Persson Karin, Selbæk Geir, Brækhus Anne, Beyer Mona, Barca Maria, Engedal Knut
1 Norwegian National Advisory Unit on Ageing and Health, Vestfold Hospital Trust, Tønsberg, Norway.
2 Department of Geriatric Medicine, Oslo University Hospital, Oslo, Norway.
Acta Radiol. 2017 Jun;58(6):740-747. doi: 10.1177/0284185116669874. Epub 2016 Sep 28.
Background The dementia syndrome has been regarded a clinical diagnosis but the focus on supplemental biomarkers is increasing. An automatic magnetic resonance imaging (MRI) volumetry method, NeuroQuant® (NQ), has been developed for use in clinical settings. Purpose To evaluate the clinical usefulness of NQ in distinguishing Alzheimer's disease dementia (AD) from non-dementia and non-AD dementia. Material and Methods NQ was performed in 275 patients diagnosed according to the criteria of ICD-10 for AD, vascular dementia and Parkinson's disease dementia (PDD); the Winblad criteria for mild cognitive impairment; the Lund-Manchester criteria for frontotemporal dementia; and the revised consensus criteria for Lewy body dementia (LBD). Receiver operating curve (ROC) analyses with calculation of area under the curve (AUC) and regression analyses were carried out. Results Forebrain parenchyma (AUC 0.82), hippocampus (AUC 0.80), and inferior lateral ventricles (AUC 0.78) yielded the highest AUCs for AD/non-dementia discrimination. Only hippocampus (AUC 0.62) and cerebellum (AUC 0.67) separated AD from non-AD dementia. Cerebellum separated AD from PDD-LBD (AUC 0.83). Separate multiple regression analyses adjusted for age and gender, showed that memory (CERAD 10-word delayed recall) (beta 0.502, P < 0.001) was more strongly associated to the hippocampus volume than the diagnostic distinction of AD versus non-dementia (beta -0.392, P < 0.001). Conclusion NQ measures could separate AD from non-dementia fairly well but generally poorer from non-AD dementia. Degree of memory impairment, age, and gender, but not diagnostic distinction, were associated to the hippocampus volume in adjusted analyses. Surprisingly, cerebellum was found relevant in separating AD from PDD-LBD.
痴呆综合征一直被视为一种临床诊断,但对补充生物标志物的关注日益增加。一种用于临床的自动磁共振成像(MRI)容积测量方法——NeuroQuant®(NQ)已被开发出来。目的:评估NQ在区分阿尔茨海默病痴呆(AD)与非痴呆及非AD痴呆方面的临床实用性。材料与方法:对275例根据国际疾病分类第10版(ICD - 10)标准诊断为AD、血管性痴呆和帕金森病痴呆(PDD);根据温布拉德标准诊断为轻度认知障碍;根据伦德 - 曼彻斯特标准诊断为额颞叶痴呆;以及根据路易体痴呆(LBD)修订共识标准诊断的患者进行NQ检查。进行了计算曲线下面积(AUC)的受试者操作特征曲线(ROC)分析和回归分析。结果:前脑实质(AUC 0.82)、海马体(AUC 0.80)和外侧脑室下部(AUC 0.78)在AD/非痴呆鉴别中曲线下面积最高。只有海马体(AUC 0.62)和小脑(AUC 0.67)能将AD与非AD痴呆区分开。小脑能将AD与PDD - LBD区分开(AUC 0.83)。经年龄和性别校正的单独多元回归分析显示,记忆(CERAD 10词延迟回忆)(β 0.502,P < 0.001)与海马体体积的相关性比AD与非痴呆的诊断区分(β -0.392,P < 0.001)更强。结论:NQ测量能较好地将AD与非痴呆区分开,但通常在区分AD与非AD痴呆方面较差。在校正分析中,记忆损害程度、年龄和性别与海马体体积相关,而非诊断区分。令人惊讶的是,发现小脑在区分AD与PDD - LBD方面具有相关性。