Nutrition outcomes of disease modifying therapies in spinal muscular atrophy: A systematic review.

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Muscle & Nerve Pub Date : 2024-11-01 Epub Date: 2024-08-11 DOI:10.1002/mus.28224
Katie O'Brien, Kay Nguo, Eppie M Yiu, Ian R Woodcock, Natassja Billich, Zoe E Davidson
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Abstract

The nutritional implications of spinal muscular atrophy (SMA) are profound. Disease modifying therapies (DMT) have improved clinical outcomes. This review describes the impact of DMT on nutrition outcomes. A systematic search strategy was applied across seven databases until May 2023. Eligible studies measured nutrition outcomes in individuals with SMA on DMT (nusinersen, risdiplam or onasemnogene abeparvovec [OA]) compared to untreated comparators. Nutrition outcomes included anthropometry, feeding route, swallowing dysfunction, dietary intake, dietetic intervention, nutritional biochemistry, metabolism, gastrointestinal issues and energy expenditure. Articles retrieved were screened in duplicate, data were extracted and appraised systematically. Sixty three articles from 54 studies were included; 41% (n = 22) investigated nusinersen in pediatric participants with SMA type 1. Anthropometry (n = 18), feeding route (n = 39), and swallowing dysfunction (n = 18) were the most commonly reported outcomes. In combined pediatric and adult cohorts, BMI z-score remained stable post nusinersen therapy. The proportion of children with SMA requiring enteral nutrition was stable post nusinersen therapy. Ability to thrive at age 1.5 years was higher in children treated in early infancy with OA compared to historical controls. Significant heterogeneity existed across study population characteristics and outcome measures. Nusinersen may prevent deterioration in some nutrition outcomes; and OA in early infancy may be associated with improved nutrition outcomes. Timing of DMT initiation is an important consideration for future nutrition research. Studies investigating nutrition as a primary outcome of DMT, using consistent outcome measures are required for nutritional management strategies for this cohort to be appropriately tailored.

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脊髓性肌萎缩症疾病调整疗法的营养结果:系统综述。
脊髓性肌萎缩症(SMA)对营养的影响非常深远。疾病调整疗法(DMT)改善了临床疗效。本综述介绍了 DMT 对营养结果的影响。在 2023 年 5 月之前,我们在七个数据库中采用了系统性检索策略。符合条件的研究测量了接受 DMT(纽西奈森、利地普兰或onasemnogene abeparvovec [OA])治疗的 SMA 患者与未接受治疗的比较者相比的营养结果。营养结果包括人体测量、进食途径、吞咽功能障碍、饮食摄入量、饮食干预、营养生化、新陈代谢、胃肠道问题和能量消耗。对检索到的文章进行了一式两份的筛选、数据提取和系统评估。共纳入 54 项研究中的 63 篇文章;41%(n = 22)的文章对患有 SMA 1 型的儿科参与者进行了纽西奈森调查。人体测量(18 例)、进食途径(39 例)和吞咽功能障碍(18 例)是最常报告的结果。在儿童和成人联合组群中,努西奈森治疗后体重指数z-score保持稳定。需要肠内营养的 SMA 患儿比例在使用纽西奈森治疗后保持稳定。与历史对照组相比,在婴儿早期接受 OA 治疗的儿童在 1.5 岁时的茁壮成长能力更高。在研究人群特征和结果测量方面存在显著的异质性。奴西那生可预防某些营养结果的恶化;婴儿早期接受OA治疗可能与营养结果的改善有关。开始使用 DMT 的时机是未来营养研究的一个重要考虑因素。将营养作为 DMT 的主要结果进行调查研究,并采用一致的结果测量方法,是为这一人群制定适当的营养管理策略所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Muscle & Nerve
Muscle & Nerve 医学-临床神经学
CiteScore
6.40
自引率
5.90%
发文量
287
审稿时长
3-6 weeks
期刊介绍: Muscle & Nerve is an international and interdisciplinary publication of original contributions, in both health and disease, concerning studies of the muscle, the neuromuscular junction, the peripheral motor, sensory and autonomic neurons, and the central nervous system where the behavior of the peripheral nervous system is clarified. Appearing monthly, Muscle & Nerve publishes clinical studies and clinically relevant research reports in the fields of anatomy, biochemistry, cell biology, electrophysiology and electrodiagnosis, epidemiology, genetics, immunology, pathology, pharmacology, physiology, toxicology, and virology. The Journal welcomes articles and reports on basic clinical electrophysiology and electrodiagnosis. We expedite some papers dealing with timely topics to keep up with the fast-moving pace of science, based on the referees'' recommendation.
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