Rizvi Saliha, Raza Syed Tasleem, Mahdi Farzana
Department of Biochemistry, Era's Lucknow Medical College and Hospital, Lucknow-226003, India.
Curr Aging Sci. 2014;7(3):161-7. doi: 10.2174/1874609808666150122153151.
Telomeres are gene sequences present at chromosomal ends and are responsible for maintaining genome integrity. Telomere length is maximum at birth and decreases progressively with advancing age and thus is considered as a biomarker of chronological aging. This age associated decrease in the length of telomere is linked to various ageing associated diseases like diabetes, hypertension, Alzheimer's disease, cancer etc. and their associated complications. Telomere length is a result of combined effect of oxidative stress, inflammation and repeated cell replication on it, and thus forming an association between telomere length and chronological aging and related diseases. Thus, decrease in telomere length was found to be important in determining both, the variations in longevity and age-related diseases in an individual. Ongoing and progressive research in the field of telomere length dynamics has proved that aging and age-related diseases apart from having a synergistic effect on telomere length were also found to effect telomere length independently also. Here a short description about telomere length variations and its association with human aging and age-related diseases is reviewed.
端粒是存在于染色体末端的基因序列,负责维持基因组完整性。端粒长度在出生时最长,并随着年龄的增长而逐渐缩短,因此被视为生物衰老的一个生物标志物。端粒长度随年龄增长而缩短与多种衰老相关疾病如糖尿病、高血压、阿尔茨海默病、癌症等及其相关并发症有关。端粒长度是氧化应激、炎症和细胞反复复制共同作用的结果,从而在端粒长度与生物衰老及相关疾病之间建立了联系。因此,发现端粒长度的缩短在决定个体寿命差异和与年龄相关疾病方面都很重要。在端粒长度动态变化领域正在进行的和不断深入的研究已经证明,衰老和与年龄相关的疾病除了对端粒长度有协同作用外,还被发现可以独立影响端粒长度。这里综述了关于端粒长度变化及其与人类衰老和年龄相关疾病关联的简短描述。