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Study 38 of 68HGH (Somatropin) literatureZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · Review2026

[Prospects and mechanistic insights into the use of recombinant human growth hormone in the treatment of pediatric inflammatory bowel disease].

Recombinant human growth hormone (rhGH) may offer a new avenue for managing growth retardation in pediatric inflammatory bowel disease, but more research is needed to confirm its efficacy and safety.

Read at Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatricsAdd to compare

Where it sits

this study against the rest of the hgh (somatropin) corpus
4
Preclinical
47
Observational
0
Open-label
10
Randomised
7
Reviews · this one

Summary and findings

This review explores the potential use of recombinant human growth hormone (rhGH) in treating growth retardation associated with pediatric inflammatory bowel disease (PIBD). It discusses the pathogenesis of growth impairment in PIBD and evaluates recent progress and challenges in rhGH application. The review aims to provide insights for clinical management of PIBD-related growth disorders.

How much of this paper we could read: full text read (0.70). We had a clear abstract, so the summary below closely tracks the paper. What this means →
2026

Abstract

The authors’ words, as Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics supplied them

Pediatric inflammatory bowel disease (PIBD) is a chronic immune-mediated inflammatory disorder of the gastrointestinal tract, with a steadily increasing global incidence. Growth retardation is one of the most common extraintestinal complications of PIBD, especially in children with Crohn's disease, severely affecting their quality of life and final adult height. The pathogenesis of this complication is complex, involving chronic intestinal inflammation, malnutrition, dysregulation of the endocrine axis, and adverse effects of glucocorticoid therapy. Current clinical management primarily focuses on controlling inflammation and optimizing nutrition, but some patients still experience persistent growth impairment. Recombinant human growth hormone (rhGH) directly promotes linear growth and its potential therapeutic value in PIBD has attracted increasing attention. This review summarizes the pathogenesis of PIBD-related growth retardation and outlines recent progress and clinical challenges in rhGH application in PIBD, aiming to provide a reference for the clinical management of PIBD-associated growth disorders.

Background

Pediatric inflammatory bowel disease (PIBD) is a chronic condition that affects the gastrointestinal tract and is increasingly prevalent worldwide. Growth retardation is a significant complication of PIBD, particularly in children with Crohn's disease, impacting their quality of life and adult height. The complexity of this issue arises from factors such as chronic inflammation, malnutrition, endocrine dysregulation, and glucocorticoid therapy. While current treatments focus on inflammation control and nutritional support, some children continue to experience growth issues, prompting interest in alternative therapies like recombinant human growth hormone (rhGH).

Methods

This paper is a review article, summarizing existing literature on the use of recombinant human growth hormone (rhGH) in pediatric inflammatory bowel disease (PIBD). It does not involve new experimental data or a specific study design. The review aims to compile and discuss the pathogenesis of PIBD-related growth retardation and the potential role of rhGH in managing this complication.

Results

Not reported in abstract.

Interpretation

The review highlights the potential of rhGH to address growth retardation in PIBD, but it does not provide new data to support its efficacy or safety. The discussion is based on existing studies, which may vary in quality and relevance. The clinical significance of rhGH in PIBD remains uncertain without robust, controlled trials demonstrating meaningful outcomes. The review underscores the need for further research to establish the therapeutic value of rhGH in this context.

Key findings

  • Not reported in abstract.
  • Not reported in abstract.
  • Not reported in abstract.

Limitations

  • No new experimental data presented
  • Relies on existing literature
  • Potential biases in reviewed studies
  • Lack of quantitative findings

Elsewhere in the HGH (Somatropin) corpus

DAdvances in Systemic Treatment of Breast Cancer.The New England journal of medicine · 2026reviewBConverging Growth Trajectories During Recombinant Human Growth Hormone Therapy in Children With Isolated and Combined Pituitary Hormone Deficiency.Clinical endocrinology · 2023 · n=120 · Cumulative height SDS gains after 48 months: 3.10 ± 1.36 for CPHD vs. 1.92 ± 0.87 for IGHD, p < 0.001.HumanBMicrostructural Vulnerability of the Tibial Tubercle Apophysis During Growth Hormone Therapy: A Multicenter Prospective Cohort Study Using Diffusion Tensor Imaging-MRI.The Journal of bone and joint surgery. American volume · 2023 · n=53 · ADC was significantly higher at 8 months compared with baseline (1.61 × 10-3 vs 1.52 × 10-3 mm2/sec, p = 0.041).HumanBA Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.Clinical genetics · 2023 · n=1 · Not reported in abstract.HumanAInteraction between vitamin D and the growth hormone/insulin-like growth factor 1 axis in children: a systematic review and meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026 · WMD: 5.83 ng/mL increase in vitamin D levels after rhGH treatment, 95% CI: 3.72 to 7.94, p<0.00001.reviewDInteraction between vitamin D and the growth hormone/insulin-like growth factor 1 axis in children: a systematic review and meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026 · WMD: 5.83 ng/mL increase in vitamin D levels after rhGH treatment, 95% CI: 3.72 to 7.94, p<0.00001.review