|Year : 2016 | Volume
| Issue : 5 | Page : 413-418
Serum level of Interleukin-8 in subjects with diabetes, diabetes plus oral lichen planus, and oral lichen planus: A biochemical study
Atefeh Tavangar1, Faezeh Khozeimeh2, Fereshtehossadat Ghoreishian3, Mahsa Abbasi Boroujeni4
1 Dental Materials Research Center and Department of Oral and Maxillofacial Medicine, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran
2 Dental Research Center and Department of Oral and Maxillofacial Medicine, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran
3 Dentist, Isfahan University of Medical Science, Isfahan, Iran
4 Department of Prosthodontics School of Dentistry, Isfahan University of Medical Science, Isfahan, Iran
|Date of Web Publication||14-Oct-2016|
Mahsa Abbasi Boroujeni
Department of Prosthodontics School of Dentistry, Isfahan University of Medical Science, Isfahan
Source of Support: None, Conflict of Interest: None
Background: Correlation between diabetes mellitus (DM) and oral lichen planus (OLP) seems probable. Since Interleukin-8 (IL-8) is an important inflammatory mediator involved in both conditions, this study aimed to measure and compare the serum level of IL-8 in DM, OLP, and DM + OLP patients in comparison with healthy individuals.
Materials and Methods: This cross sectional study was conducted on 75 patients (30 OLP, 5 OLP and type II DM, 20 type II DM, and 20 healthy controls). Serum levels of IL-8, fasting blood sugar (FBS) and 2-h postprandial blood sugar were measured in the four groups. Data were analyzed using SPSS version 20 by one-way ANOVA and post_hocleast significant difference test.
Results: Type II DM patients with OLP had the highest mean serum level of IL-8 followed by OLP, DM and control groups, respectively. Pairwise comparison of groups revealed significant differences in serum IL-8 between the control and OLP and also control and OLP+DM (P < 0.05) groups. No other significant differences were noted. The mean levels of FBS and 2-h postprandial blood sugar were the highest in OLP+DM patients followed by DM, OLP and control groups, respectively.
Conclusion: The ascending trend of serum level of IL-8 in the control, DM, OLP, and DM+OLP patients may indicate the role of this factor in the pathogenesis of DM and OLP. Moreover, it may play a synergistic role in patients suffering from both conditions.
Keywords: Diabetes mellitus, interleukin-8, lichen planus, oral, serum, type 2
|How to cite this article:|
Tavangar A, Khozeimeh F, Ghoreishian F, Boroujeni MA. Serum level of Interleukin-8 in subjects with diabetes, diabetes plus oral lichen planus, and oral lichen planus: A biochemical study. Dent Res J 2016;13:413-8
|How to cite this URL:|
Tavangar A, Khozeimeh F, Ghoreishian F, Boroujeni MA. Serum level of Interleukin-8 in subjects with diabetes, diabetes plus oral lichen planus, and oral lichen planus: A biochemical study. Dent Res J [serial online] 2016 [cited 2021 Sep 25];13:413-8. Available from: https://www.drjjournal.net/text.asp?2016/13/5/413/192277
| Introduction|| |
Oral lichen planus (OLP) is a T-cell mediated inflammatory disease of the oral mucosa. The etiology of OLP is unknown and it occurs in 0.5% -1.9% of the population. , Interleukin-8(IL-8) is an important mediator of host response to injury, trauma and inflammation  and plays a role in activation of neutrophils, neutrophil chemotactic factor, T-cells and basophils.  Interlukin-8 is produced by different cells such as monocytes/macrophages, T-cells, neutrophils, endothelial cells, fibroblasts and keratinocytes in inflammatory and pathological processes. ,, Healthy tissues have insignificant amounts of IL-8 but its concentration quickly reaches 10-100 times its baseline level in response to pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) or IL-1β, bacterial or viral products, and cellular stress. 
Keratinocytes in OLP patients can synthesize IL-1 and TNF-α., Moreover, mononuclear cells infiltrated in the tissues in mucosal OLP patients, as well as mononuclear cells in the peripheral blood of these patients, can produce TNF-α.,, Furthermore, following an increase in releasing both locally and systemically of IL-1 and TNF-α, keratinocytes, macrophages, T-cells, endothelial cells and fibroblasts in OLP lesions release significant amounts of IL-8.Interlukin-8 results in greater infiltration of T-cells such as cytotoxic T-cells at the site of OLP. Thus, IL-8 may be involved in the pathogenesis of OLP. 
Studies have shown that serum levels of IL-6 and IL-8 are higher in OLP patients compared to healthy individuals. , Moreover, serum level of IL-8 is a more specific indicator of OLP than IL-6. 
Diabetes mellitus (DM) is a metabolic disease caused by impaired insulin production or resistance to it, and is characterized by the abnormal metabolism of glucose, proteins and lipids.  In fact, type II DM is an inflammatory disease and inflammatory cytokines are involved in its pathogenesis.  Serum level of IL-8 in type II DM is significantly higher than that in healthy individuals. ,
At present, a correlation between DM and OLP seems probable.  The Prevalence of DM in OLP patients has been reported as1.6% - 85%. ,, Studies in this regard have been variable in the methodology and results. Jolly showed that 85% of patients with OLP in his study had abnormal glucose tolerance test results.  Seyhan et al., in their study stated that half of the patients with OLP had glucose metabolism impairment and one-fourth of these patients had DM.  However, other studies failed to show a higher incidence of abnormal glucose tolerance test in OLP patients compared to the healthy population. ,
Since IL8 is an important inflammatory mediator involved in both conditions, the first objective of this study was to measure and compare the serum level of IL8 in four groups of OLP, DM, OLP+DM and healthy control. Considering the existing controversies regarding the possible association of DM and OLP, the second objective of this study was to assess the fasting blood sugar (FBS) and 2-h postprandial blood sugar in OLP patients.
| Materials and Methods|| |
This analytical cross sectional study was conducted on three groups of OLP, type II DM and control. Considering the 80% power ofthe study, d = 50 and α = 0.05, thesample size was calculated to be 35 in OLP, 20 in type II DM and 20 in control groups. Samples were selected through convenience sampling among those presenting to Isfahan School of Dentistry and clinics in the city of Isfahan. The OLP group was divided into two subgroups of OLP alone and OLP + type II DM. Thus, 30 OLP,5OLP and type II DM,20 type II DM and 20healthy control individuals were evaluated. The healthy controls were selected among those presenting for check up and had no history of systemic disease or drug intake. An internal medicine specialist confirmed the health of control subjects. The DM patients were selected among subjects suspected for DM, who referredto a diabetes treatment center for a definite diagnosis. These subjects had FBS ≥110 mg/dL or 2-h postprandial blood sugar ≥200 mg/dL and reported polyphagia, polydipsia and polyuria.  These subjects had no other systemic disease and reported no drug intake. The diagnosis of type II DM was made by an internal medicine specialist.
The OLP patients were selected among those presenting to Isfahan School of Dentistry and clinics in the city of Isfahan.Following observation of white striations and red streaks and inclusion of OLP in the list of differential diagnoses (according to the clinical criteria) by an oral medicine specialist, a biopsy sample was taken from the lesion. Upon confirmation of OLP by pathologist according to the World Health Organization criteria,  the patient was included in the study. Patients with lichenoid reactions due to medications or contact and those with graft versus host disease (frequently Bone marrow graft) or cutaneous lesions were excluded. Fasting and 2-hpostprandial blood sugar tests were requested for subjects with definite diagnosis of OLP.Based on the test results, they were assigned to OLP or OLP+DM group until 35 samples were recruited.
All participants underwent a thorough physical examination to ensurethe absence of inflammation in other parts of the body. Tobacco users, alcohol consumers and patients with periodontitis were excluded. In general, patients with a history of systemic conditions other than DM and OLP and those on any type of medication were excluded from the study.
After 8 h of fasting, 3cc of blood was drawn from each subject between 7 and 9 a.m.(to prevent errors due to the circadian rhythm). Within 5-10 minutes, subjects had a usual breakfast (carbohydrate-rich) and underwent 2-h postprandial blood sugar test two hours after the breakfast. Within this 2-h period, subjects were requested to refrain from severe physical exercise. Immediately after clotting, blood samples were centrifuged at 3000 rpm for 15 minutes to isolate the serum. Immediately afterwards, the FBS and 2-h postprandial blood sugar were measured. The remaining serum isolated from the fasting blood sample was stored at 20°C for measurement of IL-8 using the ELISA Kit (Quantikine ELISA, R and D Systems, Inc., USA). The obtained data were analyzed using SPSS (IBM Stasistics 20), one-way ANOVA and post - hocleast significant difference (LSD) test. Normality of the data was checked using Kolmogorov- Smirnov test.
| Results|| |
A total of 20 DM, 20 healthy control and 35 OLP individuals were included; 14.28% of OLP patients had type II DM. Furthermore, 20% of OLP patients had impaired fasting glucose (FBS of 100- 125 mg/dL).
As seen in [Table 1], the highest mean concentration of serum IL-8 was seen in OLP+DM group followed by OLP, DM (6.1 ± 1.91 pg/mL) and control (5.3 ± 1.23 pg/mL) groups.
|Table 1: The mean (±standard deviation) and range of changes in serum interleukin-8 concentration in the four groups and result of post hoc least significant difference test|
Click here to view
One-way ANOVA showed significant differences among groups in terms of serum level of IL8 (P = 0.011). Post-hoc LSD test was then applied and showed a significant difference in serum level of IL-8 between the control and OLP groups (P = 0.002). The difference between the OLP+DM and control subjects was also significant in terms if serum level of IL-8 (P = 0.022). However, although the mean serum level of IL-8 in the DM group was higher than that in the control group, this difference was not significant (P = 0.087). The serum level of IL8 in OLP+DM patients was higher than that in DM group but this difference was not significant either (P = 0.219). The serum level of IL8 was higher in OLP+DM group compared to the OLP group but not significantly (P = 0.615).
The mean levels of FBS and 2-h postprandial blood sugar in OLP+DM patients were the highest followed by DM, OLP and control groups, respectively [Table 2].
|Table 2: The mean levels of fasting blood sugar and 2-h postprandial blood sugar in the four groups|
Click here to view
| Discussion|| |
To the best of the authors' knowledge, no previous study has compared FBS, 2-h postprandial blood sugar and IL-8 levels in the serum of OLP, type II DM, OLP+DM and control subjects simultaneously; thus, the current study is probably the first one.
The first objective of this study was comparing the serum level of IL-8 in OLP subjects and healthy individuals. The results showed that the mean serum level of IL-8 in OLP patients was significantly higher than that in controls (P < 0.05). Sun et al.,  in 2005 concluded that the serum level of IL-8 was significantly higher in OLP patients than controls and thus, IL-8 is a more sensitive marker than IL-6 for diagnosis of OLP. Rhodus et al. in 2005  and Zhang et al. in 2008  stated that the serum and salivary levels of IL8 were significantly higher than those in control group. Our findings are in agreement with the results of the above-mentioned studies. The following explanation can better elucidate the reason behind higher serum level of IL-8 in OLP patients compared to healthy controls. In general, there is a strong theory that T-cell-mediated autoimmune reactions are involved in the pathogenesis of OLP.The localand systemic release of different cytokines from the oral mucosa and blood is responsible for initiation and progression of this disease.  Histological analysis has shown band-like infiltrates of T lymphocytes in the upper lamina propriaof OLP lesions.  Inflammatory cytokines such as TNF-αand IL-1 stimulate T - cells, monocytes, macrophages, keratinocytes, neutrophils, and endothelial cells and result in secretion of IL-8 in the lesion and in the peripheral blood. , Cell culture studies have shown that OLP keratinocytes produce higher levels ofTNF-α than gingivitis keratinocytes. , Thus, greater infiltration of inflammatory cells especially T - cells as well as increased secretion of TNF-α and IL-1 in these patients can lead to higher secretion of IL-8; which explains the high serum levels of IL-8 in OLP patients compared to healthy individuals.
Based on previous studies, OLP plus DM may occur concomitantly. ,, Thus, the second objective of this study was to assess the serum level of IL-8 as a possible relevant factor in DM patients compared to healthy individuals. In the current study, the mean serum level of IL-8 in DM patients (6.1 ± 1.91 pg/mL) was higher than that in controls (5.3 ± 1.23pg/mL); however, this difference was not significant (P > 0.05). According to a study by Abou-Shousha et al.,  serum level of IL-8 in DM patients was significantly higher than that in healthy controls (P = 0.032). They suggested that serum level of IL-8 could be used as a predictor of DM-related micro- and macro-vascular diseases especially in high-risk individuals. Other studies also showed significantly higher serum level of IL-8 in type II DM compared to healthy individuals. , Although in the above-mentioned studies the serum level of IL-8 in diabetic patients was significantly higher than that in controls, this difference in our study was not significant. Such difference in results might be due to the variable sample sizes, differences in the nutritional regimens of healthy individuals, genetic variations and ethnic characteristics of subjects in different geographical locations. In general, it seems that high glucose level in diabetic patients results in attachment of monocytes to endothelial cells and subsequent production of IL-8. ,
The third objective of the current study was to measure the serum level of IL-8 in patients with OLP+DM in comparison with OLP plu DM patients as well as healthy controls. In our study, a significantly higher level of serum IL-8 was found in OLP+DM patients compared to healthy controls (despite the small sample size of the former group)-(P < 0.05). No previous study has been conducted in this regard to compare with.
Since the occurrence of DM and glucose impairments has been reported in OLP patients, ,, the fourth objective of this study was to measure the levels of FBS and 2-h postprandial blood sugar in OLP patients in comparison with other groups. The mean level of FBS and 2-h postprandial blood sugar was the highest in OLP+DM patients followed by DM, OLP and control groups, respectively. In our study, 14.28% of OLP patients had DM and 20% had impaired fasting glucose (FBS of 100-125 mg/dL). Despite the higher mean level of FBS in OLP patients compare tocontrols, this difference did not reach statistical significance.
Seyhan et al.  found a significant difference in FBS between OLP and control subjects; whereas, some other studies failed to show a higher frequency of abnormal glucose tolerance test in OLP patients compared to the general population. , Ansar et al.  reported that the mean FBS in OLP patients was 102.5 ± 32 mg/dL. This value was close to the value reported in our study (99.85 ± 14.4 mg/dL). Such controversy in the results of the afore-mentioned studies may be due to different methodology and study designs. Higher FBS levels in OLP patients compared to healthy controls points to the possible role of glucose intolerance in the pathogenesis of OLP.  In addition, the ascending trend of the serum level of IL8 in control, DM, OLP, and OLP+DM patients may indicate the role of this factor in the pathogenesis of OLP and DB; moreover, it may have a synergistic effect on both conditions.
In this study, it was not possible to detect internal inflammation (if any); thus, the IL-8 value was not exclusively indicative of OLP or DM. Small sample size in the OLP+DM group was another limitation of our study which was due to the small number of OLP patients and difficulty in encouraging them to participate in the study. Future studies with larger sample sizes are required on OLP patients to compare the serum level of IL-8 in different types of OLP and also to assess its role in the clinical course of the disease.
| Conclusion|| |
The results showed higher serum levels of IL-8 in OLP+DM and OLP patients compared to healthy controls. Thus, IL-8 should be considered as an effective inflammatory factor in the pathogenesis of this disease. Administration of medications balancing the level of IL8 and decreasing its serum level may be a step forward to alleviate the symptoms of OLP and OLP+DM patients.
| Acknowledgments|| |
This study financially supportedby the dental Research commitee of Isfahan University of MedicalSciences.
Financial support and sponsorship
Grant Number: 394661.
Conflicts of interest
The authors of this manuscript declare that they have no conflicts of interest, real or perceived, financial or non-financial in this article.
| References|| |
Porter SR, Kirby A, Olsen I, Barrett W. Immunologic aspects of dermal and oral lichen planus: A review. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997;83:358-66.
Brown RS, Bottomley WK, Puente E, Lavigne GJ. A retrospective evaluation of 193 patients with oral lichen planus. J Oral Pathol Med 1993;22:69-72.
Abboud CN, Scully SP, Lichtman AH, Brennan JK, Segel GB. The requirements for ionized calcium and magnesium in lymphocyte proliferation. J Cell Physiol 1985;122:64-72.
al-Dalaan A, al-Sedairy S, al-Balaa S, al-Janadi M, Elramahi K, Bahabri S, et al.
Enhanced interleukin 8 secretion in circulation of patients with Behçet′s disease. J Rheumatol 1995;22:904-7.
Wang LM, Kitteringham N, Mineshita S, Wang JZ, Nomura Y, Koike Y, et al.
The demonstration of serum interleukin-8 and superoxide dismutase in Adamantiades-Behçet′s disease. Arch Dermatol Res 1997;289:444-7.
Ozoran K, Aydintug O, Tokgöz G, Düzgün N, Tutkak H, Gürler A. Serum levels of interleukin-8 in patients with Behcet′s disease. Ann Rheum Dis 1995;54:610.
Zouboulis CC, Katsantonis J, Ketteler R, Treudler R, Kaklamani E, Hornemann S, et al.
Adamantiades-Behçet′s disease: Interleukin-8 is increased in serum of patients with active oral and neurological manifestations and is secreted by small vessel endothelial cells. Arch Dermatol Res 2000;292:279-84.
Karagouni EE, Dotsika EN, Sklavounou A. Alteration in peripheral blood mononuclear cell function and serum cytokines in oral lichen planus. J Oral Pathol Med 1994;23:28-35.
Yamamoto T, Osaki T, Yoneda K, Ueta E. Cytokine production by keratinocytes and mononuclear infiltrates in oral lichen planus. J Oral Pathol Med 1994;23:309-15.
Yamamoto T, Osaki T. Characteristic cytokines generated by keratinocytes and mononuclear infiltrates in oral lichen planus. J Invest Dermatol 1995;104:784-8.
Sun A, Wang JT, Chia JS, Chiang CP. Serum interleukin-8 level is a more sensitive marker than serum interleukin-6 level in monitoring the disease activity of oral lichen planus. Br J Dermatol 2005;152:1187-92.
de Moura Castro Jacques C, Cardozo Pereira AL, Cabral MG, Cardoso AS, Ramos-e-Silva M. Oral lichen planus part I: Epidemiology, clinics, etiology, immunopathogeny, and diagnosis. Skinmed 2003;2:342-7.
Desir GV. Kv1.3 potassium channel blockade as an approach to insulin resistance. Expert Opin Ther Targets 2005;9:571-9.
Abou-Shousha S, Abd El-Megeed MH, Sultan HK. Interleukin-8, ferritin and soluble transferrin receptors in type II diabetes mellitus. Egypt J Immunol 2006;13:19-25.
Srinivasan S, Hatley ME, Reilly KB, Danziger EC, Hedrick CC. Modulation of PPARalpha expression and inflammatory interleukin-6 production by chronic glucose increases monocyte/endothelial adhesion. Arterioscler Thromb Vasc Biol 2004;24:851-7.
Home P. Contributions of basal and post-prandialhyperglycaemia to micro- and macrovascular complications in people with type 2 diabetes. Curr Med Res Opin 2005;21:989-98.
Lundström IM. Incidence of diabetes mellitus in patients with oral lichen planus. Int J Oral Surg 1983;12:147-52.
Nigam PK, Sharma L, Agrawal JK, Singh G, Khurana SK. Glucose tolerance studies in lichen planus. Dermatologica 1987;175:284-9.
Conte A, Inverardi D, Loconsole F, Petruzzellis V, Rantuccio F. A retrospective study of 200 cases of lichen. G Ital Dermatol Venereol 1990;125:85-9.
Denli YG, Durdu M, Karakas M. Diabetes and hepatitis frequency in 140 lichen planus cases in Cukurova region. J Dermatol 2004;31:293-8.
Jolly M. Lichen planus and its association with diabetes mellitus. Med J Aust 1972;1:990-2.
Seyhan M, Ozcan H, Sahin I, Bayram N, Karincaoglu Y. High prevalence of glucose metabolism disturbance in patients with lichen planus. Diabetes Res Clin Pract 2007;77:198-202.
Christensen E, Holmstrup P, Wiberg-Jorgensen F, Neumann-Jensen B, Pindborg JJ. Glucose tolerance in patients with oral lichen planus. J Oral Pathol 1977;6:143-51.
Bussell SN, Smales FC, Sutton RB, Duckworth R. Glucose tolerance in patients with lesions of the oral mucosa. Br Dent J 1979;146:186-8.
Alberti KG, Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 1998;15:539-53.
Kramer IR, Lucas RB, Pindborg JJ, Sobin LH. Definition of leukoplakia and related lesions: An aid to studies on oral precancer. Oral Surg Oral Med Oral Pathol 1978;46:518-39.
Rhodus NL, Cheng B, Bowles W, Myers S, Miller L, Ondrey F. Proinflammatory cytokine levels in saliva before and after treatment of (erosive) oral lichen planus with dexamethasone. Oral Dis 2006;12:112-6.
Zhang Y, Lin M, Zhang S, Wang Z, Jiang L, Shen J, et al.
NF-kappaB-dependent cytokines in saliva and serum from patients with oral lichen planus: A study in an ethnic Chinese population. Cytokine 2008;41:144-9.
Khan A, Farah CS, Savage NW, Walsh LJ, Harbrow DJ, Sugerman PB. Th1 cytokines in oral lichen planus. J Oral Pathol Med 2003;32:77-83.
Katsantonis J, Adler Y, Orfanos CE, Zouboulis CC. Adamantiades-Behçet′s disease: Serum IL-8 is a more reliable marker for disease activity than C-reactive protein and erythrocyte sedimentation rate. Dermatology 2000;201:37-9.
Porat R, Poutsiaka DD, Miller LC, Granowitz EV, Dinarello CA. Interleukin-1 (IL-1) receptor blockade reduces endotoxin and Borrelia burgdorferi-stimulated IL-8 synthesis in human mononuclear cells. FASEB J 1992;6:2482-6.
Kaplanski G, Porat R, Aiura K, Erban JK, Gelfand JA, Dinarello CA. Activated platelets induce endothelial secretion of interleukin-8 in vitro
via an interleukin-1-mediated event. Blood 1993;81:2492-5.
Srinivasan S, Bolick DT, Hatley ME, Natarajan R, Reilly KB, Yeh M, et al.
Glucose regulates interleukin-8 production in aortic endothelial cells through activation of the p38 mitogen-activated protein kinase pathway in diabetes. J Biol Chem 2004;279:31930-6.
Ansar A, Farshchian M, Ghasemzadeh SM. Comparison of the frequency of diabetes mellitus in the patientswith lichen planus and normal controls: A case-control study. Dermatol Cosmet 2011;2:78-84.
Köse O, Lalli A, Kutulola AO, Odell EW, Waseem A. Changes in the expression of stem cell markers in oral lichen planus and hyperkeratotic lesions. J Oral Sci 2007;49:133-9.
[Table 1], [Table 2]