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帕金森病痴呆和路易体痴呆中的灰质萎缩。

Gray matter atrophy in Parkinson disease with dementia and dementia with Lewy bodies.

作者信息

Beyer Mona K, Larsen Jan P, Aarsland Dag

机构信息

Department of Radiology, Stavanger University Hospital, Stavanger, Norway.

出版信息

Neurology. 2007 Aug 21;69(8):747-54. doi: 10.1212/01.wnl.0000269666.62598.1c.

Abstract

BACKGROUND

The nosologic relationship between dementia with Lewy bodies (DLB) and Parkinson disease with dementia (PDD) is continuously being debated. We conducted a study using voxel-based morphometry (VBM) to explore the pattern of cortical atrophy in DLB and PDD.

METHODS

Seventy-four patients and healthy elderly were imaged (healthy elderly n = 20, PDD n = 15, DLB n = 18, and Alzheimer dementia [AD] n = 21).Three dimensional T1-weighted MRI were acquired, and images analyzed using VBM. The following diagnostic criteria were used: criteria proposed by the third report of the DLB Consortium for DLB, the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Diseases Association criteria for AD, and Diagnostic and Statistical Manual of Mental Disorders, fourth edition criteria for dementia in PDD.

RESULTS

Overall dementia severity was similar in the dementia groups. We found more pronounced cortical atrophy in DLB than in PDD in the temporal, parietal, and occipital lobes. Patients with AD had reduced gray matter concentrations in the temporal lobes bilaterally, including the amygdala, compared to PDD. Compared to DLB, the AD group had temporal and frontal lobe atrophy.

CONCLUSION

We found that despite a similar severity of dementia, patients with dementia with Lewy bodies (DLB) had more cortical atrophy than patients with Parkinson disease with dementia (PDD), indicating different brain substrates underlying dementia in the two syndromes. Together with previous studies reporting subtle clinical and neurobiologic differences between DLB and PDD, our findings support the hypothesis that PDD and DLB are not identical entities, but rather represent two subtypes of a spectrum of Lewy body disease.

摘要

背景

路易体痴呆(DLB)与帕金森病痴呆(PDD)之间的疾病分类关系一直存在争议。我们进行了一项基于体素的形态学测量(VBM)研究,以探索DLB和PDD的皮质萎缩模式。

方法

对74例患者和健康老年人进行了成像(健康老年人n = 20,PDD n = 15,DLB n = 18,阿尔茨海默病[AD] n = 21)。采集三维T1加权MRI图像,并使用VBM进行分析。采用以下诊断标准:DLB联盟第三份报告中提出的DLB标准、美国国立神经疾病和中风研究所及阿尔茨海默病及相关疾病协会的AD标准以及《精神疾病诊断与统计手册》第四版中PDD痴呆的标准。

结果

痴呆组的总体痴呆严重程度相似。我们发现,DLB患者在颞叶、顶叶和枕叶的皮质萎缩比PDD患者更明显。与PDD相比,AD患者双侧颞叶(包括杏仁核)的灰质浓度降低。与DLB相比,AD组存在颞叶和额叶萎缩。

结论

我们发现,尽管痴呆严重程度相似,但路易体痴呆(DLB)患者的皮质萎缩比帕金森病痴呆(PDD)患者更多,这表明这两种综合征中痴呆的脑基质不同。结合先前报道DLB和PDD之间存在细微临床和神经生物学差异的研究,我们的发现支持以下假设:PDD和DLB并非同一实体,而是路易体病谱系中的两种亚型。

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