Comparative evaluation of serum and gingival crevicular fluid levels of interleukin 21 in periodontally diseased and healthy patients
DOI:
https://doi.org/10.33393/jcb.2024.3149Keywords:
Blood samples, Cytokines, Gingival crevicular fluid, Interleukin 21, Periodontal diseases, PeriodontitisAbstract
Background: Periodontitis is an inflammatory reaction to subgingival pathogenic microorganisms that causes gradual deterioration of the gingiva, periodontal ligament, and alveolar bone. Interleukin (IL)-21 is the most recently found member of type I cytokine family that is upregulated during inflammation. The current study aims to investigate the biological plausibility of IL-21 as a biomarker for chronic periodontitis.
Materials and methods: This cross-sectional clinico-biochemical investigation included 15 systemically healthy, 15 periodontally healthy, 15 chronic gingivitis, and 15 chronic periodontitis subjects aged 25 to 60 years. Following subject enrollment, gingival crevicular fluid (GCF) and blood samples were then taken from each subject. The concentration of IL-21 in all samples was determined using enzyme-linked immunosorbent assay (ELISA) kit. The data was examined using the Kruskal-Wallis test and the Spearman correlation test.
Results: Serum IL-21 levels in chronic periodontitis patients were substantially greater than in periodontally healthy individuals. GCF IL-21 levels were substantially greater in gingivitis and chronic periodontitis patients compared to periodontally healthy individuals. In terms of clinical indicators, serum IL-21 levels correlated significantly with bleeding index (BI) in the chronic periodontitis group. In chronic periodontitis group, disease severity as evaluated by probing pocket depth (PPD) and clinical attachment loss (CAL) did not correlate with serum or GCF IL-21 levels.
Conclusion: According to the current study’s findings, periodontally involved patients had higher IL-21 levels than periodontally healthy patients, suggesting it can be used as biomarker. Further studies with larger sample size can shed more light on the clinical advantage of IL-21 as a possible marker for disease activity and progression.
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Salvi GE, Lang NP. Host response modulation in the management of periodontal diseases. J Clin Periodontol. 2005;32(s6)(suppl 6):108-129. https://doi.org/10.1111/j.1600-051X.2005.00785.x PMID:16128833
Grossi SG, Zambon JJ, Ho AW, et al. Assessment of risk for periodontal disease. I. Risk indicators for attachment loss. J Periodontol. 1994;65(3):260-267. https://doi.org/10.1902/jop.1994.65.3.260 PMID:8164120
Gemmell E, Yamazaki K, Seymour GJ. Destructive periodontitis lesions are determined by the nature of the lymphocytic response. Crit Rev Oral Biol Med. 2002;13(1):17-34. https://doi.org/10.1177/154411130201300104 PMID:12097235
Offenbacher S. Periodontal diseases: pathogenesis. Ann Periodontol. 1996;1(1):821-878. https://doi.org/10.1902/annals.1996.1.1.821 PMID:9118282
Taba M Jr, Kinney J, Kim AS, Giannobile WV. Diagnostic biomarkers for oral and periodontal diseases. Dent Clin North Am. 2005;49(3):551-571, vi. https://doi.org/10.1016/j.cden.2005.03.009 PMID:15978241
Fazal I, Shetty B, Yadalam U, Khan SF, Nambiar M. Effectiveness of periodontal intervention on the levels of N-terminal pro-brain natriuretic peptide in chronic periodontitis patients. J Circ Biomark. 2022;11:48-56. https://doi.org/10.33393/jcb.2022.2454 PMID:36381349
AlRowis R, AlMoharib HS, AlMubarak A, Bhaskardoss J, Preethanath RS, Anil S. Oral fluid-based biomarkers in periodontal disease – part 2. Gingival crevicular fluid. J Int Oral Health. 2014;6(5):126-135. PMID:25395809
Engebretson SP, Grbic JT, Singer R, Lamster IB. GCF IL-1beta profiles in periodontal disease. J Clin Periodontol. 2002;29(1):48-53. https://doi.org/10.1034/j.1600-051x.2002.290108.x PMID:11846849
Irwin CR, Myrillas TT. The role of IL-6 in the pathogenesis of periodontal disease. Oral Dis. 1998;4(1):43-47. https://doi.org/10.1111/j.1601-0825.1998.tb00255.x PMID:9655045
Harada A, Sekido N, Akahoshi T, Wada T, Mukaida N, Matsushima K. Essential involvement of interleukin-8 (IL-8) in acute inflammation. J Leukoc Biol. 1994;56(5):559-564. https://doi.org/10.1002/jlb.56.5.559 PMID:7964163
Tsai IS, Tsai CC, Ho YP, Ho KY, Wu Y-M, Hung CC. Interleukin-12 and interleukin-16 in periodontal disease. Cytokine. 2005;31(1):34-40. https://doi.org/10.1016/j.cyto.2005.02.007 PMID:15886011
de Rham C, Ferrari-Lacraz S, Jendly S, Schneiter G, Dayer JM, Villard J. The proinflammatory cytokines IL-2, IL-15 and IL-21 modulate the repertoire of mature human natural killer cell receptors. Arthritis Res Ther. 2007;9(6):R125. doi: 10.1186/ar2336. PMID: 18053164
Sarra M, Pallone F, Monteleone G. Interleukin-21 in chronic inflammatory diseases. Biofactors. 2013;39(4):368-373. https://doi.org/10.1002/biof.1105 PMID:23553807
Rasmussen TK, Andersen T, Hvid M, et al. Increased interleukin 21 (IL-21) and IL-23 are associated with increased disease activity and with radiographic status in patients with early rheumatoid arthritis. J Rheumatol. 2010;37(10):2014-2020. https://doi.org/10.3899/jrheum.100259 PMID:20682664
Gerlach K, Daniel C, Lehr HA, et al. Transcription factor NFATc2 controls the emergence of colon cancer associated with IL-6-dependent colitis. Cancer Res. 2012;72(17):4340-4350. https://doi.org/10.1158/0008-5472.CAN-11-4155 PMID:22738913
Abraham C, Cho J. Interleukin-23/Th17 pathways and inflammatory bowel disease. Inflamm Bowel Dis. 2009;15(7):1090-1100. https://doi.org/10.1002/ibd.20894 PMID:19253307
Nurieva R, Yang XO, Martinez G, et al. Essential autocrine regulation by IL-21 in the generation of inflammatory T cells. Nature. 2007;448(7152):480-483. https://doi.org/10.1038/nature05969 PMID:17581589
Onoda T, Rahman M, Nara H, et al. Human CD4+ central and effector memory T cells produce IL-21: effect on cytokine-driven proliferation of CD4+ T cell subsets. Int Immunol. 2007;19(10):1191-1199. https://doi.org/10.1093/intimm/dxm090 PMID:17698559
Pelletier M, Girard D. Biological functions of interleukin-21 and its role in inflammation. ScientificWorldJournal. 2007;7:1715-1735. https://doi.org/10.1100/tsw.2007.275 PMID:17982568
Shetty B, Fazal I, Khan SF, et al. Association between cardiovascular diseases and periodontal disease: more than what meets the eye. Drug Target Insights. 2023;17:31-38. https://doi.org/10.33393/dti.2023.2510 PMID:36761891
Persson GR. Site-based versus subject-based periodontal diagnosis. Periodontol 2000. 2005;39(1):145-163. https://doi.org/10.1111/j.1600-0757.2005.00130.x PMID:16135069
Loos BG, Tjoa S. Host-derived diagnostic markers for periodontitis: do they exist in gingival crevice fluid? Periodontol 2000. 2005;39(1):53-72. https://doi.org/10.1111/j.1600-0757.2005.00129.x PMID:16135064
Dutzan N, Rivas C, García-Sesnich J, et al. Levels of interleukin-21 in patients with untreated chronic periodontitis. J Periodontol. 2011 Oct;82(10):1483-1489. doi: 10.1902/jop.2011.100449. PMID: 21405938.
Dutzan N, Vernal R, Vaque JP, et al. Interleukin-21 expression and its association with proinflammatory cytokines in untreated chronic periodontitis patients. J Periodontol. 2012;83(7):948-954. https://doi.org/10.1902/jop.2011.110482 PMID:22181687
Lokhande RV, Ambekar JG, Bhat KG, Dongre NN. Interleukin-21 and its association with chronic periodontitis. J Indian Soc Periodontol. 2019;23(1):21-24. https://doi.org/10.4103/jisp.jisp_410_18 PMID:30692738
Zhao L, Zhou Y, Xu Y, Sun Y, Li L, Chen W. Effect of non-surgical periodontal therapy on the levels of Th17/Th1/Th2 cytokines and their transcription factors in Chinese chronic periodontitis patients. J Clin Periodontol. 2011;38(6):509-516. https://doi.org/10.1111/j.1600-051X.2011.01712.x PMID:21392046
Napimoga MH, Nunes LH, Maciel AA, et al. Possible involvement of IL-21 and IL-10 on salivary IgA levels in chronic periodontitis subjects. Scand J Immunol. 2011;74(6):596-602. https://doi.org/10.1111/j.1365-3083.2011.02605.x PMID:21815905
Vahabi S, Yadegari Z, Pournaghi S. The comparison of the salivary concentration of interleukin-17 and interleukin-18 in patients with chronic periodontitis and healthy individuals. Dent Res J (Isfahan). 2020;17(4):280-286. https://doi.org/10.4103/1735-3327.292060 PMID:33282154
Khiste SV, Ranganath V, Nichani AS, Rajani V. Critical analysis of biomarkers in the current periodontal practice. J Indian Soc Periodontol. 2011;15(2):104-110. https://doi.org/10.4103/0972-124X.84376 PMID:21976831
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Copyright (c) 2024 Shabnam Gulfishan, Suhail Ahmed Syed, Krishnanjeya Reddy Pathakota, Preethi Krishnan, Aravinda B Reddy, Ibrahim Fazal
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Accepted 2024-08-20
Published 2024-09-20