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Circulation Journal
Official Journal of the Japanese Circulation Society
http://www. j-circ.or.jp
Supplementary File 1
TableS1. Baseline Characteristics of Subjects in the LISTEN Study
Male (%)
Age (years)
BMI
Statin administration before starting the study (%)
Medical history (%)
Cardiovascular/cerebrovascular events
Myocardial infarction
Angina pectoris
Heart failure
Revascularization
Cardiac arrhythmias
Cerebral hemorrhage
Cerebral infarction
Transient ischemic attack
Complications
Diabetic complications
Diabetic retinopathy
Diabetic nephropathy
Diabetic neuropathy
Hypertension*
Lipid parameters
Non-HDL-C (mg/dl)
TC (mg/dl)
LDL-C (mg/dl)
HDL-C (mg/dl)
LDL-C/HDL-C ratio
Non-HDL-C/HDL-C ratio
TG (mg/dl)
FFA (mEq/L)
Parameters related to glucose level
HbA1c (NGSP value) (%)
Blood glucose (mg/dl)
Insulin (U/ml)
1,5-AG (g/ml)
HOMA-IR
All subjects
(n=1,018)
Rosuvastatin
(n=514)
Atorvastatin
(n=504)
466 (45.8)
66.411.1
25.354.09
241 (23.7)
235 (45.7)
66.311.6
25.504.04
121 (23.5)
231 (45.8)
66.610.6
25.194.15
120 (23.8)
206 (20.2)
14 (1.4)
62 (6.1)
18 (1.8)
12 (1.2)
57 (5.6)
9 (0.9)
51 (5.0)
9 (0.9)
103 (20.0)
7 (1.4)
31 (6.0)
8 (1.6)
9 (1.8)
26 (5.1)
6 (1.2)
30 (5.8)
4 (0.8)
103 (20.4)
7 (1.4)
31 (6.2)
10 (2.0)
3 (0.6)
31 (6.2)
3 (0.6)
21 (4.2)
5 (1.0)
0.88
116 (11.4)
13 (1.3)
34 (3.3)
46 (4.5)
645 (63.4)
67 (13.0)
9 (1.8)
21 (4.1)
23 (4.5)
338 (65.8)
49 (9.7)
4 (0.8)
13 (2.6)
23 (4.6)
307 (60.9)
0.11
0.26
0.22
168.933.3
223.934.0
139.430.0
54.914.1
2.690.86
3.301.20
152.1115.8
0.5840.298
168.935.8
223.036.0
139.231.9
54.113.6
2.730.91
3.361.31
154.5137.1
0.5840.299
169.030.6
224.831.8
139.627.9
55.814.6
2.660.81
3.251.07
149.689.1
0.5850.297
0.41
0.15
0.45
0.08
0.36
0.43
0.73
0.91
6.390.63
6.400.66
119.131.2
12.5720.07
15.398.10
3.936.32
6.380.59
118.827.0**
10.9518.66**
15.407.91**
0.80
0.54
0.13
0.97
0.19
118.929.2**
11.7719.39**
15.408.01**
3.696.97
3.447.58
P value
>0.99
0.99
0.24
0.94
>0.99
>0.99
0.64
0.14
0.50
0.51
0.25
0.75
>0.99
0.12
Atorvastatin
(n=504)
P value
0.04
61 (11.9)
83 (16.5)
29 (5.6)
54 (10.7)
Gliclazide
0 (0.0)
2 (0.4)
Glimepiride
4 (0.8)
4 (0.8)
Metformin hydrochloride
11 (2.1)
7 (1.4)
Pioglitazone hydrochloride
2 (0.4)
2 (0.4)
6 (1.2)
14 (2.8)
Alogliptin benzoate
4 (0.8)
7 (1.4)
Vildagliptin
3 (0.6)
10 (2.0)
Linagliptin
0 (0.0)
3 (0.6)
0 (0.0)
1 (0.2)
Voglibose
0 (0.0)
2 (0.4)
Miglitol
0 (0.0)
3 (0.6)
0 (0.0)
1 (0.2)
Liraglutide
1 (0.2)
0 (0.0)
Insulin glargine
0 (0.0)
2 (0.4)
Increased dosage
15 (2.9)
10 (2.0)
Gliclazide
0 (0.0)
1 (0.2)
Glimepiride
7 (1.4)
3 (0.6)
Metformin hydrochloride
5 (1.0)
4 (0.8)
Pioglitazone hydrochloride
1 (0.2)
0 (0.0)
3 (0.6)
2 (0.4)
Vildagliptin
1 (0.2)
0 (0.0)
1 (0.2)
0 (0.0)
1 (0.2)
0 (0.0)
45 (8.8)
64 (12.7)
4 (0.8)
8 (1.6)
Decrease of medication
5 (1.0)
6 (1.2)
Finishing medication
7 (1.4)
5 (1.0)
03 months
14 (2.7)
20 (4.0)
36 months
8 (1.6)
12 (2.4)
612 months
23 (4.5)
32 (6.3)
03 months
5 (1.0)
6 (1.2)
36 months
5 (1.0)
5 (1.0)
612 months
6 (1.2)
8 (1.6)
0.04
FigureS1.Analyses performed using repeated measures ANOVA for overall comparison between treatment groups. The unpaired
t-test adjusted by Holms method was used for intergroup comparison to avoid multiplicity at multiple time points. LDL-C, lowdensity lipoprotein cholesterol; TC, total cholesterol; HDL-C, high-density lipoprotein cholesterol; TG, triglyceride.
FigureS2.Analyses performed using repeated measures ANOVA for overall comparison between treatment groups. The unpaired
t-test adjusted by Holms method was used for intergroup comparison to avoid multiplicity at multiple time points.