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PMID: 16612125 Published · ppublish English Journal Article Review

Small for gestational age and the metabolic syndrome: which mechanism is suggested by epidemiological and clinical studies?

Hormone research ·Vol. 65 Suppl 3 ·2006-00-00 ·Pages 123-30

Lévy-Marchal C, Czernichow P

Abstract

The metabolic and cardiovascular complications associated with in-utero undernutrition have been identified during the past 10 years. Reduced fetal growth is independently associated with an increased risk of development of cardiovascular diseases, the insulin-resistance syndrome or one of its components (i.e., hypertension, dyslipidaemia, impaired glucose tolerance and type 2 diabetes). Insulin resistance appears to be a key component underlying these metabolic complications. Although the mechanism remains unclear, several pieces of evidence support an active role of adipose tissue in the emergence of insulin resistance (an abnormal growth pattern and repartition, hypersensitivity to catecholamines, regulation of leptin and adiponectin secretion and modulation of peroxisome proliferator-activated receptor gamma). Among individuals born SGA, those who are more at risk of gaining excess adiposity are those who are thin at birth following a period of fetal growth restriction. This period of undernutrition is followed by a neonatal period of catch-up growth and renutrition. This pattern induces important modifications in adipose tissue, with long-term consequences, among which is a high risk of early development of insulin resistance. Not all individuals born SGA will show such modifications in adipose tissue, meaning that not all of those born SGA are at risk of insulin resistance and diabetes. From a broader point of view, several hypotheses have been proposed over the past 10 years to explain this unexpected association between being born SGA and the later development of disease. Each of them points to a detrimental fetal environment, to a genetic susceptibility or to interactions between these two components playing a critical role in this context. Although not confirmed, the hypothesis suggesting that this association could be the consequence of genetic/environmental interactions remains the most attractive.

MeSH Terms
Birth Weight/physiology Body Composition Clinical Trials as Topic Diabetes Mellitus, Type 2/physiopathology Epidemiologic Studies Humans Infant, Newborn Infant, Small for Gestational Age Insulin/metabolism Insulin Secretion Metabolic Syndrome/physiopathology
Chemicals
Insulin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lévy-Marchal C
INSERM Units 457 and 690, Robert Debré Hospital, Paris, France. [email protected]
Czernichow P
Article Info
Journal
Hormone research
Abbr.
Horm Res
ISSN
0301-0163
Published
2006-00-00
Epub
2006-00-10
Pages
123-30
Language
English
Region
Switzerland
NLM ID
0366126
Subset
IM
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