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质量保证评估对大规模基于人群队列中扩散张量成像结果的影响。

The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort.

作者信息

Roalf David R, Quarmley Megan, Elliott Mark A, Satterthwaite Theodore D, Vandekar Simon N, Ruparel Kosha, Gennatas Efstathios D, Calkins Monica E, Moore Tyler M, Hopson Ryan, Prabhakaran Karthik, Jackson Chad T, Verma Ragini, Hakonarson Hakon, Gur Ruben C, Gur Raquel E

机构信息

Neuropsychiatry Section, Department of Psychiatry, USA.

Neuropsychiatry Section, Department of Psychiatry, USA.

出版信息

Neuroimage. 2016 Jan 15;125:903-919. doi: 10.1016/j.neuroimage.2015.10.068. Epub 2015 Oct 28.

DOI:10.1016/j.neuroimage.2015.10.068
PMID:26520775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4753778/
Abstract

BACKGROUND

Diffusion tensor imaging (DTI) is applied in investigation of brain biomarkers for neurodevelopmental and neurodegenerative disorders. However, the quality of DTI measurements, like other neuroimaging techniques, is susceptible to several confounding factors (e.g., motion, eddy currents), which have only recently come under scrutiny. These confounds are especially relevant in adolescent samples where data quality may be compromised in ways that confound interpretation of maturation parameters. The current study aims to leverage DTI data from the Philadelphia Neurodevelopmental Cohort (PNC), a sample of 1601 youths with ages of 8-21 who underwent neuroimaging, to: 1) establish quality assurance (QA) metrics for the automatic identification of poor DTI image quality; 2) examine the performance of these QA measures in an external validation sample; 3) document the influence of data quality on developmental patterns of typical DTI metrics.

METHODS

All diffusion-weighted images were acquired on the same scanner. Visual QA was performed on all subjects completing DTI; images were manually categorized as Poor, Good, or Excellent. Four image quality metrics were automatically computed and used to predict manual QA status: Mean voxel intensity outlier count (MEANVOX), Maximum voxel intensity outlier count (MAXVOX), mean relative motion (MOTION) and temporal signal-to-noise ratio (TSNR). Classification accuracy for each metric was calculated as the area under the receiver-operating characteristic curve (AUC). A threshold was generated for each measure that best differentiated visual QA status and applied in a validation sample. The effects of data quality on sensitivity to expected age effects in this developmental sample were then investigated using the traditional MRI diffusion metrics: fractional anisotropy (FA) and mean diffusivity (MD). Finally, our method of QA is compared with DTIPrep.

RESULTS

TSNR (AUC=0.94) best differentiated Poor data from Good and Excellent data. MAXVOX (AUC=0.88) best differentiated Good from Excellent DTI data. At the optimal threshold, 88% of Poor data and 91% Good/Excellent data were correctly identified. Use of these thresholds on a validation dataset (n=374) indicated high accuracy. In the validation sample 83% of Poor data and 94% of Excellent data was identified using thresholds derived from the training sample. Both FA and MD were affected by the inclusion of poor data in an analysis of an age, sex and race matched comparison sample. In addition, we show that the inclusion of poor data results in significant attenuation of the correlation between diffusion metrics (FA and MD) and age during a critical neurodevelopmental period. We find higher correspondence between our QA method and DTIPrep for Poor data, but we find our method to be more robust for apparently high-quality images.

CONCLUSION

Automated QA of DTI can facilitate large-scale, high-throughput quality assurance by reliably identifying both scanner and subject induced imaging artifacts. The results present a practical example of the confounding effects of artifacts on DTI analysis in a large population-based sample, and suggest that estimates of data quality should not only be reported but also accounted for in data analysis, especially in studies of development.

摘要

背景

扩散张量成像(DTI)被应用于神经发育和神经退行性疾病的脑生物标志物研究。然而,与其他神经成像技术一样,DTI测量的质量易受多种混杂因素(如运动、涡流)的影响,这些因素直到最近才受到关注。这些混杂因素在青少年样本中尤为重要,因为数据质量可能以混淆成熟参数解释的方式受到损害。本研究旨在利用来自费城神经发育队列(PNC)的DTI数据,该队列包含1601名年龄在8至21岁之间接受神经成像检查的青少年,以:1)建立用于自动识别低质量DTI图像质量的质量保证(QA)指标;2)在外部验证样本中检验这些QA措施的性能;3)记录数据质量对典型DTI指标发育模式的影响。

方法

所有扩散加权图像均在同一台扫描仪上采集。对所有完成DTI检查的受试者进行视觉QA;图像被手动分类为差、好或优。自动计算四个图像质量指标并用于预测手动QA状态:平均体素强度异常值计数(MEANVOX)、最大体素强度异常值计数(MAXVOX)、平均相对运动(MOTION)和时间信噪比(TSNR)。每个指标的分类准确率计算为受试者工作特征曲线(AUC)下的面积。为每个指标生成一个能最佳区分视觉QA状态的阈值,并应用于验证样本。然后使用传统的MRI扩散指标:分数各向异性(FA)和平均扩散率(MD),研究数据质量对该发育样本中预期年龄效应敏感性的影响。最后,将我们的QA方法与DTIPrep进行比较。

结果

TSNR(AUC = 0.94)能最好地区分差数据与好数据和优数据。MAXVOX(AUC = 0.88)能最好地区分好的DTI数据与优的DTI数据。在最佳阈值下,88%的差数据和91%的好/优数据被正确识别。在验证数据集(n = 374)上使用这些阈值显示出高准确率。在验证样本中,使用从训练样本得出的阈值识别出83%的差数据和94%的优数据。在年龄、性别和种族匹配的比较样本分析中,FA和MD均受到包含差数据的影响。此外,我们表明,在关键神经发育时期,包含差数据会导致扩散指标(FA和MD)与年龄之间的相关性显著减弱。我们发现对于差数据,我们的QA方法与DTIPrep的对应性更高,但我们发现我们的方法对于明显高质量的图像更稳健。

结论

DTI的自动QA可以通过可靠地识别扫描仪和受试者引起的成像伪影,促进大规模、高通量的质量保证。研究结果展示了伪影对基于大样本人群的DTI分析的混杂效应的一个实际例子,并表明不仅应报告数据质量估计值,而且在数据分析中也应考虑到数据质量,特别是在发育研究中。

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