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超越肌肉无力:解读杜氏肌营养不良症中的内分泌和代谢功能障碍,一篇叙述性综述

Beyond Muscle Weakness: Unraveling Endocrine and Metabolic Dysfunctions in Duchenne Muscular Dystrophy, a Narrative Review.

作者信息

Cannalire Giuseppe, Biasucci Giacomo, Sambati Vanessa, Toschetti Tommaso, Bellani Arianna Maria, Shulhai Anna-Mariia, Casadei Federica, Di Bari Erika Rita, Ferraboschi Francesca, Parenti Cecilia, Pera Maria Carmela, Esposito Susanna, Street Maria Elisabeth

机构信息

Pediatrics and Neonatology Unit, University of Parma, Guglielmo da Saliceto Hospital, 29121 Piacenza, Italy.

Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.

出版信息

Biomedicines. 2025 Jul 1;13(7):1613. doi: 10.3390/biomedicines13071613.

Abstract

Duchenne muscular dystrophy (DMD) is a severe X-linked neuromuscular disorder caused by mutations in the gene, leading to progressive muscle degeneration, loss of ambulation, and multi-systemic complications. Beyond its impact on mobility, DMD is associated with significant endocrine and metabolic dysfunctions that develop over time. To provide a comprehensive analysis of growth disturbances, endocrine dysfunctions, and metabolic complications in DMD including bone metabolism, considering the underlying mechanisms, clinical implications, and management strategies for daily clinical guidance. In this narrative review, an evaluation of the literature was conducted by searching the Medline database via the PubMed, Scopus, and Web of Science interfaces. Growth retardation is a hallmark feature of DMD, with patients exhibiting significantly shorter stature compared to their healthy peers. This is exacerbated by long-term glucocorticoid therapy, which disrupts the growth hormone/insulin-like growth factor-1 (GH/IGF-1) axis and delays puberty. Obesity prevalence follows a biphasic trend, with increased risk in early disease stages due to reduced mobility and corticosteroid use, followed by a decline in body mass index (BMI) in later stages due to muscle wasting. Metabolic complications, including insulin resistance, altered lipid metabolism, and hepatic steatosis, further characterize disease burden. Osteoporosis and increased fracture risk, primarily due to reduced mechanical loading and glucocorticoid-induced bone resorption, are major concerns, needing early screening and intervention. The RANK/RANKL/OPG signaling pathway has emerged as a critical factor in bone deterioration, providing potential therapeutic targets for improving skeletal health. Growth and endocrine disorders in DMD are complex and multifactorial, requiring proactive monitoring and early intervention. Addressing these issues requires a multidisciplinary approach integrating endocrine, nutritional, and bone health management. Further research is essential to refine treatment strategies that mitigate growth and metabolic disturbances while preserving overall patient well-being.

摘要

杜兴氏肌肉营养不良症(DMD)是一种严重的X连锁神经肌肉疾病,由该基因的突变引起,导致进行性肌肉退化、行走能力丧失和多系统并发症。除了对行动能力的影响外,DMD还与随着时间推移而出现的显著内分泌和代谢功能障碍有关。为了全面分析DMD中的生长障碍、内分泌功能障碍和代谢并发症,包括骨代谢,同时考虑其潜在机制、临床意义和日常临床指导的管理策略。在这篇叙述性综述中,通过PubMed、Scopus和Web of Science界面搜索Medline数据库对文献进行了评估。生长发育迟缓是DMD的一个标志性特征,与健康同龄人相比,患者身高明显更矮。长期糖皮质激素治疗会加剧这种情况,它会破坏生长激素/胰岛素样生长因子-1(GH/IGF-1)轴并延迟青春期。肥胖患病率呈双相趋势,疾病早期阶段由于活动减少和使用皮质类固醇,风险增加,而后期由于肌肉萎缩,体重指数(BMI)下降。代谢并发症,包括胰岛素抵抗、脂质代谢改变和肝脂肪变性,进一步加重了疾病负担。骨质疏松症和骨折风险增加,主要是由于机械负荷减少和糖皮质激素诱导的骨吸收,是主要关注点,需要早期筛查和干预。RANK/RANKL/OPG信号通路已成为骨退化的关键因素,为改善骨骼健康提供了潜在的治疗靶点。DMD中的生长和内分泌紊乱是复杂且多因素的,需要积极监测和早期干预。解决这些问题需要一种综合内分泌、营养和骨骼健康管理的多学科方法。进一步的研究对于完善治疗策略至关重要,这些策略既能减轻生长和代谢紊乱,又能维护患者的整体健康。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bdc/12292557/3a4327be8469/biomedicines-13-01613-g001.jpg

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