Journals / Türk Dermatoloji Dergisi / 2019 / Cilt: 13 - Sayı: 4

Thiol/Disulfide Homeostasis in Patients with Telogen Effluvium: Is Oxidative Stress Important in the Pathogenesis of Telogen Effluvium?

Pages
131–134
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)

There is a need for new studies that will show the possible effects of OS on TE pathogenesis and research different OS markers in addition to thiol/disulfide parameters.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: The aim of this study was to assess the correlation between telogen effluvium (TE) with the new oxidative stress (OS) indicator of thiol/disulfide balance and to research the role of OS in the pathogenesis of TE.
📊
Key Findings & Data:Methods: Our study included 101 patients with TE diagnosis and 39 healthy individuals.
💡
Conclusion & Impact:There is a need for new studies that will show the possible effects of OS on TE pathogenesis and research different OS markers in addition to thiol/disulfide parameters.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Objective: The aim of this study was to assess the correlation between telogen effluvium (TE) with the new oxidative stress (OS) indicator of thiol/disulfide balance and to research the role of OS in the pathogenesis of TE. Methods: Our study included 101 patients with TE diagnosis and 39 healthy individuals. Serum thiol/disulfide was measured with a new automated spectrometric method developed by Erel and Neselioglu, and results were compared statistically. Results: Among the six thiol/disulfide parameters, there were statistically significant differences for native thiol, total thiol, disulfide, disulfide/native thiol, disulfide/total thiol, and native thiol/total thiol studied in the patient and control groups (P = 0.042, 0.044, <0.001, 0.013, 0.026, and < 0.001, respectively). Conclusions: Based on the results of this study, it can be said that OS is closely associated with TE pathogenesis. There is a need for new studies that will show the possible effects of OS on TE pathogenesis and research different OS markers in addition to thiol/disulfide parameters.

🔖

Cite This Article

SAVCI, U., ŞAHİN, M. F., ŞENEL, E., ÖZTEKİN, A., MUSLU, U., SUNGUR, M., NESELİOĞLU, S., EREL, Ö. (2019). Thiol/Disulfide Homeostasis in Patients with Telogen Effluvium: Is Oxidative Stress Important in the Pathogenesis of Telogen Effluvium?. Türk Dermatoloji Dergisi, Cilt: 13 - Sayı: 4, 131–134. https://ajindex.com/articles/409131

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. Yavuz IH, Yavuz GO, Bilgili SG, Demir H, Demir C. Assessment of heavy metal and trace element levels in patients with telogen effluvium. Indian J Dermatol 2018;63:246‑50
  2. Hughes EC, Taneja A. Telogen Effluvium. SourceStatPearls. Treasure Island (FL): StatPearls Publishing; 2018
  3. Grover C, Khurana A. Telogen effluvium. Indian J Dermatol Venereol Leprol 2013;79:591‑603
  4. Headington JT. Telogen effluvium. New concepts and review. Arch Dermatol 1993;129:356‑63
  5. Hengl T, Herfert J, Soliman A, Schlinzig K, Trüeb RM, Abts HF, et al. Cystine‑thiamin‑containing hair‑growth formulation modulates the response to UV radiation in an in vitro model for growth‑limiting conditions of human keratinocytes. J Photochem Photobiol B 2018;189:318‑25
  6. Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem 2014;47:326‑32
  7. Tetik S, Ahmad S, Alturfan AA, Fresko I, Disbudak M, Sahin Y, et al. Determination of oxidant stress in plasma of rheumatoid arthritis and primary osteoarthritis patients. Indian J Biochem Biophys 2010;47:353‑8
  8. Matteucci E, Giampietro O. Thiol signalling network with an eye to diabetes. Molecules 2010;15:8890‑903
  9. Prabhu A, Sarcar B, Kahali S, Yuan Z, Johnson JJ, Adam KP, et al. Cysteine catabolism: A novel metabolic pathway contributing to glioblastoma growth. Cancer Res 2014;74:787‑96
  10. Circu ML, Aw TY. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med 2010;48:749‑62
  11. Sbrana E, Paladini A, Bramanti E, Spinetti MC, Raspi G. Quantitation of reduced glutathione and cysteine in human immunodeficiency virus‑infected patients. Electrophoresis 2004;25:1522‑9
  12. Rodrigues SD, Batista GB, Ingberman M, Pecoits‑Filho R, Nakao LS. Plasma cysteine/cystine reduction potential correlates with plasma creatinine levels in chronic kidney disease. Blood Purif 2012;34:231‑7 13. Smeyne M, Smeyne RJ. Glutathione metabolism and parkinson’s disease. Free Radic Biol Med 2013;62:13‑25
  13. Calabrese V, Lodi R, Tonon C, D’Agata V, Sapienza M, Scapagnini G, et al. Oxidative stress, mitochondrial dysfunction and cellular stress response in friedreich’s ataxia. J Neurol Sci 2005;233:145‑62
  14. Kuo LM, Kuo CY, Lin CY, Hung MF, Shen JJ, Hwang TL, et al. Intracellular glutathione depletion by oridonin leads to apoptosis in hepatic stellate cells. Molecules 2014;19:3327‑44
  15. Gumusyayla S, Vural G, Bektas H, Deniz O, Neselioglu S, Erel O. A novel oxidative stress marker in patient