On modeling

被引:258
作者
Novikov, Dmitry S. [1 ]
Kiselev, Valerij G. [2 ]
Jespersen, Sune N. [3 ,4 ]
机构
[1] NYU, Sch Med, Dept Radiol, Bernard & Irene Schwartz Ctr Biomed Imaging, 660 First Ave,Room 206, New York, NY 10016 USA
[2] Univ Med Ctr Freiburg, Dept Radiol, Med Phys, Fac Med, Freiburg, Germany
[3] Aarhus Univ, Dept Clin Med, CFIN MINDLab, Aarhus, Denmark
[4] Aarhus Univ, Dept Phys & Astron, Aarhus, Denmark
基金
美国国家卫生研究院;
关键词
functional form; microstructure; model; representation; validation; AXON DIAMETER DISTRIBUTION; DIFFUSION-TIME-DEPENDENCE; FREE-WATER ELIMINATION; MR SIGNAL FORMATION; IN-VIVO MEASUREMENT; WHITE-MATTER; ANOMALOUS DIFFUSION; NMR SIGNAL; GAUSSIAN APPROXIMATION; ORIENTATION DISPERSION;
D O I
10.1002/mrm.27101
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Mapping tissue microstructure with MRI holds great promise as a noninvasive window into tissue organization at the cellular level. Having originated within the realm of diffusion NMR in the late 1970s, this field is experiencing an exponential growth in the number of publications. At the same time, model-based approaches are also increasingly incorporated into advanced MRI acquisition and reconstruction techniques. However, after about two decades of intellectual and financial investment, microstructural mapping has yet to find a single commonly accepted clinical application. Here, we suggest that slow progress in clinical translation may signify unresolved fundamental problems. We outline such problems and related practical pitfalls, as well as review strategies for developing and validating tissue microstructure models, to provoke a discussion on how to bridge the gap between our scientific aspirations and the clinical reality. We argue for recalibrating the efforts of our community toward a more systematic focus on fundamental research aimed at identifying relevant degrees of freedom affecting the measured MR signal. Such a focus is essential for realizing the truly revolutionary potential of noninvasive three-dimensional in vivo microstructural mapping.
引用
收藏
页码:3172 / 3193
页数:22
相关论文
共 181 条
[1]  
Abbe E., 1873, ARCH MIKROSK ANAT, V9, P413, DOI [DOI 10.1007/BF02956173, 10.1007/BF02956173]
[2]   The use of MR-detectable reporter molecules and ions to evaluate diffusion in normal and ischemic brain [J].
Ackerman, Joseph J. H. ;
Neil, Jeffrey J. .
NMR IN BIOMEDICINE, 2010, 23 (07) :725-733
[3]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[4]  
Alexander D.C., 2017, NMR in Biomedicine
[5]   Orientationally invariant indices of axon diameter and density from diffusion MRI [J].
Alexander, Daniel C. ;
Hubbard, Penny L. ;
Hall, Matt G. ;
Moore, Elizabeth A. ;
Ptito, Maurice ;
Parker, Geoff J. M. ;
Dyrby, Tim B. .
NEUROIMAGE, 2010, 52 (04) :1374-1389
[6]   MORE IS DIFFERENT - BROKEN SYMMETRY AND NATURE OF HIERARCHICAL STRUCTURE OF SCIENCE [J].
ANDERSON, PW .
SCIENCE, 1972, 177 (4047) :393-&
[7]  
[Anonymous], ARXIV160909144
[8]  
[Anonymous], 2017, P 25 ANN M ISMRM
[9]  
[Anonymous], 2017, NEUROIMAGE
[10]  
[Anonymous], ARXIV161202059