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Software for the Diagnosis of Sarcopenia in Community-Dwelling Older Adults: Design and Validation Study

机译:社区住宅老年人诊断SARCOPENIA的软件:设计和验证研究

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Background The usual diagnosis of sarcopenia requires a dual-energy x-ray absorptiometry (DXA) exam, which has low accessibility in primary care for Latin American countries. Objective The aim of this study is to design and validate software for mobile devices (Android, IOS) and computers, based on an adapted version of the diagnostic algorithm of sarcopenia proposed by the European Working Group on Sarcopenia in Older People (EWGSOP). Methods Follow-up exams were conducted on 430 community-dwelling Chileans 60 years and older (mean 68.2 years, SD 4.9) participating in the IsaMayor and Alexandros cohorts designed to study sarcopenia and disability associated with obesity, respectively. All the participants from the cohorts were randomly selected from the registries of primary health care centers and, for this study, must have a DXA scan at baseline. The software (HTSMayor) was designed according to an adapted version of the algorithm proposed by the EWGSOP and was divided into four phases: longitudinal validation of diagnostic algorithm of sarcopenia, alpha version, beta version, and release version. The software estimates appendicular skeletal muscle mass (ASM) using an anthropometric equation or DXA measurements with Chilean cut-off points. The predictive validation of the algorithm was estimated, comparing functional limitations (at least one activity of daily living, two instrumental activities of daily living, or three mobility limitations), falls, and osteoporosis at follow-ups in patients with and without sarcopenia at baseline, using adjusted logistic models. Results After a median follow-up of 4.8 years (2078.4 person-years), 37 (9.9%) new cases of sarcopenia, out of the 374 patients without sarcopenia at baseline, were identified (incidence density rate=1.78 per 100 person-years). ASM estimated with the anthropometric equation showed both a high sensitivity and specificity as compared with those estimated by DXA measurements, yielding a concordance of 0.96. The diagnostic algorithm of sarcopenia considered in the software with the equation showed both a high sensitivity (82.1%) and specificity (94.9%) when compared with DXA (reference standard). Adults without sarcopenia (at baseline) showed better physical performance (after approximately 5 years) than adults with sarcopenia. Loss of functionality was greater in adults with sarcopenia (OR 5.0, 95% CI 2.2-11.4) than in adults without sarcopenia. In addition, the risks of falls (OR 2.2, 95% CI 1.1-4.3) and osteoporosis (OR 2.8, 95% CI 1.2-6.6) were higher in older persons with sarcopenia than those without sarcopenia. The measurements and results were completed for the beta and release tests with a mean time of 10 minutes and 11 minutes, respectively. Conclusions We developed and validated a software for the diagnosis of sarcopenia in older Chilean adults that can be used on a mobile device or a computer with good sensitivity and specificity, thus allowing for the development of programs for the prevention, delay, or reversal of this disease. To our knowledge, HTSMayor is the first software to diagnose sarcopenia.
机译:背景技术SARCOPENIA的通常诊断需要双能X射线吸收测定法(DXA)考试,其在拉丁美洲国家的初级保健可达性低。目的本研究的目的是根据欧洲工作组(EWGSOP)的SARCOPENIA提出的SARCOPENIA诊断算法的适应版本来设计和验证移动设备(Android,iOS)和计算机的软件。方法在60岁及以上的430名社区住宅智利人(平均68.2岁,SD 4.9)上进行了后续考试,参与了旨在研究与肥胖有关的嗜睡和残疾的ISAMAYOR和Alexandros队列。群组的所有参与者都是从初级医疗中心的注册管理机构中随机选择,并且对于这项研究,必须在基线上进行DXA扫描。软件(HTSMayor)根据EWGSOP提出的算法的调整版本设计,并分为四个阶段:Sarcopenia,Alpha版本,Beta版本和发布版本的诊断算法的纵向验​​证。该软件使用智利截止点使用人体测量方程或DXA测量来估计附奇骨骼肌质量(ASM)。估计算法的预测验证,比较功能限制(日常生活的至少一个活动,每日生活的两个乐曲活动,或三种流动限制),跌倒和骨质疏松患者在基线的患者的随访中的随访,使用调整后的逻辑模型。结果在4.8岁(2078.4人 - 年)的中位随访后,37(9.9%)SARCOPENIA的新病例,在374名没有SARCOPENIA的患者中被识别出(入射密度率=每100人的1.78岁)。与人类测量方程估计的ASM显示出高灵敏度和特异性,与DXA测量估计的那些相比,产生0.96的一致性。与等式的软件中考虑的SARCOPENIA的诊断算法显示出高灵敏度(82.1%)和与DXA(参考标准)相比的特异性(94.9%)。没有SARCOPENIA(基线)的成年人表现出比患有康迟病毒的成年人更好的身体表现(大约5年)。患有SARCOPENIA(或5.0,95%CI 2.2-11.4)的成年人的功能丧失比在没有SARCOPENIA的成年人的成年人更大。此外,秋季的风险(或2.2,95%CI 1.1-4.3)和骨质疏松症(或2.8,95%CI 1.2-6.6)的患者患有比没有康迟病毒的人更高。为β和释放试验完成测量和结果,平均时间分别为10分钟和11分钟。结论我们开发并验证了一个软件,用于诊断较旧的智利成年人,这些成年人可用于移动设备或计算机具有良好敏感性和特异性的计算机,从而允许开发用于预防,延迟或逆转的计划疾病。为了我们的知识,HTSMayor是诊断康迟腺的第一个软件。

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