Measurment of Serum level of Catestatin in patients with Acne vulgaris

Document Type : Original Article

Authors

1 Dermatology department, Faculty of Medicine, Beni-Suef University, Beni-Suef 62511, Egypt

2 Biochemistry department, Faculty of Medicine, Beni-Suef University, Beni-Suef 62511, Egypt

3 Dermatology department, Sheikh Zayed Specialized Hospital, Giza12511, Egypt

Abstract

Background: Acne is a persistent inflammatory condition of the pilosebaceous unit. The pathogenesis encompasses three components: hyperseborrhea, aberrant follicular keratinization, and the development of Propionibacterium acnes inside the pilosebaceous unit. Objective: To evaluate serum catestatin (CST) level in Acne vulgaris patients as an attempt to answer the question about its role in disease pathogenesis and severity.  Patients and Methods: This case-control study was carried out on 45 patients with different degrees of acne vulgaris severity (Group A) in addition to 45 age and sex matched healthy volunteers as a control group (Group B).  For all participants, thorough history taking and good general and dermatological examination were done. Serum levels of catestatin were tested. Results: The present investigation revealed that CST levels (ng/ml) in acne vulgaris patients were reported at (8.21±5.70 ng/ml), but in healthy controls, they were (3.04±0.84 ng/ml). A very substantial difference existed between the two groups. Serum levels of CST were somewhat elevated in females relative to men; however, this disparity was statistically insignificant. The levels of CST were elevated in individuals with severe lesions; nevertheless, the serum levels of CST exhibited a non-statistically significant difference concerning lesion severity. There was a significant negative correlation between CST level (ng/ml) and age (years) of the acne patients (r=-0.321, p=0.032). Conclusion: A very substantial difference existed between the two groups regarding CST level but connection to acne severity was not verified.

Keywords

Main Subjects


  1.  

    1. Dréno, B., Pécastaings, S., Corvec, S., Veraldi, S., Khammari, A., & Roques, C. (2018). Cutibacterium acnes (Propionibacterium acnes) and acne vulgaris: a brief look at the latest updates. Journal of the European Academy of Dermatology and Venereology32, 5-14.
    2. Alanazi, M. S., Hammad, S. M., & Mohamed, A. E (2018): Prevalence and psychological impact of Acne vulgaris among female secondary school students in Arar city. Electronic physician.; 10(8): 7224–7229.
    3. Bagatin, E., Freitas, T. H. P., Rivitti-Machado, M. C., Machado, M. C. R., Ribeiro, B. M., Nunes, S., & Rocha, M. A. D. D (2019): Adult female acne: a guide to clinical practice. Anais brasileiros de dermatologia.; 94(1): 62–75.
    4. González-Mondragón, E. A., Ganoza-Granados, L. D. C., Toledo-Bahena, M. E., Valencia-Herrera, A. M., Duarte-Abdala, M. R., Camargo-Sánchez, K. A., & Mena-Cedillos, C. A. (2022). Acne and diet: a review of pathogenic mechanisms. Boletín médico del Hospital Infantil de México, 79(2), 83-90.
    5. Yang, J., Yang, H., Xu, A., & He, L (2020): A Review of Advancement on Influencing Factors of Acne: An Emphasis on Environment Characteristics. Frontiers in public health.; 8, 450.
    6. Aung, G., Niyonsaba, F., Ushio, H., Kajiwara, N., Saito, H., Ikeda, S., Ogawa, H., & Okumura, K (2011): Catestatin, a neuroendocrine antimicrobial peptide, induces human mast cell migration, degranulation and production of cytokines and chemokines. Immunology.; 132(4): 527– 539.
    7. Deng, Z., & Xu, C (2017): Role of the neuroendocrine antimicrobial peptide catestatin in innate immunity and pain. Acta biochimica et biophysica Sinica.; 49(11): 967–972.
    8. Dréno B (2017): what is new in the pathophysiology of acne, an overview. Journal of the European Academy of Dermatology and Venereology.; 31 Suppl 5, 8–12.
    9. Ali Awad, E. Y., Soliman, F. E. S., & Maklad, S. A. (2022). The Effect of Acne Vulgaris on Body Image Satisfaction, Self Esteem and Quality of Life of Adolescents at Tanta city. Tanta Scientific Nursing Journal27(4), 188-206.
    10. El-Tahlawi, S. M., Mohamed, N. E., Mohamed, S. R., & Abd El Nasser, L. (2020). Serum level of vitamin D &Beta-2-defensin in patients with acne vulgaris. Fayoum University Medical Journal7(1), 134-146.
    11. Yücesoy, S. N., Ak, T., Öner, S., & Serdaroğlu, S. (2023). Serum catestatin levels in patients with acne vulgaris: single-center prospective study. Skin Appendage Disorders, 1-7.
    12. Durai, P. C. T., & Nair, D. G. (2015). Acne vulgaris and quality of life among young adults in South India. Indian journal of dermatology60(1), 33-40.
    13. George, R. M., & Sridharan, R. (2018). Factors aggravating or precipitating acne in Indian adults: a hospital-based study of 110 cases. Indian journal of dermatology63(4), 328-331.
    14. Jaber, R. M., Alnshash, B. M., Mousa, S. N., Fayoumi, H. S., Al-Qaderi, L. M., & Zant, A. M. (2020). The epidemiology of acne vulgaris among adolescents and young adults in Jordan University Hospital. Open Journal of Nursing10(4), 353-366.
    15. Shah, N., Shukla, R., Chaudhari, P., Patil, S., Patil, A., Nadkarni, N., & Goldust, M. (2021). Prevalence of acne vulgaris and its clinico‐epidemiological pattern in adult patients: Results of a prospective, observational study.Journal of cosmetic dermatology20(11), 3672-3678.
    16. Skroza N, Tolino E, Mambrin A, Zuber S, Balduzzi V, Marchesiello A, Bernardini N, Proietti I and Potenza C (2018). Adult acne versus adolescent acne. J Clin Aesthet Dermatol. 11:21–25.
    17. Al-Kubaisy, W., Abdullah, N. N., Kahn, S. M., & Zia, M. (2014). Sociodemographic characteristics of acne among university students in Damascus, Syria. Epidemiology Research International2014(1), 974019.
    18. Smithard, A., Glazebrook, C., & Williams, H. C. (2001). Acne prevalence, knowledge about acne and psychological morbidity in mid‐adolescence: a community‐based study.British Journal of Dermatology145(2), 274-279.
    19. Ogé, L. K., Broussard, A., & Marshall, M. D. (2019). Acne vulgaris: diagnosis and treatment. American family physician100(8), 475-484.
    20. Özçelik, S., Kulaç, İ., Yazıcı, M., & Öcal, E. (2018). Distribution of childhood skin diseases according to age and gender, a single institution experience. Turkish Archives of Pediatrics/Türk Pediatri Arşivi, 53(2), 105.‏
    21. Poli, F., Dreno, B., & Verschoore, M. (2001). An epidemiological study of acne in female adults: results of a survey conducted in France. Journal of the European Academy of Dermatology and Venereology, 15(6), 541-545.
    22. Nagy, I., Pivarcsi, A., Koreck, A., Széll, M., Urbán, E., & Kemény, L. (2005). Distinct strains of Propionibacterium acnes induce selective human β-defensin-2 and interleukin-8 expression in human keratinocytes through toll-like receptors. Journal of Investigative Dermatology, 124(5), 931-938.
    23. Nagy, I., Pivarcsi, A., Kis, K., Koreck, A., Bodai, L., McDowell, A., ... & Kemény, L. (2006). Propionibacterium acnes and lipopolysaccharide induce the expression of antimicrobial peptides and proinflammatory cytokines/chemokines in human sebocytes. Microbes and infection, 8(8), 2195-2205.
    24. Rokowska-Waluch, A., Pawlaczyk, M., Cybulski, M., Żurawski, J., Kaczmarek, M., Michalak, M., & Mojs, E. (2016). Stressful events and serum concentration of substance P in acne patients. Annals of dermatology28(4), 464-469.
    25. Nagiub, H., Elbayomi, Y., Mansour, M., & Zohdy, M. (2021). Serum level of the neuropeptide substance ‘P’in patients with acne vulgaris. Egyptian Journal of Dermatology and Venerology, 41(1), 10.‏
    26. El-Ramly, A. Z., Fawzi, M. M., Mahmoud, S. B., Ghaffar, M. M. A., & Shaker, O. G. (2016). Assessment of serum levels of cathelicidin and vitamin D in acne vulgaris. Journal of the Egyptian Women’s Dermatologic Society13(2), 99-105.
    27. Al‐Sudany, N. K., Mohammed, N. H., & Alrifai, S. B. (2019). Downregulation of S100a7a antimicrobial peptide in acne vulgaris patients after isotretinoin therapy. Dermatologic Therapy32(6), e13136.
    28. Borovaya, A., Dombrowski, Y., Zwicker, S., Olisova, O., Ruzicka, T., Wolf, R., ... & Sárdy, M. (2014). Isotretinoin therapy changes the expression of antimicrobial peptides in acne vulgaris. Archives of dermatological research, 306, 689-700.‏
    29. Chronnell, C. M., Ghali, L. R., Quinn, A. G., Bull, J. J., McKay, I. A., Philpott, M. P., ... & Cunliffe, W. J. (2001). Human β defensin-1 and-2 expression in human pilosebaceous units: upregulation in acne vulgaris lesions. Journal of Investigative Dermatology, 117(5), 1120-1125.‏
    30. Coates, S. J., Lee, E. H., & Granstein, R. D. (2017). Cutaneous Neuroimmunology. Clinical and Basic Immunodermatology, 179-199.
    31. Jati, S., Mahata, S., Das, S., Chatterjee, S., & Mahata, S. K. (2023). Catestatin: antimicrobial functions and potential therapeutics. Pharmaceutics15(5), 1550.
    32. Egger, M., Beer, A. G., Theurl, M., Schgoer, W., Hotter, B., Tatarczyk, T., ... & Kirchmair, R. (2008). Monocyte migration: a novel effect and signaling pathways of catestatin. European journal of pharmacology, 598(1-3), 104-111.‏
    33. Simac, P., Perkovic, D., Bozic, I., Matijas, M., Gugo, K., Martinovic, D., & Bozic, J. (2022). Serum catestatin levels in patients with rheumatoid arthritis. Scientific Reports, 12(1), 3812.‏
    34. Muntjewerff, E. M., Tang, K., Lutter, L., Christoffersson, G., Nicolasen, M. J., Gao, H., ... & Mahata, S. K. (2021). Chromogranin A regulates gut permeability via the antagonistic actions of its proteolytic peptides. Acta Physiologica, 232(2), e13655.‏
    35. Rabbi, M. F., Munyaka, P. M., Eissa, N., Metz-Boutigue, M. H., Khafipour, E., & Ghia, J. E. (2017). Human catestatin alters gut microbiota composition in mice. Frontiers in Microbiology7, 2151.
    36. Luketin, M., Mizdrak, M., Boric-Skaro, D., Martinovic, D., Tokic, D., Vilovic, M., ... & Bozic, J. (2021). Plasma catestatin levels and advanced glycation end products in patients on hemodialysis. Biomolecules, 11(3), 456.‏
    37. Ma, L. Y., Chen, W. W., Gao, R. L., Liu, L. S., Zhu, M. L., Wang, Y. J., ... & Hu, S. S. (2020). China cardiovascular diseases report 2018: an updated summary. Journal of geriatric cardiology: JGC, 17(1), 1.‏