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Author Spotlight: Studying the Impact of Maternal Dietary Deficiencies on Long-Term Offspring Health Outcomes
Published on: June 28, 2024
Impact of Maternal High-Fat Diet on Offspring Cardiovascular-Kidney-Metabolic Health: Spotlight on Oxidative Stress
Chien-Ning Hsu1,2,3, Chih-Kuang Chen4, Chih-Yao Hou5
1Department of Pharmacy, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Insights
Maternal high-fat diet (HFD) programs offspring for cardiovascular-kidney-metabolic syndrome (CKMS) largely via oxidative stress. Understanding this link is key to preventing intergenerational CKMS risk.
Area of Science:
- Integrative biology
- Developmental programming
- Metabolic disease
Background:
- Cardiovascular-kidney-metabolic syndrome (CKMS) involves interconnected cardiovascular, renal, and metabolic disorders.
- Oxidative stress is a key mediator in multi-organ dysfunction within CKMS.
- Maternal high-fat diet (HFD) exposure during gestation and lactation programs offspring for CKMS phenotypes in animal models.
Purpose of the Study:
- To review the role of oxidative stress in maternal HFD-induced CKMS programming.
- To identify critical knowledge gaps regarding oxidative stress's organ- and time-specific effects and reversibility.
- To explore interactions between oxidative stress and other programming pathways.
Main Methods:
- Literature review integrating evidence across organ systems.
- Analysis of animal model data on maternal HFD and offspring CKMS phenotypes.
- Identification of unresolved questions and future research priorities.
Main Results:
- Maternal HFD is a significant driver of offspring CKMS risk, mediated by oxidative stress.
- Oxidative stress's precise role, specificity, and reversibility in developmental programming remain incompletely understood.
- Interactions with renin-angiotensin system, epigenetics, gut microbiota, and nutrient sensing require further investigation.
Conclusions:
- Maternal HFD-induced oxidative stress is a critical mechanistic axis for CKMS programming.
- Further research is needed to clarify the nuances of oxidative stress in CKMS development.
- Targeted antioxidant strategies are essential to mitigate the intergenerational transmission of CKMS risk.
Abstract:
Cardiovascular-kidney-metabolic syndrome (CKMS) encompasses interconnected cardiovascular, renal, and metabolic disorders, including obesity, hypertension, and type 2 diabetes. Oxidative stress is increasingly recognized as a central driver of this multi-organ dysfunction. Among maternal influences, exposure to a high-fat diet (HFD) during pregnancy and lactation consistently predisposes offspring to CKMS-related phenotypes in animal models. While oxidative stress is implicated as a key mediator, its precise role in developmental programming remains unclear, and comparing the differences in its role between overt CKMS and CKM programming is critical. Critical gaps include whether oxidative stress acts uniformly or in an organ- and time-specific manner, which signals initiate long-term redox alterations, and whether these effects are reversible. Furthermore, its interactions with other programming pathways-such as renin-angiotensin system activation, epigenetic dysregulation, gut microbiota imbalance, and altered nutrient sensing-remain insufficiently explored. This review uniquely highlights maternal HFD-induced oxidative stress as a mechanistic axis of CKMS programming and delineates unresolved questions that limit translation. By integrating evidence across organ systems and proposing priorities for multi-organ profiling, refined models, and longitudinal human studies, we outline a forward-looking agenda for the field. Ultimately, clarifying how maternal HFD and oxidative stress shape offspring CKMS risk is essential to inform targeted antioxidant strategies to reduce the intergenerational transmission of CKMS risk.
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