Abstract

BackgroundEvidence from in vitro and rodent studies suggests that leptin, a key signal of long-term energy reserves, promotes IGF1 synthesis and linear growth. This effect of leptin has not been fully investigated in humans. The aim of our study was to investigate the effect of leptin substitution on growth factors and linear growth in children with congenital leptin deficiency (CLD).MethodsIn this cohort study we included eight pediatric patients (six males), age 0.9–14.8 years, who were diagnosed with CLD and received leptin substitution at our University Medical Center. We calculated standard deviation scores (SDS) for serum levels of IGF1 and IGFBP3, IGF1/IGFBP3 molar ratio, and height at baseline (T0) and 12 months (T12) after the initiation of substitution with metreleptin.ResultsAll patients had severe obesity (BMI-SDS mean ± SD: 4.14 ± 1.51) at T0 and significant BMI-SDS reduction to 2.47 ± 1.05 at T12. At T0, all patients were taller than the mid-parental median, yet had low IGF1 and IGF1/IGFBP3 molar ratios (IGF1-SDSoverline xT0: −1.58 ± 0.92, IGF1/IGFBP3 molar ratio-SDSoverline xT0: −1.58 ± 0.88). At T12, IGF1-SDS increased significantly (∆T0–12: 1.63 ± 1.40, p = 0.01), and IGFBP3-SDS and IGF1/IGFBP3 molar ratio-SDS showed a trend toward an increase. In the three children within the childhood growth period (post-infancy, pre-puberty) height-SDS increased (∆height-SDST0–12: 0.57 ± 0.06, p = 0.003) despite substantial weight loss.ConclusionsThese results in CLD patients are contrary to observations in children with idiopathic obesity who typically have above-mean IGF1 levels that decrease with weight loss, and therefore suggest that leptin increases IGF1 levels and promotes linear growth.

Highlights

  • Human data are limited to observed associations of leptin, IGF1 levels, and growth in several human conditions associated with hyper- [11] or hypoleptinemia [1, 3, 12,13,14,15,16], and their response to leptin treatment

  • After 12 months of leptin substitution, BMI-standard deviation scores (SDS) significantly decreased in all patients

  • Blood samples were obtained between 08:00 h and 09:00 h after an overnight fast and were processed by the Department of Clinical Chemistry, University Medical Center Ulm

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Summary

Introduction

Term energy availability that correlates with fat mass, has been implicated in the regulation of IGF1 secretion and linear growth during acute and chronic nutritional alterations [2,3,4]. Leptin therapy in patients with hypothalamic amenorrhea [3, 13] and lipodystrophy [14] leads to increases in IGF1 concentrations These disease models suggest a stimulatory effect of leptin on IGF1, but are confounded by other metabolic alterations that underlie or accompany the altered levels of leptin. Evidence from in vitro and rodent studies suggests that leptin, a key signal of long-term energy reserves, promotes IGF1 synthesis and linear growth. This effect of leptin has not been fully investigated in humans. We calculated standard deviation scores (SDS) for serum levels of IGF1 and IGFBP3, IGF1/IGFBP3 molar ratio, and height at baseline (T0) and 12 months (T12) after the initiation of substitution with metreleptin

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