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Association of adiposity, telomere length and mortality: data from the NHANES 1999-2002

机译:肥胖,端粒长度和死亡率的关联:来自NHANES 1999-2002的数据

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BACKGROUND/OBJECTIVES: Telomere shortening is associated with age and risk of medical comorbidity. We assessed the relationship between measures of adiposity, leukocyte telomere length, and mortality and whether it is modified by age.SUBJECTS/METHODS: Subjects with dual-energy X-ray absorptiometry measures were identified using the National Health and Nutrition Examination Survey 1999-2002. Obesity was categorized using two body fat definitions (BF1%: men ≥ 25%; females ≥ 35%; BF2% ≥ 28% and ≥ 38%, respectively), body mass index (BMI) and waist circumference (WC; men ≥ 102 cm; females ≥ 88 cm). Telomere length relative to standard reference DNA (T/S ratio) was assessed using quantitative PCR. Weighted multivariable regression models evaluated the association of telomere length with adiposity, both continuously and categorically (lowormal BF%, low/high WC and standard BMI categories). Differences in telomere length by age and adiposity were ascertained and subsequent models were stratified by age. Proportional hazard models assessed the risk of mortality by adiposity status. A telomere by adiposity interaction was tested in the entire cohort and by age category (< 60 vs ≥ 60 years; < 70 vs ≥ 70 years). RESULTS: We identified 7827 subjects. Mean age was 46.1 years. Overall telomere length was 1.05 ±0.01 (s.e.) that differed by BF1% (low/high: 1.12 ±0.02 vs 1.03 ±0.02; P< 0.001), BF2% (1.02 ±0.02 vs 1.11 ±0.02; P< 0.001), BMI (underweight 1.08 ±0.03; normal 1.09 + 0.02; overweight 1.04 ±0.02; and obese 1.03 ±0.02;P< 0.001) and WC (low/high 1.09 ±0.02 vs 1.02 ±0.02; P< 0.001). Adjusted β-coefficients evaluating the relationship between telomere length and adiposity (measured continuously) were as follows: BF1% (β = - 0.0033 ±0.0008; P< 0.001), BF2% (-0.041 ±0.008; P< 0.001), BMI (β = - 0.025 ± 0.0008; P = 0.005) and WC (β = - 0.0011 ± 0.0004; P=0.007). High BF% (BF1%: β = - 0.035 ± 0.011; P=0.002; BF2%: )3 = -0.041 ±0.008; P< 0.001) and WC (β = -0.035±0.011; P=0.008) were inversely related to telomere length (TL). Stratifying by age, high BF1% (-0.061 ±0.013), BF2% (-0.065 ±0.01), BMI-obesity (-0.07 ±0.015) and high WC (-0.048 ±0.013) were significant (all P< 0.001). This association diminished with increasing age. In older participants, TL was inversely related to mortality (hazard ratio 0.36 (0.27, 0.49)), as were those classified by BF1% (0.68 (0.56, 0.81)), BF2% (0.75 (0.65, 0.80)), BMI(0.50 (0.42, 0.60)) and WC (0.72 (0.63, 0.83)). No interaction was observed between adiposity status, telomere length and mortality.CONCLUSIONS: Obesity is associated with shorter telomere length in young participants, a relationship that diminishes with increasing age. It does not moderate the relationship with mortality.
机译:背景/目的:端粒缩短与年龄和医学合并症风险有关。我们评估了肥胖,白细胞端粒长度和死亡率的测量值之间的关系,以及死亡率是否随年龄而改变。对象/方法:使用1999-2002年美国国家健康和营养检查调查确定了采用双能X线吸收法的受试者。肥胖通过两种身体脂肪定义(分别为BF1%:男性≥25%;女性≥35%; BF2%≥28%和≥38%),体重指数(BMI)和腰围(WC;男性≥102)进行分类。厘米;女性≥88厘米)。使用定量PCR评估相对于标准参考DNA的端粒长度(T / S比)。加权多变量回归模型连续和明确地评估了端粒长度与肥胖的相关性(低/正常BF%,低/高WC和标准BMI类别)。确定端粒长度随年龄和肥胖的差异,随后的模型按年龄分层。比例风险模型通过肥胖状况评估了死亡风险。在整个队列和年龄组(<60 vs≥60岁; <70 vs≥70岁)中,通过肥胖相互作用对端粒进行了测试。结果:我们确定了7827名受试者。平均年龄为46.1岁。端粒总长度为1.05±0.01(se),相差BF1%(低/高:1.12±0.02 vs 1.03±0.02; P <0.001),BF2%(1.02±0.02 vs 1.11±0.02; P <0.001),BMI (体重不足1.08±0.03;正常体重1.09 + 0.02;体重超重1.04±0.02;肥胖者1.03±0.02; P <0.001)和WC(低/高1.09±0.02对1.02±0.02; P <0.001)。评估端粒长度与肥胖之间关系的调整后的β系数(连续测量)如下:BF1%(β=-0.0033±0.0008; P <0.001),BF2%(-0.041±0.008; P <0.001),BMI( β=-0.025±0.0008; P = 0.005)和WC(β=-0.0011±0.0004; P = 0.007)。高BF%(BF1%:β=-0.035±0.011; P = 0.002; BF2%:)3 = -0.041±0.008; P <0.001)和WC(β= -0.035±0.011; P = 0.008)与端粒长度(TL)成反比。按年龄分层,高BF1%(-0.061±0.013),高BF2%(-0.065±0.01),BMI肥胖(-0.07±0.015)和高WC(-0.048±0.013)显着(所有P <0.001)。随着年龄的增长,这种联系逐渐消失。在老年参与者中,TL与死亡率成反比(危险比0.36(0.27,0.49)),按BF1%(0.68(0.56,0.81)),BF2%(0.75(0.65,0.80)),BMI( 0.50(0.42,0.60))和WC(0.72(0.63,0.83))。结论:肥胖与年轻参与者的端粒长度较短有关,这一关系随着年龄的增长而减少。它不能缓解与死亡率的关系。

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