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Beth Israel Deaconess Medical Center, Harvard Medical School, Hospital for Sick Children, The University of Toronto, Kinderklinik UK‐Essen, The University of Duisburg‐Essen, Department of Anthropology, University of Michigan, Boston, Massachusetts, USA
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Beth Israel Deaconess Medical Center, Harvard Medical School, Hospital for Sick Children, The University of Toronto, Kinderklinik UK‐Essen, The University of Duisburg‐Essen, Department of Anthropology, University of Michigan, Boston, Massachusetts, USA
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Beth Israel Deaconess Medical Center, Harvard Medical School, Hospital for Sick Children, The University of Toronto, Kinderklinik UK‐Essen, The University of Duisburg‐Essen, Department of Anthropology, University of Michigan, Boston, Massachusetts, USA
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origins ( Rosen & Bouxsein 2006 ). As obesity and osteoporosis are examples of so-called ‘later in life diseases’, which might be programmed very early in life, their origins may lie in the perinatal environment. Previous studies have demonstrated that
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Development 8 137 – 145 . ( doi:10.1071/RD9960137 ) Guilloteau P Zabielski R Hammon HM Metges CC 2010 Nutritional programming of gastrointestinal tract development. Is the pig a good model for man? Nutrition Research Reviews 23 4 – 22
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diseases in later life ( Fernandez-Twinn et al. 2015 ). This phenomenon, called fetal programming, is known to be the cause of several diseases, including obesity, metabolic syndrome and diabetes ( Godfrey & Barker 2001 ). Several studies have reported
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Departments of, Medicine, Cell Biology, University of Virginia, PO Box 800578, Charlottesville, Virginia 22908, USA
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Departments of, Medicine, Cell Biology, University of Virginia, PO Box 800578, Charlottesville, Virginia 22908, USA
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Introduction Developmental programing by steroid hormones is important to establish sex differences in the reproductive tract and in other physiological systems. Androgen levels surge during gestation and postnatally in the male ( Tapanainen et al
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and high birth weight predisposing for the onset of later obesity. Originally called the Barker hypothesis or foetal programming, these observations have led to the Developmental Origin of Health and Disease (DOHaD) hypothesis ( Fernandez
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reproductive disorders in offspring during adulthood. This relationship is preferentially termed ‘developmental programming’ or the ‘Developmental Origins of Adult Health and Disease’ (DOHaD). Original observations by Professor David Barker highlighted the
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lactation, and future functional state is called programming ( Lucas 1994 , Barker 2004 , de Moura & Passos 2005 ). Lactation is a critical period because in this phase important cognitive and neurological development occurs, which suggests that adverse
Departmenté Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
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Departmenté Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
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Departmenté Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
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Departmenté Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
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Departmenté Nutrição Aplicada, Instituto de Nutrição, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
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, Cravo et al. 2002 , Teixeira et al. 2002 , 2003 , Vicente et al. 2004 , Lins et al. 2005 ). This association has been denominated as metabolic imprinting or programing, which is defined as a biological phenomenon that determines relationship
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Introduction Prenatal ‘programming’ of physiological responses ( Barker et al. 1993 ), which could explain the association of low birth weight with increased risk of cardiovascular and metabolic disease in adulthood ( Barker et al
School of Medical Science, Menzies Health Institute Queensland, Griffith University, Gold Coast Campus, Southport, Queensland, Australia
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Introduction Maternal stress can impair foetal growth and program offspring susceptibility to adult onset disease ( Cottrell & Seckl 2009 ). Stress-induced impairment of foetal development is mediated by elevated maternal glucocorticoids