• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脊髓性肌萎缩症患儿的营养状况及营养摄入挑战

Nutritional Status and Nutrient Intake Challenges in Children With Spinal Muscular Atrophy.

作者信息

Mehta Nilesh M, Newman Haley, Tarrant Stacey, Graham Robert J

机构信息

Division of Critical Care Medicine, Department of Anesthesiology, Perioperative, and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts; Center for Nutrition, Boston Children's Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Division of Critical Care Medicine, Department of Anesthesiology, Perioperative, and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts.

出版信息

Pediatr Neurol. 2016 Apr;57:80-3. doi: 10.1016/j.pediatrneurol.2015.12.015. Epub 2015 Dec 24.

DOI:10.1016/j.pediatrneurol.2015.12.015
PMID:26803333
Abstract

BACKGROUND

Nutrition is recognized as a core component of multidisciplinary care for patients with spinal muscular atrophy, but specific nutritional challenges in this population are not well described. We aimed to describe the nutritional status and nutrient intake in children with spinal muscular atrophy.

METHODS

We performed a retrospective medical record review of prospectively collected data from children with spinal muscular atrophy followed at a multidisciplinary clinic at a tertiary referral center. We collected data including clinical parameters; anthropometrics, including weight, height, and body mass index (BMI); and 24-hour dietary intake records in all children followed in the clinic. Available data were found in records from the dietitian as part of a standard evaluation process, and additional clinical data were acquired from patient medical records. Subjects were classified based on spinal muscular atrophy type, and nutritional intake data were compared with dietary reference intakes for gender and age. Z-scores were calculated for weight for age (WAZ), height for age, and BMI (BMIZ) using the World Health Organization AnthroPlus software with appropriate World Health Organization reference growth standards. Subjects were classified as malnourished if their WAZ was <-2 or >+2. Anthropometric measurements were obtained at first visit and at a follow-up visit at an average of a 3-year interval between the clinic visits. A decline of more than 0.5 WAZ over this period was defined a priori as significant nutritional deterioration.

RESULTS

We analyzed data from 60 subjects, 26 (43%) female, with median age 5.5 years (interquartile range 2 years to 12 years). The cohort consisted of children with spinal muscular atrophy type 1 (28 %), type 2 (45 %), and type 3 (27 %). At the first clinic visit, nine (15%) patients were malnourished. Thirteen (23%) subjects had a significant decline in WAZ from -0.35 (-1.31 to 0.58) to -1.04 (-2.15 to 0.02) at follow-up after approximately 3 years. A third of these subjects were already malnourished at first visit. A significant decline in BMIZ was noted in 47% of the cohort, and the prevalence of severe malnutrition (BMIZ < -3) increased from 2% to 17% after 3 years. In children receiving specialized enteral nutrition via a feeding tube, overfeeding was recorded in 29% and underfeeding was recorded in 35%. Suboptimal vitamin D intake was recorded in 35% of patients with enteral feeding device.

CONCLUSIONS

Malnutrition was prevalent in children with spinal muscular atrophy, and nearly half the cohort demonstrated nutritional deterioration over time. Energy, protein, and vitamin D intakes were inadequate in a majority of the cohort. Underfeeding was highly prevalent, but overfeeding was also present in a third of the enterally fed cohort. Future studies describing optimal nutrient requirements and body composition variables in this group are required.

摘要

背景

营养被认为是脊髓性肌萎缩症患者多学科护理的核心组成部分,但该人群具体的营养挑战尚未得到充分描述。我们旨在描述脊髓性肌萎缩症患儿的营养状况和营养摄入情况。

方法

我们对前瞻性收集的数据进行了回顾性病历审查,这些数据来自于一家三级转诊中心多学科诊所随访的脊髓性肌萎缩症患儿。我们收集了包括临床参数;人体测量数据,包括体重、身高和体重指数(BMI);以及该诊所随访的所有儿童的24小时饮食摄入记录。作为标准评估过程的一部分,营养师记录中的可用数据被收集,另外的临床数据则从患者病历中获取。根据脊髓性肌萎缩症类型对受试者进行分类,并将营养摄入数据与按性别和年龄划分的膳食参考摄入量进行比较。使用世界卫生组织AnthroPlus软件及适当的世界卫生组织参考生长标准,计算年龄别体重(WAZ)、年龄别身高和BMI(BMIZ)的Z评分。如果受试者的WAZ<-2或>+2,则被分类为营养不良。在首次就诊时以及平均间隔3年的随访就诊时进行人体测量。在此期间WAZ下降超过0.5被预先定义为显著的营养恶化。

结果

我们分析了60名受试者的数据,其中26名(43%)为女性,中位年龄5.5岁(四分位间距为2岁至12岁)。该队列包括1型脊髓性肌萎缩症患儿(28%)、2型(45%)和3型(27%)。在首次诊所就诊时,9名(15%)患者营养不良。在大约3年的随访后,13名(23%)受试者的WAZ从-0.35(-1.31至0.58)显著下降至-1.04(-2.15至0.02)。这些受试者中有三分之一在首次就诊时就已经营养不良。47%的队列中观察到BMIZ显著下降,严重营养不良(BMIZ<-3)的患病率在3年后从2%增加到17%。在通过喂养管接受特殊肠内营养的儿童中,29%记录为喂养过度,35%记录为喂养不足。35%使用肠内喂养装置的患者维生素D摄入不足。

结论

营养不良在脊髓性肌萎缩症患儿中普遍存在,近一半的队列随着时间推移出现营养恶化。该队列中的大多数人能量、蛋白质和维生素D摄入不足。喂养不足非常普遍,但三分之一接受肠内喂养的队列中也存在喂养过度的情况。需要进一步开展研究来描述该群体的最佳营养需求和身体成分变量。

相似文献

1
Nutritional Status and Nutrient Intake Challenges in Children With Spinal Muscular Atrophy.脊髓性肌萎缩症患儿的营养状况及营养摄入挑战
Pediatr Neurol. 2016 Apr;57:80-3. doi: 10.1016/j.pediatrneurol.2015.12.015. Epub 2015 Dec 24.
2
Comprehensive nutritional and metabolic assessment in patients with spinal muscular atrophy: Opportunity for an individualized approach.脊髓性肌萎缩症患者的全面营养代谢评估:个体化治疗的机会。
Neuromuscul Disord. 2018 Jun;28(6):512-519. doi: 10.1016/j.nmd.2018.03.009. Epub 2018 Mar 19.
3
Phenotype assessment in neurologically impaired paediatric patients: Impact of a nutrition intervention protocol.神经损伤儿科患者表型评估:营养干预方案的影响。
Clin Nutr. 2021 Dec;40(12):5734-5741. doi: 10.1016/j.clnu.2021.10.011. Epub 2021 Oct 23.
4
Nutrition status survey of type 2 and 3 spinal muscular atrophy in Chinese population.中国人群 2 型和 3 型脊肌萎缩症的营养状况调查。
Nutr Neurosci. 2022 Jul;25(7):1488-1494. doi: 10.1080/1028415X.2020.1871212. Epub 2021 Jan 23.
5
[The overall nutritional quality of the diet is reflected in the growth of Nigerian children].尼日利亚儿童的生长情况反映了其饮食的总体营养质量。
Sante. 1999 Jan-Feb;9(1):23-31.
6
Nutritional status of rural children in the Lesotho Highlands.莱索托高地农村儿童的营养状况。
East Afr Med J. 1997 Nov;74(11):680-9.
7
Dietary intake and clinical response of hospitalized patients with acute diarrhea.急性腹泻住院患者的饮食摄入与临床反应
Food Nutr Bull. 2008 Mar;29(1):25-31. doi: 10.1177/156482650802900103.
8
A high prevalence of abnormal nutrition parameters found in predialysis end-stage kidney disease: is it a result of uremia or poor eating habits?在透析前终末期肾病患者中发现高比例的营养参数异常:这是尿毒症的结果还是不良饮食习惯所致?
J Ren Nutr. 2014 Sep;24(5):292-302. doi: 10.1053/j.jrn.2014.03.008. Epub 2014 Jul 10.
9
Nutritional status and dietary intakes of children aged 6 months to 12 years: findings of the Nutrition Survey of Malaysian Children (SEANUTS Malaysia).6 个月至 12 岁儿童的营养状况和饮食摄入:马来西亚儿童营养调查(SEANUTS Malaysia)的结果。
Br J Nutr. 2013 Sep;110 Suppl 3:S21-35. doi: 10.1017/S0007114513002092.
10
Breast-feeding and the nutritional status of nursing children in Chile.智利的母乳喂养与哺乳期儿童的营养状况
Bull Pan Am Health Organ. 1996 Jun;30(2):125-33.

引用本文的文献

1
Epigenetic regulation in spinal muscular atrophy: emerging areas and future directions.脊髓性肌萎缩症中的表观遗传调控:新出现的领域和未来方向。
Orphanet J Rare Dis. 2025 Jul 10;20(1):353. doi: 10.1186/s13023-025-03857-3.
2
Adiponectin and Leptin-Considerations in Adult Patients with Spinal Muscular Atrophy Type 3.脂联素和瘦素——对成年3型脊髓性肌萎缩症患者的考量
Diagnostics (Basel). 2025 Feb 21;15(5):529. doi: 10.3390/diagnostics15050529.
3
Swallowing function in patients with spinal muscular atrophy before and after the introduction of new gene-based therapies: what has changed?
脊髓性肌萎缩症患者在引入新的基因疗法前后的吞咽功能:有哪些变化?
Neurol Sci. 2025 Mar;46(3):1137-1149. doi: 10.1007/s10072-024-07883-0. Epub 2024 Dec 4.
4
Glucose and Lipid Metabolism Disorders in Adults with Spinal Muscular Atrophy Type 3.3型脊髓性肌萎缩症成人患者的糖脂代谢紊乱
Diagnostics (Basel). 2024 Sep 19;14(18):2078. doi: 10.3390/diagnostics14182078.
5
Exploring the Influence of Concurrent Nutritional Therapy on Children with Spinal Muscular Atrophy Receiving Nusinersen Treatment.探索同步营养治疗对接受诺西那生治疗的脊髓性肌萎缩症患儿的影响。
Children (Basel). 2024 Jul 23;11(8):886. doi: 10.3390/children11080886.
6
Elucidating the role of diet in maintaining gut health to reduce the risk of obesity, cardiovascular and other age-related inflammatory diseases: recent challenges and future recommendations.阐明饮食在维持肠道健康以降低肥胖、心血管和其他与年龄相关的炎症性疾病风险方面的作用:近期的挑战和未来的建议。
Gut Microbes. 2024 Jan-Dec;16(1):2297864. doi: 10.1080/19490976.2023.2297864. Epub 2024 Jan 4.
7
Dietary Implications of the Bidirectional Relationship between the Gut Microflora and Inflammatory Diseases with Special Emphasis on Irritable Bowel Disease: Current and Future Perspective.肠道微生物群与炎症性疾病的双向关系对饮食的影响:特别强调肠易激综合征:现状和未来展望。
Nutrients. 2023 Jun 29;15(13):2956. doi: 10.3390/nu15132956.
8
Body mass index in type 2 spinal muscular atrophy: a longitudinal study.2 型脊髓性肌萎缩症患者的体重指数:一项纵向研究。
Eur J Pediatr. 2022 May;181(5):1923-1932. doi: 10.1007/s00431-021-04325-3. Epub 2022 Jan 19.
9
The Antisense Oligonucleotide Nusinersen for Treatment of Spinal Muscular Atrophy.用于治疗脊髓性肌萎缩症的反义寡核苷酸药物诺西那生钠
Orthop Rev (Pavia). 2021 Jun 19;13(2):24934. doi: 10.52965/001c.24934. eCollection 2021.
10
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth Disease.体质指数与腓骨肌萎缩症患儿残疾的相关性。
Neurology. 2021 Oct 26;97(17):e1727-e1736. doi: 10.1212/WNL.0000000000012725. Epub 2021 Sep 7.