Logan plot

A Logan plot (or Logan graphical analysis)^[1] is a graphical analysis technique based on the compartment model that uses linear regression to analyze pharmacokinetics of tracers involving reversible uptake. It is mainly used for the evaluation of nuclear medicine imaging data after the injection of a labeled ligand that binds reversibly to specific receptor or enzyme.

In conventional

extended the method to tracers with reversible kinetics.

Description

The kinetics of radiolabeled compounds in a compartmental system can be described in terms of a set of first-order, constant-coefficient, ordinary differential equations.[4]^[5] The time course of the activity in the multicompartmental system driven by a metabolite-corrected plasma input function ${\displaystyle C_{p}(t)}$ can be described by:

${\displaystyle {\frac {d\mathbf {A} }{dt}}=\mathbf {KA} +\mathbf {Q} C_{p}(t)}$

where ${\displaystyle \mathbf {A} }$ is a column vector of activity concentration for each compartment at time ${\displaystyle t}$, ${\displaystyle \mathbf {K} }$ is the matrix of the transfer constants between compartments, and ${\displaystyle \mathbf {Q} }$ is the vector of plasma-to-tissue transfer constants. Patlak and Blasberg^[3] showed that the above equation can be written as:

${\displaystyle \int _{0}^{t}A(\tau )\,d\tau =-\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {Q} \int _{0}^{t}C_{p}(\tau )\,d\tau +\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {A} }$

where ${\displaystyle \mathbf {U} _{n}^{T}}$ represents a row vector of 1s and ${\displaystyle A(t)=\mathbf {U} _{n}^{T}\mathbf {A} }$. The total activity in the region of interest, ${\displaystyle \mathrm {ROI} (t)}$, is a combination of radioactivities from all compartments plus a plasma volume fraction (${\displaystyle V_{p}}$)^[2] and thus:

${\displaystyle \int _{0}^{t}\mathrm {ROI} (\tau )\,d\tau =(-\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {Q} +V_{p})\int _{0}^{t}C_{p}(\tau )\,d\tau +\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {A} }$

By dividing both sides by ${\displaystyle \mathrm {ROI} (t)}$, one obtains the following linear equation:

${\displaystyle {{\int _{0}^{t}\mathrm {ROI} (\tau )\,d\tau } \over \mathrm {ROI} (t)}=(-\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {Q} +V_{p}){{\int _{0}^{t}C_{p}(\tau )\,d\tau } \over \mathrm {ROI} (t)}+{{\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {A} } \over {\mathbf {U} _{n}^{T}\mathbf {A} +V_{p}C_{p}}}}$

For ${\displaystyle t>t'}$, Patlak and his colleagues^[2] showed that ${\displaystyle \mathbf {A} =-\mathbf {K} ^{-1}\mathbf {Q} C_{p}(t)}$, i.e., the steady-state condition. When this condition is satisfied, the intercept has reached its constant value so that after some time a plot of ${\displaystyle {{\int _{0}^{t}C_{p}(\tau )d\tau } \over \mathrm {ROI} (t)}}$ versus ${\displaystyle {{\int _{0}^{t}\mathrm {ROI} (\tau )d\tau } \over \mathrm {ROI} (t)}}$ becomes a straight line with slope ${\displaystyle (-\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {Q} +V_{p})}$ and intercept ${\displaystyle {{\mathbf {U} _{n}^{T}\mathbf {K} ^{-1}\mathbf {A} } \over {\mathbf {U} _{n}^{T}\mathbf {A} +V_{p}C_{p}}}}$.^[1]

For a catenary two-tissue compartment model with transfer constants ${\displaystyle K_{1}}$ (forward transport from plasma to tissue), ${\displaystyle k_{2}}$ (reverse transport from tissue to plasma), ${\displaystyle k_{3}}$ (

parameter proportional to ${\displaystyle B_{\max }k_{\mathrm {on} }}$), and ${\displaystyle k_{4}}$ (dissociation constant) to analyze enzyme or receptor system, the slope represents the total (${\displaystyle V_{d}}$) and is given by ${\displaystyle {\frac {K_{1}}{k_{2}}}(1+{\frac {k_{3}}{k_{4}}})+V_{p}}$,^[1] where ${\displaystyle k_{3}=B_{\max }k_{\mathrm {on} }}$, ${\displaystyle k_{4}=k_{\mathrm {off} }}$, ${\displaystyle {\frac {k_{3}}{k_{4}}}={\frac {B_{\max }}{K_{d}}}}$, and ${\displaystyle K_{d}=k_{\mathrm {off} }/k_{\mathrm {on} }}$, in which ${\displaystyle B_{\max }}$ is the concentration of ligand binding sites, ${\displaystyle K_{d}}$ is the equilibrium dissociation constant for the ligand-binding site complex, ${\displaystyle k_{\mathrm {on} }}$ is the ligand-binding association constant, ${\displaystyle k_{\mathrm {off} }}$ is the ligand-binding dissociation constant. For a one-tissue compartment model with transfer constants ${\displaystyle K_{1}}$ and ${\displaystyle k_{2}}$, the slope is ${\displaystyle \lambda +V_{p}}$, where ${\displaystyle \lambda }$ is the partition coefficient (${\displaystyle {K_{1}}/{k_{2}}}$) and the intercept is ${\displaystyle {\frac {-1}{k_{2}(1+V_{p}/\lambda )}}}$.^[1]

See also

• Patlak plot
• Multi-compartment model
• Positron emission tomography
• Binding potential
• Distribution volume

References