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队列简介:韩国罕见儿科内分泌和代谢疾病理想结局多中心网络(OUTSPREAD研究)。

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

作者信息

Lee Yun Jeong, Cheon Chong Kun, Suh Junghwan, Moon Jung-Eun, Ahn Moon Bae, Chang Seong Hwan, Lee Jieun, Choi Jin Ho, Kim Minsun, Lim Han Hyuk, Kim Jaehyun, Kim Shin-Hye, Lee Hae Sang, Lee Yena, Kang Eungu, Kim Se Young, Hong Yong Hee, Yang Seung, Han Heon-Seok, Chung Sochung, Cho Won Kyoung, Kim Eun Young, Kim Jin Kyung, Shim Kye Shik, Yoo Eun-Gyong, Kim Hae Soon, Yang Aram, Kim Sejin, Nam Hyo-Kyoung, Cho Sung Yoon, Lee Young Ah

机构信息

Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.

Department of Pediatrics, Pusan National University Children's Hospital, Yangsan, Korea.

出版信息

Ann Pediatr Endocrinol Metab. 2024 Dec;29(6):349-355. doi: 10.6065/apem.2448272.136. Epub 2024 Dec 31.

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.

摘要

罕见内分泌疾病是复杂的病症,由于其慢性性质和相关的长期并发症,需要终身的专科护理。在韩国,缺乏关于临床实践和结果的全国性数据限制了患者护理方面的进展。因此,启动了小儿罕见内分泌和代谢疾病理想结局多中心网络(OUTSPREAD)研究。这项研究涉及韩国各地的30个中心。该研究旨在通过收集全面的临床数据、生物样本和患者报告的结果,以识别患者护理中的并发症和未满足的需求,从而改善韩国罕见内分泌疾病患者的长期预后。优先纳入患有儿童期发病的垂体、肾上腺或性腺疾病的患者,如颅咽管瘤、先天性肾上腺皮质增生症(CAH)和特纳综合征。计划在第一个研究阶段(2022 - 2024年)招募1300名患者。回顾性审查了1980 - 2023年期间诊断、治疗和随访的临床、生化和影像数据。对于同意参与前瞻性队列研究的患者,将前瞻性收集临床数据和生物样本,以发现预测疾病控制措施有效性和预后的理想生物标志物。将评估包括生活质量和抑郁量表在内的患者报告结果,以评估心理社会结果。此外,一项关于CAH患者的子研究将开发一种使用液相色谱 - 串联质谱法的类固醇激素分析方法,以改善诊断和治疗结果监测。这项研究将通过发现理想的生物标志物、引入循证治疗指南,并最终改善罕见内分泌和代谢疾病领域的长期结局,来满足未满足的临床需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76a0/11725631/25a01de61bac/apem-2448272-136f1.jpg

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