Abstract

Obesity is a risk factor associated with age-related disorders that accelerate aging, and it increases the risk of metabolic diseases. Therefore, this study was conducted to investigate the association of leukocyte telomere length (LTL) with the presence of higher body weight in middle-aged females and males. The study subjects comprised 160 (80 control and 80 higher body mass index BMI groups) with ranging ages of 30-50 years included and stratified for BMI. The physio-biochemical analysis was measured using enzymatic determination. Mean telomere length was determined by using the southern blotting technique. The association analysis revealed a significant variance (P < 0.01) in biochemical parameters between higher BMI groups and control including waist, lipid profile, and the level of estradiol, testosterone, follicle-stimulating hormone, and luteinizing hormone. Mean telomere length was shorter in middle-aged males compared to the females of higher BMI groups and control groups for both age groups. LTL was shorter in the overweight and obese patients compared with the control group, and these differences in LTL obese group were shorter compared to the overweight group. In conclusion, shorter telomere length was observed in middle-aged males associated with higher body weight and lipid abnormalities. Lipid/lipoprotein abnormalities can be used as a predictor for the shortened telomere length and the reduction in adiposity indices can improvement the telomere length in both overweight and obese subjects.

Highlights

  • Telomeres, the repetitive sequence TTAGGG at the terminal of linear chromosomes that protect deoxynucleotide acid DNA-protein structures by constituting a loop to prevent end-to-end fusions of the chromosomes [1, 2, 3]

  • Weight index The weighted index recommended by the world health organization (WHO) including body mass index (BMI) and waist circumference was included in this study

  • The results showed a significant reduction (P

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Summary

Introduction

The repetitive sequence TTAGGG at the terminal of linear chromosomes that protect deoxynucleotide acid DNA-protein structures by constituting a loop to prevent end-to-end fusions of the chromosomes [1, 2, 3]. Telomeres prevent loss of genomic DNA at the terminal of mammalian chromosomes, thereby protecting against cell death [4, 5]. Telomere length extends to [10,11,12,13,14,15] kb in humans and decreases with age 1. With each cell cycle telomeres undergo attrition leading to progressive telomere shortening with age 6. The attrition in telomere length increases with age 7. When telomeres attrition reaches a critical length, the cell cycle arrest or apoptosis is triggered 6

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