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

\( \tau_i \)

estimated reference time

tau

\( \xi_i \)

individual log speed factor

xi

\( \gamma_i(t) \)

individual trajectory

model

\( \psi_i(t) \)

latent disease age

rt

\( \mathbf{A} \)

mixing matrix

mixing_matrix

\( t_0 \)

population reference time

tau_mean

\( \mathbf{s}_i\)

sources

sources

\( w_{i,k} \)

space shift

space_shifts

\( u_{i,l} \)

survival shift

survival_shifts

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:

\[ \psi_i(t) = e^{\xi_i}(t - \tau_i) + t_0 \]

where :

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:

\[ w_{i,k} = \sum_{j=1}^{N_w} \eta_{k,j} s_{i,j} \]

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:

\[ u_{i,l} = \sum_{m=1}^{N_s} \zeta_{l,m} s_{i,m} \]

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 \( i \).