Evidence map›Paper›PMID 41143936›Full record

ArticleNeurology and therapy2025

Short-Term Outcomes and Immunologic Mechanisms of Adrenocorticotropic Hormone in Infantile Epileptic Spasm Syndrome: A Multicenter Prospective Trial in Southern China.

Yanping Ran, Bingwei Peng, Jianwei Li, Yanqun Chang, Xiuying Wang, Cuiling Zhuo, Kelu Zheng, Yani Zhang, Jie Yu, Haixia Zhu and 6 more

Abstract read
In one paragraph

Article in Neurology and therapy, 2025. 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
–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

3 citing papers in PubMed.

  1. 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

16 authors.

Yanping Ran *Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Bingwei Peng *Department of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Jianwei LiDepartment of Neurology, Dongguan Children's Hospital, Dongguan, Guangdong, China.
Yanqun ChangDepartment of Rehabilitation, Guangdong Maternal and Child Health Hospital, Guangzhou, Guangdong, China.
Xiuying WangDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Cuiling ZhuoDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Kelu ZhengDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Yani ZhangDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Jie YuDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Haixia ZhuDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Yang TianDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Chi HouDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Wenxiao WuDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Wenlin WuDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China.
Xiaojing LiDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China. lixiaojingfy@163.com.
Wen-Xiong ChenDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 9, Jinsui Road, Tianhe District, Guangzhou, 510623, Guangdong, China. gzchcwx@126.com.ORCID http://orcid.org/0000-0001-9076-2006

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAdrenocorticotropic hormone (ACTH) is a first-line drug and standard therapy in infantile epileptic spasm syndrome (IESS) with different response rates. The mechanism of ACTH for treatment of IESS remains incompletely understood. This study aimed to evaluate short-term outcomes and immunologic mechanisms of ACTH in treating pediatric patients with IESS.

methodsA multicenter prospective trial of pediatric patients with IESS treated with ACTH over 2 weeks was performed. Short-term responders were defined as those with resolution of epileptic spasms and hypsarrhythmia (if present) at day 14 without epileptic spasm recurrence over 30 days after ACTH therapy, while non-responders included those with persistent spasms or hypsarrhythmia after treatment, or recurrence within 30 days. The risk factors for short-term efficacy were analyzed. The receiver operating characteristic (ROC) curve analysis was adopted to reveal the optimal critical value of peripheral blood lymphocyte subpopulations before ACTH treatment.

resultsAmong 151 included pediatric patients, 44 (29.1%) were short-term responders. The presence of hypsarrhythmia on pre-therapy electroencephalogram (EEG) was a risk factor for the short-term efficacy (p = 0.029). A total of 81 patients accepted lymphocyte subpopulation investigation. The short-term responder group had a lower percentage of CD3

conclusionAbout 30% children with IESS were short-term responders to ACTH therapy. The presence of hypsarrhythmia on the pre-therapy EEG was a risk factor for short-term efficacy of ACTH administration. The CD3

Indexed as

Adrenocorticotropic hormoneHypsarrhythmiaImmunologic mechanismInfantile epileptic spasm syndromeLymphocyte subpopulation

Identifiers

PMID41143936
PMCPMC12623540

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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.