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儿童骨骼疾病中的肌肉-骨骼相互作用。

Muscle-Bone Interactions in Pediatric Bone Diseases.

机构信息

Shriners Hospital for Children, 1003 Boulevard Decarie, Montreal, QC, H4A 0A9, Canada.

出版信息

Curr Osteoporos Rep. 2017 Oct;15(5):425-432. doi: 10.1007/s11914-017-0396-6.


DOI:10.1007/s11914-017-0396-6
PMID:28856575
Abstract

PURPOSE: Here, we review the skeletal effects of pediatric muscle disorders as well as muscle impairment in pediatric bone disorders. RECENT FINDINGS: When starting in utero, muscle disorders can lead to congenital multiple contractures. Pediatric-onset muscle weakness such as cerebral palsy, Duchenne muscular dystrophy, spinal muscular atrophy, or spina bifida typically are associated with small diameter of long-bone shafts, low density of metaphyseal bone, and increased fracture incidence in the lower extremities, in particular, the distal femur. Primary bone diseases can affect muscles through generic mechanisms, such as decreased physical activity or in disease-specific ways. For example, the collagen defect underlying the bone fragility of osteogenesis imperfecta may also affect muscle force generation or transmission. Transforming growth factor beta released from bone in Camurati Engelman disease may decrease muscle function. FUTURE DIRECTIONS: Considering muscle-bone interactions does not only contribute to the understanding of musculoskeletal disorders but also can identify new targets for therapeutic interventions.

摘要

目的:本文回顾了儿科肌肉疾病的骨骼效应以及儿科骨骼疾病中的肌肉损伤。

最近的发现:当从子宫内开始时,肌肉疾病可能导致先天性多发性挛缩。儿科发病的肌肉无力,如脑瘫、杜氏肌营养不良症、脊髓性肌萎缩症或脊柱裂,通常与长骨干直径较小、干骺端骨密度低以及下肢,特别是股骨远端骨折发生率增加有关。原发性骨病可通过一般机制(如体力活动减少)或特定疾病机制影响肌肉。例如,成骨不全症骨脆性的胶原缺陷也可能影响肌肉力量的产生或传递。卡穆拉蒂-恩格尔曼病中从骨骼释放的转化生长因子β可能会降低肌肉功能。

未来方向:考虑肌肉-骨骼相互作用不仅有助于理解肌肉骨骼疾病,还可以确定治疗干预的新靶点。

相似文献

[1]
Muscle-Bone Interactions in Pediatric Bone Diseases.

Curr Osteoporos Rep. 2017-10

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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Inflammation-induced leg length discrepancy in children: from molecular mechanisms to clinical implications.

Front Med (Lausanne). 2025-5-20

[2]
Asymmetry in the Onset of Paraspinal Muscles Activity Differs in Adolescents With Idiopathic Scoliosis Compared With Those With a Symmetrical Spine.

Clin Orthop Relat Res. 2025-6-1

[3]
Low muscle density in children with osteogenesis imperfecta using opportunistic low-dose chest CT: a case-control study.

BMC Musculoskelet Disord. 2024-6-18

[4]
The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy.

Dis Model Mech. 2024-4-1

[5]
Bone Health Status of Children with Spinal Muscular Atrophy.

J Bone Metab. 2023-11

[6]
Compromised Muscle Properties in a Severe Hypophosphatasia Murine Model.

Int J Mol Sci. 2023-11-2

[7]
Enhanced contrast synchrotron X-ray microtomography for describing skeleton-associated soft tissue defects in zebrafish mutants.

Front Endocrinol (Lausanne). 2023

[8]
A Scoping Review of the Recent Clinical Practice Regarding the Evaluation of Bone Mineral Density in Children and Adolescents with Neuromuscular Diseases.

Medicina (Kaunas). 2023-2-8

[9]
Impact of X-Linked Hypophosphatemia on Muscle Symptoms.

Genes (Basel). 2022-12-19

[10]
Bone, fat, and muscle interactions in health and disease.

Arch Endocrinol Metab. 2022-11-11

本文引用的文献

[1]
Long-Term Outcome of Interdisciplinary Management of Patients with Duchenne Muscular Dystrophy Receiving Daily Glucocorticoid Treatment.

J Pediatr. 2017-3

[2]
The time to and determinants of first fractures in boys with Duchenne muscular dystrophy.

Osteoporos Int. 2016-10-24

[3]
Cortical bone deficit and fat infiltration of bone marrow and skeletal muscle in ambulatory children with mild spastic cerebral palsy.

Bone. 2017-1

[4]
Asfotase alfa therapy for children with hypophosphatasia.

JCI Insight. 2016-6-16

[5]
Burden of disease in adult patients with hypophosphatasia: Results from two patient-reported surveys.

Metabolism. 2016-7-19

[6]
Bone health measures in glucocorticoid-treated ambulatory boys with Duchenne muscular dystrophy.

Neuromuscul Disord. 2016-11

[7]
Fractures in spina bifida from childhood to young adulthood.

Osteoporos Int. 2017-1

[8]
Current and emerging treatment strategies for Duchenne muscular dystrophy.

Neuropsychiatr Dis Treat. 2016-7-22

[9]
Osteogenesis imperfecta in children and adolescents-new developments in diagnosis and treatment.

Osteoporos Int. 2016-12

[10]
Fracture Rates and Fracture Sites in Patients With Osteogenesis Imperfecta: A Nationwide Register-Based Cohort Study.

J Bone Miner Res. 2017-1

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