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Table 2 Baseline characteristics of responders and nonresponders to insulin glargine 100 Units/mL at 24 weeks

From: Characteristics of insulin-Naïve people with type 2 diabetes who successfully respond to insulin glargine U100 after 24 weeks of treatment: a meta-analysis of individual participant data from 3 randomized clinical trials

 

Responders at 24 weeks

(HbA1c < 7% or ≥ 1% reduction) n = 1188

Nonresponders at 24 Weeks

(HbA1c ≥ 7% and < 1% reduction)

n = 297

P value

Age, years

57.8 (9.9)

57.2 (10.1)

0.323

Age group

  

0.833

 < 65 years

893 (75.2)

225 (75.8)

 

 ≥ 65 years

295 (24.8)

72 (24.2)

Gender

  

0.012

 Women

543 (45.7)

160 (53.9)

 

 Men

645 (54.3)

137 (46.1)

 

Duration of T2DM, years

10.3 (6.6)

9.7 (6.5)

0.159

Weight, kg

87.5 (19.7)

85.8 (21.6)

0.201

BMI, kg/m2

31.3 (5.70)

30.9 (5.70)

0.213

HbA1c, %

9.1 (1.2)

8.3 (0.9)

< 0.001

HbA1c, mmol/mol

99 (13)

91 (10)

< 0.001

FBG, mg/dL

186.7 (52.0)

158.5 (42.2)

< 0.001

≥ 1 OAMs Targeting PPGa

1111 (93.5)

290 (97.6)

0.006

 SU, yes

1067 (89.8)

284 (95.6)

0.002

 2 OAMs

790 (66.5)

194 (65.3)

0.701

  MET/SU

614 (51.7)

167 (56.2)

 3 OAMs

389 (32.7)

100 (33.7)

0.761

  MET/SU/TZD

346 (29.1)

89 (30.0)

 4 OAMs

7 (0.6)

3 (1.0)

0.429

  1. Individual participant data were pooled from 3 randomized clinical trials [20,21,22] and are mean (SD) or n (%). Patients are those who were randomized to insulin glargine as the only insulin treatment and with no missing HbA1c values at 24 weeks. Two-sided P values were considered statistically significant if < 0.05 and were calculated by ANOVA model (response = subgroup) for continuous variables and by Pearson’s Chi-square or Fisher’s exact (for OAM data with less than 80% of cells with an expected value ≥5) test for categorical variables. Abbreviations: AGI alpha glucosidase inhibitor, BMI body mass index, DPP-IV dipeptidyl peptidase IV, FBG fasting blood glucose, HbA1c glycated hemoglobin, MEG meglitinides, MET metformin, OAM oral antihyperglycemic medication, PPG postprandial blood glucose, SD standard deviation, SU sulphonylurea, T2DM type 2 diabetes mellitus, TZD thiazolidinedione. aOAMs targeting postprandial glucose were SU, DPP-IV, AGI, and MEG