The Impact of Stress on Inflammatory Dermatologic Diseases: A Narrative Review
Year 2026,
Volume: 7 Issue: 1, 36 - 48, 06.01.2026
Mustafa Arslan
,
Çiçek Hocaoğlu
Abstract
In this review, the effects of stress on inflammatory dermatologic diseases were examined from a psychoneuroim-imunological perspective. The mechanisms by which psychological stress influences the relationships between the immune system and the skin have been evaluated in the context of major inflammatory skin diseases supported by current literature. The role of stress in the pathogenesis of these disorders, its effect on disease exacerbations, and its importance in treatment response were presented based on current literature findings. In addition, the effects of stress management approaches on the prognosis of inflammatory dermatological diseases were discussed. Our review particularly focused on the role of psychological stress in the exacerbation and course of psoriasis, atopic dermatitis, acne vulgaris, rosacea, urticaria, seborrheic dermatitis, and lichen planus, which constitute a substantial proportion of patients attending dermatology clinics. Findings from our study and the existing literature demonstrate that dermatologic lesions, which are readily visible on the skin, may elicit feelings of shame and guilt and consequently increase psychological stress. This heightened stress level appears to play a significant role in disease flares. Therefore, clinicians should not overlook the psychological burden associated with dermatologic diseases, as addressing this bidirectional interaction is essential for breaking the vicious cycle that perpetuates disease activity. Accordingly, dermatologic and psychological treatment approaches should be integrated. In particular, performing disease-specific severity assessments, systematically screening psychological symptoms using validated instruments, and providing individualized psychiatric support interventions especially when implemented early, may contribute to improvements in patients’ quality of life and may positively influence disease progression.
Ethical Statement
Ethical approval was not required for this review article, as it is based on previously published studies and does not involve human participants or animals.
Supporting Institution
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Project Number
Bu çalışma için bir proje numarası bulunmamaktadır.
Thanks
I would like to thank Professor Çiçek Hocaoğlu for her kind support throughout the writing process of this article.
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Stresin inflamatuar dermatolojik hastalıklar üzerine etkisi: Geleneksel bir derleme
Year 2026,
Volume: 7 Issue: 1, 36 - 48, 06.01.2026
Mustafa Arslan
,
Çiçek Hocaoğlu
Abstract
Bu derlemede, stresin inflamatuar dermatolojik hastalıklar üzerindeki etkisi psikonöroimmünolojik açıdan incelenmiştir. Psikolojik stresin bağışıklık sistemi ile deri arasındaki ilişkileri hangi mekanizmalarla etkilediği, başlıca inflamatuar deri hastalıkları özelinde literatür bilgileri eşliğinde değerlendirilmiştir. Bu hastalıkların patogenezinde stresin rolü, alevlenmeler üzerindeki etkisi ve tedaviye yanıt açısından önemi literatür bulguları eşliğinde sunulmuştur. Ayrıca stres yönetimi yaklaşımlarının inflamatuar deri hastalıklarının prognozuna etkileri değerlendirilmiştir. Çalışmamızda dermatoloji polikliniklerinde ciddi bir hasta popülasyonu oluşturan psöriazis, atopik dermatit, akne vulgaris, rozasea, ürtiker, seboreik dermatit ve liken planus hastalıklarında psikolojik stresin bu hastalık-ların alevlenmelerindeki ve seyrindeki rolleri üzerinde durulmuştur. Çalışmamızın sonuçları ve literatürdeki bulgular, ciltte kolaylıkla fark edilebilen dermatolojik lezyonların kişilerde utanç ve suçluluk duygularını tetikleyebildiğini ve psikolojik stresi artırdığını; bu artan stres düzeyinin ise hastalığın alevlenmesinde önemli bir rol oynadığını ortaya koymaktadır. Bu karşılıklı etkileşimle oluşan kısır döngünün kırılabilmesi için dermatolojik hastalıkların taşıdığı psikolojik yükün klinisyenler tarafından göz ardı edilmemesi gerektiği belirtilmiştir. Bu nedenle hem dermatolojik hem de psikolojik tedavi yaklaşımları birlikte ele alınmalıdır. Özellikle doğru hasta gruplarında, hastalığa özgü şiddet skorlamalarının yapılması ve psikolojik belirtilerin geçerli ölçeklerle taranması, ardından bireyselleştirilmiş psikiyatrik müdahalelerin uygulanması, erken dönemde gerçekleştirildiğinde hem yaşam kalitesinin iyileştirilmesine hem de hastalığın seyrinin olumlu yönde etkilenmesine katkı sağlayabilir.
Ethical Statement
Bu derleme makalesi için etik kurul onayı gerekmemiştir; çünkü çalışma daha önce yayımlanmış araştırmalara dayanmaktadır ve insan katılımcılar veya hayvanlar üzerinde herhangi bir araştırma içermemektedir.
Supporting Institution
Bu araştırma, kamu, ticari veya kâr amacı gütmeyen sektörlerdeki fon sağlayıcı kurumlardan herhangi bir özel destek (hibe) almamıştır.
Project Number
Bu çalışma için bir proje numarası bulunmamaktadır.
Thanks
Bu makaleyi yazma sürecimde desteklerini esirgemeyen saygıdeğer Çiçek Hocaoğlu’na teşekkürlerimi sunarım.
References
-
1. Chu B, Marwaha K, Sanvictores T, Awosika AO, Ayers D. Physiology, stress reaction. In: StatPearls. Trea-sure Island (FL): StatPearls Publishing; 2024.
-
2. Mifsud KR, Reul JMHM. Mineralocorticoid and glucocorticoid receptor-mediated control of genomic responses to stress in the brain. Stress. 2018;21(5):389–402.
-
3. Ketchesin KD, Stinnett GS, Seasholtz AF. Cor-ticotropin-releasing hormone-binding protein and stress: from invertebrates to humans. Stress. 2017;20(5):449–64.
-
4. Godoy LD, Rossignoli MT, Delfino-Pereira P, Garcia-Cairasco N, Umeoka EH de L. A comprehensive overview on stress neurobiology: basic concepts and clinical implications. Front Behav Neurosci. 2018;12:127.
-
5. Swaab DF, Bao AM, Lucassen PJ. The stress system in the human brain in depression and neurodege-neration. Ageing Res Rev. 2005;4(2):141–94.
-
6. Eisen AM, Bratman GN, Olvera-Alvarez HA. Susceptibility to stress and nature exposure: unveiling differential susceptibility to physical environments; a randomized controlled trial. PLoS One. 2024;19(4):e0299965.
-
7. Gu HF, Tang CK, Yang YZ. Psychological stress, immune response, and atherosclerosis. Atherosclerosis. 2012;223(1):69–77.
-
8. Tottoli EM, Dorati R, Genta I, Chiesa E, Pisani S, Conti B. Skin wound healing process and new emer-ging technologies for skin wound care and regeneration. Pharmaceutics. 2020;12(8):735.
-
9. Lumen Learning. Layers of the skin. 2025.
-
10. Tausk F, Elenkov I, Moynihan J. Psychoneuro-immunology. Dermatol Ther 2008;21(1):22–31.
-
11. Joëls M, Baram TZ. The neuro-symphony of stress. Nat Rev Neurosci 2009;10(6):459–66.
-
12. Bao AM, Meynen G, Swaab DF. The stress sys-tem in depression and neurodegeneration: focus on the human hypothalamus. Brain Res Rev 2008;57(2):531–53.
-
13. King SB, Toufexis DJ, Hammack SE. Pituitary adenylate cyclase activating polypeptide (PACAP), stress, and sex hormones. Stress 2017;20(5):465–75.
-
14. Zhang JM, An J. Cytokines, inflammation and pain. Int Anesthesiol Clin 2007;45(2):27–37.
-
15. Han QQ, Yu J. Inflammation: a mechanism of depression? Neurosci Bull 2014;30(3):515–23.
-
16. Dinarello CA. Proinflammatory cytokines. Chest 2000;118(2):503–8.
-
17. Köhler CA, Freitas TH, Stubbs B, et al. Periphe-ral alterations in cytokine and chemokine levels after antidepressant drug treatment for major depressive disor-der: systematic review and meta-analysis. Mol Neurobiol 2018;55(5):4195–206.
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18. Maes M. Evidence for an immune response in major depression: a review and hypothesis. Prog Neu-ropsychopharmacol Biol Psychiatry 1995;19(1):11–38.
-
19. Levine J, Barak Y, Chengappa KNR, Rapoport A, Rebey M, Barak V. Cerebrospinal cytokine levels in patients with acute depression. Neuropsychobiology 1999;40(4):171–6.
-
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