Evidence map›Paper›PMID 40195751›Full record

SynthesisJournal of pediatric endocrinology & metabolism : JPEM2025

Hormonal therapy for impaired growth due to pediatric-onset inflammatory bowel disease: a systematic review and meta-analysis with trial sequential analysis.

Mardhen Catunda Rocha Melo, Rian Vilar Lima, Maryana Modena Strada, João Lucas Maia Rocha, Beatriz Vieira Cavalcante, Maria Lya Pinheiro Bezerra, Lívia Vasconcelos Martins, Maria Clara Parente Torquato, Túlio Veras Veloso, Delanie Bulcao Macedo

Abstract readSystematic ReviewMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Journal of pediatric endocrinology & metabolism : JPEM, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Mardhen Catunda Rocha MeloDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.ORCID https://orcid.org/0009-0001-5334-2886
Rian Vilar LimaDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Maryana Modena StradaDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
João Lucas Maia RochaDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Beatriz Vieira CavalcanteDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Maria Lya Pinheiro BezerraDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Lívia Vasconcelos MartinsDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Maria Clara Parente TorquatoDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Túlio Veras VelosoDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.
Delanie Bulcao MacedoDepartment of Medicine, University of Fortaleza, Fortaleza, Ceará, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInflammatory bowel diseases (IBDs) have an increasing incidence in the pediatric population. The dysabsorptive effects of this condition often lead to a decrease in linear growth. However, the effectiveness and safety of growth hormone (GH) therapy in this population is still a topic of debate, with studies showing conflicting results. CONTENT: MEDLINE, Embase, and Cochrane Library databases were systematically searched according to the PRISMA guidelines. All experimental studies featuring children with IBD receiving GH therapy were included. In addition, a trial sequential analysis (TSA) was conducted to determine the sample size required for each outcome. The prospective registry was carried out under protocol CRD42024563079. The total data set comprised eight studies involving 127 patients with IBD, 78 (61.41 %) of whom received GH therapy, with a mean follow-up duration of 1.3 years. A statistically significant effect of GH was found in increasing the height standard deviation score (HtSDS) of children with IBD (standardized mean difference - SMD=1.07; CI=0.58, 1.56; p<0.0001). When comparing children who received GH with controls, no significant improvement in HtSDS was observed (SMD=0.18; CI=-0.73, 1.08; p=0.70). However, meta-regression analysis indicated that a longer follow-up was associated with a greater improvement in the HtSDS (p=0.04). Regarding height velocity (HV), a significant increase was found when comparing measurements before and after the initiation of hormone therapy (mean difference - MD=4.09; CI=2.58, 5.60; p<0.0001). An increase in HV was also noted in children receiving GH compared to the control group (MD=4.47; CI=2.03, 6.90; p=0.0003). No significant changes in the Pediatric Crohn's Disease Activity Index (PCDAI) were detected, comparing values before and after the start of treatment (MD=-10.09; CI=-22.29, 2.10; p=0.10). The overall prevalence of any adverse effect was estimated at 15.51 % (95 % CI: 2.32-58.70 %). Most common reaction was itching at injection sites. TSA indicated a low risk of overestimating or underestimating the intervention's effect on the analyzed outcomes. SUMMARY: Our study points to the effectiveness and safety of GH therapy in children with IBD and growth impairment. OUTLOOK: Further randomized controlled trials (RCT) with standardized methodologies and extended follow-up periods are necessary to confirm these findings.

Indexed as

Growth DisordersHuman Growth HormoneInflammatory Bowel DiseasesBody HeightChildHumansHuman Growth Hormonegrowth failuregrowth hormoneinflammatory bowel disease

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.