Insulin-sensitising drugs (metformin, rosiglitazone, pioglitazone, D-chiro-inositol) for women with polycystic ovary syndrome, oligo amenorrhoea and subfertility

Background ovary syndrome (PCOS) is characterised by infrequent or absent ovulation, and high levels of androgens and insulin (hyperinsulinaemia). Hyperinsulinaemia occurs secondary to insulin resistance and is associated with increased risk of cardiovascular disease and diabetes mellitus. Insulin‐sensitising agents such as metformin may be effective in treating PCOS‐related anovulation. evaluate the effectiveness and safety of insulin‐sensitising drugs in improving reproductive and metabolic outcomes for women with PCOS undergoing ovulation induction. methods searched the following databases from inception to January 2017: Cochrane Gynaecology and Fertility Group Specialised Register, CENTRAL, MEDLINE, Embase, PsycINFO and CINAHL. We searched registers of ongoing trials and reference lists from relevant studies. criteria included randomised controlled trials of insulin‐sensitising drugs compared with placebo, no treatment, or an ovulation‐induction agent for women with oligo and anovulatory PCOS. collection and analysis review authors independently assessed studies for eligibility and bias. Primary outcomes were live birth rate and gastrointestinal adverse effects. Secondary outcomes included other pregnancy outcomes, menstrual frequency and metabolic effects. We combined data to calculate pooled odds ratios (ORs) and 95% confidence intervals (CIs). We assessed statistical heterogeneity using the I2 statistic and reported quality of the evidence for primary outcomes using GRADE methodology. results assessed the interventions metformin, clomiphene citrate, metformin plus clomiphene citrate, D‐chiro‐inositol, rosiglitazone and pioglitazone. We compared these with each other, placebo or no treatment. We included 48 studies (4451 women), 42 of which investigated metformin (4024 women). Evidence quality ranged from very low to moderate. Limitations were risk of bias (poor reporting of methodology and incomplete outcome data), imprecision and inconsistency. versus placebo or no treatment evidence suggests that metformin may improve live birth rates compared with placebo (OR 1. 59, 95% CI 1. 00 to 2. 51, 4 studies, 435 women, I2 = 0%, low‐quality evidence). The metformin group experienced more gastrointestinal side effects (OR 4. 76, 95% CI 3. 06 to 7. 41, 7 studies, 670 women, I2 = 61%, moderate‐quality evidence) but had higher rates of clinical pregnancy (OR 1. 93, 95% CI 1. 42 to 2. 64, 9 studies, 1027 women, I2 = 43%, moderate‐quality evidence), ovulation (OR 2. 55, 95% CI 1. 81 to 3. 59, 14 studies, 701 women, I2 = 58%, moderate‐quality evidence) and menstrual frequency (OR 1. 72, 95% CI 1. 14 to 2. 61, 7 studies, 427 women, I2 = 54%, low‐quality evidence). There was no clear evidence of a difference in miscarriage rates (OR 1. 08, 95% CI 0. 50 to 2. 35, 4 studies, 748 women, I2 = 0%, low‐quality evidence). plus clomiphene citrate versus clomiphene citrate alone was no conclusive evidence of a difference between the groups in live birth rates (OR 1. 21, 95% CI 0. 92 to 1. 59, 9 studies, 1079 women, I2 = 20%, low‐quality evidence), but gastrointestinal side effects were more common with combined therapy (OR 3. 97, 95% CI 2. 59 to 6. 08, 3 studies, 591 women, I2 = 47%, moderate‐quality evidence). However, the combined therapy group had higher rates of clinical pregnancy (OR 1. 59, 95% CI 1. 27 to 1. 99, 16 studies, 1529 women, I2 = 33%, moderate‐quality evidence) and ovulation (OR 1. 57, 95% CI 1. 28 to 1. 92, 21 studies, 1624 women, I2 = 64%, moderate‐quality evidence). There was a statistically significant difference in miscarriage rate per woman, with higher rates in the combined therapy group (OR 1. 59, 95% CI 1. 03 to 2. 46, 9 studies, 1096 women, I2 = 0%, low‐quality evidence) but this is of uncertain clinical significance due to low‐quality evidence, and no clear difference between groups when we analysed miscarriage per pregnancy (OR 1. 30, 95% CI 0. 80 to 2. 12, 8 studies; 400 pregnancies, I2 = 0%, low‐quality evidence). versus clomiphene citrate all studies were combined, findings for live birth were inconclusive and inconsistent (OR 0. 71, 95% CI 0. 49 to 1. 01, 5 studies, 741 women, I2 = 86%, very low‐quality evidence). In subgroup analysis by obesity status, obese women had a lower birth rate in the metformin group (OR 0. 30, 95% CI 0. 17 to 0. 52, 2 studies, 500 women, I2 = 0%, very low‐quality evidence), while data from the non‐obese group showed a possible benefit from metformin, with high heterogeneity (OR 1. 71, 95% CI 1. 00 to 2. 94, 3 studies, 241 women, I2 = 78%, very low‐quality evidence). Similarly, among obese women taking metformin there were lower rates of clinical pregnancy (OR 0. 34, 95% CI 0. 21 to 0. 55, 2 studies, 500 women, I2 = 0%, very low‐quality evidence) and ovulation (OR 0. 29, 95% CI 0. 20 to 0. 43 2 studies, 500 women, I2 = 0%, low‐quality evidence) while among non‐obese women, the metformin group had more pregnancies (OR 1. 56, 95% CI 1. 05 to 2. 33, 5 studies, 490 women, I2 = 41%, very low‐quality evidence) and no clear difference in ovulation rates (OR 0. 81, 95% CI 0. 51 to 1. 28, 4 studies, 312 women, low‐quality evidence, I2=0%). There was no clear evidence of a difference in miscarriage rates (overall: OR 0. 92, 95% CI 0. 50 to 1. 67, 5 studies, 741 women, I2 = 52%, very low‐quality evidence). ‐chiro‐inositol (2 studies), rosiglitazone (1 study) or pioglitazone (1 study) versus placebo or no treatment were unable to draw conclusions regarding other insulin‐sensitising drugs as no studies reported primary outcomes.