Notations¶
This page contains the definitions and notations of the variables used in Leaspy.
Notations, concepts, and names in DAG¶
The following table displays the relationships between a variable mathematical notation, the associated concept, and the string name used in the DAG if this variable is handled this way.
Notation |
Concept |
Name in the DAG |
|---|---|---|
\( \tau_i \) |
|
|
\( \xi_i \) |
|
|
\( \gamma_i(t) \) |
|
|
\( \psi_i(t) \) |
|
|
\( \mathbf{A} \) |
|
|
\( t_0 \) |
|
|
\( \mathbf{s}_i\) |
|
|
\( w_{i,k} \) |
|
|
\( u_{i,l} \) |
|
Concept definitions¶
This section explains each mathematical concept and provides mathematical definitions when needed.
Estimated reference time¶
The estimated reference time for a given individual \( i \) is denoted as \( \tau_i \). It follows \(\tau_i \sim \mathcal{N}(t_0, \sigma^2_{\tau})\).
Individual log speed factor¶
The individual log speed factor for a given individual \( i \) is denoted as \( \xi_i \) . It follows \(\xi_i \sim \mathcal{N}(0, \sigma^2_{\xi})\).
Individual trajectory¶
The individual trajectory for a given individual \( i \) is denoted as \( \gamma_i(t) \) and represents the disease progression of the patient \(i\). It can be indexed by \(k\) when \(K\) outcomes are estimated.
Latent disease age¶
The latent disease age, for a given individual \( i \), is denoted as \( \psi_i(t) \).
It represents a transformation from chronological time \(t\) to latent disease age that is related to its stage in the disease and is defined as:
where :
\( e^{\xi_i} \) is the individual speed factor of individual \( i \).
\( \tau_i \) is the estimated reference time of individual \( i \).
\( t_0 \) is the population reference time.
Mixing matrix¶
The mixing matrix is denoted as \( \mathbf{A} \) and is defined as a matrix that describes the mixing of different sources in the model.
Population reference time¶
The population reference time is denoted as \( t_0 \) and is defined as the reference time for the entire population.
Sources¶
The sources, for a given individual \( i \), are denoted as \( \mathbf{s}_i\) and defined as the different origins of information or data that contribute to the individual’s disease progression model.
Space shift¶
The space shift, are more interpretable than sources \(\mathbf{s}_i\), as they encapsulate total spatial variability effects. for a given individual \( i \) and a given longitudinal outcome \( k \), is denoted as \( w_{i,k} \) and defined as:
where:
\( N_w \) is the number of spatial sources.
\( \eta_{k,j} \) is the weight for spatial source \( j \) in outcome \( k \).
\( s_{i,j} \) is the contribution of spatial source \( j \) for individual \( i \).
Survival shift¶
The survival shift, for a given individual \( i \) and a given event \( l \) is denoted as \( u_{i,l} \) and defined as:
where:
\( N_s \) is the number of survival sources.
\( \zeta_{l,m} \) is the weight for survival source \( m \) in event \( l \).
\( s_{i,m} \) is the contribution of survival source \( m \) for individual \( i \).