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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Clin Pharmacol Ther. 2020 Jan 25;107(6):1362–1372. doi: 10.1002/cpt.1749

Table 2.

Mixed meal tolerance test parameters for healthy pregnant control subjects (HP) study day 1 (SD1, baseline) and study day 2 (SD2)

HP (n = 28)
Parameter SD1 SD2 Δ
SI (10−4 min−1 μU−1 mL) 8 ± 6 (2 to 20) 7 ± 4 (1 to 20) −0.8 ± 4 (−9 to 6) (p=0.6)
Φtotal (10−9 min−1) 120 ± 60 (51 to 280) 110 ± 40 (46 to 190) −10 ± 50 (−100 to 20) (p=0.1)
Φstatic (10−9 min−1) 100 ± 50 (30 to 200) 80 ± 30 (30 to 200) −10 ± 40 (−100 to 30) (p=0.1)
Φdynamic 10−9) 3,000 ± 2,000 (1,000 to 7,000) 3,000 ± 1,000 (1,000 to 5,000) 2 ± 1,000 (−2,000 to 2,000) (p=1)
Φbaseline (10−9 min−1) 10 ± 4 (4.3 to 20) 14 ± 6 (6.2 to 26) 3 ± 3 (−0.2 to 9) (p < 0.001)
DI (10−13 min−2 μU−1 mL) 800 ± 500 (200 to 2,000) 600 ± 300 (200 to 1,000) −200 ± 400 (−1,000 to 400) (p=0.04)
Peak Glucose (mg/dL) 120 ± 20 (94 to 150) 120 ± 10 (96 to 150) −0.7 ± 10 (−30 to 10) (p=0.8)

Results reported as mean ± SD (95% confidence interval)

Δ = average change between study day 1 and study day 2, SI = Insulin sensitivity, Φ = β-cell responsivity and DI = Disposition index.