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. 2009 Jul 10;32(10):1783–1788. doi: 10.2337/dc09-0585

Table 1.

Baseline characteristics of the 81 subjects who completed the CFRDT trial

CFRD FH−
IGT
Total cohort Insulin Repaglinide Placebo Total cohort Insulin Repaglinide Placebo
n 61 23 22 16 20 7 4 9
n (% female) 31 (51)* 12 (52) 11 (50) 8 (50) 5 (25) 3 (43) 0 (0) 2 (22)
Age (years) 28 ± 9 29 ± 2 26 ± 2 28 ± 3 28 ± 7 27 ± 2 29 ± 5 28 ± 2
BMI (kg/m2) 21.3 ± 2.9 20.6 ± 0.6 21.3 ± 0.7 22.2 ± 0.6 22.0 ± 2.7 20.7 ± 0.7 22.9 ± 1.7 22.5 ± 0.9
% Fat-free mass 79 ± 9 79 ± 2 80 ± 2 77 ± 2 80 ± 8 81 ± 3 79 ± 5 80 ± 3
FVC (% predicted) 90 ± 22 87 ± 4 90 ± 6 94 ± 4 88 ± 17 79 ± 7 82 ± 10 98 ± 4
FEV1 (% predicted) 70 ± 25 63 ± 5 71 ± 6 78 ± 5 69 ± 21 61 ± 7 61 ± 13 78 ± 6
NIH score 83 ± 13 80 ± 3 84 ± 3 88 ± 3 82 ± 14 79 ± 6 74 ± 9 89 ± 2
A1C (%) 6.1 ± 0.6* 6.2 ± (0.1) 6.2 ± 0.1 6.0 ± 0.1 5.5 ± 0.4 5.5 ± 0.3 5.6 ± 0.1 5.5 ± 0.1

Data for the CFRD FH− and IGT total cohorts are means ± SD; data by treatment group as means ± SEM. There were no significant differences across treatment groups for CFRD FH− or IGT.

*Total cohort CFRD FH− vs. IGT, P < 0.05.