Shaoyun Li, Yuefei Li, Xiyan Xu, Jian Shao, Ruifeng Xie, Sheng Liu, Li Peng, Jin Wang, Kaixin Zhou, Huyi Feng
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AGE levels were derived with LAF along with the other demographic and laboratory parameters. After deriving the age-adjusted AGE levels (AALs), a linear regression analysis and an ordered logistic regression analysis were applied to examine the associations between osteopenia and LAF-AGEs as well as AALs.</p><p><strong>Results: </strong>Negative correlations (Pearson r = -0.16, p < 0.001) were found between LAF-AGEs and T-scores. Higher AALs were significantly associated (p = 0.004) with escalated level of osteopenia in the ordered logistic analysis.</p><p><strong>Discussion: </strong>After reviewing the relevant studies, it is concluded that LAF-AGE is a more stable measure of long-term metabolic dysfunction than circulating AGE. LAF-AGEs are a valid, practical and non-invasive parameter for osteopenia risk evaluation. 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引用次数: 0
摘要
为了预防骨质疏松相关骨折的发生,迫切需要一种简单的、无创的生物标志物来检测静默的骨质减少症。晚期糖基化终产物(AGEs)的积累与骨密度降低和骨质疏松性骨折有关。本文旨在探讨基于晶状体自身荧光(LAF)的AGEs (LAF-AGEs)测量是否可以用于评估骨质减少的风险。方法:通过常规健康检查,选取年龄在50岁以下的368人。采用双能x线骨密度仪(DXA)测量前臂骨密度(BMD),确定骨量减少。年龄水平由LAF以及其他人口统计学和实验室参数得出。在得到年龄调整后的AGE水平(AALs)后,应用线性回归分析和有序逻辑回归分析来检验骨质减少与af - ages以及AALs之间的关系。结果:LAF-AGEs与t -score呈负相关(Pearson r = -0.16, p < 0.001)。在有序逻辑分析中,较高的AALs与骨量减少的升级程度显著相关(p = 0.004)。讨论:在回顾相关研究后,我们认为与循环AGE相比,LAF-AGE是一种更稳定的长期代谢功能障碍指标。LAF-AGEs是一种有效、实用、无创的骨质减少风险评估参数。长期随访的进一步研究将有助于阐明其在骨质疏松风险评估中的有效性。
Lens Autofluorescence Based Advanced Glycation End Products (AGEs) Measurement to Assess Risk of Osteopenia Among Individuals Under the Age of 50.
Introduction: Simple non-invasive biomarker is urgently needed to detect the largely silent osteopenia in order to prevent osteoporosis-related fracture later in life. The accumulation of advanced glycation end products (AGEs) has been related to reduced bone density and osteoporotic fractures. Whether lens autofluorescence (LAF) based AGEs (LAF-AGEs) measurement could be used to assess the risk of osteopenia is aimed to investigate in this paper.
Methods: Through routine health examination, 368 individuals under the age of 50 were enrolled. A dual-energy X-ray absorptiometry (DXA) device was used to measure bone mineral density (BMD) of the forearm and determine osteopenia. AGE levels were derived with LAF along with the other demographic and laboratory parameters. After deriving the age-adjusted AGE levels (AALs), a linear regression analysis and an ordered logistic regression analysis were applied to examine the associations between osteopenia and LAF-AGEs as well as AALs.
Results: Negative correlations (Pearson r = -0.16, p < 0.001) were found between LAF-AGEs and T-scores. Higher AALs were significantly associated (p = 0.004) with escalated level of osteopenia in the ordered logistic analysis.
Discussion: After reviewing the relevant studies, it is concluded that LAF-AGE is a more stable measure of long-term metabolic dysfunction than circulating AGE. LAF-AGEs are a valid, practical and non-invasive parameter for osteopenia risk evaluation. Further studies with longer follow-up will be helpful to clarify its effectiveness for osteoporosis risk assessment.