Muscle size and density are independently associated with death after hip fracture: A prospective cohort study

IF 8.9 1区 医学
Ling Wang, Minghui Yang, Yufeng Ge, Yandong Liu, Yongbin Su, Zhe Guo, Pengju Huang, Jian Geng, Gang Wang, Glen M. Blake, Bo He, Lu Yin, Xiaoguang Cheng, Xinbao Wu, Klaus Engelke, Annegreet G. Vlug
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引用次数: 0

Abstract

Background

Mortality following hip fracture is high and incompletely understood. We hypothesize that hip musculature size and quality are related to mortality following hip fracture. This study aims to investigate the associations of hip muscle area and density from hip CT with death following hip fracture as well as assess the dependence of this association on time after hip fracture.

Methods

In this secondary analysis of the prospectively collected CT images and data from the Chinese Second Hip Fracture Evaluation, 459 patients were enrolled between May 2015 and June 2016 and followed up for a median of 4.5 years. Muscle cross-sectional area and density were measured of the gluteus maximus (G.MaxM) and gluteus medius and minimus (G.Med/MinM) and aBMD of the proximal femur. The Goutallier classification (GC) was used for qualitatively assessing muscle fat infiltration. Separate Cox models were used to predict mortality risk adjusted for covariates.

Results

At the end of the follow-up, 85 patients were lost, 81 patients (64% women) had died, and 293 (71% women) survived. The mean age of non-surviving patients at death (82.0 ± 8.1 years) was higher than that of the surviving patients (74.4 ± 9.9 years). The Parker Mobility Score and the American Society of Anesthesiologists scores of the patients that died were respectively lower and higher compared to the surviving patients. Hip fracture patients received different surgical procedures, and no significant difference in the percentage of hip arthroplasty was observed between the dead and the surviving patients (P = 0.11). The cumulative survival was significantly lower for patients with low G.MaxM area and density and low G.Med/MinM density, independent of age and clinical risk scores. The GC grades were not associated with the mortality after hip fracture. Muscle density of both G.MaxM (adj. HR 1.83; 95% CI, 1.06–3.17) and G.Med/MinM (adj. HR 1.98; 95% CI, 1.14–3.46) was associated with mortality in the 1st year after hip fracture. G.MaxM area (adj. HR 2.11; 95% CI, 1.08–4.14) was associated with mortality in the 2nd and later years after hip fracture.

Conclusion

Our results for the first time show that hip muscle size and density are associated with mortality in older hip fracture patients, independent of age and clinical risk scores. This is an important finding to better understand the factors contributing to the high mortality in older hip fracture patients and to develop better future risk prediction scores that include muscle parameters.

肌肉大小和密度与髋部骨折后死亡独立相关:一项前瞻性队列研究
背景:髋部骨折后的死亡率很高,目前还不完全清楚。我们假设髋部肌肉组织的大小和质量与髋部骨折后的死亡率有关。本研究旨在探讨髋部CT显示的髋部肌肉面积和密度与髋部骨折后死亡的关系,并评估这种关系与髋部骨折后时间的依赖关系。方法对2015年5月至2016年6月期间前瞻性收集的中国第二次髋部骨折评估的CT图像和数据进行二次分析,纳入459例患者,中位随访时间为4.5年。测量股骨近端臀大肌(G.MaxM)、臀中、小肌(G.Med/MinM)和aBMD的肌肉横截面积和密度。采用Goutallier分级法(GC)定性评价肌肉脂肪浸润。使用单独的Cox模型预测经协变量调整后的死亡风险。结果随访结束时,丢失85例,死亡81例(女性占64%),存活293例(女性占71%)。非存活患者死亡时平均年龄(82.0±8.1岁)高于存活患者(74.4±9.9岁)。与存活患者相比,死亡患者的派克活动能力评分和美国麻醉医师协会评分分别较低和较高。髋部骨折患者接受不同的手术方式,死亡和存活患者的髋关节置换术百分比无显著差异(P = 0.11)。与年龄和临床风险评分无关,低g.m max面积和密度以及低g.m med /MinM密度的患者累积生存期显著降低。GC分级与髋部骨折后的死亡率无关。G.MaxM的肌肉密度(adj. HR 1.83;95% CI, 1.06-3.17)和g.m d/MinM (adj. HR 1.98;95% CI, 1.14-3.46)与髋部骨折后1年的死亡率相关。g .最大面积(adj. HR 2.11;95% CI, 1.08-4.14)与髋部骨折后2年及以后的死亡率相关。结论我们的研究结果首次表明,老年髋部骨折患者的髋部肌肉大小和密度与死亡率相关,与年龄和临床风险评分无关。这是一个重要的发现,可以更好地了解导致老年髋部骨折患者高死亡率的因素,并开发包括肌肉参数在内的更好的未来风险预测评分。
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来源期刊
Journal of Cachexia, Sarcopenia and Muscle
Journal of Cachexia, Sarcopenia and Muscle Medicine-Orthopedics and Sports Medicine
自引率
12.40%
发文量
0
期刊介绍: The Journal of Cachexia, Sarcopenia, and Muscle is a prestigious, peer-reviewed international publication committed to disseminating research and clinical insights pertaining to cachexia, sarcopenia, body composition, and the physiological and pathophysiological alterations occurring throughout the lifespan and in various illnesses across the spectrum of life sciences. This journal serves as a valuable resource for physicians, biochemists, biologists, dieticians, pharmacologists, and students alike.
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