Evidence map›Paper›PMID 32222149›Full record

ArticleBMC pediatrics2020

Final adult height of children with idiopathic short stature: a multicenter study on GH therapy alone started during peri-puberty.

Di Wu, Rui-Min Chen, Shao-Ke Chen, Ge-Li Liu, Lin-Qi Chen, Yu Yang, Xin-Li Wang, Ya-Guang Peng, Chun-Xiu Gong

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC pediatrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact, top 100% of its field
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

12 citing papers in PubMed, 1 citations in OpenAlex.

  1. Trial
  2. Observational
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  4. Article
  5. Review
  6. Article
  7. [Discussion on the genetic mechanisms and efficacy of growth hormone therapy in children with idiopathic short stature].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2024
    Review
  8. Article
  9. Article
  10. Article
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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

9 authors at 8 institutions in 1 country.

Di WuDepartment of Endocrine and Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Centre for Children's Health, No. 56 Nanlishi Road, Xicheng District, Beijing, 100045, China.
Rui-Min ChenDepartment of Endocrinology, Fuzhou Children's Hospital of Fujian Medical University Teaching Hospital, No.145, 817 Middle Road, Gulou District, Fuzhou, Fuzhou, 350005, Fujian Province, China.
Shao-Ke ChenDepartment of Pediatric, The second Affiliated Hospital of Guangxi Medical University, No.166, Daxuedong Road, Nanning, Guangxi, Nanning, 530007, Guangxi, China.
Ge-Li LiuDepartment of Pediatric, Tianjin Medical University General Hospital, No.154, Anshan Road, Heping District, Tianjin, 300052, Tianjin, China.
Lin-Qi ChenDepatment of Endocrinology, Children's Hospital of Soochow University, No. 92, Zhongnan Street, Gongyeyuan District, Suzhou, Suzhou, 215025, Jiangsu, China.
Yu YangDepartment of Endocrinology, Children's Hospital of Jiangxi Province, No.122, Yangming Road, Donghu District, Nanchang, Jiangxi, Nanchang, 330006, Jiangxi, China.
Xin-Li WangDepartment of Pediatric, Peking University Third Hospital, No.49, Huayuanbei Road, Haidian District, Beijing, Beijing, 100191, Beijing, China.
Ya-Guang PengCenter for Clinical Epidemiology and Evidence-Based Medicine, Beijing Children's Hospital, Capital Medical University, National Centre for Children's Health, No.56, Nanlishi Raod, Xicheng District, Beijing, Beijing, 100045, Beijing, China.
Chun-Xiu GongDepartment of Endocrine and Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Centre for Children's Health, No. 56 Nanlishi Road, Xicheng District, Beijing, 100045, China. chunxiugong@sina.com.
Beijing Children’s Hospital · CNCapital Medical University · CNFujian Medical University · CNGuangxi Medical University · CNJiangxi Provincial Children's Hospital · CNPeking University · CNSoochow University · CNTianjin Medical University General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo evaluate the efficacy of GH in improving FAH in ISS children in a multicenter study.

methodsA real-world observation was carried out. Children with ISS in seven hospitals in China were enrolled. The height gains standard deviation score and the height gain over the target height were evaluated.

resultsThere were 344 ISS patients (217 boys and 127 girls). The baseline average age of boys and girls was 12.7 and 11.7 years, with bone age of 11.7 and 10.1 years, respectively. The baseline height SDS of boys and girls was - 3.07 and - 2.74, and the FAH SDS was - 1.91 and - 1.38, respectively. Compared with the baseline height SDS, the FAH SDS was significantly increased in both boys and girls (both P = 0.0000). The FAH SDS was the highest (gain by 1.54 SD) in the ≥2y treatment course group. Two hundred eighteen patients (218/344, 63.4%) had a FAH SDS > - 2 SD. Among these patients, girls in the 1-2y treatment course group and ≥ 2y group had a FAH SDS higher than TH SDS. Even in the control group, a spontaneous catch-up growth of 1.16 SD was observed. A multivariate linear regression model was used to analyze the results, with FAH SDS as the dependent variable. It was found that the treatment course and baseline height SDS in the boys' model were statistically significant (P < 0.05), whereas the baseline height SDS and baseline bone age significantly affected the girls' FAH SDS (P < 0.05).

conclusionsBoth girls and boys of ISS improved FAH by GH therapy even if treatments begin over 10 years old and majority of them reached TH. Some peri-puberty ISS will have a spontaneous height gain. We recommend the course of GH treatment more than 2 years for girls, and longer courses for boys.

Indexed as

Body HeightGrowth DisordersHuman Growth HormoneAdultChildChinaFemaleHumansMalePubertyHuman Growth HormoneBaseline heightFinal adult height (FAH)Idiopathic short stature (ISS)Standard deviation score (SDS)Target height (TH)

Identifiers

PMID32222149
PMCPMC7102429
OpenAlexW2995721569

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LicenceCC BY
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Registered trials

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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.