Kisspeptin signalling and its correlation with placental ultrastructure and clinical outcomes in pregnant South African women with obesity and gestational diabetes.
Musa. Ezekiel E; Salazar-Petres. Esteban E; Vatish. Manu M; Levitt. Naomi N; Sferruzzi-Perri. Amanda N AN; Matjila. Mushi J MJ
Key Findings
- Gestational diabetes did not alter placental kisspeptin (KISS1) or its receptor (KISS1R) mRNA or protein levels.
- Maternal obesity reduced placental KISS1R mRNA expression, even though overall kisspeptin protein levels were unchanged.
- Maternal circulating kisspeptin correlated with placenta weight in non‑GDM obese women and inversely with intervillous space volume in non‑obese non‑GDM women; cord kisspeptin linked to infant weight in GDM obese women.
Practical Outcomes
- For biohackers, the findings don't provide a new supplement or dosage strategy involving kisspeptin. The data suggest kisspeptin isn't a major driver of insulin sensitivity changes in pregnancy, so targeting it for metabolic or longevity benefits remains speculative. No actionable protocol emerges from this study.
Summary
In pregnant South African women, having gestational diabetes didn't change the amount of kisspeptin or its receptor in the placenta, but obesity lowered the receptor's gene activity. Blood kisspeptin levels stayed the same regardless of obesity or diabetes, though they showed some links to placenta size and baby weight in specific sub‑groups. Overall, the study suggests that kisspeptin signaling in the placenta is subtly affected by maternal weight and diabetes, but it doesn't point to any clear way to use kisspeptin for health hacks.
Abstract
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.
Study Information
pubmed
2024
2024-05-31T00:00:00.000Z
10.1016/j.placenta.2024.05.138
3
69