Fully-automated segmentation of muscle and inter-/intra-muscular fat from magnetic resonance images of calves and thighs: an open-source workflow in Python.

IF 5.3 2区 医学 Q2 CELL BIOLOGY Skeletal Muscle Pub Date : 2024-12-27 DOI:10.1186/s13395-024-00365-z
Kenneth Tam, Si Wen Liu, Sarah Costa, Eva Szabo, Shannon Reitsma, Hana Gillick, Jonathan D Adachi, Andy Kin On Wong
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引用次数: 0

Abstract

Background: INTER- and INTRAmuscular fat (IMF) is elevated in high metabolic states and can promote inflammation. While magnetic resonance imaging (MRI) excels in depicting IMF, the lack of reproducible tools prevents the ability to measure change and track intervention success.

Methods: We detail an open-source fully-automated iterative threshold-seeking algorithm (ITSA) for segmenting IMF from T1-weighted MRI of the calf and thigh within three cohorts (CaMos Hamilton (N = 54), AMBERS (N = 280), OAI (N = 105)) selecting adults 45-85 years of age. Within the CaMos Hamilton cohort, same-day and 1-year repeated images (N = 38) were used to evaluate short- and long-term precision error with root mean square coefficients of variation; and to validate against semi-automated segmentation methods using linear regression. The effect of algorithmic improvements to fat ascertainment using 3D connectivity and partial volume correction rules on analytical precision was investigated. Robustness and versatility of the algorithm was demonstrated by application to different MR sequences/magnetic strength and to calf versus thigh scans.

Results: Among 439 adults (319 female(89%), age: 71.6 ± 7.6 yrs, BMI: 28.06 ± 4.87 kg/m2, IMF%: 10.91 ± 4.57%), fully-automated ITSA performed well across MR sequences and anatomies from three cohorts. Applying both 3D connectivity and partial volume fat correction improved precision from 4.99% to 2.21% test-retest error. Validation against semi-automated methods showed R2 from 0.92 to 0.98 with fully-automated ITSA routinely yielding more conservative computations of IMF volumes. Quality control shows 7% of cases requiring manual correction, primarily due to IMF merging with subcutaneous fat. A full workflow described methods to export tags for manual correction.

Conclusions: The greatest challenge in segmenting IMF from MRI is in selecting a dynamic threshold that consistently performs across repeated imaging. Fully-automated ITSA achieved this, demonstrated low short- and long-term precision error, conducive of use within RCTs.

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从小腿和大腿的磁共振图像中全自动分割肌肉和肌肉间/肌肉内脂肪:Python的开源工作流程。
背景:肌间和肌内脂肪(IMF)在高代谢状态下升高,可促进炎症。虽然磁共振成像(MRI)在描绘IMF方面表现出色,但缺乏可重复的工具阻碍了测量变化和跟踪干预成功的能力。方法:我们详细介绍了一种开源的全自动迭代阈值搜索算法(ITSA),用于在三个队列(CaMos Hamilton (N = 54), AMBERS (N = 280), OAI (N = 105))中从小腿和大腿的t1加权MRI中分割IMF,这些队列选择了45-85岁的成年人。在CaMos Hamilton队列中,使用当天和1年重复图像(N = 38)评估短期和长期精度误差的均方根变异系数;并对使用线性回归的半自动分割方法进行验证。研究了利用三维连通性和部分体积校正规则改进脂肪确定算法对分析精度的影响。该算法的鲁棒性和通用性通过应用于不同的磁共振序列/磁场强度以及小腿和大腿扫描来证明。结果:在439名成年人中(319名女性,占89%),年龄:71.6±7.6岁,BMI: 28.06±4.87 kg/m2, IMF%: 10.91±4.57%),全自动ITSA在三个队列的MR序列和解剖结构中表现良好。同时应用3D连通性和部分体积脂肪校正,可将精度从4.99%提高到2.21%。对半自动方法的验证表明,在全自动ITSA常规方法下,R2为0.92至0.98,得到的IMF体积计算更为保守。质量控制显示,7%的病例需要人工矫正,主要是由于IMF与皮下脂肪合并。完整的工作流程描述了导出标签以进行手动更正的方法。结论:从MRI中分割IMF的最大挑战是选择一个动态阈值,该阈值在重复成像中始终如一。全自动ITSA实现了这一点,证明了较低的短期和长期精度误差,有利于在随机对照试验中使用。
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来源期刊
Skeletal Muscle
Skeletal Muscle CELL BIOLOGY-
CiteScore
9.10
自引率
0.00%
发文量
25
审稿时长
12 weeks
期刊介绍: The only open access journal in its field, Skeletal Muscle publishes novel, cutting-edge research and technological advancements that investigate the molecular mechanisms underlying the biology of skeletal muscle. Reflecting the breadth of research in this area, the journal welcomes manuscripts about the development, metabolism, the regulation of mass and function, aging, degeneration, dystrophy and regeneration of skeletal muscle, with an emphasis on understanding adult skeletal muscle, its maintenance, and its interactions with non-muscle cell types and regulatory modulators. Main areas of interest include: -differentiation of skeletal muscle- atrophy and hypertrophy of skeletal muscle- aging of skeletal muscle- regeneration and degeneration of skeletal muscle- biology of satellite and satellite-like cells- dystrophic degeneration of skeletal muscle- energy and glucose homeostasis in skeletal muscle- non-dystrophic genetic diseases of skeletal muscle, such as Spinal Muscular Atrophy and myopathies- maintenance of neuromuscular junctions- roles of ryanodine receptors and calcium signaling in skeletal muscle- roles of nuclear receptors in skeletal muscle- roles of GPCRs and GPCR signaling in skeletal muscle- other relevant aspects of skeletal muscle biology. In addition, articles on translational clinical studies that address molecular and cellular mechanisms of skeletal muscle will be published. Case reports are also encouraged for submission. Skeletal Muscle reflects the breadth of research on skeletal muscle and bridges gaps between diverse areas of science for example cardiac cell biology and neurobiology, which share common features with respect to cell differentiation, excitatory membranes, cell-cell communication, and maintenance. Suitable articles are model and mechanism-driven, and apply statistical principles where appropriate; purely descriptive studies are of lesser interest.
期刊最新文献
Neuromuscular electrical stimulation training induces myonuclear accretion and hypertrophy in mice without overt signs of muscle damage and regeneration. Aminoguanidine hemisulfate improves mitochondrial autophagy, oxidative stress, and muscle force in Duchenne muscular dystrophy via the AKT/FOXO1 pathway in mdx mice. Sarcolemma resilience and skeletal muscle health require O-mannosylation of dystroglycan. Fully-automated segmentation of muscle and inter-/intra-muscular fat from magnetic resonance images of calves and thighs: an open-source workflow in Python. Mll4 in skeletal muscle fibers maintains muscle stem cells.
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