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Published on: July 12, 2012
Early life programming and metabolic syndrome
1Department of Endocrinology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China. wangxiumin1019@yahoo.com.cn
Insights
Early life nutrition and environmental exposures can epigenetically program children for metabolic syndrome (MS). The perinatal period offers a critical window for interventions to prevent adult-onset diseases.
Area of Science:
- Developmental biology
- Epigenetics
- Public health
Background:
- Metabolic syndrome (MS) is a global epidemic in children.
- Early life "programming" influences the risk of obesity, type 2 diabetes, cardiovascular disease, and MS.
- Nutritional imbalances and endocrine disruptor chemicals during development are risk factors for later-life MS.
Purpose of the Study:
- To investigate the role of early life factors in the etiology of metabolic syndrome.
- To understand the molecular mechanisms of epigenetic gene regulation and transgenerational inheritance of disease phenotypes.
- To identify targets for early intervention during the perinatal period.
Main Methods:
- Analysis of epigenetic marks in response to environmental stimuli.
- Studying the impact of diet and in utero environment on gene regulation.
- Focusing on the perinatal period as a critical window for intervention.
Main Results:
- Epigenetic reprogramming occurs due to environmental stimuli like diet and the in utero environment.
- Early life exposures can influence the development of adult-onset disease phenotypes.
- The perinatal period is a key developmental stage for physiological changes.
Conclusions:
- Early life interventions can potentially alter physiological pathways and prevent adult-onset diseases.
- Understanding epigenetic mechanisms provides insight into disease inheritance.
- Targeting the perinatal period is crucial for mitigating the risk of metabolic syndrome and related conditions.
Abstract:
Metabolic syndrome (MS) has reached epidemic proportions worldwide among children. Early life "programming" is now thought to be important in the etiology of obesity, type 2 diabetes, cardiovascular disease and MS. Nutritional imbalance and exposures to endocrine disruptor chemicals during development can increase risk for MS later in life. Epigenetic marks may be reprogrammed in response to both stochastic and environmental stimuli, such as changes in diet and the in utero environment, therefore, determination of targets for early life effects on epigenetic gene regulation provides insight into the molecular mechanisms involved in the epigenetic transgenerational inheritance of a variety of adult onset disease phenotypes. The perinatal period is a crucial time of growth, development and physiological changes in mother and child, which provides a window of opportunity for early intervention that may induce beneficial physiological alternations.
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