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

Title
Cohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study)
Authors
Lee Y.J.; Cheon C.K.; Suh J.; Moon J.-E.; Ahn M.B.; Chang S.H.; Lee J.; Choi J.H.; Kim M.; Lim H.H.; Kim J.; Kim S.-H.; Lee H.S.; Lee Y.; Kang E.; Kim S.Y.; Hong Y.H.; Yang S.; Han H.-S.; Chung S.; Cho W.K.; Kim E.Y.; Kim J.K.; Shim K.S.; Yoo E.-G.; Kim H.S.; Yang A.; Kim S.; Nam H.-K.; Cho S.Y.; Lee Y.A.
Ewha Authors
김혜순
SCOPUS Author ID
김혜순scopus
Issue Date
2024
Journal Title
Annals of Pediatric Endocrinology and Metabolism
ISSN
2287-1012JCR Link
Citation
Annals of Pediatric Endocrinology and Metabolism vol. 29, no. 6, pp. 349 - 355
Keywords
Child; Cohort studies; Congenital adrenal hyperplasia; Craniopharyngioma; Endocrine system diseases; Rare disease; Treatment outcome; Turner syndrome
Publisher
Korean society of pediatric endocrinology
Indexed
SCOPUS; KCI scopus
Document Type
Article
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. © 2024 Annals of Pediatric Endocrinology & Metabolism.
DOI
10.6065/apem.2448272.136
Appears in Collections:
의과대학 > 의학과 > Journal papers
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