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Title: | Effect of nusinersen on respiratory function in paediatric spinal muscular atrophy types 1-3 | Authors: | Sly, P. D. Begum, N. Chacko, A. Ware, R. S. Gauld, L. M. Thomas, N. Deegan, S. |
Issue Date: | 2022 | Source: | 77, (1), 2022, p. 40-46 | Pages: | 40-46 | Journal: | Thorax | Abstract: | Introduction Nusinersen is used in spinal muscular atrophy (SMA) to improve peripheral muscle function; however, respiratory effects are largely unknown. Aim To assess the effects of nusinersen on respiratory function in paediatric SMA during first year of treatment. Methods A prospective observational study in paediatric patients with SMA who began receiving nusinersen in Queensland, Australia, from June 2018 to December 2019. Outcomes assessed were the age-appropriate respiratory investigations: spirometry, oscillometry, sniff nasal inspiratory pressure, mean inspiratory pressure, mean expiratory pressure, lung clearance index, as well as polysomnography (PSG) and muscle function testing. Lung function was collected retrospectively for up to 2 years prior to nusinersen initiation. Change in lung function was assessed using mixed effects linear regression models, while PSG and muscle function were compared using the Wilcoxon signed-rank test. Results Twenty-eight patients (15 male, aged 0.08-18.58 years) were enrolled: type 1 (n=7); type 2 (n=12); type 3 (n=9). The annual rate of decline in FVC z-score prior to nusinersen initiation was -0.58 (95% CI -0.75 to -0.41), and post initiation was -0.25 (95% CI -0.46 to -0.03), with a significant difference in rate of decline (0.33 (95% CI 0.02 to 0.66) (p=0.04)). Most lung function measures were largely unchanged in the year post nusinersen initiation. The total Apnoea-Hypopnoea Index (AHI) was reduced from a median of 5.5 events/hour (IQR 2.1-10.1) at initiation to 2.7 events/hour (IQR 0.7-5.3) after 1 year (p=0.02). All SMA type 1% and 75% of SMA types 2 and 3 had pre-defined peripheral muscle response to nusinersen. Conclusion The first year of nusinersen treatment saw reduced lung function decline (especially in type 2) and improvement in AHI.L6350358592021-05-21 | DOI: | 10.1136/thoraxjnl-2020-216564 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L635035859&from=exporthttp://dx.doi.org/10.1136/thoraxjnl-2020-216564 | | Keywords: | child;clinical article;drug effect;female;human;infant;Kugelberg Welander disease;linear regression analysis;lung clearance;lung function;lung function test;male;mean expiratory pressure;mean inspiratory pressure;muscle function;observational study;adult;outcome assessment;polysomnography;prospective study;rank sum test;respiratory function;respiratory tract parameters;sniff nasal inspiratory pressure;spinal muscular atrophy type 2;spirometry;Werdnig Hoffmann disease;EMBLA N7000;adolescent;polysomnographnusinersen;oscillometry;apnea hypopnea index;article | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
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