|Year : 2017 | Volume
| Issue : 2 | Page : 104-110
Salivary oxidative stress in oral lichen planus treated with triamcinolone mouthrinse
Arash Mansourian1, Farzaneh Agha-Hosseini1, Hamed Hossein Kazemi2, Nazanin Mortazavi3, Mahdieh-Sadat Moosavi1, Jalil Beytollahi4, Iraj Mirzaii-Dizgah5
1 Department of Oral Medicine, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran
2 Department of Oral Medicine, School of Dentistry, Babol University of Medical Sciences, Babol, Iran
3 Department of Oral Medicine, School of Dentistry, Golestan University of Medical Sciences, Tehran, Iran
4 Dental School, University of Toronto, Toronto, Ontario, Canada
5 Department of Physiology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran
|Date of Web Publication||8-May-2017|
Hamed Hossein Kazemi
Department of Oral Medicine, School of Dentistry, Babol University of Medical Sciences, PO Box 47135-853, Babol
Source of Support: None, Conflict of Interest: None
Background: Total antioxidant capacity (TAC) and malondialdehyde (MDA) levels have not been reported in oral lichen planus (OLP) patients treated with a topical corticosteroid. This study evaluates TAC and MDA levels in unstimulated saliva of OLP patients. Such measurements may need to be supported by clinical observation.
Materials and Methods: Twenty patients with OLP participated in a study conducted at the Department of Oral Medicine, Tehran University of Medical Sciences. Salivary TAC and MDA were determined by biochemical analyses before and after 5-week triamcinolone acetonide (0.2%) mouthrinse treatment. Subjective symptoms as well as lesion status pre- and post-treatment were measured using visual analog scale (VAS) and clinical scoring system, respectively. Wilcoxon signed rank test was used for the evaluation of MDA and TAC parameters, VASs, and rates of clinical scores. Spearman's rank correlation was used to determine the relationship between different variables.
Results: A statistically significant increase in salivary TAC was found after treatment. There was no significant difference in the reduction of salivary MDA levels in OLP patients after treatment.
Conclusion: Posttreatment analyses revealed a significant degree of recovery and pain relief of OLP lesions. Hence, triamcinolon mouthrinse by reducing oxidative stress is an appropriate treatment in OLP patients.
Keywords: Malondialdehyde, oral lichen planus, oxidative stress, triamcinolone acetonide
|How to cite this article:|
Mansourian A, Agha-Hosseini F, Kazemi HH, Mortazavi N, Moosavi MS, Beytollahi J, Mirzaii-Dizgah I. Salivary oxidative stress in oral lichen planus treated with triamcinolone mouthrinse. Dent Res J 2017;14:104-10
|How to cite this URL:|
Mansourian A, Agha-Hosseini F, Kazemi HH, Mortazavi N, Moosavi MS, Beytollahi J, Mirzaii-Dizgah I. Salivary oxidative stress in oral lichen planus treated with triamcinolone mouthrinse. Dent Res J [serial online] 2017 [cited 2017 Dec 12];14:104-10. Available from: http://www.drjjournal.net/text.asp?2017/14/2/104/205794
| Introduction|| |
Oral lichen planus (OLP) is a chronic inflammatory mucosal disease of unknown etiology which can cause symptoms ranging from a burning sensation to severe pain interfering with speaking, eating, and swallowing. The typical age of presentation is between 30 and 60 years, the disease is more frequently seen in women, and the most affected sites are the buccal mucosa, tongue, and the gingiva. There are no effective means to prevent OLP. The possible malignant transformation of OLP is the subject of current discussions in literature.,
Free radicals, including reactive oxygen species (ROS) and reactive nitrogen species (RNS), exist in normal cells at low concentrations. An uncontrolled production of ROS/RNS results in oxidative stress status. Oxidative stress may be defined as a violation in balance between oxidants and reductants in living organisms. The efficiency of antioxidants is expressed as total antioxidant capacity (TAC) parameter, summarizing overall activity of all types of antioxidants in living systems. Such a parameter may alternate the costly and time-consuming assays of individual antioxidant species as exogenous antioxidants (e.g., carotenoids, ascorbic acid, tocopherols, folic acid); endogenous antioxidants (e.g., catalase, superoxide dismutase, glutathione peroxidase, reduced glutathione, ferritin); and synthetic antioxidants (e.g., penicillinamine).
Saliva may be considered the first line of defense against free radical-mediated oxidative stress, so the antioxidant capacity of saliva is of strategic interest. As a diagnostic fluid which may be easily collected, saliva is used for the measurement of markers of oxidative stress associated with local oral conditions., Lipoperoxidation has been considered a major presentation of oxidative stress. Malondialdehyde (MDA), as the lipid peroxidation marker, increases in an oxidative stress-dependent situation  and OLP., Higher levels of MDA were reported in saliva of patients affected by OLP.,
To the best of our knowledge, pro-oxidant/antioxidant parameter change following a topical corticosteroid treatment has not been reported yet. The aim of the present study was to evaluate the changes in the status of oxidative stress and antioxidant defense system in OLP. In a prospective study, patients were treated with a triamcinolone acetonide mouthrinse. MDA and TAC in saliva of patients prior to and after treatment were measured.
| Materials and Methods|| |
This clinical trial was performed at the Department of Oral Medicine. This study was registered at IRCT. ir (IRCT2014092919133N1) which is a primary registry in the WHO Registry Network setup.
Twenty-seven patients, with clinically and pathologically proven OLP according to the revised, modified World Health Organization 2003 diagnostic criteria,, were enrolled in this study. The inclusion criteria required the following:
Presence of bilateral, frequently symmetrical lesions, erythematous, or ulcerative lesions in the presence of reticular lesions elsewhere in the oral mucosa, presence of well-defined band-like zones of inflammatory infiltration confined to the superficial part of the connective tissue consisting mainly of mature lymphocytes, signs of liquefaction degeneration in the basal layer cells, and the absence of dysplasia.
The exclusion criteria were as follows:
Not using any systemic or topical therapeutic for the past 3 months or 1 month, respectively, patients with systemic disease and systemic drug therapy such as beta-blockers, diuretics, and calcium channel blockers, also intake of immunosuppressive agents, any supplementary vitamin in the previous 3 months, and a history of smoking or alcohol intake at least 1 month prior to the study were excluded from the study., Patients with lichenoid lesions associated with drugs or restorations as well as the presence of any dermatological involvement of OLP were also excluded from the study.
A biopsy specimen was taken from each patient to confirm the diagnosis. Verified OLP patients (twenty patients) were then prepared for saliva collection.
Saliva collection and antioxidant assays
Participants in the study were evaluated under the same protocol. They attended the Department of Oral Medicine, between 10:00 and 12:00 a.m. Samples were collected at the same time of the day (10–12 a.m.) and at least 2 h after the last intake of food or drink. Prior to saliva collection, patients were asked to rinse the mouth with distilled water. Five milliliters of unstimulated whole saliva was then collected through spitting method into a graded sampling tube. Immediately after collection, saliva samples were centrifuged at 2000 g for 10 min at +4°C. The supernatants were also drawn and stored at −80°C until further analysis. All patients were prescribed a suspension of triamcinolone acetonide 0.2%, four times a day, for 5 weeks. Patients were instructed to rinse with 5 ml of mouthrinse for 3 min and then to expectorate, and were also instructed not to eat or drink until 30 min after usage. All patients were placed on follow-up period during 2, 4, and 5 weeks after starting the treatment. Saliva collection procedure was repeated at the end of 5-week therapy.
The TAC of saliva was determined by measuring its ability to decolorize 2,2'-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) radical cation (ABTS+). In brief, in this method, the ABTS is oxidized to ABTS+ (deep green) using hydrogen peroxide in acidic medium (the acetate buffer 30 mmol/L pH 3.6). Antioxidants accelerate the bleaching rate of ABTS+ in the acetate buffer 0.4 mol/L pH 5.8 medium to a degree proportional to their concentrations. This change in color is measured as a change in absorbance at 660 nm. The results were expressed as μmol trolox equivalent/L according to a standard curve, which was prepared with a serial dilution of trolox.
The saliva MDA level, which is the end product of the oxidation of polyunsaturated fatty acids, was measured based on reaction with thiobarbituric acid (TBA) at 90–100°C. MDA and TBA react together, in the TBA test reaction, to make a pink pigment with an absorption maximum at 532 nm. The reaction was completed at pH 2–3 at 90°C for 15 min. Precipitate protein was made by mixing sample with two volumes of cold 10% (w/v) trichloroacetic acid. They centrifuged and reacted with an equal volume of 0.67% (w/v) TBA in a boiling water bath for 10 min. The absorbance was read at 532 nm. The results were stated as μmol/1 consistent with a standard curve.
This study was approved by the Review Board, and written informed consent was obtained from all patients prior to saliva collection and prior to treatment. During the study, three patients who developed candidiasis were treated by an antifungal drug (nystatin). These patients were excluded from the study because their treatments might have affected the results. Four patients with poor compliance were also excluded from the study. For ethical considerations, treatment was continued for active or excluded patients who still had complaints after the 5 weeks of therapy. All patients were given instruction regarding the disease and the planned treatment.
The changes in the subjective symptoms were evaluated with the use of visual analog scale (VAS) on a 0–100 scale. Prior to the treatment and at the end of the 5-week follow-up, VAS was recorded for all the patients.
Severity of the disease (objective response) was assessed by a semi-quantitative scoring system based on site and area, with moderate modification by adding the right and left borders of the tongue, also considering gingiva as the upper and lower parts. Grading based on score was modified, and the maximum score was changed from 12 to 15. [Table 1] demonstrates the basic scoring/grading system used by Malhotra et al. but with moderate modification.
Wilcoxon signed rank test was used for the evaluation of MDA and TAC parameters prior and after treatment. This test, also, was used to analyze VASs and rates of clinical involvements (scores) prior to and after treatment. Spearman's rank correlation was used to determine the relationship between different variables.
| Results|| |
Twenty confirmed OLP patients (16 women, four men), with a mean age of 48.20 years, were evaluated in the present study. The mean duration of the disease was 11.50 months before entering the study. Distribution frequency of the lesions under the study is shown in [Table 2].
|Table 2: Distribution of absolute frequency and relative frequency of lesion forms, n (%)|
Click here to view
Mean VAS score prior to treatment was 3.90 ± 2.17, and after treatment, it was 0.90 ± 1.48. The difference was statistically significant (P < 0.001). In this study, bivariate correlations between TAC, MDA, VAS, and duration of disease were not statistically significant (P > 0.05).
The mean level of unstimulated whole saliva MDA in OLP patients prior to the treatment was higher than that of the treated patients as shown in [Table 3] and [Figure 1]. However, the difference was not statistically significant (P = 0.380). The mean level of salivary TAC in OLP patients who received the treatment was promoted. This difference was statistically significant (P = 0.028). [Table 3] and [Figure 2] represent such a significant increase in TAC level prior to and after the treatment.
|Table 3: Mean total antioxidant capacity (μmol/trolox) and malondialdehyde (μmol/L) prior to and after treatment (mean±standard deviation)|
Click here to view
|Figure 1: Concentration of malondialdehyde in unstimulated saliva of oral lichen planus patients before and after treatment with triamcinolone mouthrinse.|
Click here to view
|Figure 2: Concentration of total antioxidant capacity in unstimulated saliva of oral lichen planus patients before and after treatment with triamcinolone mouthrinse.|
Click here to view
Based on the modified scoring system (0–15), clinical scores were 2–10 (mean = 4.80 ± 1.93) before and 0–6 (mean = 2.15 ± 1.66) after the treatment. The difference was statistically significant (P < 0.001), which was an indication of clinical improvement. Out of the twenty patients who participated in our study, improvement of clinical score was noted in 14 patients (70%) at the end of 5-week treatment by mouthrinse. Grade 0 or complete healing of Grade I was observed in four patients (20%), indicating that the whole lesion resolved and normal mucosa was regained. Change of Grade II to Grade I in nine patients (45%) and Grade III to Grade II in one patient (5%) were observed.
Absolute/relative distribution frequencies of clinical grades prior to and after treatment are shown in [Table 4].
|Table 4: Distribution of absolute frequency and relative frequency of lesion grades prior to and after treatment, n (%)|
Click here to view
| Discussion|| |
According to the literature, OLP involves primarily middle-aged adults, and the lesions are more frequent in women.,, The present study revealed similar gender difference, i.e., 16 women compare to four men. Patients were in the age range between 32 and 68 years (mean = 48.20). Buccal mucosa involvement in the present study was predominantly bilateral, which is similar to other studies.,
According to van der Waal, the reticular, erythematous (erosive), plaque type, and ulcerative type are the most common types; among them, the erythematous and ulcerative types are particularly painful. A VAS recording prior to and after treatment revealed a decline in the score of the most of our patients. Differences of both VAS scores and clinical scores were statistically significant (P < 0.001) and could account for a palliative effect at the end of 5-week treatment. The clinical and symptomatic improvements observed in the present study were comparable to those of Malhotra et al's., study who compared triamcinolone acetonide (0.1%) paste with an oral steroid (Betamethasone). Their subjective responses appeared from 12th week; however, mean scores of objective responses appeared to be significant from 8th week afterward. From this viewpoint, the results of their study can be compared to ours, in which the objective mean scores are significant following a 5-week corticosteroid mouthrinse treatment. According to our findings, four completely recovered cases, as well as changing Grade III and Grade II cases to Grade II and Grade I, respectively, indicate certain degrees of recovery following treatment. Topical corticosteroids are safe when applied to mucous membrane for short periods, but prolonged use can produce side effects such as adrenal suppression, secondary candidiasis, and rarely, atrophy of oral mucosa. Corticosteroids are the most effective agents in the treatment of OLP, and topical corticosteroids have been preferred over systemic corticosteroids, except during acute exacerbations. However, there has been debate considering the application of such immunomodulating agents in OLP and oral lichenoid lesions.
Free radicals and ROS are essential for biological processes. Tissue damage can occur when antioxidants do not efficiently counteract their action. The mouth is a critical site for oxidative stress due to frequent exposure to chemical, thermal, and microbial stimulants. With the advent of new technology, a blood drop, sample of urine or saliva can provide a generic value of the patient's oxidative stress, measuring the amount of free radicals. Saliva is increasingly used and well validated in diagnosing, monitoring systemic health and disease states, predicting disease progression as well as detecting biomarkers. Since the process of mastication promotes a variety of immunological reactions such as lipid peroxidation, saliva may be considered as the first line of defense against free radical-mediated oxidative stress.
The literature shows how MDA is one of the most studied products of polyunsaturated fatty acid peroxidation, which increases in oxidative stress-dependent conditions. Previous studies shown that MDA is increased in saliva of patients affected by OLP., A systematic review published in 2014 concluded that there is a need for further studies with concentration on the prognostic value of MDA by evaluating its levels both pre- and post-treatment in OLP. Our study with a declined MDA level following a topical corticosteroid therapy (although not statistically significant) resembles a recent study in Belgium, in which the effect of curcumin intake was assessed in OLP patients. Authors claimed that the lipid peroxidation decrease in patients with precancerous lesions due to the anti-precancerous effects of curcumin was mediated by pro- and anti-oxidative pathways. A significant rise in salivary TAC level, which was found in our treated patients, was similar to a remarkable activity of total antioxidants in healthy controls of an OLP study by Ergun et al. A significant increase in salivary TAC may also account for a reinforced antioxidant defense system at the end of a 5-week clinical trial. Such a significant rise in TAC may improve the balance in the pro-oxidant/antioxidant equilibrium. Formerly, it has been hypothesized that, in lichen planus lesions, antioxidant defense mechanisms are overwhelmed resulting in an increase of oxidative damage to lipids, proteins, and DNA, which may be involved in the inflammatory processes of the disease.
Several studies have recently reported nuclear factor-kappa B (NF-κB) expression in OLP. As an inflammatory regulator, NF-κB may be activated by a variety of inflammatory signals, and some pro-inflammatory cytokines such as interleukin-1 β and tumor necrosis factor-α. NF-κB is one of the most important transcription factors whose activity can be influenced by oxidative stress., NF-κB is also inhibited by glucocorticoids and can be a target for novel anti-inflammatory therapies. Recent studies suggest that defense mechanism reduction in lichen planus and the impaired oxidant/antioxidant balance may contribute to the pathophysiology of the disease., Oxidative damage represents the main threat for the genome integrity in living organisms. ROS generation may also be prone to mutagenesis. The importance of reactive oxygen and antioxidant species to human biology came from the realization that transcription factors, such as NF-κB and activating protein-1, were redox sensitive. The activity of a redox-sensitive transcription factor is affected by oxidation. Kinases and tyrosine phosphatases, proposed as redox regulators of signaling machinery, regulate T-cell receptor signaling and successive phosphorylation cascade. Eventually, signaling complexes are formed which activate several signaling pathways such as the NF-κB pathway.,
| Conclusion|| |
Antioxidant drugs may reverse the increased oxidative stress status in lichen planus and result in clinical improvement. Based on oxidative stress modulation, the antioxidant defense must be part of a therapeutic strategy for OLP. Therefore, we propose drugs such as triamcinolone acetonide mouthrinse for such an increased oxidative stress status.
Financial support and sponsorship
Conflicts of interest
The authors of this manuscript declare that they have no conflicts of interest, real or perceived, financial or nonfinancial, in this article.
| References|| |
Agha-Hosseini F, Mirzaii-Dizgah I, Farmanbar N, Abdollahi M. Oxidative stress status and DNA damage in saliva of human subjects with oral lichen planus and oral squamous cell carcinoma. J Oral Pathol Med 2012;41:736-40.
van der Waal I. Oral lichen planus and oral lichenoid lesions; a critical appraisal with emphasis on the diagnostic aspects. Med Oral Patol Oral Cir Bucal 2009;14:E310-4.
van der Meij EH, Schepman KP, van der Waal I. The possible premalignant character of oral lichen planus and oral lichenoid lesions: A prospective study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003;96:164-71.
Gorsky M, Epstein JB. Oral lichen planus: Malignant transformation and human papilloma virus: A review of potential clinical implications. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2011;111:461-4.
Arana C, Cutando A, Ferrera MJ, Gómez-Moreno G, Worf CV, Bolaños MJ, et al.
Parameters of oxidative stress in saliva from diabetic and parenteral drug addict patients. J Oral Pathol Med 2006;35:554-9.
Ziyatdinova GK, Budnikov HC, Pogorel'tzev VI. Determination of total antioxidant capacity of human plasma from patients with lung diseases using constant-current coulometry. Eurasian J Anal Chem 2009;1:19-30.
Chapple IL, Matthews JB. The role of reactive oxygen and antioxidant species in periodontal tissue destruction. Periodontol 2000 2007;43:160-232.
Battino M, Greabu M, Totan A, Bullon P, Bucur A, Tovaru S, et al.
Oxidative stress markers in oral lichen planus. Biofactors 2008;33:301-10.
Takane M, Sugano N, Ezawa T, Uchiyama T, Ito K. A marker of oxidative stress in saliva: Association with periodontally-involved teeth of a hopeless prognosis. J Oral Sci 2005;47:53-7.
Vlková B, Stanko P, Minárik G, Tóthová L, Szemes T, Banasová L, et al.
Salivary markers of oxidative stress in patients with oral premalignant lesions. Arch Oral Biol 2012;57:1651-6.
Iannitti T, Rottigni V, Palmieri B. Role of free radicals and antioxidant defences in oral cavity-related pathologies. J Oral Pathol Med 2012;41:649-61.
Sezer E, Ozugurlu F, Ozyurt H, Sahin S, Etikan I. Lipid peroxidation and antioxidant status in lichen planus. Clin Exp Dermatol 2007;32:430-4.
Aly DG, Shahin RS. Oxidative stress in lichen planus. Acta Dermatovenerol Alp Pannonica Adriat 2010;19:3-11.
Upadhyay RB, Carnelio S, Shenoy RP, Gyawali P, Mukherjee M. Oxidative stress and antioxidant defense in oral lichen planus and oral lichenoid reaction. Scand J Clin Lab Invest 2010;70:225-8.
Ergun S, Trosala SC, Warnakulasuriya S, Özel S, Önal AE, Ofluoglu D, et al.
Evaluation of oxidative stress and antioxidant profile in patients with oral lichen planus. J Oral Pathol Med 2011;40:286-93.
Belal MH. Management of symptomatic erosive-ulcerative lesions of oral lichen planus in an adult Egyptian population using Selenium-ACE combined with topical corticosteroids plus antifungal agent. Contemp Clin Dent 2015;6:454-60.
] [Full text]
Agha-Hosseini F, Mirzaii-Dizgah I, Mikaili S, Abdollahi M. Increased salivary lipid peroxidation in human subjects with oral lichen planus. Int J Dent Hyg 2009;7:246-50.
Erel O. A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem 2004;37:277-85.
Esterbauer H, Cheeseman KH. Determination of aldehydic lipid peroxidation products: Malondialdehyde and 4-hydroxynonenal. Methods Enzymol 1990;186:407-21.
Malhotra AK, Khaitan BK, Sethuraman G, Sharma VK. Betamethasone oral mini-pulse therapy compared with topical triamcinolone acetonide (0.1%) paste in oral lichen planus: A randomized comparative study. J Am Acad Dermatol 2008;58:596-602.
Scully C, Carrozzo M. Oral mucosal disease: Lichen planus. Br J Oral Maxillofac Surg 2008;46:15-21.
Chainani-Wu N, Silverman S Jr., Reingold A, Bostrom A, Lozada-Nur F, Weintraub J. Validation of instruments to measure the symptoms and signs of oral lichen planus. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2008;105:51-8.
Mishra SS, Uma Maheswari T. Evaluation of oxidative stress in oral lichen planus using malondialdehyde: A systematic review. J Saudi Soc Dermatol Dermatol Surg 2014; 18: 2-7.
Rai B, Kaur J, Jacobs R, Singh J. Possible action mechanism for curcumin in pre-cancerous lesions based on serum and salivary markers of oxidative stress. J Oral Sci 2010;52:251-6.
Sander CS, Cooper SM, Ali I, Dean D, Thiele JJ, Wojnarowska F. Decreased antioxidant enzyme expression and increased oxidative damage in erosive lichen planus of the vulva. BJOG 2005;112:1572-5.
Zhou G, Xia K, Du GF, Chen XM, Xu XY, Lu R, et al.
Activation of nuclear factor-kappa B correlates with tumor necrosis factor-alpha in oral lichen planus: A clinicopathologic study in atrophic-erosive and reticular form. J Oral Pathol Med 2009;38:559-64.
Schoonbroodt S, Piette J. Oxidative stress interference with the nuclear factor-κB activation pathways. Biochem Pharmacol 2000;60:1075-83.
Barnes PJ. Anti-inflammatory actions of glucocorticoids: Molecular mechanisms. Clin Sci (Lond) 1998;94:557-72.
Larbi A, Kempf J, Pawelec G. Oxidative stress modulation and T cell activation. Exp Gerontol 2007;42:852-8.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4]