Chahine Mirna N, Toupance Simon, El-Hakim Sandy, Labat Carlos, Gautier Sylvie, Moussallem Toufic, Yared Pierre, Asmar Roland, Benetos Athanase
a Foundation-Medical Research Institutes, Beirut, Lebanon.
b Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon.
Can J Physiol Pharmacol. 2019 Apr;97(4):328-334. doi: 10.1139/cjpp-2018-0582. Epub 2019 Mar 15.
Short telomere length (TL) is associated with atherosclerotic cardiovascular disease (ACVD) and other age-related diseases. It is unclear whether these associations originate from having inherently short TL or a faster TL attrition before or during disease development. We proposed the blood-and-muscle model to assess TL dynamics throughout life course. Our objective was to measure TL in leukocytes (LTL) and in skeletal muscle (MTL), which served as a proxy of TL at birth. The delta (MTL-LTL) represented life-long telomere attrition. Blood draws and skeletal muscle biopsies were performed on 35 Lebanese individuals undergoing surgery. Following DNA extraction, LTL and MTL were measured by Southern blot. In every individual aged between 30 and 85 years, MTL was longer than LTL. With age, MTL and LTL decreased, but the delta (MTL-LTL) increased by 14 bp/year. We validated the blood-and-muscle model that allowed us to identify TL, TL at birth, and lifelong TL attrition in a cross-sectional study. This model can be used in larger cross-sectional studies to evaluate the association of telomere dynamics with age-related diseases onset and progression.
短端粒长度(TL)与动脉粥样硬化性心血管疾病(ACVD)及其他与年龄相关的疾病有关。目前尚不清楚这些关联是源于天生的短端粒长度,还是疾病发生之前或期间更快的端粒损耗。我们提出了血液-肌肉模型来评估整个生命过程中的端粒动态变化。我们的目标是测量白细胞中的端粒长度(LTL)和骨骼肌中的端粒长度(MTL),后者可作为出生时端粒长度的代表。差值(MTL-LTL)代表终生端粒损耗。对35名接受手术的黎巴嫩人进行了血液采集和骨骼肌活检。提取DNA后,通过Southern印迹法测量LTL和MTL。在每一位年龄在30至85岁之间的个体中,MTL均长于LTL。随着年龄增长,MTL和LTL均下降,但差值(MTL-LTL)以每年14个碱基对的速度增加。我们验证了血液-肌肉模型,该模型使我们能够在一项横断面研究中识别端粒长度、出生时的端粒长度以及终生端粒损耗。此模型可用于更大规模的横断面研究,以评估端粒动态变化与年龄相关疾病的发病和进展之间的关联。