Correlation Between Telomere Length and Biomarkers of Oxidative Stress in Human Aging.

IF 2.2 4区 医学 Q3 GERIATRICS & GERONTOLOGY
Rejuvenation research Pub Date : 2022-02-01 Epub Date: 2022-02-03 DOI:10.1089/rej.2021.0045
Somu Yadav, Pawan Kumar Maurya
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引用次数: 0

Abstract

The telomere length (TL) has increasingly been used as a biomarker of human aging because it has been shown to predict the chances of survival and longevity. Oxidative stress is presumed to be a major cause of telomere shortening, but the importance of oxidative stress as a determinant of telomere shortening remains less clear and has recently been questioned. We analyzed 105 healthy subjects of both sexes between the ages of 20-77 years. The TL and biomarkers of oxidative stress were estimated as per standard protocols. A significant (p < 0.001) age-dependent decline in TL was observed. TL was positively correlated with the ferric reducing ability of plasma value (r = 0.8811) and reduced glutathione (r = 0.8209), whereas negatively correlated with malondialdehyde (r = -0.7191). Our findings supported the idea of a possible correlation between the TL and biomarkers of oxidative stress in aging. The study has remarkable scope in medical science as the findings on correlation of TL with biomarkers of oxidative stress in aging are novel and they will help in further research against oxidative stress.

人类衰老过程中端粒长度与氧化应激生物标志物的相关性
端粒长度(TL)越来越多地被用作人类衰老的生物标志物,因为它已被证明可以预测生存和长寿的机会。氧化应激被认为是端粒缩短的主要原因,但氧化应激作为端粒缩短的决定因素的重要性仍然不太清楚,最近受到质疑。我们分析了105名年龄在20-77岁之间的男女健康受试者。根据标准方案估计氧化应激的TL和生物标志物。与还原性谷胱甘肽(r = 0.8209)显著(p r = 0.8811),而与丙二醛呈负相关(r = -0.7191)。我们的发现支持了衰老过程中TL与氧化应激生物标志物之间可能存在关联的观点。TL与衰老过程中氧化应激生物标志物相关性的研究结果新颖,对进一步研究氧化应激具有重要的医学意义。
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来源期刊
Rejuvenation research
Rejuvenation research 医学-老年医学
CiteScore
4.50
自引率
0.00%
发文量
41
审稿时长
3 months
期刊介绍: Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence. Rejuvenation Research coverage includes: Cell immortalization and senescence Pluripotent stem cells DNA damage/repair Gene targeting, gene therapy, and genomics Growth factors and nutrient supply/sensing Immunosenescence Comparative biology of aging Tissue engineering Late-life pathologies (cardiovascular, neurodegenerative and others) Public policy and social context.
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