Division of Endocrinology, Department of Medicine, University of Cape Town, Cape Town, South Africa; Department of Internal Medicine, Kaduna State University, Kaduna, Nigeria.
Carrera de Obstetricia, Facultad de Ciencias para el Cuidado de la Salud, Universidad San Sebastián, Valdivia, Chile.
Placenta. 2024 Sep 2;154:49-59. doi: 10.1016/j.placenta.2024.05.138. Epub 2024 May 31.
Gestational diabetes mellitus (GDM) is a major pregnancy metabolic disorder and is strongly linked with obesity. Kisspeptin is a hormone that increases several thousand-fold in the maternal circulation during human pregnancy, with placenta as its main source. Studies have suggested that kisspeptin regulates trophoblast invasion and promotes pancreatic insulin secretion and peripheral insulin sensitivity.
In a well-characterized cohort of pregnant South African women and molecular and histological techniques, this study explored the impact and interaction of maternal obesity and GDM on kisspeptin (KISS1) signalling in relation to placental morphology and maternal and neonatal parameters.
We found that GDM had no effect on placental KISS1 and KISS1R (KISS1 receptor) mRNA and/or protein expression. However, obesity reduced placental KISS1R mRNA expression even though overall KISS1 protein abundance or localization was not different from the non-obese group. Maternal and cord circulating KISS1 concentrations did not vary with obesity or GDM, but maternal circulating KISS1 was positively correlated with placenta weight in non-GDM obese women, and negatively correlated with placental intervillous space volume in non-GDM non-obese women. Cord serum KISS1 was positively correlated with infant weight in GDM obese women, but negatively correlated with maternal BMI in the non-obese GDM group. Placental syncytiotrophoblast extracellular vesicles exhibited detectable KISS1 and its abundance was ∼50 % lower in those from obese GDM compared to non-GDM women.
This study shows maternal obesity and GDM can modulate placental kisspeptin signalling and placental morphological development with potential pathophysiological implications for clinically-relevant pregnancy and perinatal outcomes.
妊娠糖尿病(GDM)是一种主要的妊娠代谢紊乱疾病,与肥胖密切相关。Kisspeptin 是一种在人类妊娠期间母体循环中增加数千倍的激素,胎盘是其主要来源。研究表明,Kisspeptin 调节滋养细胞侵袭,并促进胰腺胰岛素分泌和外周胰岛素敏感性。
本研究使用经过良好特征描述的南非孕妇队列和分子及组织学技术,探讨了母体肥胖和 GDM 对与胎盘形态和母婴参数相关的 Kisspeptin(KISS1)信号的影响和相互作用。
我们发现 GDM 对胎盘 KISS1 和 KISS1R(KISS1 受体)mRNA 和/或蛋白表达没有影响。然而,肥胖即使降低了胎盘 KISS1R mRNA 表达,但其整体 KISS1 蛋白丰度或定位与非肥胖组并无不同。母体和脐带循环中的 KISS1 浓度不受肥胖或 GDM 影响,但非 GDM 肥胖女性的母体循环 KISS1 与胎盘重量呈正相关,而非 GDM 非肥胖女性的母体循环 KISS1 与胎盘绒毛间隙体积呈负相关。GDM 肥胖女性的脐带血清 KISS1 与婴儿体重呈正相关,而非肥胖 GDM 组的脐带血清 KISS1 与母体 BMI 呈负相关。胎盘合体滋养细胞细胞外囊泡中可检测到 Kisspeptin,其丰度在肥胖 GDM 妇女中比非 GDM 妇女低约 50%。
本研究表明,母体肥胖和 GDM 可以调节胎盘 Kisspeptin 信号和胎盘形态发育,对具有临床相关性的妊娠和围产期结局具有潜在的病理生理学意义。