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Different states of clinical control are associated with changes in IGF‐I and IGFBPs in children with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency
Author(s) -
Cunha Heloisa Marcelina,
Elias Lucila Leico Kagohara,
CamachoHübner Cecilia,
Moreira Ayrton Custódio,
Martinelli Carlos Eduardo
Publication year - 2004
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/j.1365-2265.2004.02075.x
Subject(s) - congenital adrenal hyperplasia , medicine , endocrinology , bone age , 21 hydroxylase , androgen , hyperplasia , androgen excess , insulin , hormone , insulin resistance , polycystic ovary
Summary objective Congenital adrenal hyperplasia (CAH) due to 21‐hydroxylase deficiency (21‐OHD) is characterized by high androgen levels, ambiguous genitalia or premature pubarche, increased height velocity and skeletal maturation. Considering the possibility of changes in the IGF system components depending on the state of clinical control, the objective of the present study was to analyse serum IGF‐I, IGF‐II and IGFBP levels in children with 21‐OHD under two states of clinical control. patients and design We studied 12 prepubertal children with 21‐OHD CAH aged 4·0 ± 0·7 years. They were classified as good (GC) or poor control (PC) based on growth rate, signs of adrenal insufficiency or Cushing syndrome, progression of sexual characteristics and serum androgens levels. Blood samples were obtained from each patient in two different states of clinical control (GC and PC) for biochemical measurements. measurements IGF‐I, IGF‐II, IGFBP‐1, IGFBP‐2 and IGFBP‐3 were determined by immunoassays. IGFBPs were also analysed by Western ligand blotting (WLB). results Levels of IGF‐I ( P = 0·03) and IGFBP‐3 ( P = 0·01) were higher in GC than in PC while IGFBP‐1 ( P = 0·004) concentrations were lower in GC patients. A trend towards higher levels of IGF‐II ( P = 0·08) and lower levels of IGFBP‐2 ( P = 0·08) was observed in GC children. Increased IGFBP‐4 band intensity was observed in GC children ( P = 0·03). conclusion Higher levels of IGF‐I, IGFBP‐3 and IGFBP‐4, but lower levels of IGFBP‐1, were associated with better control in children with 21‐OHD CAH. These findings are different from those observed in children with other causes of increasing androgens levels and are likely to be related to the insufficient glucocorticoid status.