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Sex and gender differences in developmental programming of metabolism.
Dearden, Laura; Bouret, Sebastien G; Ozanne, Susan E.
Affiliation
  • Dearden L; University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Treatment Centre, Addenbrooke's Hospital, Level 4, Box 289, Cambridge, CB2 0QQ, United Kingdom.
  • Bouret SG; The Saban Research Institute, Developmental Neuroscience Program & Diabetes and Obesity Program, Center for Endocrinology, Diabetes and Metabolism, Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA, 90027, USA; Inserm, Jean-Pierre Aubert Research Center, U1172, University Lille 2, Lille, 59045, France.
  • Ozanne SE; University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Addenbrooke's Treatment Centre, Addenbrooke's Hospital, Level 4, Box 289, Cambridge, CB2 0QQ, United Kingdom. Electronic address: Seo10@cam.ac.uk.
Mol Metab ; 15: 8-19, 2018 09.
Article de En | MEDLINE | ID: mdl-29773464
ABSTRACT

BACKGROUND:

The early life environment experienced by an individual in utero and during the neonatal period is a major factor in shaping later life disease risk-including susceptibility to develop obesity, diabetes, and cardiovascular disease. The incidence of metabolic disease is different between males and females. How the early life environment may underlie these sex differences is an area of active investigation. SCOPE OF REVIEW The purpose of this review is to summarize our current understanding of how the early life environment influences metabolic disease risk in a sex specific manner. We also discuss the possible mechanisms responsible for mediating these sexually dimorphic effects and highlight the results of recent intervention studies in animal models. MAJOR

CONCLUSIONS:

Exposure to states of both under- and over-nutrition during early life predisposes both sexes to develop metabolic disease. Females seem particularly susceptible to develop increased adiposity and disrupted glucose homeostasis as a result of exposure to in utero undernutrition or high sugar environments, respectively. The male placenta is particularly vulnerable to damage by adverse nutritional states and this may underlie some of the metabolic phenotypes observed in adulthood. More studies investigating both sexes are needed to understand how changes to the early life environment impact differently on the long-term health of male and female individuals.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Caractères sexuels / Développement embryonnaire / Métabolisme énergétique / Maladies métaboliques Type d'étude: Prognostic_studies Aspects: Determinantes_sociais_saude Limites: Female / Humans / Male Langue: En Journal: Mol Metab Année: 2018 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Caractères sexuels / Développement embryonnaire / Métabolisme énergétique / Maladies métaboliques Type d'étude: Prognostic_studies Aspects: Determinantes_sociais_saude Limites: Female / Humans / Male Langue: En Journal: Mol Metab Année: 2018 Type de document: Article Pays d'affiliation: Royaume-Uni