Pulse Brain · Growing Health Evidence Index
Tier 4 — Narrative / commentaryPeer-reviewed

Genetics, epigenetics and transgenerational transmission of obesity in children

Nadia Panera, Claudia Mandato, Annalisa Crudele, S. Bertrando, Pietro Vajro, Anna Alisi

Frontiers in Endocrinology · 2022

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Summary

This narrative review examines the contribution of heritable genetic and epigenetic patterns to childhood obesity susceptibility. The authors synthesise evidence that maternal obesity, overnutrition during pregnancy and lactation, and pre-conception environmental exposures can reprogram epigenetic architecture and transmit obesity susceptibility to offspring independently of purely genetic inheritance. The review emphasises that environmental factors such as maternal malnutrition, hypoxia, and endocrine disruptor exposure during critical developmental windows may programme childhood adipose tissue and influence long-term obesity risk.

Regional applicability

The findings are directly applicable to UK clinical practice and public health, as the mechanisms of epigenetic inheritance and maternal environmental influences on childhood obesity are universal biological phenomena. Understanding these pathways could inform UK prevention strategies targeting pregnant women and early childhood nutrition, though the review does not assess UK-specific prevalence data or policy implementation.

Key measures

Obesity prevalence; genetic predisposition; epigenetic inheritance mechanisms; maternal obesity/overnutrition effects; environmental exposure factors (malnutrition, hypoxia, hormones, endocrine disruptors); adipose tissue programming

Outcomes reported

The narrative review synthesised evidence on how inherited genetic and epigenetic patterns contribute to obesity susceptibility in children, with emphasis on maternal nutritional and environmental factors during pregnancy and early postnatal periods.

Theme
Nutrition & health
Subject
Maternal, infant & child nutrition
Study type
Narrative Review
Study design
Narrative review
Source type
Peer-reviewed study
Status
Published
System type
Human clinical
DOI
10.3389/fendo.2022.1006008
Catalogue ID
SNmoj1yugd-vhipvs

Topic tags

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