Abstract
Purpose
It has been known that noise correlation plays an important role in the determination of the performance of spectral imaging based on two‐material decomposition (2‐MD). To further understand the basics of spectral imaging in photon‐counting CT toward optimal design and implementation, we study the noise correlation in multi‐MD (m‐MD) and its impact on the performance of spectral imaging.
Method
We derive the equations that characterize the noise and noise correlation in the material‐specific (basis) images in m‐MD, followed by a simulation study to verify the derived equations and study the noise correlation's impact on the performance of spectral imaging. Using a specially designed digital phantom, the study of noise correlation runs over the cases of two‐, three‐, and four‐MD (2‐MD, 3‐MD, and 4‐MD). Then, the noise correlation's impact on the performance of spectral imaging in photon‐counting CT is investigated, using a modified Shepp–Logan phantom.
Results
The results in 2‐MD show that, in‐line with what has been reported in the literature, the noise correlation coefficient between the material‐specific images corresponding to the basis materials approaches −1. The results in m‐MD (m ≥ 3) are more complicated and interesting, as the noise correlation coefficients between a pair of the material‐specific images alternate between ±1, and so do in the case of 4‐MD. The m‐MD data show that the noise in virtual monochromatic imaging (a form of spectral imaging) is moderate even though the noises in material‐specific (basis) images vary drastically.
Conclusions
The observation of noise correlation in 3‐MD, 4‐MD, and beyond (i.e., m‐MD) is informative to the community. The relationship between noise correlation and the performance of spectral imaging revealed in this work may help clinical medical physicists understand the fundamentals of spectral imaging based on MD and optimize the performance of spectral imaging in photon‐counting CT and other X‐ray imaging modalities.
Keywords: CT, material‐specific imaging, multi‐material decomposition, noise correlation; noise, photon‐counting CT, spectral CT, virtual monochromatic imaging
1. INTRODUCTION
As a quantitative imaging method that is well balanced over its contrast, spatial and temporal resolutions, CT has become one of the most widely used modalities for diagnostic imaging in clinics, with more than 80 million procedures carried out annually in the United States alone. 1 However, the challenges in clinical applications are demanding CT to be more potent in contrast resolution for early detection and characterization of pathologies in soft tissues. Owing to its capability of material‐specific and virtual monochromatic imaging, the spectral imaging implemented in photon‐counting CT offers the opportunity for scientists and researchers in the field to make CT more potent in detection and characterization of vascular and parenchymal lesions, especially in concert with administration of contrast agents, either state‐of‐the‐art iodinated 2 or other novel contrast agents 3 in the future.
Contrast agent has been indispensable in conventional CT since the very beginning and will continue to be the case in photon‐counting CT, especially in light of the prospect that novel contrast agents in the form of biodegradable nanoparticles may play more important roles. The spectral imaging in photon‐counting CT with administration of one or multiple contrast agents 4 demands in‐depth studies of multi‐material decomposition (m‐MD). Recently, based on an in‐depth revisiting of the physics underlying photon‐counting CT, we have carried out studies on the condition of basis materials (functions) and spectral channelization (energy binning) for spectral imaging. Using the approach based on singular value decomposition and analysis, 5 , 6 , 7 , 8 we have shown how the condition of basis materials and spectral channelization can affect the performance of spectral imaging in photon‐counting CT 2 , 3 based on multi‐MD (m‐MD). In this work, we address another fundamental issue in photon‐counting CT ‐ the correlation of noise and its impact on the performance of spectral imaging.
It has been known from the beginning that the noise in the projection data acquired at two distinct peak tube voltages are of relevance in determining spectral CT's imaging performance. 8 , 9 With resort to maximum likelihood estimation, Alvarez and Macovski showed that the Jacobian of the transform from projection space to A‐space 10 determines the noise property that is governed by the Cramér–Rao lower bound. 5 Alternatively, Kelcz et al. studied the same issue by taking noise as the uncertainty in estimating the basis materials’ mass density. 11 Using the first‐order Taylor expansion, Kelcz et al. found that the so‐called R‐quantity, which is the ratio of mass attenuation coefficients associated with the two interested materials at the two distinct peak voltages, plays a key role that is almost identical to the Jacobian of the transform from projection space to A‐space. 12
Initially, Alvarez and Macovski assumed no correlation in noise between the projection data acquired at the two peak voltages (correlation‐vanishing henceforth), as this is the cases in data acquisition implemented via photon‐counting under ideal spectral response or voltage‐switching (termed as fast kV‐switching nowadays). 8 , 9 , 13 They showed that though the noise correlation in projection data vanishes, there still exists a negative noise correlation in the image corresponding to each basis material 8 , 9 , 13 , 14 (material‐specific image henceforth). Notably, the assumption of correlation‐vanishing seems invalid in the case of data acquisition via layered (sandwiched) detector. However, through an in‐depth statistical analysis, it turns out that the noise correlation in the data acquired by the first and second layers is in fact negligibly small and thus can be treated as another case of correlation‐vanishing. 15 Nevertheless, the correlation‐vanishing assumption is actually not valid in the data acquisition by photon‐counting if realistic detector response is considered, as the spectral distortion inevitably induces correlation in the projection data acquired at the low and high peak voltage. 5 , 6 , 7
In spectral imaging based on 2‐MD, an investigation to reveal the effect of noise correlation in the projection data on noise and noise correlation in the material‐specific images has been reported in the literature. 16 Analytically, it was shown that the correlation between the noise in the two material‐specific images is negative, and, if the correlation in the projection data vanishes, the analytics degenerates to the case that was initially derived by Alvarez and Macovski. 8 , 9 , 13 Notably, the work in Ref. [ 16 ] was focused on the counting‐integration mode in data acquisition, and only analytic plots were given, though the conclusion is in fact general and applicable to other cases of 2‐MD‐based spectral imaging implemented via different schemes of data acquisition. 16
With the engagement of multispectral channels and multi‐basis materials, the dimension of Jacobian increases accordingly. This case, in turn, complicates the way at which the noise correlation in projection data acquired in each spectral channel impacts the noise correlation in the material‐specific images. Specifically, the sign of the off‐diagonal elements in the inverse of an M × M (M > 2) matrix may vary, implying that the noise correlation corresponding to each material‐specific image in the m‐MD‐based spectral imaging may not be always negative, as has been the case in 2‐MD‐based spectral imaging. 14 Via analytical derivation, phantom studies, and quantitative analysis, we have investigated the noise correlation in the material‐specific (basis) images via m‐MD and reported the preliminary data. 17 In this work, we extend our effort to further investigate the noise correlation and study its impact on the performance of m‐MD‐based spectral imaging in photon‐counting CT, in which we focus on the cases of m‐MD (m ≥ 3) that are carried out in the projection domain, with the goal to provide the information for further understanding of the basics of m‐MD‐based spectral imaging in photon‐counting CT and other X‐ray imaging. Purposely, our work is designed to be a phantom study supported by computer simulation, so that any adverse effects, which may be induced by the imperfection in photon‐counting CT's imaging chain, on the investigation and its conclusion can be ruled out.
2. METHOD
2.1. Modeling of signal detection and material decomposition in photon‐counting CT
The modeling of signal and its detection in photon‐counting CT have been detailed in our recent publication 5 , 6 , 7 and are only reiterated here briefly for reader's convenience. If the noise in data acquisition is taken into consideration, the detection of signal in photon‐counting CT can be analytically expressed as
| (1) |
where denotes the spectrum of X‐ray source, and L is the path penetrated by the X‐ray beam. Subscript k indexes the spectral channel in which the raw data are acquired, whereas is defined in the kth spectral channel [] that takes detector's efficiency η(E) and spectral response into account. 5 , 6 , 7 Poisson(⋅) denotes the numerical operation that generates random numbers to observe the Poisson distribution. 18 In MD, we can write
| (2) |
Then, Equation (1) is converted into
| (3) |
Given p = 1, 2, …, P, denotes the line integral of associated with the mass distribution of material p, which can be obtained from (k = 1, 2, …, K) by solving the set of integral equations specified in Equation (3) through numerical methods, for example, the iterative Newton–Raphson algorithm, 9 , 19 in which the integral equations’ initial conditions are obtained by system calibration via polynomial data fitting. 9 , 19 , 20
2.2. Data acquisition and image formation in photon‐counting CT
In simulation, 21 the X‐ray technique is set at 1000 mA/140 keV, and the gantry of photon‐counting CT rotates at 1 rot/s. The spectral channels are defined as [1–58, 59–140] keV in 2‐MD (Figure 1a,a′), [1–51, 52–68, 69–140] keV in 3‐MD (Figure 1b,b′), and [1–43, 44–58, 59–72, 73–140] keV in 4‐MD (Figure 1c,c′). The goal in spectral channelization is to ensure that the photon counts in each channel be about the same at the incident surface of the object to be imaged, in spite of other criteria that have been used in practice. 22 For illustration, the spectral channels under ideal detector response are plotted in Figure 1a–c, whereas their counterparts under realistic detector response in Figure 1a′–c′. The material in the photon‐counting detector assumed in the simulation is cadmium zinc telluride (CZT) or cadmium telluride, which is associated with the Compton scattering, charge‐sharing, and fluorescent‐escaping that may distort the detector's spectral response. 6 , 7 The photon‐counting detector is designed as a curved two‐dimensional array at 864 × 16 dimension and 1.024 × 1.092 mm2 pitch. The source‐to‐iso and source‐to‐detector distances are 541.0 and 949.0 mm, respectively, consistent to one of the multi‐detector row CT scanners in the clinic. After MD, each basis image is in turn reconstructed from (p = 1, 2, …, P) via an FBP image reconstruction algorithm. 23
FIGURE 1.

Two (a), three (b), and four (c) spectral channels under ideal detector spectral response and their counterparts (a′–c′) under realistic detector response (keV is the unit of abscissa)
2.3. Noise propagation in m‐MD‐based spectral imaging
By treating Ik(L) (k = 1, …, K) and Ap(L) (p = 1, …, P) as random variables in the projection space and A‐space, respectively, the mapping from the former to the latter can be written as
| (4) |
Then, we have the covariance matrix of A as 16 , 24
| (5) |
where each entry of the mapping matrix F is defined as . In analog to the way in Ref. [16], we define the effective attenuation coefficient, signal‐to‐noise ratio (SNR), correlation coefficient in the projection space, and A‐space, respectively, as
| (6) |
| (7) |
2.3.1. Noise propagation in 2‐MD‐based spectral imaging
In 2‐MD, we have the Jacobian
| (8) |
According to Equation (5), the covariance matrix V[A] becomes
| (9) |
where the entries are
| (10) |
| (11) |
| (12) |
Furthermore, we have the cross‐correlation
| (13) |
If there is no correlation between the projection data acquired at the two peak voltages, the following equations degenerate into
| (10′) |
| (11′) |
| (12′) |
| (13′) |
which is exactly the same as that given by Alvarez and Macovski at the very beginning. 8 , 9 In general, an interchannel spectral overlapping under realistic detector spectral response induces positive correlation between the data acquired in each channel, that is, , which decreases the magnitude of nominators in Equations (10)–(13). Meanwhile, however, the interchannel overlapping may decrease the magnitude of in the denominator to a larger extent. Jointly, these changes may increase the magnitude of noise and noise correlation in the data denoted by A 1 and A 2 that are obtained via MD.
2.3.2. Noise propagation in 3‐MD‐based spectral imaging and beyond
In 3‐MD, we have the Jacobian
| (14) |
Again starting from Equation (5), the covariance matrix V[A] becomes
| (15) |
with the entries being derived in the Appendix. Similarly, the interchannel spectral overlap induces positive correlation between the data acquired in different channels, that is, , , and , which, in general, decreases the magnitude of nominators in Equations (A1)–(A6). Moreover, the interchannel overlap may decrease the magnitude of in the denominator to a larger extent. Jointly, these changes may increase the magnitude of noise and noise correlation in the data denoted by A 1–A 3 after MD.
As shown in the Appendix, the analytic expression of each entry of matrix V 3×3[A] becomes exhaustively complicated in 3‐MD, though their derivation can be carried out according to Equation (5). Hence, an analysis of the noise and noise correlation via simulation study makes more sense in terms of feasibility in the case of 4‐MD‐ (and beyond) based spectral imaging in photon‐counting CT.
2.4. Analysis of noise correlation and imaging performance via simulation study
The noise correlation and its impact on the performance of spectral imaging are assessed via simulation study, in which the imaging chain of photon‐counting CT is modeled and simulated using a software kit. 5 , 6 , 7 , 21
2.4.1. Analysis of noise correlation
A cylinder of water at 20 cm diameter, which consists of three rods at 7 cm diameter, is designed as the phantom to assess the correlation of noise in material‐specific images in photon‐counting CT (henceforth, the noise correlation phantom). The materials that make rods 1–3 corresponding to the cases of 2‐MD, 3‐MD, and 4‐MD are listed in Table 1. Specifically, two materials (soft tissue and cortical bone) are assumed in the 2‐MD case, whereas iodine and gadolinium are added into the cases of 3‐MD and 4‐MD, respectively. The fraction of each material in the rods are chosen for quantitative purpose without any implication toward clinical or preclinical applications, as such the difference in material composition is adequate to ensure the accuracy in quantitative measurement. A sectional view of the phantom is presented in Figure 2a, in which a region of interest (ROI) at 6 cm diameter within rod 3 is defined for illustration of noise and noise correlation measurement.
TABLE 1.
Material configuration (fraction in weight) of the three rods in the phantom used for evaluation and verification of noise correlation in the material‐specific (basis) images in 2‐material decomposition (MD), 3‐MD, and 4‐MD, respectively
| 2‐MD | 3‐MD | 4‐MD | |
|---|---|---|---|
| Rod 1 |
1/3 soft tissue 2/3 cortical bone |
2/7 soft tissue 4/7 iodine (10 mg/ml) 1/7 cortical bone |
2/7 soft tissue 2.5/7 iodine (10 mg/ml) 2/7 gadolinium (10 mg/ml) 0.5/7 cortical bone |
| Rod 2 |
1/2 soft tissue 1/2 cortical bone |
3/7 soft tissue 3/7 iodine (10 mg/ml) 1/7 cortical bone |
3/7 soft tissue 2/7 iodine (10 mg/ml) 1.5/7 gadolinium (10 mg/ml) 0.5/7 cortical bone |
| Rod 3 |
2/3 soft tissue 1/3 cortical bone |
4/7 soft tissue 2/7 iodine (10 mg/ml) 1/7 cortical bone |
3/7 soft tissue 2.5/7 iodine (10 mg/ml) 1/7 gadolinium (10 mg/ml) 0.5/7 cortical bone |
FIGURE 2.

Sectional view of the noise correlation phantom (a) and the head phantom for assessment of imaging performance (b)
A number of basis materials have been investigated in our previous studies. 5 , 6 , 7 In the study of analyzing noise correlation, we choose soft tissue and cortical bone as the basis materials for 2‐MD 28 , and soft tissue, 10 mg/ml gadolinium, and cortical bone for 3‐MD. In the case of 4‐MD, the basis materials are chosen as soft tissue, 10 mg/ml iodine, 10 mg/ml gadolinium, and cortical bone.
Once the material‐specific images are generated, ROIs are drawn in each of them as illustrated in Figure 2a. The Pearson correlation coefficient (R‐coefficient), as defined in the following, is adopted to quantitatively assess the correlation of noise in those images:
| (16) |
where and denote the pixels at identical location in each of the two material specific images. and are the averaged intensities of all the pixels in each of the two ROIs, and N is the total number of pixels in each ROI.
2.4.2. Assessment of spectral imaging performance
A humanoid head modified from the Shepp–Logan phantom (henceforth the head phantom) is used to study the noise correlation's impact on the performance of virtual monochromatic imaging (a form of spectral imaging) in photon‐counting CT. Presented in Figure 2b is a sectional view of the head phantom, wherein two ROIs are defined as the areas of signal (big dashed circle) and background (small dashed circle) for measurement of contrast, noise, and contrast‐to‐noise ratio (CNR):
| (17) |
where and are the mean and standard deviation gauged in the signal ROI, and and are the counterparts in the background ROI. The mass attenuation coefficients of the materials in the head phantom are determined according to authoritative publications, for example, Refs. [25, 26] and the EPDL library. 27 The readers who are interested in the configuration details of the phantom are referred to Refs. [6, 7]. The study of noise correlation's impact on the performance of spectral imaging is focused on the 3‐MD case, in which four sets of basis materials are selected: (i) BM‐1: adipose, PMMA, and Teflon; (ii) BM‐2: adipose, PMMA, and 20 mg/ml iodine; (iii) BM‐3: soft tissue, 20 mg/ml iodine, and cortical bone; (iv) BM‐4: adipose, 20 mg/ml iodine, and Teflon.
3. RESULTS
3.1. Noise and noise correlation in 2‐MD material‐specific images
The material‐specific images corresponding to basis materials soft tissue and cortical bone obtained via 2‐MD under ideal and realistic detector spectral response are presented in the top and bottom rows of Figure 3, whereas the noise correlation corresponding to these two material‐specific images are displayed in the scatterplot in Figure 4a,b, respectively. The noise in the material‐specific images under 2‐MD is in negative correlation, which is consistent to what has been reported in the literature 13 , 14 , 16 and serves as a validation of the MD implemented in our study. Moreover, it is observed that, in addition to increasing the magnitude of noise in each material‐specific image markedly (Figure 3), the interchannel overlapping in detector's spectral response increases the magnitude of noise correlation coefficient modestly (Figure 4).
FIGURE 3.

Material‐specific (tissue [a,a′] and bone [b,b′]) images acquired via two‐material decomposition (2‐MD), whereas the detector response is ideal (top) or realistic (bottom).
FIGURE 4.

Correlation of noise between material‐specific images acquired via two‐material decomposition (2‐MD) under ideal (a) and realistic (b) detector spectral response
3.2. Noise and noise correlation in 3‐MD material‐specific images
The material‐specific images corresponding to basis materials soft tissue, 10 mg/ml iodine, and cortical bone acquired via 3‐MD under ideal detector spectral response are presented in Figure 5a–c. Overall, given identical X‐ray dose, the basis images acquired via 3‐MD (Figure 5) are noisier than those via 2‐MD (Figure 3), as fewer X‐ray photons fall into each spectral channel in the former than that in the latter. It is also noted that the interchannel overlap in detector's response increases the magnitude of noise in each material‐specific image significantly (Figure 5), which is within anticipation according to Equations (A1)–(A3).
FIGURE 5.

Material‐specific (tissue [left], 10 mg/ml I [middle] and bone [right]) images of the noise correlation phantom acquired via three‐material decomposition (3‐MD), whereas the detector response is ideal (a–c) or realistic (a′–c′)
The correlation of noise in the material‐specific images corresponding to basis materials soft tissue, 10 mg/ml iodine, and cortical bone under ideal detector spectral response are presented in the scatterplots in Figure 6a–c. The polarity of noise correlation over the material‐specific images in 3‐MD‐based spectral imaging alternates between ±1. The interchannel overlap induced by the spectral distortion in a realistic detector's spectral response increases the magnitude of noise correlation modestly, which is again within expectation according to Equations (A1′)–(A3′).
FIGURE 6.

Correlation of noise between the material‐specific images acquired via three‐material decomposition (3‐MD) under both ideal (a–c) and realistic (a′–c′) detector response
3.3. Noise and noise correlation in 4‐MD material‐specific images
The material‐specific images corresponding to basis materials soft tissue, 10 mg/ml gadolinium, 10 mg/ml iodine, and cortical bone via 4‐MD under ideal detector spectral response are displayed in Figure 7a–c. Overall, given the same X‐ray dose, the noise in the 4‐MD basis images is much stronger than that in the 3‐MD case, as the number of X‐ray photons falling into each spectral channel is further fewer, as demonstrated by visual comparison between Figures 5a–c and 7a–d. Similar to what has been observed in the cases of 2‐MD and 3‐MD, the interchannel overlap in detector's response in 4‐MD makes the noise in each material‐specific image much stronger (Figure 7a′–d′) over their counterparts under ideal detector spectral response (Figure 7a′–d′).
FIGURE 7.

Material‐specific (left to right: soft tissue, [10 mg/ml] Gd, [10 mg/ml] I and cortical bone) images of the noise correlation phantom acquired via four‐material decomposition (4‐MD) under ideal (a–d) and realistic (a′–d′) detector response
The correlation of noise between the material‐specific images in 4‐MD are presented in the scatterplots in Figure 8a–f. Similar to the cases in 3‐MD, the polarity of noise correlation between those material‐specific images in 4‐MD alternates between ±1. Obviously, the interchannel spectral overlap induced by the spectral distortion in realistic detector's spectral response in 4‐MD increases the magnitude of noise correlation considerably (compare Figures 8a–f and 9a–f), similar to what happens in the cases of 2‐MD and 3‐MD. Moreover, it is observed in Figure 7 that the noise in the material‐specific image corresponding to gadolinium (Figure 7c,c′) is the strongest in comparison to other material‐specific images. Consequently, the Person correlation coefficient decreases significantly whenever gadolinium is involved, as illustrated in Figure 8a,d,e in comparison to Figures 8b,c,f, and 9a,d,e compared to Figure 8b,c,f as well. We believe that the underlying reason is that gadolinium is much more attenuating than other materials in the phantom. In particular, the K‐edge of gadolinium is at 50.2 keV, which is very close to the effective energy of the polychromatic X‐ray source utilized in the simulation study.
FIGURE 8.

Noise correlation in four‐material decomposition (4‐MD): (a) soft tissue versus gadolinium, (b) soft tissue versus iodine, (c) soft tissue versus bone, (d) gadolinium versus iodine, (e) gadolinium versus bone, and (f) iodine versus bone
FIGURE 9.

Noise correlation in four‐material decomposition (4‐MD): (a) soft tissue versus gadolinium, (b) soft tissue versus iodine, (c) soft tissue versus bone, (d) gadolinium versus iodine, (e) gadolinium versus bone, and (f) iodine versus bone
3.4. Impact of noise correlation on the performance of spectral imaging
Shown in the first row of Figure 10 are material‐specific images of the head phantom (columns 1–3) acquired via 3‐MD with basis material set BM‐1 and the virtual monochromatic image (VMI) formed at 45 keV (column 4) under ideal detector spectral response, whereas those in rows 2–4 are their counterparts acquired with basis material sets BM‐2, BM‐3, and BM‐4. It is observed that, in contrast to the drastic variation of noise in the material‐specific images over the four basis material sets, the noise in the VMIs formed at 45 keV only varies modestly. Similar observation can be made on their counterparts acquired under realistic detector spectral response (Figure 11).
FIGURE 10.

Basis images (columns 1–3) of the head phantom acquired with basis material sets BM‐1, BM‐2, BM‐3, and BM‐4 (rows 1–4) and resultant virtual monochromatic images (VMIs) at 45 keV (column 4) under ideal detector response
FIGURE 11.

Basis images (columns 1–3) of the head phantom acquired with basis material sets BM‐1, BM‐2, BM‐3, and BM‐4 (rows 1–4) and resultant virtual monochromatic images (VMIs) at 45 keV (column 4), under realistic detector response
The noises gauged in each of the material‐specific images in Figure 10 under ideal detector spectral response are charted in Figure 12a, showing that the variation of noise within the basis material sets BM‐1 and BM‐2 is drastic. Similar phenomenon is observed under realistic detector spectral response (Figures 11 and 12a′), except for the markedly increased magnitude in noise. Moreover, an inspection of Figure 12a,a′ reveals that the variation of noise in the material‐specific images across the basis material sets BM‐1, BM‐2, BM‐3, and BM‐4 is drastic too. On the other hand, under both ideal and realistic detector spectral response, the noise in the VMIs at 45 keV only varies modestly across the four basis material sets (Figure 12b,b′), leading to moderate variation in the CNR (Figure 12c,c′) that is consistent to visual inspection of the images displayed in Figures 10d1–d4 and 11d1–d4 .
FIGURE 12.

Noise in the material‐specific images of each basis material set (row 1), and the resultant noise (row 2) and contrast‐to‐noise ratio (CNR) (row 3) in each virtual monochromatic image at 45 keV under ideal (left) and realistic (right) detector spectral response
4. DISCUSSION
Recognizing the momentum in R&D of photon‐counting CT and the potential of m‐MD‐based spectral imaging, we derived the equations governing the behavior of noise and noise correlation in the material‐specific images for spectral imaging in photon‐counting CT based on m‐MD. As the analytic expression for noise and noise correlation in the cases beyond 2‐MD becomes complicated, we carried out a simulation with phantoms to assess the noise correlation between the material‐specific images, and it impact on the performance of m‐MD‐based spectral imaging in photon‐counting CT. Specifically, by extending the study of noise correlation from 2‐MD‐based spectral imaging to the m‐MD‐ (3‐MD, 4‐MD and beyond) based cases in photon‐counting CT, we characterized the quantitative relation in noise correlation between the material‐specific (basis) images in m‐MD‐based spectral imaging, which is significantly more complicated than its counterpart in the 2‐MD‐based case. To the best of our knowledge, such an attempt in the paradigm of m‐MD‐based spectral imaging in photon‐counting CT has not been reported in the literature.
As reported in the literature, 13 , 14 , 16 the noise correlation in the material‐specific images of 2‐MD is negative (Figure 4). However, as demonstrated in Figures 6, 8, and 9, the polarity of noise correlation in the material‐specific images of 3‐MD and 4‐MD alternates between ±1, and such an alternation makes the noise property in m‐MD‐based spectral imaging complicated in photon‐counting CT. Meanwhile, it may bring about the opportunity for us to design and implement sophisticated algorithms for de‐noising in m‐MD‐based spectral imaging in photon‐counting CT, for example, similar to what has been reported in the literature, 14 or in particular, using neural network or deep learning–based approaches. 29 , 30 For example, the material‐specific images with their noise in negative correlation should be preferably utilized in de‐noising, whereas caution needs to be exercised if the images are in positive noise correlation.
In the case of 2‐MD, Equations (10)–(13) show that the magnitude of noise in each material‐specific image is jointly determined by the SNR of the data acquired in each spectral channel, the interchannel data correlation and (), the effective attenuation coefficients μ11, μ12, μ21, and μ22, and the Jacobians that is depending on μ11, μ12, μ21, and μ22. Similarly, in the case of 3‐MD, Equations (A1)–(A6) show that the magnitude of noise in each material‐specific image is jointly determined by the SNR of the data acquired in each spectral channel, the interchannel data correlation , the effective attenuation coefficients (), and the Jacobian that is dependent on (. In the case of either 2‐MD or 3‐MD, the distortion in a realistic detector's spectral response induces interchannel data correlation, that is, or > 0 . Meanwhile, the distortion in a realistic detector's spectral response also alters the effective attenuation coefficients μ11, μ12, μ21, and μ22 or (, and accordingly the Jacobian or . In reality, the role played by the Jacobian in the denominator is dominant over that by the interchannel data correlation in the nominator. Consequently, the material‐specific images under realistic detector spectral response is noisier than their counterparts under ideal detector spectral response, as we have observed visually in Figures 3, 5, and 7 and quantitatively in Figure 12a–a′. Similar observation can be made on the noise in 4‐MD if we compare the results shown in Figure 7a–d and a′–d′, though the analytic equations that characterizing the noise behavior in 4‐MD is not presented due to its complexity in expression.
The polarity of noise correlation in the material‐specific images depends on their order in the set of basis materials. Specifically, the order is determined by the attenuating property of the basis materials at the low‐energy end (see Figure 12 and its related context in Ref. [6] for in‐depth analysis and discussion), which in turn determines the sign of the cofactors in getting the inverse matrixes according to Equation (5). The magnitude of noise correlation between the material‐specific images in 2‐MD and 3‐MD, regardless of its polarity, approaches unity, implying that the correlation is actually very strong. As illustrated in Equations (10)–(13) and (A1)–(A6), the interchannel data correlation () and the effective attenuation coefficients (pth material in kth energy bin) play important roles in determining the magnitude of noise correlation in 2‐MD and 3‐MD, in a manner that is similar to their influence on the magnitude of noise just explained earlier. A close inspection of Figures 4 and 6 shows that the distortion in detector's spectral response, which may be induced by charge‐sharing, the Compton scattering, and florescence‐escaping, 8 , 9 , 10 , 11 , 12 , 13 indeed increases the magnitude of noise correlation between the material‐specific images in comparison to their counterparts under ideal detector spectral response. Similar observation can be made on the noise correlation in the case of 4‐MD if we compare the results displayed in Figures 8a–f and 9a–f, in spite of the fact that the analytic equations that characterizing the behavior of noise correlation in 4‐MD is not explicitly given due to its complexity in expression.
The drastic variation of noise in each of the material‐specific images in 3‐MD Figure 12a,a′ is attributed to the similarity in attenuation between the basis materials adipose and PMMA and thus poor conditioning in the basis material sets BM‐1 and BM‐2. 5 , 6 With improvement in the conditioning of basis materials in BM‐3 and BM‐4, the variation of noise in the material‐specific images becomes much more tractable. Hence, for material‐specific imaging, attention should be paid to basis materials selection 5 , 6 (see Figure 12a,a′). On the other hand, despite the noise varies radically over the material‐specific images across the basis material sets BM‐1, BM‐2, BM‐3, and BM‐4 (Figure 12a,a′), the variation of noise in virtual monochromatic image is moderate (Figure 12b,b′), leading to moderate variation in the imaging performance assessed by CNR (Figure 12c,c′). It is believed that the tolerance to the conditioning of basis materials in virtual monochromatic imaging is partially attributable to the fact that there exist negative noise correlations between the material‐specific images.
Only 3‐MD and 4‐MD are considered in our study as the examples to evaluate and verify the property of noise and noise correlation in m‐MD. However, it should be straightforward to apply Equation (5) and its derivatives over the cases, wherein more than four basis materials are engaged in MD. Fortunately, as indicated in our recent investigation on the conditioning of basis materials and spectral channelization and their impacts on the performance of photon‐counting spectral imaging in CT, 6 , 7 the chance for more than four basis materials (and accordingly four spectral channels) is really limited, in light of the fact that more basis materials (and thus more spectral channels) may radically impact the imaging performance, for example, the occurrence of severe noise with increasing number of spectral channels, as we have observed in the cases presented in Figure 7a′–d′. Finally, we would like to state that the data acquired in this work are informative to the clinical medical physicists who are interested in spectral imaging in either photon‐counting or energy‐integration spectral CT. The information may also beneficiary to the clinical medical physicists who are working in other X‐ray imaging modalities, such as digital radiography and tomosynthesis, because, basically, there is no difference in carrying out the MD between them and CT.
5. CONCLUSIONS
By taking 3‐ and 4‐MD as the examples, we investigated the noise correlation in material‐specific (basis) images and its effect on the performance of spectral imaging in photon‐counting CT based on multi‐MD. The obtained results and conveyed information may help clinical medical physicists further understand the fundamentals of spectral imaging in either photon‐counting or energy‐integration CT based on multi‐MD, and other X‐ray imaging modalities, such as digital radiography and tomosynthesis.
AUTHOR CONTRIBUTIONS
Xiangyang Tang: Study conception, study design, literature research, data analysis, manuscript writing, and study integrity; Yan Ren: Study design, data acquisition, data analysis, and manuscript editing; Huiqiao Xie: Data analysis and manuscript editing.
CONFLICTS OF INTEREST
The authors have no relevant conflicts of interest to disclose.
FUNDING INFORMATION
XT is a recipient of research grant from SinoVision Technologies, which is not relevant to the work presented herein. The authors have no other relevant financial interests to disclose.
ACKNOWLEDGMENTS
The authors express their appreciation to Leonardo Tang at Georgia Institute of Technology for his proofreading of the manuscript as a volunteer.
APPENDIX A.
A.1.
Starting from Equation (5) and following with algebra, we can specifically and deliberately arrive at the results presented below, though the results may be analytically expressed in a more compact form.
| (A1) |
| (A2) |
| (A3) |
| (A4) |
| (A5) |
| (A6) |
where
| (A7) |
If no correlation exists in projection data, , Equations (A1)–(A6) degenerate into
| (A1′) |
| (A2′) |
| (A3′) |
| (A4′) |
| (A5′) |
| (A6′) |
Tang T, Ren Y, Xie H. Noise correlation and its impact on the performance of multi‐material decomposition‐based spectral imaging in photon‐counting CT. J Appl Clin Med Phys. 2023;24:e13830. 10.1002/acm2.13830
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
