基于图像减影的多发性硬化症二维质子密度加权扫描病灶体积变化半自动量化方法的验证

Q4 Neuroscience Neuroimage. Reports Pub Date : 2023-12-21 DOI:10.1016/j.ynirp.2023.100194
Rozemarijn M. Mattiesing , Serena Stel , Alysha S. Mangroe , Iman Brouwer , Adriaan Versteeg , Ronald A. van Schijndel , Bernard M.J. Uitdehaag , Frederik Barkhof , Hugo Vrenken , Joost P.A. Kuijer
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引用次数: 0

摘要

背景检测和量化脑白质病变的变化对于监测多发性硬化症(MS)患者的治疗效果非常重要。现有的自动工具主要需要 FLAIR 图像作为输入,而 FLAIR 图像并不总是可用的,或者只关注新的/增大的活动。因此,我们开发并验证了一种基于二维质子密度(PD)加权图像和图像减影的半自动方法,用于量化病灶体积的变化。这种半自动方法可以深入了解 "阳性 "活动(定义为新增和扩大的病灶)和 "阴性 "活动(消失和缩小的病灶)。随访时间最长为 5 年。对两张 PD 加权图像进行归一化处理,将其注册到一个共同的半空间,进行强度匹配,然后进行减法。在手动病变掩膜内,使用减影强度阈值量化病变变化,并计算病变总体积变化(TLVC)。再现性是通过评估横向性来衡量的,具体来说,我们计算了两次就诊之间 TLVC 的一步直接测量和多步间接测量的绝对一致的类内相关系数 (ICCtrans) 和差值 (Δtrans)。通过计算绝对一致的类内相关系数(ICCacc)和两次就诊之间一步式半自动 TLVC 与人工测量的病变体积变化(数值差异)之间的差异(Δacc)来评估准确性。斯皮尔曼相关性(rs)用于评估整体和中心萎缩、人工测量的 T2 病灶体积以及病灶体积变化与该方法性能的关系,该性能通过差值测量 |Δtrans| 和 Δacc 反映出来。结果重现性非常好,ICCtrans 值在 0.90 到 0.96 之间。准确性总体良好,ICCacc 值在 0.67 到 0.86 之间。Δtrans 的标准偏差在 0.25 至 0.86 mL 之间。Δacc 的平均值在 0.11 到 0.37 mL 之间,与零有显著差异。整体萎缩和中心萎缩都与较低的再现性明显相关(|Δtrans|与整体萎缩的相关性,rs = -0.19 至 -0.28;|Δtrans|与中心萎缩的相关性,rs = 0.22 至 0.34)。总体/中心萎缩与准确性之间一般没有明显的相关性。病变体积越大,可重复性越低(rs = 0.62)。病灶体积变化越大,可重复性越低(rs = 0.22),准确性越低(Δacc 与病灶体积变化的相关性,rs = -0.52)。结论总的来说,半自动减影法可以对(早期)多发性硬化症随时间变化的病灶体积变化进行有效、可靠的定量研究,随访时间最长可达 5 年。
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Validation of a semi-automated method to quantify lesion volume changes in multiple sclerosis on 2D proton-density-weighted scans based on image subtraction

Background

The detection and quantification of changes in white matter lesions in the brain is important to monitor treatment effects in patients with multiple sclerosis (MS). Existing automatic tools predominantly require FLAIR images as input which are not always available, or only focus on new/enlarging activity. Therefore, we developed and validated a semi-automated method to quantify lesion volume changes based on 2D proton-density (PD)-weighted images and image subtraction. This semi-automated method provides insight in both “positive” activity (defined as new and enlarging lesions) and “negative” activity (disappearing and shrinking lesions).

Methods

Yearly MRI scans of patients with early MS from the REFLEX/REFLEXION studies were used. The maximum follow-up period was 5 years. Two PD-weighted images were normalized, registered to a common halfway-space, intensity-matched, and subsequently subtracted. Within manual lesion masks, lesion changes were quantified using a subtraction intensity threshold and total lesion volume change (TLVC) was calculated. Reproducibility was measured by assessing transitivity, specifically, we calculated the intraclass correlation coefficient for the absolute agreement (ICCtrans) and the difference (Δtrans) between the direct one-step and indirect multi-step measurements of TLVC between two visits. Accuracy was assessed by calculating both the intraclass correlation coefficient for absolute agreement (ICCacc) and the difference (Δacc) between the one-step semi-automated TLVC and manually measured lesion volume change (numerical difference) between two visits. Spearman's correlations (rs) were used to assess the relation of global and central atrophy, manually measured T2 lesion volume, and lesion volume change with the method's performance as reflected by the difference measures |Δtrans| and Δacc. An alpha of 0.05 was used as the cut-off for significance.

Results

Reproducibility was excellent, with ICCtrans values ranging from 0.90 to 0.96. Accuracy was good overall, with ICCacc values ranging from 0.67 to 0.86. The standard deviation of Δtrans ranged from 0.25 to 0.86 mL. The mean of Δacc ranged from 0.11 to 0.37 mL and was significantly different from zero. Both global and central atrophy significantly correlated with lower reproducibility (correlation of |Δtrans| with global atrophy, rs = −0.19 to −0.28, and correlation of |Δtrans| with central atrophy, rs = 0.22 to 0.34). There was generally no significant correlation between global/central atrophy and accuracy. Higher lesion volume was significantly correlated with lower reproducibility (rs = 0.62). Higher lesion volume change was significantly correlated with lower reproducibility (rs = 0.22) and lower accuracy (correlation of Δacc with lesion volume change, rs = −0.52).

Discussion

The semi-automated method to quantify lesion volume changes has excellent reproducibility and overall good accuracy. The amount of atrophy and especially lesion volume (change) should be taken into account when applying this method, as an increase in these variables might affect the quality of the results.

Conclusion

Overall, the semi-automated subtraction method allows a valid and reliable quantitative investigation of lesion volume changes over time in (early) MS for follow-up periods up to 5 years.

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来源期刊
Neuroimage. Reports
Neuroimage. Reports Neuroscience (General)
CiteScore
1.90
自引率
0.00%
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0
审稿时长
87 days
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