scholarly journals Sustained High Insulin-Like Growth Factor-Binding Protein 3 Levels after Suppression of Gonadal Steroids in Central Idiopathic Precocious Puberty

1994 ◽  
Vol 3 (Supple4) ◽  
pp. 183-186 ◽  
Author(s):  
Atsushi Murata ◽  
Yasuyuki Kobayashi ◽  
Toshiyuki Yasuda ◽  
Yukihiro Hasegawa ◽  
Masanori Minagawa ◽  
...  
2021 ◽  
pp. 1-8
Author(s):  
Patricia Diaz Escagedo ◽  
Cheri L. Deal ◽  
Andrew A. Dwyer ◽  
Michael Hauschild

<b><i>Background:</i></b> Central precocious puberty (CPP) in females is characterized by thelarche before 8 years of age. Evidence of reproductive axis activation confirms the diagnosis (basal serum luteinizing hormone (LH) ≥0.3 IU/L or LH-releasing hormone (LHRH)-stimulated LH ≥5 IU/L). Stimulation testing is the diagnostic gold standard but is time-consuming and costly. Serum levels of insulin-like growth factor-1 (IGF-1) and insulin-like growth factor-binding protein 3 (IGFBP-3) are increased in girls with CPP. <b><i>Objective:</i></b> The aim of the study was to assess the utility of serum IGF-1 and IGFBP-3 in identifying CPP in girls aged 6–8 years. <b><i>Methods:</i></b> The study was a single-center retrospective study. Girls with confirmed CPP (<i>n</i> = 44) and isolated premature precocious adrenarche/ precocious thelarche (PA/PT, <i>n</i> = 16) had baseline biochemical profiling and LHRH stimulation testing. Serum IGF-1 and IGFBP-3 results were converted to standard deviation scores (SDS). Correlations were calculated and receiver operating characteristic curves were plotted. <b><i>Results:</i></b> Girls with CPP had higher basal and peak LH, IGF-1 SDS, and growth velocity (<i>p</i> &#x3c; 0.05). IGF-1 SDS correlated positively with basal and peak LH (<i>p</i> &#x3c; 0.05). IGF-1 SDS (1.75–2.15) differentiated CPP and PA/PT with 89% sensitivity and 56% specificity (basal LH) and 94% specificity and 55% sensitivity (peak LH). IGFBP-3 SDS did not differ between groups or by CPP parameters. <b><i>Conclusions:</i></b> In clinical practice, IGF-1 SDS may be an additional tool for identifying CPP in girls aged 6 to 8 years when baseline clinical and laboratory diagnostic criteria are inconclusive, possibly avoiding more time-consuming and costly procedures.


Hepatology ◽  
1996 ◽  
Vol 24 (1) ◽  
pp. 127-133 ◽  
Author(s):  
E Shmueli ◽  
J P Miell ◽  
M Stewart ◽  
K G Alberti ◽  
C O Record

Metabolism ◽  
2017 ◽  
Vol 73 ◽  
pp. 36-42 ◽  
Author(s):  
Frej Stilling ◽  
Sara Wallenius ◽  
Karl Michaëlsson ◽  
Christine Dalgård ◽  
Kerstin Brismar ◽  
...  

Diabetes ◽  
1994 ◽  
Vol 43 (2) ◽  
pp. 232-239 ◽  
Author(s):  
M. S. Lewitt ◽  
H. Saunders ◽  
J. L. Phyual ◽  
R. C. Baxter

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