Low Birth Weight and Male Reproductive Function

Scientific interest in morbidity in children born small for gestational age (SGA) has increased considerably over the last few decades. The elevated risk of cardiovascular and metabolic diseases in adulthood in individuals born SGA has been well documented, whereas data on gonadal development are li...

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Veröffentlicht in:Hormone research 2006-01, Vol.65 (Suppl 3), p.116-122
Hauptverfasser: Main, K.M., Jensen, R.B., Asklund, C., Hoi-Hansen, C.E., Skakkebaek, N.E.
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container_end_page 122
container_issue Suppl 3
container_start_page 116
container_title Hormone research
container_volume 65
creator Main, K.M.
Jensen, R.B.
Asklund, C.
Hoi-Hansen, C.E.
Skakkebaek, N.E.
description Scientific interest in morbidity in children born small for gestational age (SGA) has increased considerably over the last few decades. The elevated risk of cardiovascular and metabolic diseases in adulthood in individuals born SGA has been well documented, whereas data on gonadal development are limited. Prospective studies, case-control investigations and registry surveys show that impaired intrauterine growth increases the risks of congenital hypospadias, cryptorchidism and testicular cancer approximately two- to threefold. Although few studies focus on the effect of intrauterine growth on male pubertal development, testicular hormone production or sperm quality, available evidence points towards a subtle impairment of both Sertoli cell and Leydig cell function. Animal studies support the hypothesis that impaired perinatal growth restriction, depending on the timing, can affect postnatal testis size and function into adulthood. Current human data, however, are often based on highly selected hospital populations and lack precise distinctions between low birth weight, SGA, timing of growth restriction and a differentiation of catch-up growth patterns. Despite the methodological inadequacies of individual study results, the combined evidence from all data leaves little doubt that fetal growth restriction is associated with increased risk of male reproductive health problems, including hypospadias, cryptorchidism and testicular cancer.
doi_str_mv 10.1159/000091516
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The elevated risk of cardiovascular and metabolic diseases in adulthood in individuals born SGA has been well documented, whereas data on gonadal development are limited. Prospective studies, case-control investigations and registry surveys show that impaired intrauterine growth increases the risks of congenital hypospadias, cryptorchidism and testicular cancer approximately two- to threefold. Although few studies focus on the effect of intrauterine growth on male pubertal development, testicular hormone production or sperm quality, available evidence points towards a subtle impairment of both Sertoli cell and Leydig cell function. Animal studies support the hypothesis that impaired perinatal growth restriction, depending on the timing, can affect postnatal testis size and function into adulthood. Current human data, however, are often based on highly selected hospital populations and lack precise distinctions between low birth weight, SGA, timing of growth restriction and a differentiation of catch-up growth patterns. 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Current human data, however, are often based on highly selected hospital populations and lack precise distinctions between low birth weight, SGA, timing of growth restriction and a differentiation of catch-up growth patterns. 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The elevated risk of cardiovascular and metabolic diseases in adulthood in individuals born SGA has been well documented, whereas data on gonadal development are limited. Prospective studies, case-control investigations and registry surveys show that impaired intrauterine growth increases the risks of congenital hypospadias, cryptorchidism and testicular cancer approximately two- to threefold. Although few studies focus on the effect of intrauterine growth on male pubertal development, testicular hormone production or sperm quality, available evidence points towards a subtle impairment of both Sertoli cell and Leydig cell function. Animal studies support the hypothesis that impaired perinatal growth restriction, depending on the timing, can affect postnatal testis size and function into adulthood. 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source MEDLINE; Karger Journals; Alma/SFX Local Collection
subjects Birth Weight - physiology
Cryptorchidism - epidemiology
Cryptorchidism - physiopathology
Female
Fetal Growth Retardation - physiopathology
Genitalia, Male - abnormalities
Genitalia, Male - physiology
Germinoma - epidemiology
Gonadotropins, Pituitary - physiology
Humans
Hypospadias - epidemiology
Hypospadias - physiopathology
Infant, Low Birth Weight
Infant, Newborn
Influence of Size at Birth on Postnatal Endocrine Function
Male
Pregnancy
Puberty - physiology
Testicular Neoplasms - epidemiology
title Low Birth Weight and Male Reproductive Function
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