From: Diagnostic markers based on a computational model of lipoprotein metabolism
Subject group | Number of subjects | Ref. | Included in 'normo-lipidemic' group | Included in 'dys-lipidemic' group |
---|---|---|---|---|
Normolipidemic controls | 3 (in: N1, N3, N5) | [19] | x | Ā |
Normolipidemic controls | 6 | [20] | x | Ā |
Normolipidemic controls: apoE 3/3 subjects. | 5 | [17] | x | Ā |
Normolipidemic controls | 9 | [21] | x | Ā |
All subjects | 12 | [22] | x | Ā |
phenotype 'A' (large LDL particle size) | 9 | [18] | x | Ā |
mixed dyslipidemia prior to treatment (Baseline) | 5 (in: P2, P3, P5, P7, P8) | [24] | Ā | x |
mixed dyslipidemia prior to treatment (Baseline) | 11 | [25] | Ā | x |
kidney patients | 9 | [21] | Ā | x |
hypothyroid subjects before and during T4 therapy | 10 (excluded before T4: 6; during T4: 3) | [26] | Ā | x |
HIV treatment-associated hyperlipidemic subjects | 5 | [23] | Ā | x |
phenotype 'B' subjects, with small LDL particle size | 4 (in: subjects 17-20) | [18] | Ā | x |
LPL -/- | 3 | [16] | Ā | Ā |
apoE 2/2 | 4 | [17] | Ā | Ā |
apoE 4/4 | 5 | [17] | Ā | Ā |
homozygous familial hypercholesterolemia | 3 (in: FH1, FH2, FH4) | [19] | Ā | Ā |
familial defective apoB | 3 | [29] | Ā | Ā |
S447X; a single nucleotide polymorphism in the LPL gene | 5 | [30] | Ā | Ā |
Total used for normolipidemic group | 44 | Ā | Ā | Ā |
Total used for dyslipidemic group | 44 | Ā | Ā | Ā |