Magris Riccardo, Uchytil Jaroslav, Cipryan Lukáš, Skýpala Jiří, Jandacka Daniel, Monte Andrea
Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Human Motion Diagnostic Center, Department of Human Movement Studies, University of Ostrava, 70200, Ostrava, Czech Republic.
Sci Rep. 2025 May 8;15(1):16077. doi: 10.1038/s41598-025-01219-4.
The aim of this study was to test the hypothesis that individuals with an increase in HbA1c (i.e. above the regular but below the diabetic threshold) exhibit an impairment in the Achilles tendon structure and walking capacity, due to the adverse effect of the advanced glycation end-product. One hundred fifty-eight participants matched for gender, age, physical activity and BMI, were divided in two cohorts based on the HbA1c level: normal HbA1c (NGH; <39 mmol/molHb; n = 79) and altered HbA1c (AGH; >=39 mmol/molHb; n = 79). Each participant performed several walking trials to evaluate the kinematic parameters during walling at the self-selected speed and a quantitative MRI scan of the Achilles tendon (AT) to obtain its intrinsic characteristics (i.e. T2* relaxation time short and long component). The AT T2* relaxation time short component (a parameter related to the tendon collagen quality) was reduced in AGH compared to NGH. Furthermore, AGH exhibited a slower self-selected walking speed (NGH: 1.59 ± 0.18 m/s; AGH:1.54 ± 0.16 m/s) and a shorter stride length (NGH: 1.59 ± 0.13 m; AGH:1.55 ± 0.11 m). Our data suggest that a non-pathological increase in HbA1c is able to negatively affect AT collagen quality and walking capacity in healthy people. These results highlight the importance of glycemic control, even below the pathological threshold. Since diabetes could alter several biological pathways, further studies are necessary to determine which mechanisms and their timing, regarding the HbA1c rise, affect tendon composition and, consequently, walking capacity.
糖化血红蛋白(HbA1c)升高(即高于正常水平但低于糖尿病阈值)的个体,由于晚期糖基化终产物的不良影响,其跟腱结构和行走能力会出现损伤。158名在性别、年龄、身体活动和体重指数方面相匹配的参与者,根据HbA1c水平被分为两个队列:正常HbA1c(NGH;<39 mmol/molHb;n = 79)和改变的HbA1c(AGH;>=39 mmol/molHb;n = 79)。每位参与者进行了多次行走试验,以评估自选速度行走时的运动学参数,并对跟腱进行定量磁共振成像扫描,以获取其内在特征(即T2弛豫时间的短成分和长成分)。与NGH相比,AGH的跟腱T2弛豫时间短成分(一个与肌腱胶原蛋白质量相关的参数)降低。此外,AGH的自选行走速度较慢(NGH:1.59±0.18 m/s;AGH:1.54±0.16 m/s),步幅较短(NGH:1.59±0.13 m;AGH:1.55±0.11 m)。我们的数据表明,在健康人群中,HbA1c的非病理性升高能够对跟腱胶原蛋白质量和行走能力产生负面影响。这些结果凸显了血糖控制的重要性,即使在低于病理阈值的情况下。由于糖尿病可能会改变多种生物学途径,因此有必要进一步研究,以确定HbA1c升高影响肌腱成分进而影响行走能力的具体机制及其时间。