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1.
J Clin Endocrinol Metab ; 98(3): E518-27, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23430788

RESUMO

CONTEXT AND OBJECTIVE: Information on the correlation of normative reproductive hormone levels with physical development (Tanner stages) during puberty and on the influences of genes and environment on variation in these hormones and Tanner stages is limited. DESIGN, SETTING, AND PARTICIPANTS: One hundred twelve healthy 9-year-old twin pairs (n = 224) took part in a longitudinal study, of which 89 pairs participated again at age 12 years (n = 178). MAIN OUTCOME MEASURES: Morning urinary LH, FSH, estradiol, and salivary testosterone levels, determined by competitive immunoassays, were measured. Tanner stages were determined through physical examination. RESULTS: Over the 3-year interval, all hormone levels showed a 2- to 9-fold increase. LH and FSH at age 9 years predicted sex-specific Tanner stages at age 12 years in both boys and girls. Most of the associations between hormone levels at age 9 years and physical development at 12 years were explained by genetic influences. FSH in 9-year-old boys correlated with all hormone levels and Tanner stages at age 12 years. Moderate to high heritability estimates were found for hormone levels at both ages and in both sexes. In girls a shift from environmental (age 9 years) to genetic influences (age 12 years) was found for estradiol and pubic hair development, and for breast development a shift in the opposite direction was seen. CONCLUSIONS: During development LH and FSH (and testosterone in boys) levels predict secondary sexual characteristics in boys and girls 3 years later. These correlations are largely due to genes that are involved in both early pubertal hormone levels and subsequent physical development.


Assuntos
Desenvolvimento Infantil/fisiologia , Sistema Endócrino/crescimento & desenvolvimento , Hormônios Esteroides Gonadais/sangue , Hormônios Esteroides Gonadais/genética , Criança , Sistema Endócrino/metabolismo , Meio Ambiente , Estradiol/sangue , Estradiol/genética , Feminino , Hormônio Foliculoestimulante Humano/sangue , Hormônio Foliculoestimulante Humano/genética , Seguimentos , Humanos , Estudos Longitudinais , Hormônio Luteinizante/sangue , Hormônio Luteinizante/genética , Masculino , Puberdade/genética , Puberdade/fisiologia , Desenvolvimento Sexual/genética , Desenvolvimento Sexual/fisiologia , Testosterona/sangue , Testosterona/genética
2.
Neuroimage ; 59(4): 3871-80, 2012 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-22155028

RESUMO

During development from childhood to adulthood the human brain undergoes considerable thinning of the cerebral cortex. Whether developmental cortical thinning is influenced by genes and if independent genetic factors influence different parts of the cortex is not known. Magnetic resonance brain imaging was done in twins at age 9 (N = 190) and again at age 12 (N = 125; 113 repeated measures) to assess genetic influences on changes in cortical thinning. We find considerable thinning of the cortex between over this three year interval (on average 0.05 mm; 1.5%), particularly in the frontal poles, and orbitofrontal, paracentral, and occipital cortices. Cortical thinning was highly heritable at age 9 and age 12, and the degree of genetic influence differed for the various areas of the brain. One genetic factor affected left inferior frontal (Broca's area), and left parietal (Wernicke's area) thinning; a second factor influenced left anterior paracentral (sensory-motor) thinning. Two factors influenced cortical thinning in the frontal poles: one of decreasing influence over time, and another independent genetic factor emerging at age 12 in left and right frontal poles. Thus, thinning of the cerebral cortex is heritable in children between the ages 9 and 12. Furthermore, different genetic factors are responsible for variation in cortical thickness at ages 9 and 12, with independent genetic factors acting on cortical thickness across time and between various brain areas during childhood brain development.


Assuntos
Córtex Cerebral/anatomia & histologia , Córtex Cerebral/crescimento & desenvolvimento , Imageamento por Ressonância Magnética , Criança , Feminino , Hereditariedade/genética , Humanos , Estudos Longitudinais , Masculino , Modelos Genéticos , Tamanho do Órgão , Gêmeos/genética
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