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Table 1 Overview of state variables, variables, parameters and constants used in this paper

From: Diagnostic markers based on a computational model of lipoprotein metabolism

Ā Ā 

State Variables - determine the system state

d i, j

nm

Lipoprotein particle diameter in the i-th step of a lipolysis cascade, in the j-th subclass of the size range covered by that cascade step

Q ss (d i, j )

Particles * dL-1

Steady-state particle pool size in a pool with mean particle diameter d i, j

Ā Ā 

Variables - specify processes and output

d i , j r

nm

the radius of the subclass with average diameter d i, j

J l (d i, j )

Particles *

dL-1 * day-1

Particle flux into the pool with mean particle diameter d i, j due to extrahepatic lipolysis

J l, liver (d i, j )

Particles *

dL-1 * day-1

Particle flux into the pool with mean particle diameter d i, j due to hepatic lipolysis

k l (d)

day-1

Particle size dependent extrahepatic lipolysis rate

k a, liver

day-1

Particle size dependent liver attachment rate

(attachment is followed by either lipolysis or uptake)

k l, liver (d)

day-1

Particle size dependent liver lipolysis rate

k u, liver (d)

day-1

Particle size dependent liver uptake rate

n tg (d i, j )

Molecules * particle-1

Number of triglyceride molecules in a lipoprotein particle with diameter d i, j

Q *

Particles * dL-1

Steady-state particle pool size in the size range called *

k u , l i v e r * ĀÆ

day-1

Particle size dependent liver uptake rate, averaged per particle over the size range called *

k l ĀÆ

day-1

Particle size dependent extrahepatic lipolysis rate, averaged per particle over all particles in the model

k a , l i v e r ĀÆ

day-1

Particle size dependent liver attachment rate, averaged per particle over all particles in the model

J p,*

Particles * dL-1*day-1

Particle production flux into the size range called *

J in, *

Particles *

dL-1 * day-1

Particle production influx (production + lipolysis) into the size range called *

Q out ([d a d b ])

Particles * dL-1

Steady state particle pool size in interval from d a todbin the final particle concentration profile.

Ā Ā 

Parameters - are optimized using data

k l, max

day-1

maximum rate at which extrahepatic lipolysis takes place

k a, apoEmax

day-1

maximum rate at which liver binding mediated by ApoE takes place

k a, apoB

day-1

rate at which liver binding mediated by ApoB takes place

A

nm

shape parameter for liver binding mediated by ApoE

B

-

shape parameter for liver binding mediated by ApoE

Ļƒ u, liver

nm

shape parameter describing fraction of liver attachment which is taken up (instead of lipolyzed) - with changing particle size

Ā Ā 

Model constants and derived variables - calibrated in this paper

d a, apoEmin

17 nm

minimum particle diameter at which liver binding mediated by ApoE takes place

dhl, peak

31.33 nm

Hepatic lipase lipolysis peak size (see Eq. 5)

s u, liver

7.87

Liver uptake shape constant (see Eq. 2)

d l, min

25.13 nm

minimum size at which extrahepatic lipolysis occurs (see Eq. 4 in [13])

Ļƒ l

77.35 nm

shape constant for extrahepatic lipolysis (see Eq. 4 in [13])