Evidence map›Paper›PMID 42902698›Full record

ArticlePediatric endocrinology, diabetes, and metabolism2026

Efficacy of recombinant growth hormone therapy in children born small for gestational age (SGA): a retrospective analysis.

Aleksandra Pałysa, Monika Kopiec-Burdecka, Beata Pyrżak

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Article in Pediatric endocrinology, diabetes, and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Aleksandra Pałysa<p>Department of Paediatrics and Endocrinology, Medical University of Warsaw, Poland</p>.
Monika Kopiec-Burdecka<p>Department of Paediatrics and Endocrinology, Medical University of Warsaw, Poland</p>.
Beata Pyrżak<p>Department of Paediatrics and Endocrinology, Medical University of Warsaw, Poland</p>.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChildren born small for gestational age (SGA) present with a birth weight or length below -2 standard deviations (SD) relative to population norms for gestational age and sex. In Poland, such patients are eligible for recombinant human growth hormone (rhGH) therapy reimbursed by the National Health Fund.

aimTo retrospectively assess the effectiveness of rhGH therapy in children diagnosed with SGA based on clinical data from 39 patients treated with rhGH between 2016 and 2025. MATERIAL AND

methodsAnthropometric data were analysed at therapy initiation and completion. Treatment duration and changes in height and weight SD score (SDS) were evaluated. The influence of age at treatment initiation and sex on therapy outcomes was also assessed.

resultsThe mean treatment duration was 3 years and 9 months. The average annual height gain was 6.9 cm/year and weight gain 5.3 kg/year. Boys showed a significantly higher annual height gain than girls (p = 0.013), while weight gain differences were not significant (p = 0.08). An improvement in both height and weight SDS was observed across all age groups, with the most pronounced benefits among children who began therapy before the age of 10 years. The most frequent reason for treatment discontinuation was reduced growth velocity.

conclusionsrhGH therapy in children born SGA is effective and safe, resulting in an improvement in growth parameters. The best outcomes are achieved when treatment is initiated in early childhood. The therapy is safe when accompanied by appropriate metabolic monitoring.

Indexed as

Growth DisordersHuman Growth HormoneInfant, Small for Gestational AgeBody HeightChildChild, PreschoolFemaleHumansInfant, NewbornMalePolandRecombinant ProteinsRetrospective StudiesTreatment OutcomeWeight GainHuman Growth HormoneRecombinant Proteinsgrowth deficiencygrowth hormone therapyrecombinant human growth hormonerhGH.SGAsmall for gestational age

Identifiers

PMID42902698
PMCPMC13628192

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