患有肾病性胱氨酸沉积症的儿童和年轻人皮质受损,肌肉质量下降。

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2024-08-21 DOI:10.1093/jbmr/zjae092
Susanne Bechtold-Dalla Pozza, Simon Lemster, Nadine Herzig, Katharina Vill, Ilja Dubinski, Katharina Hohenfellner
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引用次数: 0

摘要

肾病性胱氨酸病是一种孤儿型常染色体隐性遗传溶酶体储积病,其特点是缺乏胱氨酸转运蛋白--胱抑素,从而导致组织损伤,主要是肾脏和角膜损伤。随着半胱胺胱氨酸消耗疗法的引入以及患者有可能存活至成年,骨骼并发症带来的新挑战令人担忧,而有关骨骼发育的数据却十分稀少。本研究旨在获得更多有关这些患者骨密度和几何形状的信息。研究人员对 51 名经遗传证实患有肾病性胱氨酸沉积症的患者(29 名男性,22 名女性)进行了临床评估,包括病史、体格检查、握力测量、生化和影像学研究。对骨质密度、骨骼几何形状和肌肉横截面积进行了测量,并对肌肉进行了评估。结果与特定年龄和性别的参考数据进行了比较。身高(平均值[M] = -1.75, 标准差[SD] = 1.43)、体重(平均值[M] = -1.67, 标准差[SD] = 1.29)和体重指数(平均值[M] = -0.98,标准差[SD] = 1.29)的 Z 值均低于参考数据。髓质横截面积(CSA)和皮质密度 z 值没有受到影响(分别为中=0.12,标度=1.56 和中=-0.25,标度=1.63),但皮质 CSA z 值和力量应变指数(SSI)有所降低(中=-2.16,标度=1.08,中=-2.07,标度=1.08)。肌肉缺损表现为肌肉CSA(中值=-2.43,标度值=1.27)和握力(中值=-3.01,标度值=1.10)的z值降低,以及跳跃力(比参考值低34%)降低。多元回归分析表明,肌肉质量与髓质CSA和SSI有关,但与皮质CSA无关。虽然骨密度参数正常,但骨骼几何形状发生了改变,导致皮质变薄,可能会影响骨强度。肌肉无力是导致骨几何形状改变的部分原因,可能成为潜在的治疗目标。
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Cortical impairment and reduced muscle mass in children and young adults with nephropathic cystinosis.

Nephropathic cystinosis is an orphan autosomal recessive lysosomal storage disease characterized by a deficiency of cystinosin, a cystine transporter protein, leading to tissue damage, primarily in the kidney and cornea. With the introduction of cystine-depleting therapy with cysteamine and the possibility to survive to adulthood, new challenges of skeletal complications are a concern, with sparse data available regarding bone development. The aim of the current study was to gain more information on bone density and geometry in these patients. Fifty-one patients (29 males, 22 females) with genetically proven nephropathic cystinosis were clinically evaluated with a medical history, physical examination, grip strength measurements, and biochemical and imaging studies. Bone mineral density, bone geometry, and muscle cross sectional area were measured, and muscle was evaluated. Results were compared with age- and gender-specific reference data. Z-scores for height (mean [M] = -1.75, standard deviation [SD] = 1.43), weight (M = -1.67, SD = 1.29), and BMI (M = -0.98, SD = 1.29) were lower than reference data. Medullary cross-sectional area (CSA) and cortical density z-scores were not compromised (M = 0.12, SD = 1.56 and M = -0.25, SD = 1.63, respectively), but cortical CSA z-scores and Strength-Strain Index (SSI) were reduced (M = -2.16, SD = 1.08, M = -2.07, SD = 1.08). Muscular deficits were reflected by reduced z-scores for muscle CSA (M = -2.43, SD = 1.27) and grip strength (M = -3.01, SD = 1.10), along with jump force (34% lower than reference value). Multiple regression analyses indicated an association of muscle mass with medullary CSA and SSI, but not with cortical CSA. While bone density parameters were normal, bone geometry was altered, resulting in a thinner cortex with possible impact on bone strength. Muscle weakness be partially responsible for altered bone geometry and could provide a potential treatment target.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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