Journals / Erciyes Medical Journal / 2018 / Cilt: 40 - Sayı: 3

Evaluation of Oxidative Stress and Thiol-Disulfide Parameters According to the Body Mass Index in Adult Individuals

Pages
155–161
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In addition to this, the oxidative stress and thiol–disulfide homeostasis markers are observed to be further increased in the overweight group than the obese (≥30) group due to body’s reaction to first inconsistency.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: In this study, the parameters of oxidative stress markers and thiol–disulfide homeostasis as a novel biomarker were evaluated in experimental groups of adult individuals, which were formed according to the body mass index (BMI).
📊
Key Findings & Data:Materials and Methods: A total of 165 adult patients were grouped as normal weight (BMI 18.5–24.9, n=39), preobese or overweight (BMI 25–29.9, n=47), obese (BMI 30–34.9; n=44), and severely obese (BMI >35, n=35).
💡
Conclusion & Impact:In addition to this, the oxidative stress and thiol–disulfide homeostasis markers are observed to be further increased in the overweight group than the obese (≥30) group due to body’s reaction to first inconsistency.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Objective: In this study, the parameters of oxidative stress markers and thiol–disulfide homeostasis as a novel biomarker were evaluated in experimental groups of adult individuals, which were formed according to the body mass index (BMI). Materials and Methods: A total of 165 adult patients were grouped as normal weight (BMI 18.5–24.9, n=39), preobese or overweight (BMI 25–29.9, n=47), obese (BMI 30–34.9; n=44), and severely obese (BMI >35, n=35). In addition to thiol–disulfide homeostasis parameters, the total oxidant status (TOS), total antioxidant status (TAS), oxidative stress index (OSI), ischemia-modified albumin (IMA), albumin, and ceruloplasmin levels were determined. Results: Native thiol, total thiol, and native thiol/total thiol % levels were significantly decreased in the overweight, obese, and severely obese groups compared to the normal weight group (p<0.001). Disulfide levels were elevated in the overweight group compared to the normal weight group (p<0.01). While the TOS and OSI levels of the normal weight group were elevated compared to the overweight (p<0.001) and obese/severely obese groups (p<0.05), albumin levels of the normal weight group were reduced compared to other groups (p<0.001). The IMA levels of the overweight group were elevated compared to the normal weight and severely obese groups (p<0.05 and p<0.001, respectively). Ceruloplasmin levels of the severely obese group were increased compared to the normal weight and overweight groups (p<0.001 and p<0.01, respectively). Conclusion: In our study, oxidative stress was increased in groups with a BMI greater than normal (≥25). In addition to this, the oxidative stress and thiol–disulfide homeostasis markers are observed to be further increased in the overweight group than the obese (≥30) group due to body’s reaction to first inconsistency.

🔖

Cite This Article

SÖĞÜT, İ., AYDIN, A. Ş., GÖKMEN, E. S., ATAK, P. G., EREL, Ö. (2018). Evaluation of Oxidative Stress and Thiol-Disulfide Parameters According to the Body Mass Index in Adult Individuals. Erciyes Medical Journal, Cilt: 40 - Sayı: 3, 155–161. https://ajindex.com/articles/195367

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. Hill JO, Wyatt HR, Peters JC. Energy balance and obesity. Circulation 2012
  2. 126(1): 126-32. [CrossRef] Kaila B, Raman M. Obesity: a review of pathogenesis and management strategies. Can J Gastroenterol 2008
  3. 22(1): 61-8. [CrossRef] Matsuda M, Shimomura I. Increased oxidative stress in obesity: implications for metabolic syndrome, diabetes, hypertension, dyslipidemia, atherosclerosis, and cancer. Obes Res Clin Pract 2013
  4. 7(5): e330-41. [CrossRef] Kruk J. Overweight, obesity, oxidative stress and the risk of breast cancer. Asian Pac J Cancer Prev 2014
  5. 15(22): 9579-86. [CrossRef] Manna P, Jain SK. Obesity, Oxidative stress, adipose tissue dysfunction, and the associated health risks: causes and therapeutic strategies. Metab Syndr Relat Disord 2015
  6. 13(10): 423-44. [CrossRef] Birben E, Sahiner UM, Sackesen C, Erzurum S, Kalayci O. Oxidative stress and antioxidant defense. World Allergy Organ J 2012
  7. 5(1): 9-19. [CrossRef] Pisoschi AM, Pop A. The role of antioxidants in the chemistry of oxidative stress: A review. Eur J Med Chem 2015
  8. [CrossRef] Ates I, Kaplan M, Yüksel M, Meşe D, Alışık M, Erel Ö, et al. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine 2016
  9. 51(1): 47-51. [CrossRef] Elmas B, Karacan M, Dervişoğlu P, Kösecik M, İşgüven ŞP, Bal C. Dynamic thiol/disulphide homeostasis as a novel indicator of oxidative stress in obese children and its relationship with inflammatory-cardiovascular markers. Anatol J Cardiol 2017
  10. 18(5): 361-9. [CrossRef] Hanikoglu F, Hanikoglu A, Kucuksayan E, Alisik M, Gocener AA, Erel O, et al. Dynamic thiol/disulphide homeostasis before and after radical prostatectomy in patients with prostate cancer. Free Radic Res 2016
  11. 50(sup1): S79-S84. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem 2014
  12. 47(18): 326-32. [CrossRef] Erel O. A new automated colorimetric method for measuring total oxidant status. Clin Biochem. 2005
  13. 38(12): 1103-11. [CrossRef] Erel O. A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem 2004
  14. 37(4): 277-85. [CrossRef] Daş M, Çevik Y, Erel Ö, Çorbacıoğlu ŞK. Ischemia-modified albumin levels in the prediction of acute critical neurological findings in carbon monoxide poisoning. Kaohsiung J Med Sci 2016
  15. 32(4): 201-6. [CrossRef] Knight JA. Diseases and disorders associated with ex