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CLN2和CLN3型贝敦氏病对英国各家庭影响的证据。

Evidence of the impact of CLN2 and CLN3 Batten disease on families in the United Kingdom.

作者信息

Mole Sara E, Gissen Paul, Nordstrom Shannon, Wait Suzanne, Allen Louise, Antonini Mathilda, Brownnutt Liz, Brown Richard, Cole Barbara, Gibbon Frances, Henderson Robert H, Kenrick Sarah, Sisic Zlatko, Thompson Bob, Nightingale Joanna

机构信息

UCL Great Ormond Street Institute of Child Health, 30 Guilford St, London, WC1N 1EH, UK.

NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond St, London, WC1N 3JH, UK.

出版信息

Orphanet J Rare Dis. 2025 May 12;20(1):223. doi: 10.1186/s13023-025-03747-8.

Abstract

BACKGROUND

Neuronal Ceroid Lipofuscinoses (NCLs), also known as Batten disease, are a group of inherited neurodegenerative disorders that mostly arise in childhood. Each of the NCLs is a genetically distinct disease caused by variants in at least 13 different genes (CLN1-CLN14). NCLs are neurodegenerative, and symptoms can include a combination of childhood dementia, epileptic seizures, motor decline and vision loss, and eventually lead to premature death. There is currently no cure for any subtype of NCL, however, enzyme replacement therapy is available for CLN2 disease, and several treatment strategies are being explored for other NCL subtypes. Early diagnosis and initiation of supportive services (e.g. health, education, social services) are essential to preserve quality of life. Only a few studies have investigated family experiences with NCL, many of which are international in scope.

METHODS

A mixed-method research study was conducted in the UK to understand family experiences in CLN2 and CLN3 disease. It involved an initial literature review, followed by in-depth qualitative interviews. Interview data were analysed using a thematic analysis. Thirteen families (n = 13) participated in the interviews. This represented 16 parents (11 mothers and 5 fathers) of 18 children (10 diagnosed with CLN3 disease and 8 diagnosed with CLN2 disease). Findings were analysed jointly across CLN2 and CLN3 disease.

RESULTS

Six overarching themes emerged from the analysis: difficulty in recognising early symptoms; the shock of a diagnosis; the demands of caring for complex and ever-changing needs; a constant battle to access appropriate and timely support services; the extensive impact on the unaffected sibling; and the all-encompassing impact on the family.

CONCLUSIONS

This study contributes novel UK specific data on family experiences and unmet needs in CLN2 and CLN3 disease. More needs to be done to ensure NCLs are diagnosed early, and timely local support services are made available to protect quality of life for both the affected children and their families.

摘要

背景

神经元蜡样脂褐质沉积症(NCLs),也被称为巴顿病,是一组主要在儿童期出现的遗传性神经退行性疾病。每种NCL都是由至少13种不同基因(CLN1 - CLN14)的变异引起的基因独特的疾病。NCLs具有神经退行性,症状可能包括儿童期痴呆、癫痫发作、运动功能衰退和视力丧失等多种症状,并最终导致过早死亡。目前尚无任何NCL亚型的治愈方法,不过,CLN2疾病可采用酶替代疗法,并且正在为其他NCL亚型探索多种治疗策略。早期诊断并启动支持性服务(如医疗、教育、社会服务)对于维持生活质量至关重要。仅有少数研究调查了NCL患者家庭的经历,其中许多研究范围是国际性的。

方法

在英国开展了一项混合方法研究,以了解CLN2和CLN3疾病患者家庭的经历。该研究首先进行了文献综述,随后进行了深入的定性访谈。访谈数据采用主题分析法进行分析。13个家庭(n = 13)参与了访谈。这代表了18名儿童的16位家长(11位母亲和5位父亲)(10名被诊断为CLN3疾病,8名被诊断为CLN2疾病)。对CLN2和CLN3疾病的研究结果进行了联合分析。

结果

分析得出了六个总体主题:难以识别早期症状;诊断带来的震惊;照顾复杂且不断变化的需求的压力;为获得适当和及时的支持服务而持续进行的斗争;对未受影响的兄弟姐妹的广泛影响;以及对家庭的全方位影响。

结论

本研究提供了关于CLN2和CLN3疾病患者家庭经历及未满足需求的新的英国特定数据。需要做更多工作以确保NCLs得到早期诊断,并提供及时的本地支持服务,以保护患病儿童及其家庭的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/341b/12067959/91d9b8504bb7/13023_2025_3747_Fig1_HTML.jpg

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