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Auxological and metabolic effects of long-term treatment with recombinant growth hormone in children born small for gestational age: a retrospective study.
Ferrigno, Rosario; Savanelli, Maria Cristina; Cioffi, Daniela; Pellino, Valeria; Klain, Antonella.
Afiliación
  • Ferrigno R; UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Napoli, Italy. ferrignoro@gmail.com.
  • Savanelli MC; UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Napoli, Italy.
  • Cioffi D; UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Napoli, Italy.
  • Pellino V; UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Napoli, Italy.
  • Klain A; UOSD di Auxologia ed Endocrinologia, AORN Santobono-Pausilipon, Napoli, Italy.
Endocrine ; 84(1): 213-222, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38214878
ABSTRACT
RATIONALE Children born small for gestational age (SGA) not showing catch-up during the first two years of life reportedly show an impaired growth rate and adult height, as well as a worse metabolic outcome, mainly in terms of glycemic and lipid profile, compared to general population. In SGA children with short stature, treatment with recombinant growth hormone (GH) is currently recommended until adolescence; therefore, it may last long-term. STUDY

METHODS:

The aim of the current study was to evaluate the auxological and metabolic effects and the safety of long-term recombinant GH treatment in SGA children. The study included 15 SGA children (5 F, 10 M; mean age 6.78 yrs) treated with GH for at least 48 months. Growth and metabolic parameters, including glycemic and lipid profile, transaminases, and urycemia, were collected every six months.

RESULTS:

Compared to baseline, SGA children showed a significant improvement in height, weight, and growth rate after four yaers of treatment with GH (p ≤ 0.002), being already evident after six months of treatment (p < 0.001). Noteworthy, patients showed a constant, significant improvement in height throughout the treatment, as it was significantly higher at each follow-up compared to the previous one, until 42 months of treatment, except at 30 months of treatment (p < 0.001 T6VST12; p < 0.01 T12VST18, T18VST24; p < 0.05 T30VST36, T36VST42). Considering metabolic parameters, compared to baseline, a recurring increase in glycemia (p ≤ 0.028 vs T30, T36, and T48) and decrease in AST (p ≤ 0.035 vs T36, T42, and T48) and an occasional decrease in LDL cholesterol (p ≤ 0.04 vs T24 and T42) and triglycerides (p = 0.008 vs T18) and increase in urycemia (p = 0.034 vs T42). Considering safety profile, treatment was well tolerated, as the most frequently reported adverse event was poor compliance (20%); no hyperglycemia, hypercholesterolemia or hyperstransaminasemia occurred throughout the treatment,

CONCLUSIONS:

Long-term GH treatment showed to be effective in improving height and growth rate in SGA children, with a positive impact of metabolic profile and a safety profile, although glycemia should be carefully monitored over time.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hormona del Crecimiento / Hormona de Crecimiento Humana Tipo de estudio: Observational_studies Límite: Child / Humans Idioma: En Revista: Endocrine Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hormona del Crecimiento / Hormona de Crecimiento Humana Tipo de estudio: Observational_studies Límite: Child / Humans Idioma: En Revista: Endocrine Asunto de la revista: ENDOCRINOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Italia
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