Easy-to-use and easy-to-interpret quality control of 3D gradient echo T1-weighted MR acquisition sequences for improved test-retest stability of MRI-based hippocampus volumetry

模式识别(心理学) 核医学 再现性 人工智能 计算机科学 医学 数学 统计
作者
Ralph Buchert,Per Suppa,Babak A. Ardekani,Fuensanta Bellvís Bataller,Pierrick Bourgeat,Pierrick Coupé,Robert Dahnke,Gabriel A. Devenyi,Simon Fristed Eskildsen,Clara Fischer,Jose Vincente Manjón Herrera,Christian Ledig,Andreas Lemke,Bénédicte Maréchal,Roland Opfer,Diana M. Sima,Lothar Spies,Aziz M. Uluğ,Hans‐Jürgen Huppertz
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
标识
DOI:10.1177/13872877251380301
摘要

Background MRI-based hippocampus volume (HV) is widely used as neurodegeneration marker in Alzheimer's disease. Objective An easy-to-use and easy-to-interpret method to categorize T1-weighted MR sequences with respect to test-retest stability of hippocampus volumetry based on general image quality metrics (IQM). Methods The study included 446 3D T1-weighted MRI scans of one healthy middle-aged man obtained during 32 months in 122 scanning sessions performed with 96 different scanners at 76 different sites. Each scanning session represented a different acquisition sequence of ≥2 back-to-back repeat scans (3.7 ± 0.7 on average). Unilateral HVs were determined with 18 different tools for automatic volumetry. An acquisition sequence was considered “poor” if the z-score of the within-session coefficient-of-variation of the HV estimates from the session, averaged across all volumetry tools and both hemispheres, exceeded one standard deviation. General IQM were computed for each scanning session using the freely available MRI Quality Control Tool. A classification-and-regression tree (CART) was trained to discriminate between good and poor acquisition sequences using the IQM as input. Results The CART selected the left-right width of the acquisition field-of-view and the contrast-to-noise ratio as predictor variables. Overall accuracy of the CART was 79.5%. CART-based classification increased the ratio of good-to-poor acquisition sequences from 3.5 among all sequences to 7.4 among the sequences predicted to be good. This was at the expense of losing 15% of the good sequences. Conclusions The IQM-based decision tree model provides useful performance for the differentiation of T1-weighted sequences associated with good versus poor test-retest stability of hippocampus volumetry.

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