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. 2014 Jun 13;14:48. doi: 10.1186/1472-6823-14-48

Table 1.

Clinical and biochemical characteristics of the study cohort

  Patients who survived (n = 7697) Patients who died (n = 1070)  
 
Median (25th to 75th) or n(%)
Median (25th to 75th) or n(%)
P value†
Age, years
57(47–66)
69(62–75)
<0.0001
Male gender
3586(46.6%)
533(49.8%)
0.0477
Smoking status
 
 
<0.0001
Ex-smoker
1094(14.2%)
256(23.9%)
 
Current smoker
1310(17.0%)
197(18.4%)
 
Alcohol intake
 
 
<0.0001
Ex-drinker
846(11.0%)
206(19.3%)
 
Current drinker
720(9.4%)
57(19.3%)
 
Body mass index, kg/m2
24.9(22.6-27.6)
24.2(21.8-26.6)
<0.0001
Duration of diabetes, years
5(1-10)
9(4–15)
<0.0001
Systolic BP, mmHg
132(120–145)
144(128–159)
<0.0001
Diastolic BP, mmHg
75(68–82)
75(68–83)
0.4583
HbA1c, %
7.2(6.3-8.4)
7.5(6.5-8.9)
<0.0001
LDL-C, mmol/L
2.98(2.40-3.60)
3.14(2.50-3.90)
<0.0001
HDL-C, mmol/L
1.28(1.09-1.52)
1.25(1.03-1.54)
0.0108
Triglyceride, mmol/L
1.37(0.97-1.99)
1.36(0.98-2.00)
0.6668
Spot urinary ACR, mg/mmol
1.69(2.72)
13.42(2.06-120.20)
<0.0001
Prior cardiovascular disease
972(12.6%)
321(30.0%)
<0.0001
Prior cancer
193(2.9%)
69(6.5%)
<0.0001
Medication use at enrollment
Renin-angiotensin system inhibitors
1687(21.9%)
306(28.6%)
<0.0001
Lipid lowering drugs
1509(19.6%)
170(15.9%)
0.0038
Oral anti-diabetes drugs
5335(69.3%)
626(58.5%)
<0.0001
Insulin
1197(15.6%)
311(29.1%)
<0.0001
CKD events at baseline
eGFR, ml min-1 1.73 m-2 at baseline
105.6(86.2-126.0)
79.0(51.7-104.7)
<0.0001
eGFR < 60 ml min-1 1.73 m-2 at baseline
571(7.4%)
326(30.5%)
<0.0001
Major hyopglycaemia events
12 months prior to enrollment
146(1.9%)
63(5.9%)
<0.0001
During follow-up only§
122(1.6%)
57(5.3%)
<0.0001
Either of them 268(3.5%) 120(11.2%) <0.001

Abbreviations: HbA1c, glycated haemglobin; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol; BP, blood pressure; ACR, albumin:creatinine ratio; eGFR, estimated glomerular filtration rate;

†, Derived from Wilcoxon Two-Sample test or Chi-squared test where appropriate;

§, Defined as hypoglycaemia events that required hospitalisations. For patients who developed the event during follow-up, the time period from enrollment to the time of hospitalisation was removed as the immortal time period so that the follow-up started at the time of admission for hypoglycaemia. In these patients, all baseline values of continuous covariables and prior cancer and cardiovascular disease were re-estimated by treating the time of admission for hypoglycaemia as the enrollment date.