Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity
Language English Country Germany Media electronic-print
Document type Journal Article
PubMed
40080424
DOI
10.1515/jpem-2024-0463
PII: jpem-2024-0463
Knihovny.cz E-resources
- Keywords
- BMI, Prader–Willi syndrome, growth, growth hormone treatment, obesity,
- MeSH
- Child MeSH
- Body Mass Index MeSH
- Infant MeSH
- Humans MeSH
- Human Growth Hormone * therapeutic use MeSH
- Obesity, Morbid * prevention & control etiology MeSH
- Follow-Up Studies MeSH
- Pediatric Obesity * prevention & control MeSH
- Prader-Willi Syndrome * drug therapy complications MeSH
- Child, Preschool MeSH
- Prognosis MeSH
- Body Height drug effects MeSH
- Age of Onset MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Names of Substances
- Human Growth Hormone * MeSH
OBJECTIVES: Subsequent to early life feeding issues, children with Prader-Willi syndrome (PWS) develop hyperphagia and severe obesity. Growth hormone (GH) therapy has been approved in PWS to improve growth, body composition, and BMI. We aimed to clarify the role of age at GH therapy onset on growth and BMI trajectories in children with PWS. METHODS: We analyzed height and BMI in 114 patients (58 boys) from REPAR - Czech national GH registry. From them, 69 started GH therapy prior to 2 y/o (age 0.8 ± 0.4 years; mean ± SD; early-onset group [EO]), and 45 later (age 7.1 ± 4.1 years; late-onset group [LO]). RESULTS: Height-SDS before therapy was similar in all (EO: -1.9 ± 1.2 [mean ± SD]; LO: -1.7 ± 1.1). After the first year of GH therapy, height-SDS in the EO group increased to -1.0 ± 1.2, in the LO group to -0.9 ± 1.1. After 5 years, height fully normalized in all (-0.1 ± 1.1 SDS). The LO children were already obese at treatment initiation (BMI-SDS: 2.9 ± 2.2), and their BMI-SDS decreased after 1 year of GH therapy by 0.9 (p=0.003). The weight in EO children was below average before GH treatment (BMI-SDS: -0.9 ± 1.2) and their BMI-SDS increased to the overweight range of 1.3 ± 2.2 (p<0.001) within the oncoming 3 years. Albeit BMI-SDS was around the obesity limit in most children after 5 years on GH therapy, the highest lifetime BMI-SDS was lower in EO (2.2 ± 2.6) than in LO (3.7 ± 2.2; p<0.001). CONCLUSIONS: GH treatment in PWS normalizes body height. After 5 years of GH therapy, BMI-SDS in EO and LO groups are similar; however, the EO group is exposed to lower maximal BMI-SDS values.
Department of Pediatrics Masaryk Hospital Ústí nad Labem Czech Republic
Institute of Biostatistics and Analyzes s r o Brno Czech Republic
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