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. 2013 Dec 15;4(6):365–371. doi: 10.4239/wjd.v4.i6.365

Table 2.

Laboratory parameters at baseline and 3 mo later

Baseline 3 mo Percentage change
Fasting plasma glucose, mg/dL (mmol/L)
Switch to the highest dose rosuvastatin 91 ± 26 (5.1 ± 1.4) 95 ± 19 (5.3 ± 1.1) 4%b
Add-on-statin ER-NA/LRPT 93 ± 17 (5.2 ± 0.9) 102 ± 27 (5.7 ± 1.5) 10%bdf
Add-on-statin fenofibrate 94 ± 10 (5.2 ± 0.6) 94 ± 11 (5.2 ± 0.6) 0%
HbA1c, %
Switch to the highest dose rosuvastatin 6.1 ± 0.5 6.3 ± 0.5 0.2%b
Add-on-statin ER-NA/LRPT 6.3 ± 1.1 6.6 ± 1.2 0.3%bdf
Add-on-statin fenofibrate 6.1 ± 0.8 6.2 ± 1.0 0.10%
HOMA-IR index
Switch to the highest dose rosuvastatin 1.4 (1.2-2.1) 1.6 (1.5-2.6) 14%bf
Add-on-statin ER-NA/LRPT 1.5 (1.4-2.1) 2.5 (1.5-2.8) 65%bdf
Add-on-statin fenofibrate 1.7 (1.5-2.3) 1.6 (1.4-2.2) -6%b

Values are expressed as mean ± SD [except for fasting plasma insulin and HOMA-IR index which are expressed as median (range)]. No significant differences in baseline data were found across groups.

b

P < 0.01 vs baseline;

d

P < 0.01 vs switch to the highest dose rosuvastatin group;

f

P < 0.01 vs add-on-statin fenofibrate group. ER-NA/LRPT: Extended release nicotinic acid/laropiprant; HOMA-IR index: Homeostasis model assessment of insulin resistance index; HbA1c: Glycosylated haemoglobin.