Skip to main content
Log in

Oxidative Stress in Alopecia Areata: A Case–Control Study

  • Original Research Article
  • Published:
American Journal of Clinical Dermatology Aims and scope Submit manuscript

Abstract

Background

Increased reactive oxygen species (ROS) and lipid peroxidation are seen in many dermatologic disorders, including atopic dermatitis, psoriasis, vitiligo, acne vulgaris, pemphigus vulgaris, and lichen planus. In alopecia areata (AA), there is increased production of ROS from perifollicular inflammatory cells.

Objective

The aim of this study was to determine the oxidative stress index (OSI) and lipid peroxidation by studying serum total oxidant capacity (TOC), total antioxidant capacity (TAC), and malondialdehyde (MDA) values in AA patients.

Methods

The study included 35 AA patients and a control group consisting of 30 age- and sex-matched healthy volunteers. The serum TOC, TAC, and MDA values were measured, and the OSIs were calculated and compared in both groups.

Results

The mean serum TOC (p < 0.001), MDA (p < 0.001), and OSI (p < 0.001) values were found to be significantly higher in AA patients than in the control group. The mean serum TAC value was significantly lower (p < 0.05) in cases than in controls. Significantly higher MDA (p < 0.001), TOC (p < 0.001), and OSI values (p < 0.001) and lower TAC values (p < 0.01) were found in severe AA than in mild or moderate AA.

Conclusion

The demonstrated results confirmed the presence of oxidative stress and lipid peroxidation in AA. Whether these changes play a role in disease pathogenesis or result from the inflammatory process requires further investigation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Madani S, Shapiro J. Alopecia areata update. J Am Acad Dermatol. 2000;42:549–66.

    CAS  PubMed  Google Scholar 

  2. McDonagh AJ, Tazi-Ahnini R. Epidemiology and genetics of alopecia areata. Clin Exp Dermatol. 2002;27:405–9.

    Article  CAS  PubMed  Google Scholar 

  3. Duvic M, Nelson A, de Andrade M. The genetics of alopecia areata. Clin Dermatol. 2001;19:135–9.

    Article  CAS  PubMed  Google Scholar 

  4. Lontz W, Sirsjo A, Liu W, et al. Increased mRNA expression of manganese superoxide dismutase in psoriasis skin lesions and in cultured human keratinocytes exposed to IL-1 beta and TNF-alpha. Free Radic Biol Med. 1995;18:349–55.

    Article  CAS  PubMed  Google Scholar 

  5. Therond P, Gerbaud P, Dimon S, et al. Antioxidant enzymes in psoriatic fibroblasts and erythrocytes. J Invest Dermatol. 1996;106:1325–8.

    Article  CAS  PubMed  Google Scholar 

  6. Niwa Y, Kanoh T, Sakane T, et al. Detection of enhanced lipid peroxide levels in patients with inflammatory skin diseases. J Clin Biochem Nutr. 1987;2:245–51.

    Article  Google Scholar 

  7. Emerit I. Free radicals and aging of the skin. EXS. 1992;62:328–41.

    CAS  PubMed  Google Scholar 

  8. Miyachi Y. Photoaging from an oxidative standpoint. J Dermatol Sci. 1995;9:79–86.

    Article  CAS  PubMed  Google Scholar 

  9. Schallreuter K, Wood J. Free radical reduction in the human epidermis. Free Radic Biol Med. 1989;6:519–32.

    Article  CAS  PubMed  Google Scholar 

  10. Fuchs J, Huflejt ME, Rothfuss LM, et al. Impairment of enzymic and nonenzymic antioxidants in skin by UVB irradiation. J Invest Dermatol. 1989;93:769–73.

    Article  CAS  PubMed  Google Scholar 

  11. Bacchetti T, Campanati A, Ferretti G, et al. Oxidative stress and psoriasis: the effect of antitumour necrosis factor-α inhibitor treatment. Br J Dermatol. 2013;168:984–9.

    Article  CAS  PubMed  Google Scholar 

  12. Grange A, Weill B, Dupin N, et al. Does inflammatory acne result from imbalance in the keratinocyte innate immune response? Microbes Infect. 2010;12:1085–90.

    Article  CAS  PubMed  Google Scholar 

  13. Yesilova Y, Ucmak D, Selek S, et al. Oxidative stress index may play a key role in patients with pemphigus vulgaris. J Eur Acad Dermatol Venereol. 2013;27:465–7.

    Article  CAS  PubMed  Google Scholar 

  14. Sapuntsova SG, Lebed’ko OA, Shchetkina MV, et al. Status of free-radical oxidation and proliferation processes in patients with atopic dermatitis and lichen planus. Bull Exp Biol Med. 2011;150:690–2.

    Article  CAS  PubMed  Google Scholar 

  15. Akoglu G, Emre S, Metin A, et al. Evaluation of total oxidant and antioxidant status in localized and generalized vitiligo. Clin Exp Dermatol. 2013 (Epub ahead of print).

  16. Briganti S, Picardo M. Antioxidant activity, lipid peroxidation and skin diseases: what’s new. J Eur Acad Dermatol Venereol. 2003;17:663–9.

    Article  CAS  PubMed  Google Scholar 

  17. Naziroglu M, Kokcam I. Antioxidants and lipid peroxidation status in the blood of patients with alopecia. Cell Biochem Funct. 2000;18:169–73.

    Article  CAS  PubMed  Google Scholar 

  18. Portugal M, Barak V, Ginsburg I, et al. Interplay among oxidants, antioxidants, and cytokines in skin disorders: present status and future considerations. Biomed Pharmacother. 2007;61:412–22.

    Article  CAS  PubMed  Google Scholar 

  19. Akar A, Arca E, Erbil H, et al. Antioxidant enzymes and lipid peroxidation in the scalp of patients with alopecia areata. J Dermatol Sci. 2002;29:85–90.

    Article  CAS  PubMed  Google Scholar 

  20. Koca R, Armutcu F, Altinyazar CH, et al. Evaluation of lipid peroxidation, oxidant/antioxidant status, and serum nitric oxide levels in alopecia areata. Med Sci Monit. 2005;11:296–9.

    Google Scholar 

  21. Kavak A, Baykal C, Ozarmağan G, et al. HLA in alopecia areata. Int J Dermatol. 2000;39:589–92.

    Article  CAS  PubMed  Google Scholar 

  22. Draper H, Hadley M. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990;186:421–31.

    CAS  PubMed  Google Scholar 

  23. Erel O. A novel automated method to measure total antioxidant response against potent free radical reactions. Clin Biochem. 2004;37:112–29.

    Article  CAS  PubMed  Google Scholar 

  24. Cakmak A, Zeyrek D, Atas A, et al. Oxidative status and paraoxonase activity in children with asthma. Clin Invest Med. 2009;32:327–34.

    Google Scholar 

  25. Erel O. A new automated colorimetric method for measuring total oxidant status. Clin Biochem. 2005;38:1103–11.

    Article  CAS  PubMed  Google Scholar 

  26. Demirbag R, Gur M, Yilmaz R, et al. Influence of oxidative stress on the development of collateral circulation in total coronary occlusions. Int J Cardiol. 2007;116:14–9.

    Article  PubMed  Google Scholar 

  27. Valko M, Leibfritz D, Moncol J, et al. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 2007;39:44–84.

    Article  CAS  PubMed  Google Scholar 

  28. Devasagayam TPA, Tilak JC, Boloor KK, et al. Free radicals and antioxidants in human health: current status and future prospects. J Assoc Physicians India. 2004;52:794–804.

    CAS  PubMed  Google Scholar 

  29. Sies H. Oxidative stress: oxidants and antioxidants. Exp Physiol. 82:291–95.

  30. Alp R, Selek S, Alp SI, et al. Oxidative and antioxidative balance in patients of migraine. Eur Rev Med Pharmacol Sci. 2010;14:877–82.

    Google Scholar 

  31. Weiss SJ. Tissue destruction by neutrophils. N Engl J Med. 1989;320:365–76.

    Article  CAS  PubMed  Google Scholar 

  32. Kannan K, Jain SK. Oxidative stress and apoptosis. Pathophysiology. 2000;7:153–63.

    Article  CAS  PubMed  Google Scholar 

  33. Kim SW, Kim BJ, Youn SW, et al. Evaluation of free oxygen radical and antioxidant capacity in alopecia areata. J Dermatol. 2010;37:762–4.

    Article  PubMed  Google Scholar 

  34. Eken A, Dogan P, Karaoglu S, et al. Selenium and glutathione peroxidase in patients with alopecia. Turk Derm. 1996;30:23–34.

    Google Scholar 

  35. Mussalo-Rauhamaa H, Lakomaa EL, Kianto U, et al. Element concentrations in serum, erythrocytes, hair and urine of alopecia patients. Acta Derm Venereol. 1986;66:103–9.

    CAS  PubMed  Google Scholar 

  36. Abdel Fattah NSA, Ebrahim AA, El Okda ES. Lipid peroxidation/antioxidant activity in patients with alopecia areata. JEADV. 2011;25:403–8.

    CAS  PubMed  Google Scholar 

  37. Tobin DJ. Morphological analysis of hair follicles in alopecia areata. Microsc Res Tech. 1997;38:443–51.

    Article  CAS  PubMed  Google Scholar 

  38. Reid MB, Li YP. Cytokines and oxidative signaling in skeletal muscle. Acta Physiol Scand. 2001;171:225–32.

    Article  CAS  PubMed  Google Scholar 

  39. Latha B, Babu M. The involvement of free radicals in burn injury: a review. Burns. 2001;27:309–17.

    Article  CAS  PubMed  Google Scholar 

  40. Khan MF, Wu X, Ansari GA. Anti-malondialdehyde antibodies in MRL +/+ mice treated with trichloroethene and dichloroacetyl chloride: possible role of lipid peroxidation in autoimmunity. Toxicol Appl Pharmacol. 2001;170:88–92.

    Article  CAS  PubMed  Google Scholar 

  41. Wang L, Muxin G, Nishida H, et al. Psychological stress-induced oxidative stress as a model of sub-healthy condition and the effect of TCM. Evid Based Complement Alternat Med. 2007;4:195–202.

    Article  PubMed Central  PubMed  Google Scholar 

  42. Manolache L, Benea V. Stress in patients with alopecia areata and vitiligo. J Eur Acad Dermatol Venereol. 2007;21:921–8.

    Article  PubMed  Google Scholar 

  43. Al-Mutairi N, Eldin ON. Clinical profile and impact on quality of life: seven years experience with patients of alopecia areata. Indian J Dermatol Venereol Leprol. 2011;77:489–93.

    Article  PubMed  Google Scholar 

  44. Sheu MY, Fowler AJ, Kao J, et al. Topical peroxisome proliferator activated receptor-alpha activators reduce inflammation in irritant and allergic contact dermatitis models. J Invest Dermatol. 2002;118:94–101.

    Article  CAS  PubMed  Google Scholar 

  45. Sertznig P, Seifert M, Tilgen W, Reichrath J. Peroxisome proliferator activated receptors (PPARs) and the human skin: importance of PPARs in skin physiology and dermatologic diseases. Am J Clin Dermatol. 2008;9:15–31.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

This manuscript has been read and approved by all authors, the requirements for authorship have been met, and each author believes that the manuscript represents honest work. The authors have no conflicts of interest that are directly relevant to the content of this study. No sources of funding were used to conduct this study or to prepare this manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ola Ahmed Bakry.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bakry, O.A., Elshazly, R.M.A., Shoeib, M.A.M. et al. Oxidative Stress in Alopecia Areata: A Case–Control Study. Am J Clin Dermatol 15, 57–64 (2014). https://doi.org/10.1007/s40257-013-0036-6

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40257-013-0036-6

Keywords

Navigation