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Peer-reviewedCC BYPLOS One

Effects of a maternal ketogenic diet on maternal and offspring metabolic health in mice

  1. 1Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, United States of America.

Abstract

Ketogenic (keto) diets have gained popularity due to their potential benefits on weight loss and metabolic conditions. However, the consequences of consuming a keto diet before, during, and after pregnancy on maternal and offspring health remain incompletely understood. To investigate this, female Swiss Webster mice were randomly assigned to either a keto or control diet. After 6 weeks on diet, females were mated and maintained on their respective diets throughout pregnancy and lactation. In experiment 1, glucose tolerance tests (GTT) were performed on pregnant dams at gestational day (GD) 16.5. At GD 17.5, dams were euthanized, urine was collected for ketone analysis, and fetal and placental weights were recorded. In experiment 2, dams delivered naturally and one male and one female offspring per dam were retained and weighed weekly. At 12 weeks of age, offspring underwent GTT, followed by euthanasia and serum collection for insulin and leptin analysis. Compared with controls, keto dams exhibited increased body weight, impaired glucose tolerance, elevated urinary ketones, and reduced circulating insulin during late gestation (p < 0.05). Fetuses from keto dams were significantly smaller (p < 0.05), whereas placental weight and placental efficiency were unchanged. Offspring from keto dams tended to have lower body weights during early postnatal development; however, longitudinal analysis did not identify a significant overall effect of maternal diet or a maternal diet x time interaction. At 12 weeks, keto offspring exhibited a modest but statistically significant improvement in glucose tolerance compared to control offspring (p < 0.05). Male keto offspring had significantly decreased serum insulin (p < 0.05) compared to male control offspring, while no differences were observed in females. Serum leptin levels did not differ between diet groups, although sex differences present in control offspring were not observed in keto offspring. In this exploratory mouse study, ketogenic diet consumption was associated with altered maternal glucose homeostasis during pregnancy and reduced fetal growth, although these maternal and fetal findings were derived from a limited number of independent pregnancies and require confirmation in larger studies. Offspring exposed to maternal ketogenic diet demonstrated modest metabolic differences at 12 weeks of age. Together, these findings support further investigation of the maternal and developmental consequences of ketogenic diet exposure during pregnancy.

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BibTeX
@article{ruano2026effects,
  title = {{Effects of a maternal ketogenic diet on maternal and offspring metabolic health in mice}},
  author = {Antonio H Ruano and Rachel A Kracaw and Isabella A Cervantes and Simone Hernandez Ruano and Moises J Tacam and Kathleen A Pennington},
  journal = {PLOS One},
  year = {2026},
  month = oct,
  doi = {10.1371/journal.pone.0356015},
  url = {https://doi.org/10.1371/journal.pone.0356015},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Effects of a maternal ketogenic diet on maternal and offspring metabolic health in mice
AU  - Antonio H Ruano
AU  - Rachel A Kracaw
AU  - Isabella A Cervantes
AU  - Simone Hernandez Ruano
AU  - Moises J Tacam
AU  - Kathleen A Pennington
PY  - 2026
DA  - 2026/10/21
JO  - PLOS One
DO  - 10.1371/journal.pone.0356015
UR  - https://doi.org/10.1371/journal.pone.0356015
AB  - Ketogenic (keto) diets have gained popularity due to their potential benefits on weight loss and metabolic conditions. However, the consequences of consuming a keto diet before, during, and after pregnancy on maternal and offspring health remain incompletely understood. To investigate this, female Swiss Webster mice were randomly assigned to either a keto or control diet. After 6 weeks on diet, females were mated and maintained on their respective diets throughout pregnancy and lactation. In experiment 1, glucose tolerance tests (GTT) were performed on pregnant dams at gestational day (GD) 16.5. At GD 17.5, dams were euthanized, urine was collected for ketone analysis, and fetal and placental weights were recorded. In experiment 2, dams delivered naturally and one male and one female offspring per dam were retained and weighed weekly. At 12 weeks of age, offspring underwent GTT, followed by euthanasia and serum collection for insulin and leptin analysis. Compared with controls, keto dams exhibited increased body weight, impaired glucose tolerance, elevated urinary ketones, and reduced circulating insulin during late gestation (p < 0.05). Fetuses from keto dams were significantly smaller (p < 0.05), whereas placental weight and placental efficiency were unchanged. Offspring from keto dams tended to have lower body weights during early postnatal development; however, longitudinal analysis did not identify a significant overall effect of maternal diet or a maternal diet x time interaction. At 12 weeks, keto offspring exhibited a modest but statistically significant improvement in glucose tolerance compared to control offspring (p < 0.05). Male keto offspring had significantly decreased serum insulin (p < 0.05) compared to male control offspring, while no differences were observed in females. Serum leptin levels did not differ between diet groups, although sex differences present in control offspring were not observed in keto offspring. In this exploratory mouse study, ketogenic diet consumption was associated with altered maternal glucose homeostasis during pregnancy and reduced fetal growth, although these maternal and fetal findings were derived from a limited number of independent pregnancies and require confirmation in larger studies. Offspring exposed to maternal ketogenic diet demonstrated modest metabolic differences at 12 weeks of age. Together, these findings support further investigation of the maternal and developmental consequences of ketogenic diet exposure during pregnancy.
SN  - 1932-6203
ER  -