期刊论文详细信息
Orphanet Journal of Rare Diseases
Growth patterns in children with spinal muscular atrophy
Claudio Bruno1  Jonathan C. Wells2  Mary Fewtrell2  Ester Giaquinto3  Caterina Agosto4  Alessandro Leone5  Ramona De Amicis5  Giorgio Bedogni5  Andrea Foppiani5  Alberto Battezzati5  Simone Ravella5  Simona Bertoli6  Marina Pedemonte7  Chiara Mastella8  Giovanni Baranello9  Adele D’Amico1,10  Enrico Bertini1,10 
[1] Center of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, Genoa, Italy;Childhood Nutrition Research Group, Population, Policy and Practice Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK;Dietetic and Nutrition Center, M. Bufalini Hospital, Cesena, Italy;Dipartimento di Salute della Donna e del Bambino, Università di Padova, Padua, Italy;International Center for the Assessment of Nutritional Status (ICANS), Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan, Via Sandro Botticelli 21, 20133, Milan, Italy;International Center for the Assessment of Nutritional Status (ICANS), Department of Food, Environmental and Nutritional Sciences (DeFENS), University of Milan, Via Sandro Botticelli 21, 20133, Milan, Italy;Obesity Unit and Laboratory of Nutrition and Obesity Research, Department of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano, Milan, Italy;Pediatric Neurology and Muscle Disease Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy;SAPRE-UONPIA, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy;UO Neurologia dello Sviluppo, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy;The Dubowitz Neuromuscular Centre, UCL NIHR GOSH Biomedical Research Centre, UCL Great Ormond Street Institute of Child Health, London, UK;Unità di Malattie Neuromuscolari e Neurodegenerative, Laboratorio di Medicina Molecolare, Dipartimento di Neuroscienze e Neuroriabilitazione, IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy;
关键词: Spinal muscular atrophy;    Growth;    Percentiles;    Nutritional status;   
DOI  :  10.1186/s13023-021-02015-9
来源: Springer
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【 摘 要 】

BackgroundSpinal muscular atrophy (SMA) is a neuromuscular disorder characterized by muscle atrophy and weakness. SMA type 1 (SMA1) is the most severe form: affected infants are unable to sit unaided; SMA type 2 (SMA2) children can sit, but are not able to walk independently. The Standards of Care has improved quality of life and the increasing availability of disease-modifying treatments is progressively changing the natural history; so, the clinical assessment of nutritional status has become even more crucial. Aims of this multicenter study were to present the growth pattern of treatment-naïve SMA1 and SMA2, and to compare it with the general growth standards.ResultsBody Weight (BW, kg) and Supine Length (SL, cm) were collected using a published standardized procedure. SMA-specific growth percentiles curves were developed and compared to the WHO reference data. We recruited 133 SMA1 and 82 SMA2 (48.8% females). Mean ages were 0.6 (0.4–1.6) and 4.1 (2.1–6.7) years, respectively. We present here a set of disease-specific percentiles curves of BW, SL, and BMI-for-age for girls and boys with SMA1 and SMA2. These curves show that BW is significantly lower in SMA than healthy peers, while SL is more variable. BMI is also typically lower in both sexes and at all ages.ConclusionsThese data on treatment-naïve patients point toward a better understanding of growth in SMA and could be useful to improve the clinical management and to assess the efficacy of the available and forthcoming therapies not only on motor function, but also on growth.

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