TY - JOUR
T1 - Why Do Normal Children Have Acromegalic Levels of IGF-I During Puberty?
AU - Juul, Anders
AU - Skakkebæk, Niels E
N1 - Copyright © 2019 Endocrine Society.
PY - 2019/3/21
Y1 - 2019/3/21
N2 - The rapid pubertal height growth is unique to humans, but why do we have it? Although the spurt contributes 13% to 15% to the final adult height, we hypothesized that the biological significance of the high acromegalic levels of GH and IGF-I, which are behind the pubertal growth spurt, might primarily occur to stimulate the reproductive organs. Evidence Synthesis: Animal data have demonstrated that adult Igf1 and Igf2 gene knockoutmice that survive show a dramatic reduction in the size of the reproductive organs and are infertile. In humans, case reports ofmutations in the genes affecting the GH-IGF axis and growth (GH, GHRH, GH-R, STAT5b, IGF-I, IGF-II, IGF-1R, PAPPA2) are also characterized by delayed pubertal onset and micropenis. Furthermore, GH treatment will tend to normalize the penile size in patients with GH deficiency. Thus, the endocrine effects of high IGF-I levels might be needed for the transition of the sexual organs, including the secondary sex characteristics, from the dormant stages of childhood into fully functioning reproductive systems. The peak IGF-I levels, on average, occur 2 years after the peak height growth velocity, suggesting reasons other than longitudinal growth for the high IGF-I levels, and remain high in the years after the height spurt, when the reproductive systems become fully functional.
AB - The rapid pubertal height growth is unique to humans, but why do we have it? Although the spurt contributes 13% to 15% to the final adult height, we hypothesized that the biological significance of the high acromegalic levels of GH and IGF-I, which are behind the pubertal growth spurt, might primarily occur to stimulate the reproductive organs. Evidence Synthesis: Animal data have demonstrated that adult Igf1 and Igf2 gene knockoutmice that survive show a dramatic reduction in the size of the reproductive organs and are infertile. In humans, case reports ofmutations in the genes affecting the GH-IGF axis and growth (GH, GHRH, GH-R, STAT5b, IGF-I, IGF-II, IGF-1R, PAPPA2) are also characterized by delayed pubertal onset and micropenis. Furthermore, GH treatment will tend to normalize the penile size in patients with GH deficiency. Thus, the endocrine effects of high IGF-I levels might be needed for the transition of the sexual organs, including the secondary sex characteristics, from the dormant stages of childhood into fully functioning reproductive systems. The peak IGF-I levels, on average, occur 2 years after the peak height growth velocity, suggesting reasons other than longitudinal growth for the high IGF-I levels, and remain high in the years after the height spurt, when the reproductive systems become fully functional.
U2 - 10.1210/jc.2018-02099
DO - 10.1210/jc.2018-02099
M3 - Journal article
C2 - 30840065
SN - 0021-972X
VL - 104
SP - 2770
EP - 2776
JO - The Journal of clinical endocrinology and metabolism
JF - The Journal of clinical endocrinology and metabolism
IS - 7
ER -