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. Author manuscript; available in PMC: 2017 Mar 2.
Published in final edited form as: Diabetologia. 2013 Sep 10;56(12):2609–2618. doi: 10.1007/s00125-013-3031-9

Table 1.

Clinical characteristics of families a, b and c

Family ID Diagnosis BMI (kg/m2) Glucose (mmol/l) C-peptide (nmol/l) Insulin (pmol/l)


FPG 2 h PG FINS 2 h INS
a II-1 DM 21.0 16.0 0.03
II-2 DM 18.4 14.4 0.07
II-4 DM 20.6 8.1 12.7 50.0 104.9
III-1 IGT 20.3 5.1 8.1 61.8 200.0
III-2 DM 21.0 5.9 11.5 43.1 134.0
b II-1 DM 24.5 14.0 0.13
III-1 DM 32.4 12.0 0.10
III-2 DM 28.4 5.2 13.0 68.8 137.5
III-3 DM 25.2 7.8 16.7 59.7 175.0
c II-1 DM 23.6 7.2 11.8 0.13
III-1 DM 26.2 8.3 13.1 41.0 150.0
IV-1 IGT 22.8 5.8 8.2 55.6 224.3
166 cases DM 24.3±3.4 9.5±4.1 15.4±4.8 0.70±0.05 127.8±97.2 304.2±192.4

Other clinical characteristics of the mutation carriers are shown. For comparison, means ± SD for the same characteristics in a group of 166 individuals with type 2 diabetes are shown. DM, diabetes mellitus; 2 h INS, 2 h plasma insulin; FINS, fasting plasma insulin; 2 h PG, 2 h plasma glucose; FPG, fasting plasma glucose