Evidence map›Paper›PMID 35083513›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2022

Long-term administration of sirolimus does not affect the physical development of children with tuberous sclerosis complex.

Jian Chen, Wen He, Yang-Yang Wang, Meng-Na Zhang, Qian Lu, Qiu-Hong Wang, Xiao-Mei Luo, Bin Wang, Li-Ping Zou

Abstract read
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In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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 2 institutions in 1 country.

Jian Chen *Faculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Wen He *Faculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Yang-Yang WangFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Meng-Na ZhangFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Qian LuFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Qiu-Hong WangFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Xiao-Mei LuoCenter for Brain Disorders Research, Capital Medical University, Beijing Institute for Brain Disorders, Beijing, China.
Bin WangFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China.
Li-Ping ZouFaculty of Pediatrics, Department of Pediatrics, The First Medical Center of Chinese, Chinese PLA General Hospital, PLA General Hospital, 28 Fuxing road, Haidian district, Beijing, 100853, China. zouliping21@hotmail.com.ORCID 0000-0001-7233-9378
Chinese PLA General Hospital · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThere was no evidence whether the mammalian/mechanistic target of rapamycin pathway hyperactivation and long-term use of mTOR inhibitors have any effects on the physical development of children. The aim was to evaluate these effects by comparing the physical development of children with TSC and normal children.

methodsA total of 120 eligible children were enrolled. They were administered sirolimus and followed for at least 12 months. Height, weight, BMI and lipid metabolism index were collected during treatment. Pearson's chi-square and Fisher's exact test were used for comparison of proportions of patients exhibiting normal and abnormal physical growth before and after 1 year of treatment. Logistic regression was used to evaluate the influence of age, sex and abnormal lipid metabolism on the increased BMIs of TSC patients after treatment.

resultsMost of the enrolled TSC children were in the normal height, weight and BMI ranges at baseline (91.7%, 95.8% and 78.3%, respectively). Most remained in the normal height, weight and BMI ranges after 1 year of sirolimus treatment (94.2%, 95% and 76.7%, respectively). There was no significant difference in the proportion of physical development before and after treatment (p > 0.05). Thirty-eight (38/106, 35.8%) patients had increased BMIs after 1 year of treatment, but there was no significant correlation between age, sex and lipid metabolism and increased BMI.

conclusionsOveractivation of the mTOR pathway and long-term administration of sirolimus does not affect the physical development of children with TSC.

Indexed as

Tuberous SclerosisAnimalsChildHumansMammalsSirolimusSirolimusPaediatricPhysical developmentSirolimusTuberous sclerosis

Identifiers

PMID35083513
OpenAlexW4210678815

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.