Evidence map›Paper›PMID 39778403›Full record

ArticleAnnals of pediatric endocrinology & metabolism2024

Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study).

Yun Jeong Lee, Chong Kun Cheon, Junghwan Suh, Jung-Eun Moon, Moon Bae Ahn, Seong Hwan Chang, Jieun Lee, Jin Ho Choi, Minsun Kim, Han Hyuk Lim and 21 more

Abstract read
In one paragraph

Article in Annals of pediatric endocrinology & metabolism, 2024. 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
  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

31 authors.

Yun Jeong LeeDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Chong Kun CheonDepartment of Pediatrics, Pusan National University Children's Hospital, Yangsan, Korea.
Junghwan SuhDepartment of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.
Jung-Eun MoonDepartment of Pediatrics, Kyungpook National University Chilgok Hospital, Daegu, Korea.
Moon Bae AhnDepartment of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Seong Hwan ChangDepartment of Pediatrics, Chonnam National University Hospital, Gwangju, Korea.
Jieun LeeDepartment of Pediatrics, Inha University Hospital, College of Medicine, Inha University, Incheon, Korea.
Jin Ho ChoiDepartment of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
Minsun KimDepartment of Pediatrics, Jeonbuk National University Medical School, Jeonju, Korea.
Han Hyuk LimDepartment of Pediatrics, Chungnam National University College of Medicine, Daejeon, Korea.
Jaehyun KimDepartment of Pediatrics, Seoul National University Bundang Hospital, Seongnam, Korea.
Shin-Hye KimDepartment of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea.
Hae Sang LeeDepartment of Pediatrics, Ajou University School of Medicine, Suwon, Korea.
Yena LeeDepartment of Pediatrics, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Korea.
Eungu KangDepartment of Pediatrics, Korea University Ansan Hospital, Ansan, Korea.
Se Young KimDepartment of Pediatrics, Bundang Jesaeng General Hospital, Daejin Medical Center, Seongnam, Korea.
Yong Hee HongDepartment of Pediatrics, Soonchunhyang University Bucheon Hospital, Soonchunhyang University College of Medicine, Bucheon, Korea.
Seung YangDepartment of Pediatrics, Hanyang University Hospital, Hanyang University College of Medicine, Seoul, Korea.
Heon-Seok HanDepartment of Pediatrics, Chungbuk National University Hospital, Cheongju, Korea.
Sochung ChungDepartment of Pediatrics, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea.
Won Kyoung ChoDepartment of Pediatrics, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Eun Young KimDepartment of Pediatrics, Chosun University Hospital, Chosun University College of Medicine, Gwangju, Korea.
Jin Kyung KimDepartment of Pediatrics, Daegu Catholic University Medical Center, Daegu Catholic University School of Medicine, Daegu, Korea.
Kye Shik ShimDepartment of Pediatrics, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
Eun-Gyong YooDepartment of Pediatrics, CHA University Bundang Medical Center, Seongnam, Korea.
Hae Soon KimDepartment of Pediatrics, College of Medicine, Ewha Womans University, Seoul, Korea.
Aram YangDepartment of Pediatrics, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Sejin KimDepartment of Pediatrics, Kyemyung University Dongsan Hospital, Daegu, Korea.
Hyo-Kyoung NamDepartment of Pediatrics, Korea University College of Medicine, Seoul, Korea.
Sung Yoon ChoDepartment of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Young Ah LeeDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.

Funding

SNUH Lee Kun-Hee Child Cancer & Rare Disease Project 22C-007-0000
6 · The paper itself

Abstract

Rare endocrine diseases are complex conditions that require lifelong specialized care due to their chronic nature and associated long-term complications. In Korea, a lack of nationwide data on clinical practice and outcomes has limited progress in patient care. Therefore, the Multicenter Networks for Ideal Outcomes of Pediatric Rare Endocrine and Metabolic Disease (OUTSPREAD) study was initiated. This study involves 30 centers across Korea. The study aims to improve the long-term prognosis of Korean patients with rare endocrine diseases by collecting comprehensive clinical data, biospecimens, and patient-reported outcomes to identify complications and unmet needs in patient care. Patients with childhood-onset pituitary, adrenal, or gonadal disorders, such as craniopharyngioma, congenital adrenal hyperplasia (CAH), and Turner syndrome were prioritized. The planned enrollment is 1,300 patients during the first study phase (2022-2024). Clinical, biochemical, and imaging data from diagnosis, treatment, and follow-up during 1980-2023 were retrospectively reviewed. For patients who agreed to participate in the prospective cohort, clinical data and biospecimens will be prospectively collected to discover ideal biomarkers that predict the effectiveness of disease control measures and prognosis. Patient-reported outcomes, including quality of life and depression scales, will be evaluated to assess psychosocial outcomes. Additionally, a substudy on CAH patients will develop a steroid hormone profiling method using liquid chromatography-tandem mass spectrometry to improve diagnosis and monitoring of treatment outcomes. This study will address unmet clinical needs by discovering ideal biomarkers, introducing evidence-based treatment guidelines, and ultimately improving long-term outcomes in the areas of rare endocrine and metabolic diseases.

Indexed as

ChildCohort studiesCongenital adrenal hyperplasiaCraniopharyngiomaEndocrine system diseasesRare diseaseTreatment outcome

Identifiers

PMID39778403
PMCPMC11725631

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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.