Dodd Jodie M, Grivell Rosalie M, Deussen Andrea R, Hague William M
School of Paediatrics and Reproductive Health, Discipline of Obstetrics and Gynaecology, The University of Adelaide, Women's and Children's Hospital, 72 King William Road, Adelaide, South Australia, Australia, 5006.
Cochrane Database Syst Rev. 2018 Jul 24;7(7):CD010564. doi: 10.1002/14651858.CD010564.pub2.
There has been considerable interest in providing antenatal dietary and lifestyle advice for women with obesity or who are overweight during pregnancy, as a strategy to limit gestational weight gain and improve maternal and infant health. However, such antenatal interventions appear to have a modest effect on gestational weight gain and other clinical pregnancy and birth outcomes and additional strategies are required.Metformin is an oral insulin-sensitising medication that acts to decrease blood glucose concentrations. Metformin is commonly used in the treatment of type 2 diabetes mellitus and polycystic ovarian syndrome, and is being used increasingly in the treatment of gestational diabetes, having been shown to result in decreased rates of caesarean birth and neonatal hypoglycaemia. Metformin may be an adjuvant therapy to current antenatal strategies in pregnant women with obesity or who are overweight, acting to reduce glucose production in the liver and improve glucose uptake in smooth muscle cells, and therefore improve the overall metabolic health of women in pregnancy and reduce the risk of known adverse pregnancy outcomes.
To evaluate the role of metformin in pregnant women with obesity or who are overweight, on maternal and infant outcomes, including adverse effects of treatment and costs.
We searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) (11 October 2017), and reference lists of retrieved studies.
All published and unpublished randomised controlled trials evaluating metformin use (compared with placebo or no metformin) in women with obesity or who are overweight in pregnancy for improving outcomes, alone or in combination with other interventions were eligible for inclusion.
Two review authors independently assessed trials for inclusion and risk of bias, extracted data and checked them for accuracy. We used the GRADE approach to assess the quality of the evidence.
We included three studies which randomised women (1099) with a body mass index (BMI) of 30 kg/m (1 study) and 35 kg/m (2 studies), with outcomes available for 1034 participants. None of the studies assessed women with a BMI between 25 kg/mand 29.9 kg/m, therefore we could not assess the use of metformin in women considered overweight. We did not identify studies of metformin in combination with another treatment. Two other studies are ongoing.All three included studies were randomised controlled trials and compared metformin with placebo, commencing early in the second trimester. Doses ranged from 500 mg twice daily to 3.0 g per day. All three studies (two in the UK, one in Egypt) included women attending hospitals for antenatal care.Two studies were generally at a low risk of bias across the majority of domains. We assessed the third study as being at an unclear risk of selection bias, performance and detection bias due to insufficient information in the report. We assessed the trial as being at a low risk of attrition bias and other bias; we felt it was at a high risk of reporting bias.The primary outcome for this review was infant birthweight large-for-gestational-age (> 90th centile for gestational age and infant sex). Women who received metformin or placebo had a similar risk of their baby being born large for his or her gestational age (risk ratio (RR) 0.95, 95% confidence interval (CI) 0.70 to 1.30; 2 studies, 831 infants; high-quality evidence).Women who received metformin may have a slightly lower gestational weight gain (mean difference (MD) -2.60 kg, 95% CI -5.29 to 0.10; 3 studies, 899 women; low-quality evidence).Metformin may make little or no difference in the risk of women developing gestational hypertension (average RR 1.02, 95% CI 0.54 to 1.94; 3 studies, 1040 women; low-quality evidence) or pre-eclampsia (RR 0.74, 95% CI 0.09 to 6.28; 2 studies, 840 women; low-quality evidence). Metformin probably makes little or no difference in the risk of women developing gestational diabetes (RR 0.85, 95% CI 0.61 to 1.19; 3 studies, 892 women; moderate-quality evidence).One study of 400 women reported women receiving metformin were more likely to experience any adverse effect compared with women receiving placebo (RR 1.63, 95% CI 1.27 to 2.08; 1 study, 400 women). Adverse effects included abdominal pain, diarrhoea, or headache. When considering individual side effects, women receiving metformin were more likely to experience diarrhoea than women receiving placebo (RR 2.34, 95% CI 1.74 to 3.14; 797 women; 2 studies, 797 women; high-quality evidence). No other important differences were identified between Metformin and placebo for other maternal secondary outcomes, including: caesarean birth, birth before 37 weeks of pregnancy, shoulder dystocia, perineal tear, or postpartum haemorrhage.In terms of other infant outcomes, there was little or no difference in the infant birthweight (MD 6.39 g, 95% CI -81.15 to 93.92; 2 studies, 834 infants; high-quality evidence). There were no other important differences identified for other infant secondary outcomes in this review: hypoglycaemia (low blood sugar); hyperbilirubinaemia (jaundice); Apgar score less than 7 at five minutes; or stillbirth and neonatal death. Only one study reported admission to the neonatal intensive care unit (NICU), indicating similar rates of admission between women receiving metformin or placebo; no other admission data were reported to assess differences in costs.
AUTHORS' CONCLUSIONS: There is insufficient evidence to support the use of metformin for women with obesity in pregnancy for improving maternal and infant outcomes. Metformin was, however, associated with increased risk of adverse effects, particularly diarrhoea. The quality of the evidence in this review varied from high to low, with downgrading decisions based on study limitations and inconsistency.There were only a small number of studies included in this review. Furthermore, none of the included studies included women categorised as 'overweight' and no trials looked at metformin in combination with another treatment.Future research is required in order to further evaluate the role of metformin therapy in pregnant women with obesity or who are overweight, as a strategy to improve maternal and infant health, alone or as an adjuvant to dietary and lifestyle advice.
为肥胖或孕期超重的女性提供产前饮食和生活方式建议,作为限制孕期体重增加和改善母婴健康的一种策略,已引起了广泛关注。然而,这种产前干预措施对孕期体重增加以及其他临床妊娠和分娩结局的影响似乎不大,因此需要其他策略。二甲双胍是一种口服胰岛素增敏药物,可降低血糖浓度。二甲双胍常用于治疗2型糖尿病和多囊卵巢综合征,并且越来越多地用于治疗妊娠期糖尿病,已证明其可降低剖宫产率和新生儿低血糖发生率。二甲双胍可能是目前针对肥胖或超重孕妇产前策略的辅助治疗方法,它可减少肝脏中的葡萄糖生成并改善平滑肌细胞对葡萄糖的摄取,从而改善孕期女性的整体代谢健康状况,并降低已知不良妊娠结局的风险。
评估二甲双胍对肥胖或超重孕妇的母婴结局的作用,包括治疗的不良反应和成本。
我们检索了Cochrane妊娠与分娩试验注册库、ClinicalTrials.gov、世界卫生组织(WHO)国际临床试验注册平台(ICTRP)(2017年10月11日)以及检索到的研究的参考文献列表。
所有已发表和未发表的随机对照试验,评估二甲双胍(与安慰剂或不使用二甲双胍相比)在肥胖或孕期超重女性中单独使用或与其他干预措施联合使用以改善结局的情况,均符合纳入标准。
两位综述作者独立评估试验是否纳入以及偏倚风险,提取数据并检查其准确性。我们使用GRADE方法评估证据质量。
我们纳入了三项研究,这些研究将体重指数(BMI)为30kg/m²(1项研究)和35kg/m²(2项研究)的女性进行随机分组,1034名参与者有结局数据。没有一项研究评估BMI在25kg/m²至29.9kg/m²之间的女性,因此我们无法评估二甲双胍在超重女性中的使用情况。我们未找到二甲双胍与另一种治疗联合使用的研究。另外两项研究正在进行中。
所有三项纳入研究均为随机对照试验,将二甲双胍与安慰剂进行比较,于孕中期早期开始。剂量范围为每日两次500mg至每日3.0g。所有三项研究(两项在英国,一项在埃及)均纳入了到医院接受产前护理的女性。
两项研究在大多数领域的偏倚风险通常较低。由于报告中的信息不足,我们将第三项研究评估为选择偏倚风险、实施和检测偏倚风险不明确。我们评估该试验的失访偏倚和其他偏倚风险较低;我们认为其报告偏倚风险较高。
本综述的主要结局是婴儿出生体重为大于胎龄儿(大于胎龄和婴儿性别的第90百分位数)。接受二甲双胍或安慰剂的女性,其婴儿出生时大于胎龄的风险相似(风险比(RR)0.95,95%置信区间(CI)0.70至1.30;2项研究,831名婴儿;高质量证据)。
接受二甲双胍的女性孕期体重增加可能略低(平均差(MD)-2.60kg,95%CI -5.29至0.10;3项研究,899名女性;低质量证据)。二甲双胍对女性发生妊娠期高血压(平均RR 1.02,95%CI 0.54至1.94;3项研究,1040名女性;低质量证据)或先兆子痫(RR 0.74,95%CI 0.09至6.28;2项研究,840名女性;低质量证据)的风险可能几乎没有影响。二甲双胍对女性发生妊娠期糖尿病的风险可能几乎没有影响(RR 0.85,95%CI 0.61至1.19;3项研究,892名女性;中等质量证据)。
一项对400名女性的研究报告称,与接受安慰剂的女性相比,接受二甲双胍的女性更有可能出现任何不良反应(RR 1.63,95%CI 1.27至2.08;1项研究,400名女性)。不良反应包括腹痛、腹泻或头痛。在考虑个体副作用时,接受二甲双胍的女性比接受安慰剂的女性更有可能出现腹泻(RR 2.34,95%CI 1.74至3.14;797名女性;2项研究,797名女性;高质量证据)。在其他孕产妇次要结局方面,二甲双胍与安慰剂之间未发现其他重要差异,包括:剖宫产、妊娠37周前分娩、肩难产、会阴撕裂或产后出血。
在其他婴儿结局方面,婴儿出生体重几乎没有差异(MD 6.39g,95%CI -81.15至93.92;2项研究,834名婴儿;高质量证据)。本综述在其他婴儿次要结局方面未发现其他重要差异:低血糖(低血糖);高胆红素血症(黄疸);5分钟时Apgar评分低于7分;或死产和新生儿死亡。只有一项研究报告了新生儿重症监护病房(NICU)的入院情况,表明接受二甲双胍或安慰剂的女性入院率相似;未报告其他入院数据以评估成本差异。
没有足够的证据支持在孕期肥胖女性中使用二甲双胍来改善母婴结局。然而,二甲双胍与不良反应风险增加有关,尤其是腹泻。本综述中的证据质量从高到低不等,降级决策基于研究局限性和不一致性。
本综述仅纳入了少数研究。此外,纳入的研究均未纳入被归类为“超重”的女性,也没有试验研究二甲双胍与另一种治疗联合使用的情况。需要进一步的研究来评估二甲双胍治疗在肥胖或超重孕妇中的作用,作为改善母婴健康的一种策略,单独使用或作为饮食和生活方式建议的辅助手段。