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One of the most common problems in edentulous patients is the low stability of lower dentures. The most effective method to overcome this problem is implant-supported overdentures. After placing an implant, for the process of osseointegration to be complete and successful, it is better that patients do not use their denture for few months. This may be nonconvenient for patient because they are unable to speak and eat properly. The aim of this study was to evaluate the effect of low level laser (LLL) and light-emitting diode (LED) photobiomodulation on implant stability as well as their effect on interleukin-1 beta (IL-1β) and prostaglandin E2 (PGE2) biomarkers around implant in lower anterior region (over denture).
In this clinical trial, 36 implants were placed in fully edentulous mandibles (12 people per person - three implants in areas of midline and canine). Each of the implants was randomly placed in one of three groups of laser, LED, and control. LLL (power of 50 mw and the amount of 20 J/cm 2for each implant) and LED with dose (20 mw/cm 2) were irradiated on the day of surgery (zero), 3, 7, 10, and 14 days. The stability of implants was measured on the day of surgery and weeks 3, 4, and 8 after surgery with Periotest. The inflammatory biomarkers of IL-1β and PGE2 were also collected from gingival crevicular fluid around implants in 4 and 8 weeks. The collected data were analyzed by ANOVA statistical tests.pvalue<0.05 considered significant.
The amounts of Periotest significantly increased 3 rdweek after surgery in the control group (P < 0.001). However, the laser group and LED group were associated with minimal changes, which indicates lower stability of implant in 3 rdweek in control group but no changes in stability of test groups (laser and LED). Laser and LED had no effect on the level of IL-1β and PGE2 in 4 and 8 weeks.
The use of LLL or LED has a positive effect on the stability of the implants 3 weeks after surgery.
After surgical phase of implant placement, it usually needs few months before prosthetic loading. This period is for the “Osseointegration process” to be completed. In this regard, it is recommended to patients not to wear any temporary prostheses, which may interfere with the process of osseointegration. This transitional period of edentulism causes nutritional and verbal problems, which are unpleasant and unacceptable for many patients. In this regard, immediate loading of dental implants has been recommended; however, the success of this method is subject to certain conditions. One of the main issues for immediate loading is some measures to improve bone to implant contact (BIC) in early healing periods.
The use of light-emitting diode photobiomodulation (LED PBM) light source and low-level laser (LLL) has been suggested with the aim to accelerate the osseointegration and BIC.
The mechanism of action of LED and LLL is based on energy photon irradiation by light in the far red to near-infrared (NIR) spectrum (630–1000 nm) using low energy lasers or LEDs. In general, all cell metabolisms are controlled through the redox state of the cell. Cellular response to the energy of photons stimulated by light varies according to the redox quality. The response is low in normal or near the normal states, while the response is higher in cases of transfer to tendency toward the reduction. Normal cells show lower reaction to the energy of photons stimulated by light, which is of the advantages of these photons. In this method, the photons' energy is absorbed by the cells and stimulates them, which is called “PBM”. According to a review of the literature, LLL and LED application could have additional benefits on bone healing process following implant therapy.
The aim of the present study was to evaluate the effect of LLL and LED PBM on implant stability (measured by Periotest), acceleration of osseointegration process, and their possible effects on BIC. The possible effects of LED and LLL on IL-1β and PGE2 biomarkers around implant were also evaluated in patients with implants placed in the lower anterior region (over denture).
This randomized controlled clinical trial was conducted by “Split Mouth” method on patients referred to the Periodontics unit, School of Dentistry, Isfahan Islamic Azad University (Khorasgan Branch). The inclusion criteria were Type II or III bone quality based on Lekholm and Zarb classification, sufficient amount of bone (no need for augmentation), at least 6 months passed of any tooth extraction, good oral hygiene, and nonsmoker. The exclusion criteria were systemic diseases including diabetes, cardiovascular diseases, hormonal disorders, blood disorders, history of jaundice, kidney failure, asthma, allergies, cancer, weakened immune system, pregnancy and lactation, history of using bisphosphonates, history of radiotherapy of head and neck in past 2 years, history of chemotherapy, and administration of immunosuppressive agents.
Three DIO implants (invasive fungal infections-tissue level) with resorbable blast media surface, made in Korea, with the same diameter and length were placed in the mandible (one in the midline and the other two at the left and right canine teeth positions). Using coin drawing, one implant was considered as control and other two were exposed to LED or laser radiation, respectively.
The LLL (diode laser doctor smile 810 nm, Italy) was radiated in the relevant group on the days of surgery (zero), 3, 7, 10, and 14 with the power of 50 mw and the amount of 20 J/cm 2for each implant by gently pressing on the buccal mucosa of the implant inside the mouth. Irradiation index information are as follows: 50 mW = 0.05W W = J/cm 2× s 0.05 = 20/S S = 400 according to this formula for each of 20 J/cm 2with 50 mW, we apply 400 s. Laser irradiation applied from buccal aspect. Time: 400 s, power density 50 mW, laser diameter: 1 cm 2(fiber 400 and apply low level head with 1 cm 2surface according). Beam shape around laser type was a continuous wave.
The LED PBM radiation (OsseopulseTM AR 300, Biolux Research, Vancouver, British Columbia, Canada) was carried out at a dose of 20 mw/cm 2on the days of surgery (zero), 3, 7, 10, and 14, each time for 20 min, on the skin of the other implants outside of the mouth (During LED radiation, the other two implants were protected by aluminum foil covering them from inside the mouth). The LED devise type and information are as follows: the LED device (Osseopuise TMAR 300, Biolux Research Vancouver, British Columbia, Canada) at the wavelength of 626 nm in the NIR region was applied for 20 min over the surgical area after suturing the flap. The treatment parameters were as follows: treatment array area: 4.80 cm 2, average intensity: 38.5 mW/cm 2, total power: 185 mW, total energy: 222 J, and average density: 46.2 J/cm 2.
The led device had eight emitters with a power of 23.125 mW each. The LED device consisted of a headset that was adjusted on the patient face. A 3-point contact on the ears and nose was provided for device stability.
The third implant was considered as control. The stability of the implants at the day of surgery, 3, 4, and 8 weeks after surgery was evaluated with Periotest Device (Gulden-Medizinteknik, Bensheim an der Bergstrasse, Germany). For any implant, three Periotest measurements were performed at each time, and the mean was recorded.
The gingival crevicular fluid samples were also collected at weeks 4 and 8 by placing a paper point inside the peri-implant sulcus for 30 s. Then, the samples were transferred into the tubes containing storage solution (neutral tris-buffered saline) and sent to the laboratory inside ice bag on the same day. The levels of IL-1β and PGE2 markers were measured by ELISA method and Thermofisher Kit.
Data analysis was done using the SPSS version 22 software (SPSS Inc. Chicago, IL, USA). The ANOVA test was used for quantitative variables within a group (implant stability and levels of inflammatory markers), while the repeated measures were applied for intergroup quantitative variables. P < 0.05 considered significant
The mean of implant stability rate at four times (periotest).
Furthermore, according to
The IL1β and PGE2 values were compared in the 1
stand 2
ndmonth after surgery separately for laser, LED PBM, and control groups. First, Kolmogorov–Smirnov test was performed to examine the normality of data distribution in the 1
stmonth, based on which, their normality was not rejected. Then, using the ANOVA method for repeated data, the three methods were compared, according to which, as shown in
Comparing calculations of IL-1β and PGE2 in the 1 stmonth with the 2 ndmonth, using ANOVA repeated measures with two methods and time variables, the data were analyzed simultaneously, which showed no significant difference between methods in the total of the two times (P = 0.765), but there was a significant difference between the two time periods (P < 0.001). In other words, the amount of IL1β in the 2 ndmonth decreased in all groups compared to the 1 stmonth, which represents a reduction of inflammatory process over the time. Meanwhile, there was no interaction between the methods and materials (P = 0124). This suggests that the changes in these three methods were the same at both times, occurring in the normal range (10–45 ng/ml).
The results of this study showed that application of LLL and LED PBM had positive effects on stability of implants placed on mandibular anterior region in subjects with fully edentulous lower jaw. Based on (S. Roghondro, M. Wood, T. D. Taylor) curve, there is a significant reduction of implant stability between 3 rdand 4 thweek after implant placement. This usual reduction of stability during 3 rdand 4 thweek after implant placement was not observed in implants treated with laser and LED PBM.
The possible effect of laser is mainly on cellular level. It is known that light wavelength stimulates cellular energy metabolism by the activation of mitochondrial respiratory chain components. The light absorbed by cytochrome c oxidase, a photoacceptor molecule in the mitochondria, alters the cellular mechanism and causes an increased adenosine triphosphate production that results in improved wound healing in ischemic and wounded tissues.
The results of this study on the stability of the implant are consistent with the studies by Lopes et al.,
The results of this study are inconsistent with the clinical trial of García-Morales et al.
Considering the impact of LED on the implant stability, the results of this study are consistent with Gokmenoglu et al.'s studies.
Regarding the inflammatory factors, there was a significant reduction of both PGE2 and IL1B after 2 months. This is natural phenomenon due to the reduction of inflammatory processes while healing is completed. However, LLL and LED had no impact on the level of these inflammatory markers at different time interval compare to control group. The results of this study are consistent with the studies by de Jesus et al.
LLL had a positive effect on the stability of implants at 3–4-week time after implant placement.
Financial support and sponsorship
This project was sponsored by research committee of Islamic azad university Isfahan (khorasgan) Branch.
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.