杜氏肌营养不良患者骨密度与心血管功能的关系:一项回顾性队列研究。

Tara Kervin, Mathula Thangarajh
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引用次数: 1

摘要

杜氏肌营养不良症(DMD)是一种x连锁遗传疾病,导致男孩进行性骨骼和心肌无力。心功能障碍是DMD患者常见的死亡原因。糖皮质激素是治疗DMD的标准药物。长期使用口服糖皮质激素的DMD是复杂的骨质健康状况不佳。流行病学研究表明,骨密度(BMD)的丧失与心血管疾病(包括冠状动脉和脑血管疾病)之间存在生物学联系。低骨密度与心功能障碍是否发生在DMD男孩中还没有研究。本回顾性队列研究的目的是研究DMD患者骨密度与心血管健康之间的关系。方法:回顾性分析某三级学术医疗中心的去识别病历。采用双能x线吸收仪(DEXA)扫描测量全身骨密度,超声心动图测量左室射血分数(LVEF)。采用线性回归评价BMD与LVEF之间的关系。结果:对32例患有DMD的男孩进行数据分析。获得基线骨密度测量的平均年龄为11±3 (SD)岁。最差LVEF在基线BMD测量后平均23.7±21.8 (SD)个月测量。基线BMD z-score与最差LVEF之间的最终调整线性回归关系无统计学意义(ß=0.41, p值=0.6455)。讨论:在这组患有DMD的男孩中,直到79个月后,BMD与LVEF功能障碍无关。未来的研究需要更长的纵向随访期来评估DMD患者骨密度与心血管疾病之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Relationship Between Bone Mineral Density and Cardiovascular Function in Duchenne Muscular Dystrophy: A Retrospective Cohort Study.

The Relationship Between Bone Mineral Density and Cardiovascular Function in Duchenne Muscular Dystrophy: A Retrospective Cohort Study.

Introduction: Duchenne muscular dystrophy (DMD) is an X-linked genetic disorder that causes progressive skeletal and cardiac muscle weakness in boys. Cardiac dysfunction is a frequent cause of death in DMD. Glucocorticoids are the standard of care in DMD. The long-term use of oral glucocorticoids in DMD is complicated by poor bone health. Epidemiological studies suggest a biological link between the loss of bone mineral density (BMD) and cardiovascular disease, including coronary artery and cerebrovascular diseases. Whether an association between low BMD and cardiac dysfunction occurs in DMD boys has not yet been studied. The objective of this retrospective cohort study was to examine the relationship between BMD and cardiovascular health in DMD.

Methods: Retrospective data analyses was performed from de-identified medical records from a tertiary academic medical center. Whole body BMD was measured using dual-energy xray absorptiometry (DEXA) scan and left ventricular ejection fraction (LVEF) was measured using echocardiogram. Linear regression was used to evaluate the relationship between BMD and LVEF.

Results: Data was analyzed from a total of 32 boys with DMD. The mean age at which baseline BMD measurements was obtained of 11±3 (SD) years. The worst LVEF was measured at a mean of 23.7±21.8 (SD) months after the baseline BMD measurement. The final adjusted linear regression of the relationship between baseline BMD z-score and worst LVEF was not statistically significant (ß=0.41, p‑value=0.6455).

Discussion: In this cohort of boys with DMD, BMD was not associated with LVEF dysfunction up to 79 months later. Future research with a longer longitudinal follow-up period is warranted to evaluate the relationship between BMD and cardiovascular disease in DMD.

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