BMI and Contraceptives Affect New Age-, Sex-, and Puberty-adjusted IGF-I and IGFBP-3 Reference Ranges Across Life Span

CONTEXT: Various clinical factors influencing serum levels of insulin-like growth factor I (IGF-I) and its binding protein 3 (IGFBP-3) are not entirely consistently described. OBJECTIVE: We asked whether body mass index (BMI), contraceptive drugs (CDs), and hormone replacement therapy (HRT) have pot...

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Main Authors: Ceglarek, U. (Author), Hörenz, C. (Author), Kiess, W. (Author), Kratzsch, J. (Author), Pfäffle, R. (Author), Thiery, J. (Author), Vogel, M. (Author), Wirkner, K. (Author)
Format: Article
Language:English
Published: NLM (Medline) 2022
Subjects:
BMI
Online Access:View Fulltext in Publisher
LEADER 03755nam a2200637Ia 4500
001 10.1210-clinem-dgac157
008 220630s2022 CNT 000 0 und d
020 |a 19457197 (ISSN) 
245 1 0 |a BMI and Contraceptives Affect New Age-, Sex-, and Puberty-adjusted IGF-I and IGFBP-3 Reference Ranges Across Life Span 
260 0 |b NLM (Medline)  |c 2022 
520 3 |a CONTEXT: Various clinical factors influencing serum levels of insulin-like growth factor I (IGF-I) and its binding protein 3 (IGFBP-3) are not entirely consistently described. OBJECTIVE: We asked whether body mass index (BMI), contraceptive drugs (CDs), and hormone replacement therapy (HRT) have potential effects on data for interpreting new age-, sex-, and puberty-adjusted reference ranges for IGF-I and IGFBP-3 serum levels. DESIGN AND SETTING: Subjects were mainly participants from 2 population-based cohort studies: the LIFE Child study of children and adolescents and the LIFE Adult study. PARTICIPANTS: We investigated 9400 serum samples from more than 7000 healthy and 1278 obese subjects between 3 months and 81 years old. MAIN OUTCOME MEASURES: Associations between IGF-I or IGFBP-3, measured with a new electrochemiluminescence immunoassay, and the predictors BMI and CDs were estimated using hierarchical linear modeling. RESULTS: During infancy, obese children had up to 1 SD score (SDS) higher mean predicted IGF-I values, converging with levels of normal-weight subjects up to 13 years old. Between 20 and 40 years of age, obesity was related to up to -0.5 lower IGF-I SDS values than the predicted values. Obesity had less impact on IGFBP-3. Estrogen- and progestin-based CDs, but not HRT, decreased IGF-I and increased IGFBP-3 (P < 0.01) in adolescents (β IGF-I = -0.45, β IGFBP-3  = 0.94) and adults (β IGF-I = -0.43, β IGFBP-3  = 1.12). Conversely, progestin-based CDs were significantly positive associated with IGF-I (β IGF-I  =0.82). CONCLUSIONS: BMI and CDs must be considered when assessing and interpreting the clinical relevance of IGF-I and IGFBP-3 measurements. © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 
650 0 4 |a adolescent 
650 0 4 |a Adolescent 
650 0 4 |a adult 
650 0 4 |a Adult 
650 0 4 |a BMI 
650 0 4 |a body mass 
650 0 4 |a Body Mass Index 
650 0 4 |a child 
650 0 4 |a Child 
650 0 4 |a childhood obesity 
650 0 4 |a contraceptive agent 
650 0 4 |a Contraceptive Agents 
650 0 4 |a contraceptive drugs 
650 0 4 |a gestagen 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a IGFBP-3 
650 0 4 |a IGF-I 
650 0 4 |a Insulin-Like Growth Factor Binding Protein 3 
650 0 4 |a Insulin-Like Growth Factor Binding Proteins 
650 0 4 |a Insulin-Like Growth Factor I 
650 0 4 |a longevity 
650 0 4 |a Longevity 
650 0 4 |a metabolism 
650 0 4 |a obesity 
650 0 4 |a Pediatric Obesity 
650 0 4 |a Progestins 
650 0 4 |a puberty 
650 0 4 |a Puberty 
650 0 4 |a reference ranges 
650 0 4 |a reference value 
650 0 4 |a Reference Values 
650 0 4 |a somatomedin binding protein 
650 0 4 |a somatomedin binding protein 3 
650 0 4 |a somatomedin C 
700 1 0 |a Ceglarek, U.  |e author 
700 1 0 |a Hörenz, C.  |e author 
700 1 0 |a Kiess, W.  |e author 
700 1 0 |a Kratzsch, J.  |e author 
700 1 0 |a Pfäffle, R.  |e author 
700 1 0 |a Thiery, J.  |e author 
700 1 0 |a Vogel, M.  |e author 
700 1 0 |a Wirkner, K.  |e author 
773 |t The Journal of clinical endocrinology and metabolism 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1210/clinem/dgac157