Impact of particle size on R 2 * and fat fraction estimation for accurate assessment of hepatic iron overload and steatosis using MRI.

IF 3 3区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Utsav Shrestha, Sarah Brasher, Zachary Abramson, Cara E Morin, Aaryani Tipirneni-Sajja
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引用次数: 0

Abstract

Purpose: To investigate the impact of iron particle size on R 2 * $$ {R}_2^{\ast } $$ and fat fraction (FF) estimations for coexisting hepatic iron overload and steatosis condition using Monte Carlo simulations and phantoms.

Methods: Three iron particle sizes (0.38, 0.52, and 0.71 μm) were studied using simulations and phantoms. Virtual liver models mimicking in vivo spatial distribution of fat droplets and iron deposits were created, and MRI signals were synthesized using Monte Carlo simulations for FF 1%-30% and liver iron concentration (LIC) 1-20 mg/g. Seventy-five fat-iron phantoms with varying iron (0-8 μg/mL) and fat (0%-40%) concentrations and particle sizes were constructed. Three-way analysis of variance was used to assess the effect of iron particle size on R 2 * $$ {R}_2^{\ast } $$ and FF estimations.

Results: In simulations, estimated and true FF were in excellent agreement (slope: 0.93-1.09) for liver iron concentration ≤ 13 mg/g. For both simulations and phantoms, FF estimation bias increased as iron concentration increased and particle size decreased, with 0.71μm iron particle having the lowest bias (≤ 20%), and 0.52 μm and 0.38 μm iron particles producing higher bias (≥ 20%) for higher iron concentrations and lower FFs. Additionally, R 2 * $$ {R}_2^{\ast } $$ increased linearly with increasing iron concentration (r ≥ 0.87) and decreasing particle size. Iron particle size significantly influenced the estimated versus true FF (simulations: p = 0.04; phantoms: p = 0.03) and R 2 * $$ {R}_2^{\ast } $$ -iron concentration (simulations: p < 0.001; phantoms: p < 0.01) relationships. Heatmap demonstrated broader region with higher FF estimation bias as iron particle size decreased, especially at higher iron concentration.

Conclusion: R 2 * $$ {R}_2^{\ast } $$ and FF estimations are affected by iron particle size, with smaller particles leading to higher R 2 * $$ {R}_2^{\ast } $$ values and increased FF estimation bias.

颗粒大小对r2 *和脂肪分数估算的影响,用于MRI准确评估肝铁超载和脂肪变性。
目的:通过蒙特卡罗模拟和模拟研究铁粒度对肝脏铁超载和脂肪变性共存状态下r2 * $$ {R}_2^{\ast } $$和脂肪分数(FF)估计的影响。方法:采用模拟和模拟的方法研究了3种铁颗粒尺寸(0.38、0.52和0.71 μm)。建立了模拟体内脂肪滴和铁沉积空间分布的虚拟肝脏模型,并用蒙特卡罗模拟方法合成了FF 1的MRI信号%-30% and liver iron concentration (LIC) 1-20 mg/g. Seventy-five fat-iron phantoms with varying iron (0-8 μg/mL) and fat (0%-40%) concentrations and particle sizes were constructed. Three-way analysis of variance was used to assess the effect of iron particle size on R 2 * $$ {R}_2^{\ast } $$ and FF estimations.Results: In simulations, estimated and true FF were in excellent agreement (slope: 0.93-1.09) for liver iron concentration ≤ 13 mg/g. For both simulations and phantoms, FF estimation bias increased as iron concentration increased and particle size decreased, with 0.71μm iron particle having the lowest bias (≤ 20%), and 0.52 μm and 0.38 μm iron particles producing higher bias (≥ 20%) for higher iron concentrations and lower FFs. Additionally, R 2 * $$ {R}_2^{\ast } $$ increased linearly with increasing iron concentration (r ≥ 0.87) and decreasing particle size. Iron particle size significantly influenced the estimated versus true FF (simulations: p = 0.04; phantoms: p = 0.03) and R 2 * $$ {R}_2^{\ast } $$ -iron concentration (simulations: p Conclusion: R 2 * $$ {R}_2^{\ast } $$ and FF estimations are affected by iron particle size, with smaller particles leading to higher R 2 * $$ {R}_2^{\ast } $$ values and increased FF estimation bias.
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来源期刊
CiteScore
6.70
自引率
24.20%
发文量
376
审稿时长
2-4 weeks
期刊介绍: Magnetic Resonance in Medicine (Magn Reson Med) is an international journal devoted to the publication of original investigations concerned with all aspects of the development and use of nuclear magnetic resonance and electron paramagnetic resonance techniques for medical applications. Reports of original investigations in the areas of mathematics, computing, engineering, physics, biophysics, chemistry, biochemistry, and physiology directly relevant to magnetic resonance will be accepted, as well as methodology-oriented clinical studies.
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