The present invention relates generally to Positron Emission Tomography (PET). More particularly, the invention relates to a method of PET image reconstruction by obtaining intra-patient tissue activity distribution and photon attenuation map and implementing a Maximum Likelihood Expectation Maximization (MLEM) method.
Quantitative Positron Emission Tomography (PET) requires the knowledge of the intra-patient photon attenuation map. This attenuation map may be obtained via a priori transmission scan. However, a transmission scan exposes the patient to additional ionizing radiation, prolongs the overall scan time and requires dedicated equipment. Moreover, such transmission scan is unavailable in combined PET and Magnetic Resonance Imaging (PET/MRI) scanners. To avoid these shortcomings, several groups proposed obtaining the attenuation map from the PET emission data alone.
Furthermore, PET image reconstruction assumes “true” coincidences, where both photons originate from the same radionuclide decay and do not scatter inside the tissue. Thus, in many cases over half of the detected coincidences are discarded, rather than used in the reconstruction process. Moreover, around 60% of such discarded coincidences have a rather simple structure, comprising just a single tissue scattered photon. Some recent work targeted the incorporation of such simple structured coincidences into activity reconstruction in PET and into activity and attenuation reconstruction in Single Photon Emission Tomography (SPECT).
What is needed is a method of reconstructing the intra-patient tissue activity distribution and photon attenuation map, using true- and tissue scattered coincidences using the Maximum Likelihood Expectation Maximization (MLEM) method in conjunction with a new set of latent random variables.
To address the needs in the art, a method of PET image reconstruction is provided that includes obtaining intra-patient tissue activity distribution and photon attenuation map using a PET/MRI scanner, and implementing a Maximum Likelihood Expectation Maximization (MLEM) method in conjunction with a specific set of latent random variables, using an appropriately programmed computer and graphics processing units, wherein the set of latent random variables comprises the numbers of photon pairs emitted from an electron-positron annihilation inside a voxel that arrive into two given voxels along a Line of Response (LOR), where the set of latent random variables results in a separable joint emission activity and a photon attenuation distribution likelihood function.
According to one aspect, the invention further comprises incorporating Time of Flight (TOF) data and Magnetic Resonance Imaging (MRI) data to the MLEM method, where detector scatter with partial energy deposition that creates a degeneracy for the identification of tissue scattered coincidences is accounted for by (i) setting an appropriate low energy threshold for data acquisition, or (ii) incorporating the detector scatter events into the MLEM method, or (i) and (ii).
According to another aspect, the invention further comprises incorporating Single Scatter Approximation (SSA) that defines tissue scatter coincidences as events where only one of the two photons is scattered and is scattered only once, wherein the tissue scatter coincidence affects attenuation coefficients of the photon defined by a distribution of possible scatter points forming a hollow shell-shape in the detector's field of view and the emission activity coefficients inside a corresponding solid shell.
The current invention provides a method of reconstructing the intra-patient tissue activity distribution and photon attenuation map, using true- and tissue scattered coincidences. To that end, the Maximum Likelihood Expectation Maximization (MLEM) method is employed in conjunction with a new set of latent random variables.
The method according to the current invention has some advantages: (i) It results in a separable activity distribution and photon attenuation map likelihood function, which simplifies maximization (
The log-likelihood maximization procedure poses a computational challenge, due to the non-separability of the joint tissue activity distribution, and photon attenuation map-likelihood function. Some researchers proposed to address this challenge by maximizing the log-likelihood via the Gradient Ascent or the Newton-Raphson methods.
However, a similar challenge for CT and SPECT was addressed differently by obtaining a separable likelihood function using an alternative set of latent random variables. The method according to the current invention extends the previous work for PET and incorporates the use of some of the tissue scattered coincidences. It results in a separable likelihood function, which is easier to maximize than a non-separable likelihood function.
Another challenge with PET image reconstruction is the measurement errors. These errors propagate into the reconstruction process, due to the coupling between the observables and reconstructed parameters. This error propagation may be addressed via the use of Time of Flight (TOF) data, which decouples some of the parameters and observables. However, error propagation is particularly challenging for the use of tissue scattered coincidences. This is due to the large number of voxels directly affected by a tissue scattered coincidence, compared with a smaller number of voxels directly affected by a true coincidence (grey line in
A further challenge with the use of tissue scattered coincidences, is detector scatter with partial energy deposition (see
Furthermore, the current invention allows for the incorporation of a priori information, with no further coupling of the update equations. For instance, such information regarding the photon attenuation map may be obtained via a priori Magnetic Resonance Imaging (MRI) scan, available in combined PET/MRI scanners.
In summary, the current invention is a method for a joint PET reconstruction of the intra-patient tissue activity distribution and photon attenuation map, and represents the first method which results in a separable joint activity and attenuation map likelihood function for PET.
According to the invention, the three-dimensional field of view is divided into voxels.
The model incorporates “true” and “scattered” coincidences. As illustrated in
As shown in
Particularly, a “true” LOR has the form of a straight tube. As shown in
LOR d∈LOS s (1)
indicates that LOR d and LOS s correspond to the same detector pair and scattering angle. Particularly, several LORs may contribute to the same observed coincidence number nd:
d,d′∈LOS snd≡nd′ (2)
The model contains observed and latent variables, shown in
where d1 and d2 denote the indices of the two detectors associated with LOR d. The symbol Γd denotes the set of possible emission locations along LOR d. As illustrated in
The model parameters are the activity distribution, θi, and the attenuation coefficients, μi, per voxel i. The activity is defined as the mean number of intra-voxel annihilations. An attenuation coefficient is defined as the intra-voxel photon scattering cross section. These parameters are determined via the MLEM method. In this method, the likelihood function is maximized by an iterative solution of a set of update equations. As derived below and shown in
where {circumflex over (N)}ni and Δ{circumflex over (N)}ni are, respectively, the mean number of detected and attenuated photon pairs, emitted from voxel i. In the absence of attenuation, Pi is the total detection probability of a photon pair emitted in voxel i. It depends on the scanner's geometry and on its specifications, such as the detector's quantum efficiencies.
As derived below and shown in
where d indicates only the observed LORs, as opposed to all possible LORs. The parameters {circumflex over (M)}jnd and Δ{circumflex over (M)}jnd are the expected cardinality of a subset of the photons emitted into LOR d, which respectively traversed- and scattered inside-voxel j. The parameter rdj is defined as follows:
where, as shown in
where the second line holds for small attenuation, when ΔMknd<<Mknd. Since Eq. (5) is monotonic in μjn+1, it has a unique solution. Since for small voxels, μjrdj is also small, Eq. (5) may be approximated via the following Taylor series expansion:
Moreover, since for x>0,
the exact solution is bounded by
The use of the first order expansion from Eq. (8), results in the following update rule for the attenuation coefficients:
It was found that for such first order expansion, the SPECT likelihood begins to decrease after about 100 iterations, following an initial increase. To address this issue, a second order expansion is used, which results in a quadratic equation in μjn+1. This approximate solution and the bounds on the exact solution from Eq. (10), may be farther refined via a higher order Taylor series expansion. Moreover, since the attenuation coefficient update equation (5) is one-dimensional, it may be solved numerically, using approaches, such as Ollingers' method.
Turning now to the model details, the following section provides sufficient details for the calculation of the model parameters defined above. Moreover, some supplementary derivations are given below. The reconstruction equations are summarized below.
The variables {circumflex over (N)}ni, Δ{circumflex over (N)}ni and Pi from Eq. (4) (
where the parameters Xjkdi denote the numbers of photon pairs reaching voxels j and k along LOR d, after being emitted inside voxel i. The symbol ∀d indicates all possible-, as opposed to just detected-, LORs. The parameters cdit are given by the following expression:
where, in the absence of attenuation, cdi is the probability for an emitted photon pair to be detected in LOR d. Particularly, it accounts for the geometric effects and for the detector's quantum efficiencies. The symbol N denotes the Gaussian distribution. The parameter t denotes the TOF time difference. σd is the standard deviation associated with the time resolutions of detectors d1 and d2. rdi is the distance between the center of voxel i and the center of LOR d. The expectations of the parameters Xjkdi are given by
where γjkd denotes the probability for a photon pair emitted between voxels j and k along LOR d, reaching these voxels:
and the symbol I denotes the indicator function. As discussed below, the second term in the denominator of the conditional expectation in Eq. (17), accounts for detector scatter with partial energy deposition. Pd is the probability for exactly one photon of a coincidence pair emitted along LOR d, depositing part of its energy inside a detector. As shown in
As also discussed below, the parameter Δ{circumflex over (M)}jnd from Eq. (5) is given by the following expression:
where δi,j is the Kronecker delta, and the voxel indices increase monotonically towards detector d2. The conditional expectations {circumflex over (X)}jkdi are derived below:
As discussed below, the symbol jkd denotes the set of LORs containing the variable Xjkdi. As discussed below, the parameter {circumflex over (M)}jnd from Eq. (5) is given by the following expression:
As shown in
j,i∈Γdji,i>j (22)
As described below, this computation may be accomplished incrementally with two projections.
As discussed below, if the scattering cross sections are sufficiently small, the Single Scatter Approximation may be applied. It may reduce noise propagation (see above) and accelerate the reconstruction process. In this approximation, γjkd from Eq. (18) simplifies into the following form:
Additionally, for scattered coincidences, Δ{circumflex over (M)}jnd and {circumflex over (M)}jnd from Eqs. (19) and (21) respectively, are simplified into the following expressions:
In conclusion, the reconstruction algorithm is defined by Eqs. (4) and (11) in conjunction with Eqs. (12)-(21). The Single Scatter Approximation alters the attenuation reconstruction, as described by Eqs. (23)-(25). Particularly, the calculation of μj no longer involves all the LORs containing voxel j. Instead, it involves only the LORs corresponding to a photon scattering inside voxel j. Additionally, as described in Eqs. (24) and (25), a scattered LOR no longer involves the calculation of γjkd for various j and k, but only the calculation of γd
Turning now to the implementation of the details, described herein is the method for the numerical calculation of the reconstruction update equations. Additionally, it references a Graphics Processing Units (GPU) based computing formulation, appropriate for the method according to the current invention. Further, discussed are the considerations in approximating the normalization parameter Pi. For simplicity, only true-, as opposed to scattered-, coincidences are treated here.
The reconstruction update equations, which were introduced above, are given by the following expressions:
where Gnd denotes the difference between the detected- and expected-number of counts along LOR d, and Rjnd denotes the cardinality of a subset of the photons entering voxel j along LOR d. Notably, when Gnd<<Rjnd and μjnldj<<1, Eq. (27) reduces into μjn+1=μjn, and the photon attenuation map reconstruction process converges. The computation of Eq. (26) requires a single forward- and back-projection. As described below, the computation of Eq. (27) requires two projections along each LOR. To that end, Eqs. (27)-(29) are formulated in terms of the following parameters:
which results in the following expressions:
As illustrated in
Particularly, the parameters Sjd and Δjd may be calculated by a projection directed towards detector d2, while the parameters Sjd may be calculated by a second, oppositely directed, projection. Therefore, as described below, the photon attenuation map update requires two projections along each LOR, after which the attenuation coefficient μjn+1 may be calculated by a single voxel traversal.
The independence of the nth-iteration tissue activity distribution, θin, and photon attenuation map, μjn, enables a parallel GPU based reconstruction. The speed of such reconstruction depends on its memory latency and branch divergence. Memory latency slows down the execution due to the data access time. Branch divergence serializes the, otherwise parallel, program, due to the Single-Instruction-Multiple-Data (SIMD) GPU operation principle.
A GPU based tissue activity distribution reconstruction method reduced branch divergence by processing the LORs according to their principal directions. This resulted in a balanced load distribution among GPU threads. Memory latency was reduced by caching parallel image-space slices into the GPU's shared memory. The current implementation adapts this method for the calculation of Eqs. (26)-(29).
Furthermore, in cylindrical scanners, the probability Pi from Eq. (26) is fairly uniform across the field of view. Hence, for a qualitative non-attenuated tissue activity distribution reconstruction, Pi could be assigned an arbitrary value, rather than calculated. However, in the presence of photon attenuation, a too small Pi value would destabilize the iterative reconstruction. This would cause a divergence of the reconstructed activity values, since the terms γd
Hence, in the presence of attenuation, a large enough Pi value is required to stabilize the iterative reconstruction. Moreover, Pi may be approximated consistently as
where the summation is over the measured LORs, rather than over all the possible LORs as in Eq. (14).
As shown in
∀s∈jkdXjksi≡Xjkdi (38)
The reconstruction equations use the non-degenerate-, as opposed to the complete-, variable set. Practically, this requires the identification of degenerate variables, which might be computationally demanding. However, this identification might be accelerated via an approximation, which is more accurate for low scattering cross sections. This approximation assumes that all degenerate variable groups, jkd, contain scattered- and true-, as opposed to only scattered-, coincidences:
∀jkd:jkd\LOS≠ø (39)
With this assumption, the non-degenerate reconstruction parameters are determined only by true-, as opposed to true- and scattered-, coincidences.
In some cases, notably with combined PET/MRI scanners, a priori information regarding the attenuation map is known. Such a priori information may be incorporated into the statistical model via the Maximum a Posteriori (MAP) method. When combined with the proposed statistical model, the MAP method does not couple the update equations, but rather results in an addition of a regularization term to the log-likelihood function.
Moreover, as mentioned above, TOF data may be incorporated into the statistical model via Eq. (15). This effectively restricts the emission and scatter loci, as illustrated in
As described below, the incorporation of detector scatter into the statistical model, involves the coupling of LORs d and d4. Such coupling is straightforward in the proposed method and was accomplished by altering the MLEM conditional probabilities. A similar approach may help generating random and scatter corrections.
With the appropriate assumptions, the current reconstruction method reduces into three other methods: A reduction into the unattenuated PET activity distribution reconstruction; A reduction into the SPECT joint activity distribution and photon attenuation map reconstruction; The CT photon attenuation map reconstruction.
The method according to the current invention uses scattered and true coincidences for joint tissue activity distribution and photon attenuation map reconstruction. It is based on a new set of latent random variables. This variable set results in a separable joint tissue activity distribution- and photon attenuation map-likelihood function, which simplifies maximization. This is the first method to result in a separable joint likelihood function for PET. The corresponding update equations have a unique solution, which may be bounded with an arbitrary precision. These equations are computationally tractable and are consistent with the PET model, the CT model and the SPECT model.
The method according to the current invention addresses detector scatter with partial energy deposition, which creates a degeneracy for the identification of tissue scattered coincidences.
Experimental error propagation is addressed via the use of Time of Flight (TOF) data (if available) and by the Single Scatter Approximation. A priori information, such as that obtained with Magnetic Resonance Imaging (MRI), may be readily incorporated into the statistical model.
Turning now to the statistical model, as mentioned above, the latent variables constitute the following subset of the complete variable set {Xjkdi}:
{Xjkdi|j,k∈di} (A1)
where, as illustrated in
di={d1,k≥i}∪{j>i,i} (A2)
The indices of each LOR increase monotonically towards detector d2. As shown below, Xjkdi are independent Poisson variables:
Xjkdi˜Pois(λjkdi) (A3)
where λjkdi were defined in Eq. (16). Since, the latent variables completely determine the variable space via Eq. (3),
P(Xjkdi,n)=P(Xjkdi) (A4)
The variables Xjkdi are independent for different d or i. The dependence for the same d and i arises since the number of photons cannot grow downstream (e.g. Xjkdi≥Xjk+1di). As shown in
where the index d3 was defined following Eq. (6). For voxels not adjacent to scatter locations, d3, the second Binomial parameter corresponds to the probability of a photon not scattering inside an upstream voxel. For voxels adjacent to scatter locations, it corresponds to the scattering probability.
Using Eq. (A5) and the independence properties of Xjkdi, the likelihood function is given
where the symbol ∀d was defined following Eq. (14). Omitting the terms irrelevant for the maximization of the likelihood with respect to θ and μ, the corresponding log-likelihood, (θ; μ), is given by the following expression:
As mentioned in section II, the log-likelihood is maximized via the MLEM method. This method is iterative, where each iteration consists of two steps, denoted “Expectation” and “Maximization”. In a given iteration n, the Expectation step calculates the form of the auxiliary function Q(θ, ν|n; θn, μn), defined by the following expression:
The Maximization step, calculates the new parameters, θn+1 and μn+1, maximizing this function:
These steps are described below.
The auxiliary function, Q(θ, ν|n; θn, μn), has the form of Eq. (A9), with the random variables Xjkdi replaced by their conditional expectations,
As shown above, these conditional expectations are given by the following expression:
where the set Djkd was defined following Eq. (20) and the index n denotes the previous reconstruction iteration. Note that generally, cdit≠csit, since the parameter cdit might depend on the detector incidence angles of the coincidence photons. The summation in Eq. (A9) is overall-, not only the detected-, LORs. Addressing so many LORs involves a high computational load. However, this load may be reduced, assuming a low emission of photon pairs into non-detected LORs:
nd=0∀i∈Γd,{circumflex over (X)}jkdi≈0 (A13)
This assumption is used in the rest of the paper. It is more valid for low photon attenuation values.
Turning now to the activity maximization step, setting the derivative of Q(θ, ν|n; θn, μn), with respect to θi to zero, yields the following update rule for the activity parameters:
where Pi was defined in Eq. (14) and {circumflex over (X)}iidi was given in Eq. (A12). In the absence of attenuation, jkd=d and γd
Regarding the attenuation maximization step, setting the derivative of Q(θ, μ|n; θn, μn), with respect to μj to zero, yields Eq. (5). As shown in
Ignoring scattered coincidences, the activity distribution and photon attenuation map reconstruction equations are respectively reduced.
Moreover, this SPECT model may be further reduced into a CT model, by representing the CT irradiation sources by the activity inside voxels d2−1. This further reduces the photon attenuation map reconstruction equation.
With respect to the derivation of condition expectations, due to the possible degeneracy in the presence of scattered coincidences, described above, a random variable Xjkdi depends on the observables
{ns|s∈jkd} (A16)
The conditional probability of Xjkdi is given by
Hence, the conditional expectations, {circumflex over (X)}jkdi, are given by
where the last equality follows since
Similarly,
is the probability for a photon not scattering inside the LOR segments Γdd
This implies that
Hence, the conditional expectation E(Xjkdi|Xd
Substitution of Eq. (A23) into Eq. (A18) yields Eq. (20). Using Eq. (3), the conditional probabilities of Xs
Hence, the conditional expectation E(Xs
Finally, substitution of Eq. (A24) into Eq. (20) yields Eq. (A12). Note that since for scattered coincidences, Γs overlaps several LORs, the terms γs
Turning now to addressing the detector scattering with partial energy deposition, as mentioned above, some of the detector scatter with partial energy deposition may be filtered out during data acquisition. Thus, it can be distinguished from tissue scatter in the reconstruction of tissue activity distribution and photon attenuation map. This may be done by setting an appropriate low energy threshold, using the following considerations: according to the kinematics of Compton scatter, a photon cannot deposit more than ⅔ of its energy via a single Compton scatter inside the detector. On the other hand, a photon cannot lose more than ⅔ of its energy via a single Compton scatter inside the tissue. Hence, with detector energy resolution of ΔEξ KeV at photon energy ξ, detector scatter corresponds to detected energies, Edetector scatter, in the range
and tissue scatter corresponds to detected energies, Etissue scatter, in the range
Hence, as shown in
Moreover, the intra-detector scatter may be incorporated into the statistical model: let ηd denote the number of photon pairs emitted along LOR d4 (
Given the number of coincidences detected along LOR d4, the conditional distribution of ηd is given by
where the probability Pd was defined in the paragraph following Eq. (18). This probability may be determined experimentally or numerically by a Monte-Carlo simulation. However, it may be approximated via the known detector attenuation coefficients, μd1 and μd2:
Since Σi∈Γd
as shown below (Eq. (D6)), the variable ηd may be treated as an independent Poisson variable:
Hence, detector scatter with partial energy deposition, may be incorporated into the statistical model via the following modification of the MLEM conditional expectations:
As mentioned above, other effects, such as random- and undesired low-energy scatter-coincidences, may be incorporated into the statistical model via similar modifications of the conditional expectations.
Turning now to single scatter approximation, as mentioned above, experimental error propagation may be reduced by decoupling the observables from some of the reconstructed parameters.
Assuming small photon attenuation, both Δ1 and Δ2 are small for d3∈Γdjk. Hence, the term Δ1 Δ2 may be neglected in the sums over Γd. This approximation is denoted as the Single Scatter Approximation (SSA). It implies that for tissue scattered coincidences, only one of the two photons scatters and it scatters only once. Nevertheless, according to Monte-Carlo simulations of a 511 KeV photon point source positioned inside a water cylinder, around 40% of the scattered photons scatter more than once. Hence, the SSA might not be accurate in such cases. With the SSA assumptions, each LOS contributes only the following latent variables:
Hence, the photon attenuation coefficient in voxel j is affected only by the true LORs and LOS intersecting this voxel. Moreover, since in this approximation, there is no need for the calculation of the parameters γjid in Eq. (29) for voxel indices i>j, the computational load is reduced, compared with the exact calculation above.
Regarding the representation of multinomial variables as independent Poisson variables, some of the dependent Multinomial variables, such as Xjkdi for different LOR indices d, but the same voxel index i, are treated as independent Poisson variables. This may be justified by consider the Multinomial vector r, with the parameters n and p, where n≡Σiri is a Poisson variable:
r˜Mult(n,p)
n˜Pois(N) (D1)
The total probability of r is given by
Since n≡Σiri and Σipi=1, this expression simplifies to
A further summation over r\ri yields:
ri˜Pois(piN) (D4)
Hence, ri are independent Poisson variables. Particularly, a Binomial variable r, with a Poisson parameter n,
r˜Bin(n,p)
n˜Pois(n) D5
may be treated as a Poisson variable with the mean pN:
r˜Pois(pN) (D6)
To see this, evaluate P(r)=ΣnP(r|n)P(n).
The present invention has now been described in accordance with several exemplary embodiments, which are intended to be illustrative in all aspects, rather than restrictive. Thus, the present invention is capable of many variations in detailed implementation, which may be derived from the description contained herein by a person of ordinary skill in the art. All such variations are considered to be within the scope and spirit of the present invention as defined by the following claims and their legal equivalents.
This application claims priority from U.S. Provisional Patent Application 61/897,294 filed Oct. 30, 2013, which is incorporated herein by reference.
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20060163485 | Stearns | Jul 2006 | A1 |
20110303835 | Fenchel | Dec 2011 | A1 |
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WO 2013164731 | Nov 2013 | WO |
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