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. 2001 Dec;45(12):3393–3402. doi: 10.1128/AAC.45.12.3393-3402.2001

TABLE 4.

Main biological side effects

Side effect Result for the following group (no. of patients):
P valuea
Ritonavir (25) Ritonavir + saquinavir (22)
Triglyceride increaseb, no. (%) 23 (92) 20 (91) 1.00
 Mean ± SD at baseline (mmol/liter) 2.1 ± 1.6 1.7 ± 1.4 0.32
 Range at baseline (mmol/liter) 0.6–8.1  0.5–5.8 
 Mean ± SD at wk 24 (mmol/liter) 4.2 ± 1.7 3.9 ± 3.2 0.88
 Range at wk 24 (mmol/liter) 0.9–7.4  0.8–13.1
Cholesterol increaseb, no. (%) 7 (28) 6 (27) 0.96
 Mean ± SD at baseline (mmol/liter) 4.7 ± 0.9 4.3 ± 0.9 0.09
 Range at baseline (mmol/liter) 3.5–6.7  2.5–6.6 
 Mean ± SD at wk 24 (mmol/liter) 6.4 ± 1.7 5.7 ± 1.3 0.39
 Range at wk 24 (mmol/liter) 4.4–10.4 4.2–8.8 
ALAT increasec, no. (%)
 Overall 15 (60) 16 (73) 0.36
 At least grade 2 7 (28) 5 (23) 0.68
ASAT increased, no. (%)
 Overall 10 (40) 10 (45) 0.71
 At least grade 2 3 (12) 4 (18) 0.69
Glutamyl transpeptidase increase,  no. (%)
 Overall 19 (76) 16 (73) 0.80
 At least grade 2 11 (44) 10 (45) 0.92
a

The P values correspond to the statistics of Student's t test (baseline values) and of ANCOVA (week 24 values, the comparison being adjusted to baseline values) for quantitative variables and of the chi-square test or Fisher's exact test, when appropriate, for categorical variables. 

b

Lipid measurements were not always obtained in a fasting state. However, to limit intraindividual variations, blood samples were collected for each patient at similar times along the follow-up and thus at similar intervals after food intake. 

c

ALAT, alanine aminotransferase. 

d

ASAT, aspartate aminotransferase.