho (P 〉 0. 05). Conclusion ^1H MRS may be a valuable tool for monitoring disease progression in PDD and further studies should investigate its utility for the early diagnosis.
分 类 号:R749.16[医药卫生—神经病学与精神病学]
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