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      Long-term metabolic risk among children born premature or small for gestational age

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          Abstract

          <p class="first" id="d14470439e131">Accumulating evidence suggests that both the intrauterine environment and growth during early life can influence the development of chronic noncommunicable diseases, such as type 2 diabetes mellitus and cardiovascular disease, in adulthood. Here, we review the available human data supporting increased metabolic risk among children born premature or small for gestational age; the adrenal and pubertal modifications that contribute to this risk; metabolic changes that occur during adolescence and early adulthood; and approaches to potentially modify or decrease risk of metabolic disease. The risks associated with delivery at term or preterm are compared for each period of life. Knowledge of these associations is fundamental for the paediatric community to develop preventive strategies early during postnatal life. </p>

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          Most cited references2

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          The fetal and infant origins of adult disease.

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            Natural growth in children born small for gestational age with and without catch-up growth.

            This first report from a population-based postnatal growth study of 3650 healthy Swedish subjects born at full term provides new reference values for height and weight and shows that over the last 20 years there has been a small secular trend in height (0.2-0.4 SDS over the whole age range) in Sweden in both boys and girls. Within this cohort, 111 (3.1%) were of low birth weight (below -2 SDS) and 141 (3.5%) were of low birth length (below -2 SDS); 54 (1.5%) were both light and short at birth. Of the children born small for gestational age, 87% showed full catch-up growth within 2 years of life. They attained puberty at a normal or early age and reached a mean final height of -0.7 SDS. The remaining subgroup of 13% born small for gestational age remained below -2 SDS throughout childhood and reached puberty somewhat early. Their mean final height was -1.7 SDS. The current data set is too small to identify possible background factors, but it is being expanded with this objective in mind.
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              Author and article information

              Journal
              Nature Reviews Endocrinology
              Nat Rev Endocrinol
              Springer Nature
              1759-5029
              1759-5037
              January 2017
              August 19 2016
              : 13
              : 1
              : 50-62
              Article
              10.1038/nrendo.2016.127
              27539244
              65047ef5-2219-4d42-8fb7-f1b890705bab
              © 2016

              http://www.springer.com/tdm

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