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1
Oxidative Stress-induced Telomere Length Shortening of Circulating Leukocyte in Patients with Obstructive Sleep Apnea.阻塞性睡眠呼吸暂停患者氧化应激诱导的循环白细胞端粒长度缩短
Aging Dis. 2016 Oct 1;7(5):604-613. doi: 10.14336/AD.2016.0215. eCollection 2016 Oct.
2
Telomere attrition and diabetes mellitus.端粒损耗与糖尿病
Geriatr Gerontol Int. 2016 Mar;16 Suppl 1:66-74. doi: 10.1111/ggi.12738.
3
The influence of oxidative stress induced by iron on telomere length.铁诱导的氧化应激对端粒长度的影响。
Environ Toxicol Pharmacol. 2015 Nov;40(3):931-5. doi: 10.1016/j.etap.2015.10.002. Epub 2015 Oct 23.
4
Oxidative stress, telomere shortening, and DNA methylation in relation to low-to-moderate occupational exposure to welding fumes.与低至中度职业性接触焊接烟尘相关的氧化应激、端粒缩短和DNA甲基化
Environ Mol Mutagen. 2015 Oct;56(8):684-93. doi: 10.1002/em.21958. Epub 2015 May 27.
5
Patients with multiple sclerosis show increased oxidative stress markers and somatic telomere length shortening.多发性硬化症患者表现出氧化应激标志物增加和体细胞端粒长度缩短。
Mol Cell Biochem. 2015 Feb;400(1-2):183-7. doi: 10.1007/s11010-014-2274-1. Epub 2014 Nov 26.
6
Blood α-tocopherol, γ-tocopherol levels and risk of prostate cancer: a meta-analysis of prospective studies.血液 α-生育酚、γ-生育酚水平与前列腺癌风险:前瞻性研究的荟萃分析。
PLoS One. 2014 Mar 25;9(3):e93044. doi: 10.1371/journal.pone.0093044. eCollection 2014.
7
The vitamin E isoforms α-tocopherol and γ-tocopherol have opposite associations with spirometric parameters: the CARDIA study.维生素 E 异构体 α-生育酚和 γ-生育酚与肺量计参数呈相反关联:CARDIA 研究。
Respir Res. 2014 Mar 15;15(1):31. doi: 10.1186/1465-9921-15-31.
8
Telomere shortening and increased oxidative stress are restricted to venous tissue in patients with varicose veins: A merely local disease?端粒缩短和氧化应激增加仅限于静脉曲张患者的静脉组织:这仅仅是一种局部疾病吗?
Vasc Med. 2014 Apr;19(2):125-130. doi: 10.1177/1358863X14525002. Epub 2014 Feb 20.
9
Isoforms of Vitamin E Differentially Regulate PKC and Inflammation: A Review.维生素E的异构体对蛋白激酶C和炎症具有不同的调节作用:综述
J Clin Cell Immunol. 2013 Mar 14;4(137). doi: 10.4172/2155-9899.1000137.
10
Two faces of vitamin E in the lung.维生素 E 在肺部的两面性。
Am J Respir Crit Care Med. 2013 Aug 1;188(3):279-84. doi: 10.1164/rccm.201303-0503ED.

美国5768名男性和女性体内的α-生育酚、γ-生育酚与端粒长度:一项美国国家健康与营养检查调查研究

Alpha- and Gamma-Tocopherol and Telomere Length in 5768 US Men and Women: A NHANES Study.

作者信息

Tucker Larry A

机构信息

Department of Exercise Sciences, Brigham Young University, Provo, UT 84602, USA.

出版信息

Nutrients. 2017 Jun 13;9(6):601. doi: 10.3390/nu9060601.

DOI:10.3390/nu9060601
PMID:28629117
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5490580/
Abstract

Antioxidants have a number of potential health benefits. The present investigation was designed to determine the relationship between serum alpha- and gamma-tocopherol levels (powerful antioxidants), and leukocyte telomere length (a biomarker of biological aging). A cross-sectional design was employed to study 5768 adults from the National Health and Nutrition Examination Survey (NHANES). DNA was obtained via blood samples. Telomere length was assessed using the quantitative polymerase chain reaction method. Serum concentrations of alpha- and gamma-tocopherol were measured using high performance liquid chromatography (HPLC). Results showed that for each one-year increase in age, telomeres were 15.6 base pairs shorter ( = 410.4, < 0.0001). After adjusting for differences in the demographic covariates, for each µg/dL higher level of gamma-tocopherol, telomeres were 0.33 base pairs shorter ( = 7.1, = 0.0126). Telomeres were approximately 1 year shorter (15.6 base pairs) for each increment of 47.3 to 55.7 µg/dL of gamma-tocopherol in the blood, depending on the variables controlled. Adults at the 75th percentile of gamma-tocopherol had 2.8-3.4 years greater cellular aging than those at the 25th percentile, depending on the covariates in the model. However, alpha-tocopherol was not related to telomere length. Evidently, gamma-tocopherol levels, but not alpha-tocopherol, account for meaningful increases in biological aging.

摘要

抗氧化剂具有许多潜在的健康益处。本研究旨在确定血清α-生育酚和γ-生育酚水平(强效抗氧化剂)与白细胞端粒长度(生物衰老的生物标志物)之间的关系。采用横断面设计,对来自美国国家健康与营养检查调查(NHANES)的5768名成年人进行研究。通过血液样本获取DNA。使用定量聚合酶链反应方法评估端粒长度。采用高效液相色谱法(HPLC)测量血清α-生育酚和γ-生育酚的浓度。结果显示,年龄每增加一岁,端粒缩短15.6个碱基对(β = 410.4,P < 0.0001)。在调整人口统计学协变量差异后,γ-生育酚水平每升高1μg/dL,端粒缩短0.33个碱基对(β = 7.1,P = 0.0126)。根据所控制的变量,血液中γ-生育酚每增加47.3至55.7μg/dL,端粒大约缩短1年(15.6个碱基对)。根据模型中的协变量,γ-生育酚处于第75百分位数的成年人比处于第25百分位数的成年人细胞衰老程度高2.8 - 3.4年。然而,α-生育酚与端粒长度无关。显然,是γ-生育酚水平而非α-生育酚水平导致了生物衰老的显著增加。