Elyounssi Safia, Kunitoki Keiko, Clauss Jacqueline A, Laurent Eline, Kane Kristina, Hughes Dylan E, Hopkinson Casey E, Bazer Oren, Sussman Rachel Freed, Doyle Alysa E, Lee Hang, Tervo-Clemmens Brenden, Eryilmaz Hamdi, Gollub Randy L, Barch Deanna M, Satterthwaite Theodore D, Dowling Kevin F, Roffman Joshua L
Department of Psychiatry, Massachusetts General Hospital and Harvard Medical School.
Martinos Center for Biomedical Imaging, Massachusetts General Hospital.
bioRxiv. 2023 Mar 1:2023.02.28.530498. doi: 10.1101/2023.02.28.530498.
Large, population-based MRI studies of adolescents promise transformational insights into neurodevelopment and mental illness risk . However, MRI studies of youth are especially susceptible to motion and other artifacts . These artifacts may go undetected by automated quality control (QC) methods that are preferred in high-throughput imaging studies, 5 and can potentially introduce non-random noise into clinical association analyses. Here we demonstrate bias in structural MRI analyses of children due to inclusion of lower quality images, as identified through rigorous visual quality control of 11,263 T1 MRI scans obtained at age 9-10 through the Adolescent Brain Cognitive Development (ABCD) Study6. Compared to the best-rated images (44.9% of the sample), lower-quality images generally associated with decreased cortical thickness and increased cortical surface area measures (Cohen's d 0.14-2.84). Variable image quality led to counterintuitive patterns in analyses that associated structural MRI and clinical measures, as inclusion of lower-quality scans altered apparent effect sizes in ways that increased risk for both false positives and negatives. Quality-related biases were partially mitigated by controlling for surface hole number, an automated index of topological complexity that differentiated lower-quality scans with good specificity at Baseline (0.81-0.93) and in 1,000 Year 2 scans (0.88-1.00). However, even among the highest-rated images, subtle topological errors occurred during image preprocessing, and their correction through manual edits significantly and reproducibly changed thickness measurements across much of the cortex (d 0.15-0.92). These findings demonstrate that inadequate QC of youth structural MRI scans can undermine advantages of large sample size to detect meaningful associations.
基于大规模人群的青少年MRI研究有望为神经发育和精神疾病风险带来变革性的见解。然而,针对青少年的MRI研究特别容易受到运动和其他伪影的影响。这些伪影可能无法被高通量成像研究中首选的自动质量控制(QC)方法检测到,并且可能会在临床关联分析中引入非随机噪声。在此,我们通过对青少年大脑认知发展(ABCD)研究在9至10岁时获得的11263份T1 MRI扫描进行严格的视觉质量控制,证明了由于纳入质量较低的图像,儿童结构MRI分析中存在偏差。与评级最高的图像(占样本的44.9%)相比,质量较低的图像通常与皮质厚度减小和皮质表面积测量值增加相关(科恩d值为0.14 - 2.84)。图像质量的变化导致在将结构MRI与临床测量相关联的分析中出现违反直觉的模式,因为纳入质量较低的扫描会以增加假阳性和假阴性风险的方式改变表观效应大小。通过控制表面空洞数量,部分减轻了与质量相关的偏差,表面空洞数量是拓扑复杂性的自动指标,在基线时(0.81 - 0.93)以及在1000份第二年的扫描中(0.88 - 1.00),该指标能以良好的特异性区分质量较低的扫描。然而,即使在评级最高的图像中,图像预处理过程中也会出现细微的拓扑错误,通过手动编辑对其进行校正会显著且可重复地改变大部分皮质的厚度测量值(d值为0.15 - 0.92)。这些发现表明,对青少年结构MRI扫描的质量控制不足会削弱大样本量在检测有意义关联方面的优势。