Three-dimensional, Bayesian image reconstruction from sparse and noisy data sets: Near-infrared fluorescence tomography

被引:126
作者
Eppstein, MJ
Hawrysz, DJ
Godavarty, A
Sevick-Muraca, EM
机构
[1] Univ Vermont, Dept Comp Sci, Burlington, VT 05405 USA
[2] Texas A&M Univ, Photon Migrat Lab, College Stn, TX 77845 USA
关键词
D O I
10.1073/pnas.112217899
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A method for inverting measurements made on the surfaces of tissues for recovery of interior optical property maps is demonstrated for sparse near-infrared (NIR) fluorescence measurement sets on large tissue-simulating volumes with highly variable signal-to-noise ratio. A Bayesian minimum-variance reconstruction algorithm compensates for the spatial variability in signal-to-noise ratio that must be expected to occur in actual NIR contrast-enhanced diagnostic medical imaging. Image reconstruction is demonstrated by using frequency-domain photon migration measurements on 256-cm(3) tissue-mimicking phantoms containing none, one, or two 1-cm(3) heterogeneities with 50- to 100-fold greater concentration of Indocyanine Green dye over background levels. The spatial parameter estimate of absorption owing to the dye was reconstructed from only 160 to 296 surface measurements of emission light at 830 nm in response to incident 785-nm excitation light modulated at 100 MHz. Measurement error of acquired fluence at fluorescent emission wavelengths is shown to be highly variable. Convergence and quality of image reconstructions are improved by Bayesian conditioning incorporating (i) experimentally determined measurement error variance, (h) recursively updated estimates of parameter uncertainty, and (iii) dynamic zonation. The results demonstrate that, to employ NIR fluorescence-enhanced optical imaging for large volumes, reconstruction approaches must account for the large range of signal-to-noise ratio associated with the measurements.
引用
收藏
页码:9619 / 9624
页数:6
相关论文
共 23 条
[1]   Novel receptor-targeted fluorescent contrast agents for in vivo tumor imaging [J].
Achilefu, S ;
Dorshow, RB ;
Bugaj, JE ;
Rajagopalan, R .
INVESTIGATIVE RADIOLOGY, 2000, 35 (08) :479-485
[2]   Simultaneous estimation of transmissivity values and zonation [J].
Eppstein, MJ ;
Dougherty, DE .
WATER RESOURCES RESEARCH, 1996, 32 (11) :3321-3336
[3]   Three-dimensional Bayesian optical image reconstruction with domain decomposition [J].
Eppstein, MJ ;
Dougherty, DE ;
Hawrysz, DJ ;
Sevick-Muraca, EM .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 2001, 20 (03) :147-163
[4]   Optimal 3-D traveltime tomography [J].
Eppstein, MJ ;
Dougherty, DE .
GEOPHYSICS, 1998, 63 (03) :1053-1061
[5]   BOUNDARY-CONDITIONS FOR THE DIFFUSION EQUATION IN RADIATIVE-TRANSFER [J].
HASKELL, RC ;
SVAASAND, LO ;
TSAY, TT ;
FENG, TC ;
MCADAMS, MS ;
TROMBERG, BJ .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1994, 11 (10) :2727-2741
[6]   Error consideration in contrast-enhanced three-dimensional optical tomography [J].
Hawrysz, DJ ;
Eppstein, MJ ;
Lee, JW ;
Sevick-Muraca, EM .
OPTICS LETTERS, 2001, 26 (10) :704-706
[7]   Developments toward diagnostic breast cancer imaging using near-infrared optical measurements and fluorescent contrast agents [J].
Hawrysz, DJ ;
Sevick-Muraca, EM .
NEOPLASIA, 2000, 2 (05) :388-417
[8]   Use of penalty terms in gradient-based iterative reconstruction schemes for optical tomography [J].
Hielscher, AH ;
Bartel, S .
JOURNAL OF BIOMEDICAL OPTICS, 2001, 6 (02) :183-192
[9]   Fluorescence-enhanced absorption imaging using frequency-domain photon migration: tolerance to measurement error [J].
Lee, J ;
Sevick-Muraca, E .
JOURNAL OF BIOMEDICAL OPTICS, 2001, 6 (01) :58-67
[10]   Synthesis, characterization, and biological properties of cyanine-labeled somatostatin analogues as receptor-targeted fluorescent probes [J].
Licha, K ;
Hessenius, C ;
Becker, A ;
Henklein, P ;
Bauer, M ;
Wisniewski, S ;
Wiedenmann, B ;
Semmler, W .
BIOCONJUGATE CHEMISTRY, 2001, 12 (01) :44-50