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Published on: April 7, 2023
Early postnatal life as a critical time window for determination of long-term metabolic health
Andreas Plagemann1, Thomas Harder, Karen Schellong
1Division of 'Experimental Obstetrics', Clinic of Obstetrics, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany. andreas.plagemann@charite.de
Insights
Neonatal nutrition significantly impacts long-term health, influencing cardiometabolic risk regardless of birth weight. Early overfeeding and nutrition type (breastfeeding vs. formula) can lead to later health issues like obesity and metabolic syndrome.
Area of Science:
- Developmental biology
- Metabolic research
- Nutritional science
Background:
- Epidemiological studies link low birth weight to increased cardiometabolic risk, similar to high birth weight.
- Neonatal overfeeding is a potential etiological factor for later metabolic dysfunction.
Purpose of the Study:
- To explore the role of neonatal nutrition in long-term health and disease programming.
- To investigate the mechanisms linking neonatal nutrition to cardiometabolic risk.
Main Methods:
- Review of epidemiological and animal studies on birth weight and neonatal nutrition.
- Analysis of human studies comparing breastfeeding and formula feeding outcomes.
- Consideration of epigenetic mechanisms, such as DNA methylation.
Main Results:
- Neonatal over-nutrition in animal models leads to overweight, impaired glucose tolerance, and cardiometabolic alterations, irrespective of birth weight.
- Human studies confirm the long-term impact of neonatal nutrition, highlighting differences between breastfeeding and formula feeding.
- Alterations in DNA methylation patterns of key metabolic genes are implicated as a mediating mechanism.
Conclusions:
- Neonatal nutrition quality and quantity play a critical role in long-term health programming beyond prenatal development.
- Understanding these mechanisms offers opportunities for primary prevention of chronic diseases like metabolic syndrome.
Abstract:
Epidemiological studies demonstrated a clear phenomenological association between low birth weight and increased cardiometabolic risk later in life, very similar to that in high birth weight subjects. Pre- and/or neonatal overfeeding appears to be an etiological clue. In animal studies, irrespective of birth weight neonatal over-nutrition leads to later overweight, impaired glucose tolerance and cardiometabolic alterations. Probably, perinatally acquired alterations of DNA methylation patterns of gene promoters of central nervous regulators of body weight and metabolism play a key role in mediating these relationships. In humans, the long-term impact of neonatal nutrition is conclusively demonstrated by studies on the consequences of breastfeeding vs. formula-feeding. Taken together, the quantity and quality of nutrition during neonatal life plays a critical role, beyond prenatal development, in the long-term programming of health and disease. This opens a variety of opportunities and challenges to primarily prevent chronic diseases, e.g. the metabolic syndrome.
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