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The Impact of Weight on Insulin-like Growth Factor-1 Levels in Short-Statured Children Treated With Growth Hormone
Keren Smuel Zilberberg1, Michal Yackobovitch-Gavan2, Ariel Tenenbaum3
1The Jesse Z and Sara Lea Shafer Institute for Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Insights
Weight status significantly impacts insulin-like growth factor-1 (IGF-1) levels in children receiving growth hormone (GH) therapy. Overweight children have higher IGF-1 levels, indicating a normal physiological response, not overtreatment.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Metabolic Health
Background:
- Short stature affects children with GH deficiency or idiopathic short stature.
- Growth hormone (GH) therapy is used to improve growth outcomes.
- The influence of weight status on treatment response requires further investigation.
Purpose of the Study:
- To investigate the relationship between weight status and insulin-like growth factor-1 (IGF-1) levels.
- To assess how weight influences growth outcomes in children treated with GH.
- To determine if weight status affects GH dosing and IGF-1 response.
Main Methods:
- Retrospective cohort study of 293 children treated with GH.
- Data collected at baseline and years 1-3 included auxological parameters, pubertal staging, GH dose, and IGF-1 levels.
- Mixed-model analyses examined the effects of weight on height standard deviation score (Ht-SDS), IGF-1-SDS, and GH dosing.
Main Results:
- Body mass index-SDS positively correlated with IGF-1-SDS.
- Overweight/obese children had higher IGF-1 SD scores than normal-weight children, despite lower GH doses.
- Both weight groups showed comparable height-SDS improvements and growth response.
Conclusions:
- Weight status significantly influences IGF-1 levels in children receiving GH therapy.
- Elevated IGF-1 in overweight children likely represents a normal physiological response.
- Clinical practice should consider weight when monitoring IGF-1 levels and adjusting GH doses.
Objective:
To examine how weight status influences insulin-like growth factor-1 (IGF-1) levels and growth outcomes in short statured children treated with growth hormone (GH) for GH deficiency or idiopathic short stature.
Methods:
This retrospective cohort study analyzed 293 children (95 GH deficiency, 197 idiopathic short stature) treated with GH in an endocrine clinic at a tertiary pediatric referral center (2016-2021). Data were collected at baseline and years 1-3, including auxological parameters, pubertal staging, GH dose, and IGF-1 levels. Mixed-model analyses examined the effects of weight on height standard deviation score (Ht-SDS), IGF-1-SDS, and GH dosing over a 3-year period.
Results:
Body mass index-SDS positively correlated with IGF-1-SDS (B = 0.150, P < .001). Overweight/obese children consistently demonstrated higher IGF-1 SD scores than normal-weight children (P < .001), despite receiving lower GH doses (P = .034). Both weight groups showed comparable height-SDS improvements over time (P < .001), with no significant difference in growth response (P = .685). Body surface area was positively associated with IGF-1-SDS at all-time points. Pubertal status significantly influenced IGF-1 levels.
Conclusions:
Weight status has a significant influence on IGF-1 levels in children treated with GH, with overweight/obese children exhibiting elevated IGF-1 levels despite receiving lower GH doses. These elevations likely represent a normal physiological response rather than overtreatment. Our findings underscore the importance of considering weight when monitoring IGF-1 levels and adjusting GH doses in clinical practice.
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