Table 6.
COC formulation | Number of studies | Before Md (1st – 3rd) |
After Md (1st – 3rd) |
∆ | p* |
---|---|---|---|---|---|
Glucose (mg/dl) | |||||
EE 35 μg / CPA 2 mg | 12 | 86.6 (81.0–92.0) | 85.6 (84.3–91.9) | −1.0 | 0.514 |
EE 30 μg / DRSP 3 mg | 10 | 84.4 (78.7–91.2) | 85.7 (80.6–90.6) | +1.3 | 0.998 |
EE 30 μg / CMA 2 μg | 2 | 86.0(84.5–87.5) | 81.8 (80.5–83.1) | −4.2 | 0.010 |
EE 30 μg / DSG 75–150 μg | 5 | 84.5 (81.3) – 88.9) | 85.2 (81.9–88.0) | +0.7 | 0.892 |
Insulin (μUI/ml) | |||||
EE 35 μg / CPA 2 mg | 11 | 17.9 (10.8–22.8) | 17.1 (10.0–18.6) | −0.8 | 0.213 |
EE 30 μg / DRSP 3 mg | 08 | 13.9 (11.3–18.1) | 12.1 (10.1–18.5) | −1.8 | 0.865 |
EE 30 μg / CMA 2 mg | 03 | 7.3 (5.2–9.4) | 7.8 (6.1–9.5) | +0.5 | 0.285 |
EE 30 μg / DSG 75–150 μg | 04 | 15.7 (13.0–19.0) | 17.1 (13.1–22.1) | +1.4 | 0.144 |
EE 30 μg / 180–250 μg NGM | 02 | 8.9 (7.6–10.2) | 9.1(7.2–11.0) | +0.2 | 0.788 |
C-peptide (mg/dl) | |||||
EE 35 μg / CPA 2 mg | 03 | 2.6 (2.0–3.2) | 3.0 (2.9–3.9) | +0.4 | 0.179 |
EE 30 μg / DRSP 3 mg | 03 | 1.2 (0.7–1.7) | 1.3 (0.7–1.9) | +0.1 | 0.654 |
EE 30 μg / DSG 75–150 μg | 02 | 1.6 (1.5–1.7) | 2.4 (2.0–2.8) | +0.8 | 0.179 |
HOMA-IR | |||||
EE 35 μg / CPA 2 mg | 09 | 3.6 (2.0–4.4) | 2.2 (1.8–3.9) | −1.4 | 0.213 |
EE 30 μg / DRSP 3 mg | 10 | 3.1 (2.2–3.7) | 2.8 (2.5–3.8) | −0.3 | 0.593 |
EE 30 μg / CMA 2 mg | 03 | 1.6 (1.2–2.0) | 1.6 (1.3–2.0) | 0 | 0.592 |
EE 30 μg / DSG 75–150 μg | 03 | 3.0 (2.3–3.7) | 2.6 (2.2–3.0) | −0.4 | 0.285 |
HbA1C (%) | |||||
EE 35 μg / CPA 2 mg | 04 | 5.0 (4.6–5.4) | 5.1 (4.7–5.6) | +0.1 | 0.422 |
EE 30 μg / DRSP 3 mg | 02 | 3.5 (2.7–4.3) | 3.5 (1.7–7.3) | 0 | 0.653 |
COC combined oral contraceptive, Md (1st – 3rd) median, first and third quartiles, HOMA-IR homeostatic model assessment for insulin resistance, HbA1C glycated hemoglobin, EE ethinylestradiol, CPA cyproterone acetate, DRSP drospirenone, CMA chlormadinone acetate, DSG desogestrel, NGM norgestimate
p* Wilcoxon signed- ranks test