Department of Pediatrics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Department of Biomolecular Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands.
J Physiol. 2023 May;601(10):1761-1780. doi: 10.1113/JP284061. Epub 2023 Apr 18.
Hyperglycaemia in pregnancy (HIP) is a pregnancy complication characterized by mild to moderate hyperglycaemia that negatively impacts short- and long-term health of mother and child. However, relationships between severity and timing of pregnancy hyperglycaemia and postpartum outcomes have not been systemically investigated. We investigated the impact of hyperglycaemia developing during pregnancy (gestational diabetes mellitus, GDM) or already present pre-mating (pre-gestational diabetes mellitus, PDM) on maternal health and pregnancy outcomes. GDM and PDM were induced in C57BL/6NTac mice by combined 60% high fat diet (HF) and low dose streptozotocin (STZ). Animals were screened for PDM prior to mating, and all underwent an oral glucose tolerance test on gestational day (GD)15. Tissues were collected at GD18 or at postnatal day (PN)15. Among HFSTZ-treated dams, 34% developed PDM and 66% developed GDM, characterized by impaired glucose-induced insulin release and inadequate suppression of endogenous glucose production. No increased adiposity or overt insulin resistance was observed. Furthermore, markers of non-alcoholic fatty liver disease (NAFLD) were significantly increased in PDM at GD18 and were positively correlated with basal glucose levels at GD18 in GDM dams. By PN15, NAFLD markers were also increased in GDM dams. Only PDM affected pregnancy outcomes such as litter size. Our findings indicate that GDM and PDM, resulting in disturbances of maternal glucose homeostasis, increase the risk of postpartum NAFLD development, related to the onset and severity of pregnancy hyperglycaemia. These findings signal a need for earlier monitoring of maternal glycaemia and more rigorous follow-up of maternal health after GDM and PDM pregnancy in humans. KEY POINTS: We studied the impact of high-fat diet/streptozotocin induced hyperglycaemia in pregnancy in mice and found that this impaired glucose tolerance and insulin release. Litter size and embryo survival were compromised by pre-gestational, but not by gestational, diabetes. Despite postpartum recovery from hyperglycaemia in a majority of dams, liver disease markers were further elevated by postnatal day 15. Maternal liver disease markers were associated with the severity of hyperglycaemia at gestational day 18. The association between hyperglycaemic exposure and non-alcoholic fatty liver disease signals a need for more rigorous monitoring and follow-up of maternal glycaemia and health in diabetic pregnancy in humans.
妊娠高血糖症(HIP)是一种妊娠并发症,其特征为轻度至中度高血糖,对母婴的短期和长期健康均有不良影响。然而,妊娠高血糖的严重程度和发生时间与产后结局之间的关系尚未被系统地研究过。我们研究了妊娠期间发生的高血糖(妊娠期糖尿病,GDM)或交配前已存在的高血糖(孕前糖尿病,PDM)对母亲健康和妊娠结局的影响。通过联合使用 60%高脂肪饮食(HF)和低剂量链脲佐菌素(STZ),在 C57BL/6NTac 小鼠中诱导 GDM 和 PDM。在交配前对 PDM 动物进行筛查,所有动物在妊娠第 15 天(GD15)进行口服葡萄糖耐量试验。在 GD18 或产后第 15 天(PN15)采集组织。在 HFSTZ 处理的孕鼠中,34%发生 PDM,66%发生 GDM,表现为葡萄糖诱导的胰岛素释放受损和内源性葡萄糖生成抑制不足。未观察到明显的肥胖或明显的胰岛素抵抗。此外,在 GD18 时 PDM 中观察到非酒精性脂肪性肝病(NAFLD)的标志物显著增加,并且与 GDM 孕鼠 GD18 时的基础血糖水平呈正相关。到 PN15 时,GDM 孕鼠的 NAFLD 标志物也增加了。只有 PDM 影响了妊娠结局,如胎仔数。我们的研究结果表明,导致母体葡萄糖稳态紊乱的 GDM 和 PDM 增加了产后 NAFLD 发展的风险,与妊娠高血糖的发生和严重程度有关。这些发现表明,在人类中,需要更早地监测母体血糖,并在 GDM 和 PDM 妊娠后更严格地监测母体健康。重点:我们研究了高脂饮食/链脲佐菌素诱导的妊娠高血糖症对小鼠的影响,发现这种情况会损害葡萄糖耐量和胰岛素释放。与妊娠糖尿病相比,孕前糖尿病会降低胎仔数和胚胎存活率。尽管大多数孕鼠在产后恢复了高血糖,但在产后第 15 天,肝脏疾病标志物进一步升高。母体肝疾病标志物与 GD18 时的高血糖严重程度相关。高血糖暴露与非酒精性脂肪性肝病之间的关联表明,在人类糖尿病妊娠中,需要更严格地监测和随访母体血糖和健康状况。