医学
组内相关
神经影像学
海马结构
磁共振成像
阿尔茨海默病神经影像学倡议
成像生物标志物
生物标志物
核医学
阿尔茨海默病
队列
放射科
内科学
疾病
心理测量学
临床心理学
生物化学
化学
精神科
作者
Jill Abrigo,Lin Shi,Yishan Luo,Qianyun Chen,Chiu‐Wing Winnie Chu,Vincent Mok
出处
期刊:Acta Radiologica
[SAGE Publishing]
日期:2018-09-05
卷期号:60 (6): 769-776
被引量:59
标识
DOI:10.1177/0284185118795327
摘要
Background One significant barrier to incorporate Alzheimer’s disease (AD) imaging biomarkers into diagnostic criteria is the lack of standardized methods for biomarker quantification. The European Alzheimer’s Disease Consortium-Alzheimer’s Disease Neuroimaging Initiative (EADC-ADNI) Harmonization Protocol project provides the most authoritative guideline for hippocampal definition and has produced a manually segmented reference dataset for validation of automated methods. Purpose To validate automated hippocampal volumetry using AccuBrain™, against the EADC-ADNI dataset, and assess its diagnostic performance for differentiating AD and normal aging in an independent cohort. Material and Methods The EADC-ADNI reference dataset comprise of manually segmented hippocampal labels from 135 volumetric T1-weighted scans from various scanners. Dice similarity coefficient (DSC), intraclass correlation coefficient (ICC), and Pearson’s r were obtained for AccuBrain™ and FreeSurfer. The magnetic resonance imaging (MRI) of a separate cohort of 299 individuals (150 normal controls, 149 with AD) were obtained from the ADNI database and processed with AccuBrain™ to assess its diagnostic accuracy. Area under the curve (AUC) for total hippocampal volumes (HV) and hippocampal fraction (HF) were determined. Results Compared with EADC-ADNI dataset ground truths, AccuBrain™ had a mean DSC of 0.89/0.89/0.89, ICC of 0.94/0.96/0.95, and r of 0.95/0.96/0.95 for right/left/total HV. AccuBrain™ HV and HF had AUC of 0.76 and 0.80, respectively. Thresholds of ≤ 5.71 mL and ≤ 0.38% afforded 80% sensitivity for AD detection. Conclusion AccuBrain™ provides accurate automated hippocampus segmentation in accordance with the EADC-ADNI standard, with great potential value in assisting clinical diagnosis of AD.
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