临床儿科杂志 ›› 2022, Vol. 40 ›› Issue (3): 235-240.doi: 10.12372/jcp.2022.21e1244
• 继续医学教育 • 上一篇
收稿日期:
2021-08-30
出版日期:
2022-03-15
发布日期:
2022-03-09
通讯作者:
马鸣
E-mail:maming73@zju.edu.cn
基金资助:
WANG Wenqiao1, MAO Shanshan2, MA Ming1()
Received:
2021-08-30
Published:
2022-03-15
Online:
2022-03-09
Contact:
MA Ming
E-mail:maming73@zju.edu.cn
摘要:
脊髓性肌萎缩症(SMA)是一种严重的神经肌肉疾病,因运动神经元存活基因1(SMN1)缺陷引起。由于肌肉无力、活动量少、消化道症状以及吞咽困难等原因,患儿发生营养不足和营养过剩的概率常明显高于正常儿童,因此SMA的营养管理至关重要。文章就SMA患儿的营养评估、可能出现的营养问题以及相关营养干预策略进行阐述。
王文俏, 毛姗姗, 马鸣. 脊髓性肌萎缩症患儿营养管理研究进展[J]. 临床儿科杂志, 2022, 40(3): 235-240.
WANG Wenqiao, MAO Shanshan, MA Ming. Research progress in nutritional management of children with spinal muscular atrophy[J]. Journal of Clinical Pediatrics, 2022, 40(3): 235-240.
[1] |
Ogino S, Leonard DG, Rennert H, et al. Genetic risk assessment in carrier testing for spinal muscular atrophy[J]. Am J Med Genet, 2002, 110(4): 301-307.
doi: 10.1002/(ISSN)1096-8628 |
[2] |
Pearn J. Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy[J]. J Med Genet, 1978, 15(6): 409-413.
pmid: 745211 |
[3] |
Wei X, Tan H, Yang P, et al. Notable carrier risks for individuals having two copies of SMN1 in spinal muscular atrophy families with 2-copy alleles: estimation based on Chinese meta-analysis data[J]. J Genet Couns, 2017, 26(1): 72-78.
doi: 10.1007/s10897-016-9980-7 |
[4] |
Bharucha-Goebel D, Kaufmann P. Treatment advances in spinal muscular atrophy[J]. Curr Neurol Neurosci Rep, 2017, 17(11): 91.
doi: 10.1007/s11910-017-0798-y |
[5] |
Moore GE, Lindenmayer AW, McConchie GA, et al. Describing nutrition in spinal muscular atrophy: a systematic review[J]. Neuromuscul Disord, 2016, 26(7): 395-404.
doi: 10.1016/j.nmd.2016.05.005 |
[6] | 北京医学会罕见病分会, 北京医学会医学遗传学分会, 北京医学会神经病学分会神经肌肉病学组, 等. 脊髓性肌萎缩症多学科管理专家共识[J]. 中华医学杂志, 2019, 99(19): 1460-1467. |
[7] |
Corkins MR, Griggs KC, Groh-Wargo S, et al. Standards for nutrition support: pediatric hospitalized patients[J]. Nutr Clin Pract, 2013, 28(2): 263-276.
doi: 10.1177/0884533613475822 pmid: 23449773 |
[8] |
McCarthy H, Dixon M, Crabtree I, et al. The development and evaluation of the Screening Tool for the Assessment of Malnutrition in Paediatrics (STAMP©) for use by healthcare staff[J]. J Hum Nutr Diet, 2012, 25(4): 311-318.
doi: 10.1111/j.1365-277X.2012.01234.x pmid: 22568534 |
[9] |
Hulst JM, Zwart H, Hop WC, et al. Dutch national survey to test the STRONGkids nutritional risk screening tool in hospitalized children[J]. Clin Nutr, 2010, 29(1): 106-111.
doi: 10.1016/j.clnu.2009.07.006 |
[10] |
Bertoli S, Foppiani A, De Amicis R, et al. Anthropometric measurement standardization for a multicenter nutrition survey in children with spinal muscular atrophy[J]. Eur J Clin Nutr, 2019, 73(12): 1646-1648.
doi: 10.1038/s41430-019-0392-2 pmid: 30647441 |
[11] | WHO Multicentre Growth Reference Study Group. Reliability of anthropometric measurements in the WHO Multicentre Growth Reference Study[J]. Acta Paediatr Suppl, 2006, 450: 38-46. |
[12] |
Mehta NM, Newman H, Tarrant S, et al. Nutritional status and nutrient intake challenges in children with spinal muscular atrophy[J]. Pediatr Neurol, 2016, 57: 80-83.
doi: 10.1016/j.pediatrneurol.2015.12.015 |
[13] |
Davis RH, Miller EA, Zhang RZ, et al. Responses to fasting and glucose loading in a cohort of well children with spinal muscular atrophy type II[J]. J Pediatr, 2015, 167(6): 1362-1368.e1.
doi: 10.1016/j.jpeds.2015.09.023 |
[14] |
Li YJ, Chen TH, Wu YZ, et al. Metabolic and nutritional issues associated with spinal muscular atrophy[J]. Nutrients, 2020, 12(12): 3842.
doi: 10.3390/nu12123842 |
[15] |
Fosbøl MØ, Zerahn B. Contemporary methods of body composition measurement[J]. Clin Physiol Funct Imaging, 2015, 35(2): 81-97.
doi: 10.1111/cpf.2015.35.issue-2 |
[16] |
Liu J, Yan Y, Xi B, et al. Skeletal muscle reference for Chinese children and adolescents[J]. J Cachexia Sarcopenia Muscle, 2019, 10(1): 155-164.
doi: 10.1002/jcsm.v10.1 |
[17] |
Dong H, Yan Y, Liu J, et al. Reference centiles for evaluating total body fat development and fat distribution by dual-energy x-ray absorptiometry among children and adolescents aged 3-18 years[J]. Clin Nutr, 2021, 40(3): 1289-1295.
doi: 10.1016/j.clnu.2020.08.012 |
[18] |
Martinez EE, Quinn N, Arouchon K, et al. Comprehensive nutritional and metabolic assessment in patients with spinal muscular atrophy: opportunity for an individualized approach[J]. Neuromuscul Disord, 2018, 28(6): 512-519.
doi: 10.1016/j.nmd.2018.03.009 |
[19] |
Baranello G, De Amicis R, Arnoldi MT, et al. Evaluation of body composition as a potential biomarker in spinal muscular atrophy[J]. Muscle Nerve, 2020, 61(4): 530-534.
doi: 10.1002/mus.26823 pmid: 32012296 |
[20] |
Sproule DM, Montes J, Montgomery M, et al. Increased fat mass and high incidence of overweight despite low body mass index in patients with spinal muscular atrophy[J]. Neuromuscul Disord, 2009, 19(6): 391-396.
doi: 10.1016/j.nmd.2009.03.009 |
[21] |
Weber DR, Moore RH, Leonard MB, et al. Fat and lean BMI reference curves in children and adolescents and their utility in identifying excess adiposity compared with BMI and percentage body fat[J]. Am J Clin Nutr, 2013, 98(1): 49-56.
doi: 10.3945/ajcn.112.053611 |
[22] |
Bertoli S, De Amicis R, Mastella C, et al. Spinal muscular atrophy, types I and II: what are the differences in body composition and resting energy expenditure?[J]. Clin Nutr, 2017, 36(6): 1674-1680.
doi: S0261-5614(16)31312-7 pmid: 27890489 |
[23] |
Burrows T, Goldman S, Rollo M. A systematic review of the validity of dietary assessment methods in children when compared with the method of doubly labelled water[J]. Eur J Clin Nutr, 2020, 74(5): 669-681.
doi: 10.1038/s41430-019-0480-3 pmid: 31391548 |
[24] |
Poruk KE, Davis RH, Smart AL, et al. Observational study of caloric and nutrient intake, bone density, and body composition in infants and children with spinal muscular atrophy type I[J]. Neuromuscul Disord, 2012, 22(11): 966-973.
doi: 10.1016/j.nmd.2012.04.008 |
[25] |
Zhou Y, Chen J, Gong X, et al. Nutrition status survey of type 2 and 3 spinal muscular atrophy in Chinese population[J]. Nutr Neurosci, 2021, 23: 1-7.
doi: 10.1080/1028415X.2018.1461459 |
[26] |
Baranello G, Vai S, Broggi F, et al. Evolution of bone mineral density, bone metabolism and fragility fractures in Spinal Muscular Atrophy (SMA) types 2 and 3[J]. Neuromuscul Disord, 2019, 29(7): 525-532.
doi: 10.1016/j.nmd.2019.06.001 |
[27] |
Wasserman HM, Hornung LN, Stenger PJ, et al. Low bone mineral density and fractures are highly prevalent in pediatric patients with spinal muscular atrophy regardless of disease severity[J]. Neuromuscul Disord, 2017, 27(4): 331-337.
doi: 10.1016/j.nmd.2017.01.019 |
[28] |
van Bruggen HW, Wadman RI, Bronkhorst EM, et al. Mandibular dysfunction as a reflection of bulbar involvement in SMA type 2 and 3[J]. Neurology, 2016, 86(6): 552-559.
doi: 10.1212/WNL.0000000000002348 |
[29] |
Messina S, Pane M, De Rose P, et al. Feeding problems and malnutrition in spinal muscular atrophy type II[J]. Neuromuscul Disord, 2008, 18(5): 389-393.
doi: 10.1016/j.nmd.2008.02.008 |
[30] |
Chen YS, Shih HH, Chen TH, et al. Prevalence and risk factors for feeding and swallowing difficulties in spinal muscular atrophy types II and III[J]. J Pediatr, 2012, 160(3): 447-451.
doi: 10.1016/j.jpeds.2011.08.016 |
[31] |
van der Heul AMB, Wijngaarde CA, Wadman RI, et al. Bulbar problems self-reported by children and adults with spinal muscular atrophy[J]. J Neuromuscul Dis, 2019, 6(3): 361-368.
doi: 10.3233/JND-190379 pmid: 31476167 |
[32] |
Choi YA, Suh DI, Chae JH, et al. Trajectory of change in the swallowing status in spinal muscular atrophy type I[J]. Int J Pediatr Otorhinolaryngol, 2020, 130: 109818.
doi: 10.1016/j.ijporl.2019.109818 |
[33] | 中华预防医学会儿童保健分会. 中国儿童钙营养专家共识(2019年版)[J]. 中国妇幼健康研究, 2019, 30(3): 262-269. |
[34] | 罗明, 覃洪金, 黄玉珠, 等. 儿童口腔运动及进食能力评估工具研究进展[J]. 护士进修杂志, 2020, 35(13): 1176-1179. |
[35] |
van den Engel-Hoek L, Erasmus CE, van Bruggen HW, et al. Dysphagia in spinal muscular atrophy type II: more than a bulbar problem?[J]. Neurology, 2009, 73(21): 1787-1791.
doi: 10.1212/WNL.0b013e3181c34aa6 pmid: 19933981 |
[36] |
Mercuri E, Finkel RS, Muntoni F, et al. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care[J]. Neuromuscul Disord, 2018, 28(2): 103-115.
doi: 10.1016/j.nmd.2017.11.005 |
[37] |
Davis RH, Godshall BJ, Seffrood E, et al. Nutritional practices at a glance: spinal muscular atrophy type I nutrition survey findings[J]. J Child Neurol, 2014, 29(11): 1467-1472.
doi: 10.1177/0883073813503988 |
[38] |
Wang CH, Finkel RS, Bertini ES, et al. Consensus statement for standard of care in spinal muscular atrophy[J]. J Child Neurol, 2007, 22(8): 1027-1049.
doi: 10.1177/0883073807305788 |
[39] |
Rattanachaiwong S, Singer P. Indirect calorimetry as point of care testing[J]. Clin Nutr, 2019, 38(6): 2531-2544.
doi: S0261-5614(18)32603-7 pmid: 30670292 |
[40] |
Bendavid I, Lobo DN, Barazzoni R, et al. The centenary of the Harris-Benedict equations: how to assess energy requirements best? Recommendations from the ESPEN expert group[J]. Clin Nutr, 2021, 40(3): 690-701.
doi: 10.1016/j.clnu.2020.11.012 pmid: 33279311 |
[41] |
Amano Y. Estimated basal metabolic rate and maintenance fluid volume in children: a proposal for a new equation[J]. Pediatr Int, 2020, 62(5): 522-528.
doi: 10.1111/ped.v62.5 |
[42] |
Bertoli S, De Amicis R, Bedogni G, et al. Predictive energy equations for spinal muscular atrophy type I children[J]. Am J Clin Nutr, 2020, 111(5): 983-996.
doi: 10.1093/ajcn/nqaa009 pmid: 32145012 |
[43] | 中国营养学会. 中国居民膳食营养素参考摄入量(2013版) [M]. 北京: 科学出版社, 2014: 652-660. |
[44] |
Deguise MO, Baranello G, Mastella C, et al. Abnormal fatty acid metabolism is a core component of spinal muscular atrophy[J]. Ann Clin Transl Neurol, 2019, 6(8): 1519-1532.
doi: 10.1002/acn3.v6.8 |
[45] |
Deguise MO, Chehade L, Tierney A, et al. Low fat diets increase survival of a mouse model of spinal muscular atrophy[J]. Ann Clin Transl Neurol, 2019, 6(11): 2340-2346.
doi: 10.1002/acn3.v6.11 |
[46] |
Chou E, Lindeback R, Sampaio H, et al. Nutritional practices in pediatric patients with neuromuscular disorders[J]. Nutr Rev, 2020, 78(10): 857-865.
doi: 10.1093/nutrit/nuz109 |
[47] | 中华预防医学会儿童保健分会. 中国儿童维生素A、维生素D临床应用专家共识[J]. 中国儿童保健杂志, 2021, 29(1): 110-116. |
[48] |
Laheij RJ, Sturkenboom MC, Hassing RJ, et al. Risk of community-acquired pneumonia and use of gastric acid-suppressive drugs[J]. JAMA, 2004, 292(16): 1955-1960.
doi: 10.1001/jama.292.16.1955 |
[49] |
Durkin ET, Schroth MK, Helin M, et al. Early laparoscopic fundoplication and gastrostomy in infants with spinal muscular atrophy type I[J]. J Pediatr Surg, 2008, 43(11): 2031-2037.
doi: 10.1016/j.jpedsurg.2008.05.035 pmid: 18970936 |
[50] |
Singh NN, Hoffman S, Reddi PP, et al. Spinal muscular atrophy: broad disease spectrum and sex-specific phenotypes[J]. Biochim Biophys Acta Mol Basis Dis, 2021, 1867(4): 166063.
doi: 10.1016/j.bbadis.2020.166063 |
[1] | 罗明静, 余嘉明, 王晓东, 张小玲, 余阅, 张瑜, 文飞球, 刘四喜. 424例地中海贫血患儿异基因造血干细胞移植后继发侵袭性真菌病临床分析[J]. 临床儿科杂志, 2025, 43(1): 21-28. |
[2] | 刘冬霞, 金蓉, 林荣军. 儿童重症难治性肺炎支原体肺炎并发闭塞性支气管炎危险因素分析[J]. 临床儿科杂志, 2025, 43(1): 29-34. |
[3] | 罗智强, 陈黎, 路新国, 廖建湘, 罗序峰. 中国大陆首例症状前治疗脊髓性肌萎缩症患儿43月龄随访报告[J]. 临床儿科杂志, 2025, 43(1): 40-44. |
[4] | 钟瑾虹, 王灿, 陈芳. 婴幼儿纤维支气管镜诊疗中镇静技术的研究进展[J]. 临床儿科杂志, 2025, 43(1): 50-55. |
[5] | 吴献, 刘艳, 刘昕竹, 黄晓会, 马婧, 徐阿晶, 幸小东, 蒋文高, 张健. 脊髓性肌萎缩症疾病修正治疗真实世界研究进展[J]. 临床儿科杂志, 2025, 43(1): 61-69. |
[6] | 幸小东, 刘艳, 刘昕竹, 蒋文高, 张健. 脊髓性肌萎缩症患者脊柱矫形围手术期治疗药物管理[J]. 临床儿科杂志, 2025, 43(1): 70-76. |
[7] | 蒋卫芹, 王静, 程安娜, 陈婷婷, 黄玉娟. 儿童热性惊厥急性期惊厥复发的危险因素分析[J]. 临床儿科杂志, 2025, 43(1): 8-13. |
[8] | 邱琇, 韦冬梅, 林珊珊, 夏慧敏, 周文浩. 广州出生队列研究的理念与实践[J]. 临床儿科杂志, 2024, 42(9): 747-752. |
[9] | 陈倩, 田英, 孙锟, 张军. 关注环境、立足疾病的大型出生队列研究平台[J]. 临床儿科杂志, 2024, 42(9): 753-757. |
[10] | 范建霞. 健康生命轨迹计划缘起与发展:社区-家庭-母婴多层面儿童超重与肥胖干预研究队列[J]. 临床儿科杂志, 2024, 42(9): 768-773. |
[11] | 姜涛, 李双杰, 唐莲, 欧阳文献. 慢性乙型肝炎患儿外周血MAIT细胞的免疫生物学特性[J]. 临床儿科杂志, 2024, 42(9): 787-790. |
[12] | 周洁, 刘克强, 王金玲, 王莹. MYH11延长突变导致巨膀胱-小结肠-肠蠕动不良综合征1例报告及文献复习[J]. 临床儿科杂志, 2024, 42(9): 798-804. |
[13] | 褚思嘉, 汤继宏. 儿童急性淋巴细胞白血病及其治疗所伴发的中枢神经系统损伤研究进展[J]. 临床儿科杂志, 2024, 42(9): 811-816. |
[14] | 丁亚平, 夏姗姗, 张晨美. 《2023年国际儿童肾脏营养工作组临床实践建议:儿童急性肾损伤的营养管理》解读[J]. 临床儿科杂志, 2024, 42(8): 667-672. |
[15] | 李怡蓉, 李惠萍, 高靖瑜, 肖玉华, 陈小敏, 卢艳玲, 赵娜娜, 冯晓勤. FLAG-IDA诱导化疗方案中不同剂量阿糖胞苷治疗儿童急性髓系白血病疗效比较[J]. 临床儿科杂志, 2024, 42(8): 673-677. |
|