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Effect of orthodontic forces on cytokine and receptor levels in gingival crevicular fluid: a systematic review
Progress in Orthodontics volume 15, Article number: 65 (2014)
This systematic review aimed to generate evidence on role of potent markers of inflammation [cytokines, chemokines, their associated receptors and antagonists] following the application of orthodontic forces. Subsequent to registration with PROSPERO, literature search followed a predetermined search strategy to key databases along with hand search (HS). Seventy-seven articles from PubMed (P), 637 from Scopus (S), 51 from Embase (E), and 3 from hand search (HS) were identified. A total of 39 articles were shortlisted that met strict inclusion and exclusion criteria and quality assessment. Each study was evaluated for participant characteristics, study design, oral hygiene regimen, and gingival crevicular fluid (GCF) handling. Among these studies, biomarkers in the order of frequency were interleukin (IL)-1β (N = 21), tumor necrosis factor (TNF)-α (N = 10), IL-8,IL-6(N=8), receptor activator of nuclear factor kappa-B ligand (RANKL) (N = 7), monocyte chemoattractant protein (MCP)-1 (N = 3), IL-2 (N=4), IL-4, IL-10, RANTES (N = 2), IL-1, IL-5, IL-1α, IP-10, osteopontin (OPN) (N = 1) and receptors and their antagonists in the order of osteoprotegerin (OPG) (N = 8), IL-1RA (N = 5), and RANK (N = 1). Results revealed an immediate release of inflammatory bone-resorptive mediators, IL-1β and TNF-α, where IL-1β increased as early as 1 min to 1 h reaching peak at 24 h while TNF-α increased at 1 h or 1 day. This was accompanied by a fall in bone-protective mediator (OPG) levels at 1 h and 24 h after orthodontic force application. Continuous forces were accompanied by a decrease in mediator levels after attaining peak levels (most commonly at 24 h) while repeated activations in interrupted force upregulated their secretion. Significant correlations of IL-1β levels with pain intensity, rate of orthodontic tooth movement (OTM) and of activity index (AI) (IL-1β/IL-1RA) with velocity of tooth movement and growth status of individuals have also been deduced. A greater AI and RANKL/OPG ratio was seen in juveniles as compared to adults or non-growers that were associated with faster rate of OTM in juveniles. None of the studies addressed the effect of estrous cycle in female subjects. Lack of homogeneity in several parameters calls for a better controlled research on the biology of OTM.
Orthodontic tooth movement (OTM) is considered an epiphenomenon of the gene expression of the periodontal ligament (PDL) and neighboring cells resulting from a series of orchestrated cellular and molecular events in alveolar bone and periodontal tissue initiated by the application of orthodontic force . A chemical cascade that mediates the transmission of signals from extracellular matrix leading to genetic modulation is interceded by the release of mediators in paracrine environment. These signals are responsible for a change in the cytoskeletal structure, leading to alteration of nuclear protein matrix and eventually gene activation or suppression ,. These events initiate the process of bone remodeling, leading to effective tooth movement. The biochemical mediators released sequentially at multiple stages during orchestration of tooth movement can be detected in gingival crevicular fluid (GCF). GCF is a unique biological exudate that has been found as a convenient medium to study these mediators with reasonable sensitivity. GCF can be collected noninvasively  with specifically designed filter paper or a micropipette (1 to 10 μl) or through magnetic beads placed in gingival crevice. GCF once collected may be cryopreserved or directly sent for chemical analysis. GCF can also be collected repeatedly at various stages of orthodontic treatment and therefore provides useful insight to biological events over the entire duration of observation.
Clinically demonstrable success of OTM is associated with expression of numerous regulatory molecules, of which cytokines have been most widely documented. Cytokines are low-molecular weight proteins (mw < 25 kDa) released in autocrine or paracrine environment in response to local signals like application of stress  and are involved in normal physiological bone turnover and remodeling -. Cytokine biology as a retort to forces applied for OTM is difficult to comprehend due to sheer number and complexity of these factors exhibiting redundancy as well as pleiotropy . Although cytokines have been extensively evaluated in GCF as quantitative biochemical indicators of inflammatory periodontal status , there has been an increasing interest on understanding their contributions as mediators of OTM owing to their role in bone and tissue remodeling. Among these cytokines, interleukins (ILs) (IL-1α, IL-1β, IL-1RA, IL-8, IL-2, IL-6, and IL-15), tumor necrosis factors (TNFs), interferons (IFNs), growth factors (GFs), and colony-stimulating factors (CSFs) have been extensively studied in relation to OTM.
The secretion of these mediators in the local environment by cells activated on application of orthodontic force varies according to the force levels and functional state of available target cells. The rate of OTM depends on recruitment of mature osteoclasts and precursors, osteoclast differentiation and number of functional osteoclasts at the bone-PDL interface, where bone resorption is considered a rate-limiting step . The earliest identified marker of bone resorption is IL-1β, closely followed by prostaglandin E2 (PGE2), nitric oxide, IL-6, and other inflammatory cytokines . TNF is also believed to have synergistic effects with IL-1 . Osteoclast differentiation and activation is mediated by the binding of receptor activator of nuclear factor kappa-B to its ligand expressed by osteoblasts and PDL cells (RANK and RANKL, respectively) ,-. This interaction and osteoclast activity is prevented by a decoy receptor for RANKL called osteoprotegerin (OPG) . Thus, the relative balance between RANK-RANKL and OPG may be critical to the magnitude and rate of OTM.
The first experimental evidence supporting role of cytokines in OTM was documented in periodontal tissues of cat canine teeth where IL-1α and IL-1β were identified after the application of a tipping force . One of the earliest noninvasive studies on IL-1β in GCF was done by Grieve et al.  where significant elevations from baseline in IL-1β and PGE levels supported initial release of proinflammatory mediators on application of orthodontic forces, followed by a decrease in 7 days (d). Since then, numerous studies in humans have focused on alterations in IL-1β levels in GCF in an attempt to understand the underlying inflammatory process during OTM. The studies have now diversified to include other interleukins like IL-1α, IL-2, IL-6, IL-8, and receptor antagonist IL-1RA. More recently, the presence of other mediators including TNF-α, TGF-β, leptin, RANK/RANKL, and OPG have also been explored in OTM.
This systematic review aims to determine effect of orthodontic forces on levels of markers of inflammation namely cytokines, chemokines, receptors and their antagonists, which have been widely documented in GCF. The present study looks into literature to generate evidence on the role of these mediators in relation to the force levels, applied mechanics, age, sex and pain intensity during orthodontic treatment. This systematic review provides insights into possible biomarkers for tooth movement and their potential contributions to modulating orthodontic bone turnover that could prove useful in designing future approaches to modulating OTM.
Material and methods
This review was registered in PROSPERO on 3 June, 2014 (registration number CRD42014009302). The systematic review was conducted strictly adhering to guidelines suggested by PROSPERO. A search strategy was finalized utilizing MESH terms, Boolean terminology, and free text terms (Additional file 1: Annexure 1). This search strategy was applied to key databases PubMed, Scopus, and Embase in April 2014 by two reviewers PK and NM which followed a cross check by third reviewer OPK. Apart from that, hand search of journals was performed for article retrieval. Segregation of articles to be considered for review was based on stringent inclusion and exclusion criteria. Seventy-seven articles in PubMed, 637 in Scopus, 51 in Embase, and 3 from hand searching were retrieved (Figure 1). Duplicates were removed before final screening of articles for inclusion in the review. The titles and abstracts of these manuscripts were studied, considering exclusion and inclusion criteria specific to each database (Figure 1). The relevant articles were obtained. These were PubMed - 41, Scopus - 17, Embase - 2 and hand searched - 3. Further, a few articles had to be excluded for non-availability of full text. These were PubMed (N = 4), Scopus (N = 15), and Embase (N = 1). Further, four articles had to be excluded since full text revealed no mention of orthodontic force (N = 1) or study was not performed in crevicular fluid (N = 3). A consensus has arrived among reviewers for final inclusion of 39 articles comprising of 33 articles from PubMed, 2 from Scopus, 1 from Embase, and 3 from hand search (Figure 1).
The inclusion and exclusion criterion were as under.
Inclusion Criteria: Participants/population -Human studies, age groups (if specified), male to female ratio (if specified), controls (either internal where baseline levels are taken as control or external where contralateral or antagonistic tooth is taken as control), sample size >5 (refers to sample size not number of teeth studied).
Intervention(s), exposure(s)-Studies on cytokines [including interleukins (ILs), tumor necrosis factor (TNF) and growth factors (GFs), colony-stimulating factors (CSFs), interferons (IFNs)], chemokines, receptors and their antagonists (RANK, RANKL, OPG, OPN) with specified orthodontic mechanics, proper oral hygiene control, no use of antibiotic/anti-inflammatory drugs before or during orthodontic force application, GCF sample collection via periopaper or micropipette placed in sulcus.
Exclusion criteria Participants/population- In vitro studies, animal studies, sample size <5, no control. Intervention(s), exposure(s)- Studies on mediators other than cytokines or chemokines or receptors, cytokine or chemokine or receptor measurement in periodontal tissue and not GCF, cytokine or chemokine or receptor levels consequent to periodontal inflammation and not orthodontic force application, cytokine levels measured in peri-implant fluid.
This is a followed data extraction by two reviewers (PK and NM). The data was recorded in a tabular form based on the following criteria:
Participant characteristics (Table 1): number of study subjects (not the number of teeth), teeth considered for study (if specified), sites (if mentioned), age of study subjects (either range or mean age ± standard deviation (SD)), sex, controls, and studied mediators. Apart from these, following inclusion criteria were also considered (if mentioned) no history of drug intake, no bone loss, no gingival inflammation, and pocket depth <2 mm.
Study characteristics (Table 2): these were nature of applied force, force magnitudes, force reactivations (if studied), total study duration, observation intervals, and type of tooth movement.
Oral hygiene regimen and assessment of gingival health (Table 3): recommendation and frequency of mouthwash intake, oral prophylaxis schedule, use of indices for gingival and periodontal assessment, and their frequency.
GCF characteristics (Table 4): time, room temperature and humidity during GCF collection, site, method of collection of GCF, storage and handling characteristics, and technique of mediator analysis.
Quality assessment of the articles included in the review was done based on a Quality Assessment Instrument (QAI) modified and developed from relevant articles in literature , given in Additional file 2: Annexure 2.
Thirty stringent criteria for evaluation of quality included relevant study design (N = 19), study measurements (N = 3), statistical analysis (N = 5), study results, and conclusions (N = 3). (Additional file 2: Annexure 2). For objective assessment of quality determination, a scoring system was incorporated where scores of 1 to 10 were considered minimal, 10 to 20 were considered moderate, and 20 to 30 were considered highly sensitive. QAI revealed 26 moderately sensitive and 13 highly sensitive studies. None of the studies fell in the score of 1 to 10.
The results were compiled after grouping of observations from similar studies to arrive at conclusions with relevant clinical implications.
Thirty-nine shortlisted studies ,- were scrutinized for inclusion and exclusion criteria. Two studies that evaluated mediators both in peri-implant crevicular fluid (PMICF) as well as GCF were included , but one study that evaluated the levels of mediators directly in sulcus and not GCF was excluded .
The studies were categorized based on participant characteristics (Table 1), study characteristics (Table 2), oral hygiene regimen and assessment of gingival health (Table 3), and GCF characteristics (Table 4). All studies displayed control, either internal/external. The levels of biomarkers assessed at baseline level (0 day) were taken as control in the former while in the later, contralateral or antagonistic teeth were taken as control. GCF sampling was done with either using periopaper or micropipette that were placed in the gingival sulcus. An overview of the results obtained has been summarized in Table 5.
Of the 39 studies, the sample size varied, smallest being 7 subjects  to a maximum of 84 subjects . The studies were categorized in four groups, with sample size up to 10 (N = 15), 11 to 20 (N = 16), 21 to 30 (N = 5), and 31 and above (N = 3). Average sample size taken was 10 subjects (N = 10).
Information on sex of the subjects was mentioned in N = 36 studies. One study (N = 1) included only male subjects. Equal numbers of male and female subjects constituted the sample in ten studies (N = 10).
Age was expressed as either range or as mean with standard deviation. There was no mention of age in one (N = 1) study. Comparative evaluation of juvenile and adults was reported in two studies (N = 2) and adolescent vs. adults in one study (N = 1). Age groups of male and females subjects were managed separately in three studies (N = 3). Age group of up to 15 years was considered in 19 (N = 19) studies and 15 years and above was considered in 20 (N = 20) studies. One study (N = 1) considered a large age group interval of 18 to 45 years .
Mediators of orthodontic tooth movement
Cytokines, receptors and their antagonists included in the review have been listed in Table 1. The cytokines have been studied singularly or in combination with other mediators. The most often studied cytokines in tooth movement are IL-1β (N = 21), TNF-α (N = 10), IL-8 (N = 8), IL-6 (N = 8), IL-2 (N=4), IL-4, IL-10 (N = 2), IL-1, IL-5, IL-1α (N = 1), OPN (N = 1), and RANKL (N = 7).
Receptors and their antagonists have been studied in the frequency of OPG (N = 8), IL 1RA (N = 5), and RANK (N = 1). Chemokines have been studied in the order of monocyte chemoattractant protein (MCP)-1 (N = 3), RANTES (N = 2), and IP-10 (N = 1). Studies related to growth factors were GMCSF (N = 3), TGF-β (N = 2), and IFN-γ (N = 2) and there was only one (N = 1) study on Leptin.
Time period and observation intervals
The total time duration for studies exhibited large variation from as low as 24 h to as high as 70 weeks. Studies were performed for a duration of 24 h (N = 3), 1 week (N = 10), 2 weeks (N = 2), 3 weeks (N = 2), approximately 1 month (N = 5), 2 months (N = 1), approximately 3 months (N = 10), 4 months (N = 2), 5 months (N = 1), and 6 months and above (N = 4).
GCF collection was done at multiple observation times ranging from a maximum of 11 times (N = 2) to minimum at 2 times (N = 4). Nine studies (N = 9) used 4 observation times; eight (N = 8) studies used 6 observation times; four (N = 4) studies used 2, 5, and 7 observation times; three (N = 3) studies used 3, 9, and 10 observation times; and two (N = 2) studies used 8 observation times.
Thirty-seven (N = 37) studies took observation point before activation as ‘zero’ or baseline. The protocol followed for GCF collection was 0, 1 h, 24 h, and 7 days (N = 14) and of 0, 1 h, and 24 h (N = 15). An additional observation point at 14 days (N = 7) and 21 days (N = 6) was also considered. An internal control (baseline levels) was considered in N = 12 studies while other studies (N = 27) took an external control that was either contralateral or antagonistic tooth or tooth other than experimental tooth.
Mechanics of force application
Twenty-seven studies considered retraction of canine (N = 27) which included NiTi coil spring (N = 18), vertical loop (N = 5), screw-based retractors (N = 3), and segmental mechanics (N = 14). Other methods of force applications were separators (N = 4), expansion with hyrax screw (N = 2), labial tipping with offsets in wire (N = 2), bracket placement (N = 1), and leveling of arches (N = 5).
Type of force application
Twenty-six studies (N = 26) used continuous force and 12 (N = 12) employed interrupted force. There was no mention of type of force in two (N = 2) studies. Four studies used continuous and interrupted force on different index teeth (N = 4).
Levels of force
Twenty-eight studies (N = 28) mentioned levels of force applied while eleven studies (N = 11) have no mention of it. One-hundred fifty-gram force was used in eight studies (N = 8), followed by 250 g (N = 5) and 100 g (N = 4). One study (N = 1) each employed 50, 120, 130, and 200 g; 70 cN; and 2 to 2.5 N of force. A range of force was applied from 4 to 13 kPa (N = 1), 90 to 115 g (N = 1), and 4, 13, 26, 52, or 78 kPa in N = 2 studies. Force reactivation was considered in three (N = 3) studies to compare continuous and interrupted force.
Oral hygiene regimen and gingival health assessment
Professional oral prophylaxis was performed before treatment (N = 28) and at every observation point (N = 23) but was not mentioned in the remaining studies. Oral hygiene regimen with recommendation of chlorhexidine mouthwash was mentioned in 11 studies (N = 11) and its frequency (N = 10) studies. Indices for assessment of gingival and periodontal health were employed before the treatment (N = 30) and at every observation point in N = 24 studies.
The GCF samples were collected at a particular time of the day (N = 11), preferably 9 AM to 12 PM and early morning (N = 2). Twenty-eight (N = 28) studies had no mention of time for GCF collection. The room temperature conditions were considered in six (N = 6) studies and humidity in five (N = 5) studies.
The sites for GCF sample collection were either mesial (N = 5) or distal (N = 21) or both mesial and distal (N = 12). GCF collection was done by periopaper (N = 33) studies, filter paper (N = 3), or filter membrane (N = 2). One study (N = 1) did not mention the technique by which GCF was collected.
Depth of insertion of paper for GCF collection was mentioned in 27 studies with the most common practice being a 1-mm depth (N = 26). One study used 2-mm depth of insertion. Duration of GCF collection was specified to be 30 s in most studies (N = 29) followed by 60 s (N = 4), 3 min (N = 1), 10 s (N = 1), and 20 s (N = 1). Repeated measurements were considered in 19 studies (N = 19) with collection repeated once in N = 11 studies, twice in N = 5 studies, and 3 times in N = 3 studies. The interval was 60 s (N = 14), 90 s (N = 1), and 120 s (N = 1).
The samples were stored at −20°C (N = 7), −30°C (N = 6), −70°C (N = 10), and −80°C (N = 9). The GCF from periopaper was retrieved by Periotron (PT)8000 (N = 18), PT6000 (N = 5), PT (N = 2), or electronic scale (N = 3) and was not mentioned in some studies (N = 11). Mediators were analyzed by ELISA (N = 27), immunoassay (IA) (N = 8), Luminex multianalyte technology (LMAT) (N = 1), Bio-Plex human cytokine assay (BHCA) (N = 1), custom protein array (CPA) (N = 1), or Quantibody Ar kit (QAK) (N = 1). Protein concentration in GCF was measured in pg/μl (N = 12), pg (N = 5), pg/mg (N = 1), pg/ml (N = 5), pg/mg (N = 1), pg/μg (N = 30), pg/30 s (N = 2), pg/20 s (N = 1), and pg/site (N = 1) and was not mentioned in N = 3 studies.
The total number of studies included in this review are 39. However in the result section, some of the variables showing number of studies may be more than 39, as few parameters have been divided into subgroups that have been considered as a separate variable.
Mediator levels in GCF
Twenty-one studies on IL-1β were evaluated. Of these, ten studies (N = 10) reported that the peak levels of IL-1β were attained at 24 h ,,,,,,,,,. The peak levels in other studies have also been reported at 4 h , 3 days ,, 7 days, 21 days , 2 months , around 3 months ,, and 6 months . One study mentioned peak for different teeth at different observation points  that resulted in peak for molars at 67 days, for premolars at 32 days and for central incisors at 39 days. Another study did not mention peak but fluctuation in IL-1β levels on application of different stresses of teeth that were correlated with velocity .
One study mentioned IL-1β levels on application of 150-g force to be twice that on application of 50-g force at 24 h and 2 months . Studies have shown decrease in levels of IL-1β, 14 days after prophylaxis, followed by an increase upon activation of orthodontic appliance (N = 2) ,. Forces of short duration show an increase in IL-1β at 7 and 21 days . Levels of IL-1β in experiment teeth were shown to be greater than control teeth at 1 h ,, 4 h , 8 h , 24 h ,,,,72 h , 7 days , 25 days ,, 32 days ,, 33 days , 39 days ,, 42 days , 46 days ,, 67 days ,, and 81 days ,.
A comparison of continuous and interrupted force was evident in one study  where it was shown that IL-1β levels in continuous force is greater than baseline at 24 h while in interrupted force, levels were greatest at first reactivation.
Difference in IL-1β levels according to site specification was mentioned in one study  where levels at distal site of tooth retraction were greater than mesial site at both 4 and 13 kPa of force application. Placement of elastic separators in molars led to an increase in levels at 1 min, 1 h, 24 h, and 7 days  at mesial site while at distal site, increase was seen at 1 h, 24 h, and 7 days .
An upregulation in IL-1β levels from baseline levels was evident at 1 min , 1 h , 24 h ,,,,, 48 h , 7 days , 3 months , and 6 months  and downregulation was seen in 48 h, 168 h, 14 days, and 21 days .
IL-8 also increased on application of continuous force for retraction at 1 h , both on tension and pressure sites  and also at 4 h , 24 h, and 48 h . Placement of separators led to an increase in levels at 24 h . Fall in levels was observed at 7 days of leveling and an increase was seen at 7 days, 21 days of retraction .
Application of interrupted force witnessed an increase in levels at 1 h  and 24 h , while continuous force application led to increase in levels at 24 h , or 4 h to 42 days . There was a decrease in levels in 1 week on continuous force retraction by hybrid retractor (HG) . TNF-α levels also increased at 1 day , at 3 months  of leveling, and at 6 months, just before retraction . A comparison of continuous force application by hybrid retractor (HG) by HG to interrupted force by rapid canine distalizer (RDG) showed higher values at 1 h in RDG group compared to HG .
Levels of receptor and their antagonists in GCF
RANKL showed an increase in levels at 24 h ,, greater than control as well as baseline with specific mention of levels in juveniles and adults ,. Two studies (N = 2) mentioned increase in levels greater than baseline, one at 48 h  and other at 42 days  at 24 h greater than control , at 48 h , 42 days  greater than baseline. Correlation with age was established with levels in adults being less than juveniles ,, an increase in RANKL/OPG ratio in 6 weeks in adolescents .
Lower value IL-1RA was shown to be associated with higher velocity of tooth movement (Vt) . It was also a determinant of activity index (AI) that is ratio of concentrations of IL-1β and IL-1RA in GCF, known to correlate with Vt ,,,. One study mentioned distinction of site where levels at distal site of retraction were greater than mesial and control on application of 4 and 13 kPa force . A comparison between levels in adults and adolescents revealed a decrease in ratio of IL1/(IL1 + IL-1RA) in 3 weeks .
The levels were decreased in experimental teeth at 1 h , 24 h ,,, 168 h , 1 month , and 3 months  than baseline levels. A distinction of age-specified levels of OPG as well as ratio of RANKL/OPG was found to be lower in adults than in juveniles . The levels of OPG in experimental teeth were found to be lower in adolescents in 6 weeks compared to control teeth . Its values were less in adolescents in 6 weeks . Site specification determined levels to increase on tension site (mesial) and to decrease on compression site (distal) .
Chemokines [CCL-2 (MCP1), CCL-3, CCL-5 (RANTES), IL-8 (CXCL8)] showed an increase in both experimental and control teeth at 24 h of force application . Levels of IL-8 were increased when force was applied for a short duration in separator placement , or longer duration in initial alignment , 1 to 2 days of leveling , increase from 4 h to 42 days , at 1 h, 24 h, and 48 h  when continuous forces were applied for retraction. Levels also showed a decrease in 7 days of leveling . A difference in levels was observed with distinction of site, with levels increased at both mesial and distal sites at 1 h of force application, between 24 h and 6 days at tension site and a statistically significant increase at tension site greater than compression site . Two studies (N = 2) on chemokines did not reveal any significant findings ,.
This systematic review was primarily aimed to conjure substantial evidence regarding the cytokine, chemokine, receptor and their antagonist (RANK, RANKL, OPG) levels in GCF consequent to application of orthodontic force. The literature revealed heterogeneity in study designs pertaining to participant characteristics, force application, levels of force, GCF collection methods and collection protocol, storage, and oral hygiene maintenance regimen. To draw logical conclusions each of the variables was tabulated and analyzed separately. Associations of change in levels of mediators were established with mechanics of applied orthodontic force, amount of force, force reactivations, differentiation in levels between tension and compression sites, age groups (juveniles and adults, growers and non-growers), and velocity of tooth movement (Vt).
The altering levels, rise, and fall of the mediators in GCF are suggestive of underlying intricate biological remodeling processes in bone and periodontal tissues that eventually leads to OTM. The forces employed for OTM or midpalatal expansion led to an initial increase in levels of bone-resorptive mediators as well as associated receptors namely IL-1β, IL-8, RANKL, and TNF-α as early as 1 min  or 1 h  and attained peak in 24 h ,,,-,,,,,,,. These mediators slowly decrease to baseline in subsequent observation points at 48 h, 168 h, 14 days, and 21 days ,,. On the contrary, bone-forming mediators like OPG show an immediate decrease in levels on application of orthodontic forces at 1 h on distal site of retraction ,, at 24 h ,,,. The role of RANK, RANKL, and OPG system in governing osteoclastogenesis has also been corroborated in animal studies , and in vitro studies - on periodontal ligament cells. When compressive orthodontic force is applied, upregulation of RANKL occurs which leads to stimulation of PGE2 pathway and finally, osteoclastic activity is initiated which results in bone resorption ,. OPG, a RANKL decoy receptor generated by osteoblastic cells and cells of the periodontal ligament, binds to RANKL and inhibits RANK/RANKL interaction that is the mainstay of osteoclastogenesis .
Besides these receptors, other factors that are directly or indirectly responsible for differentiation, survival, and activity of osteoclasts are cytokines (IL-1β, TNFα, IL-6) and chemokines (CCL2, CCL3, CCL5, CCL7, CCL9, IL-8) ,. The literature search in the present review found an increase in levels of these mediators in GCF on orthodontic force application. Evidence proves that mechanical stress induces acute inflammatory changes that alter the microvascular environment, with studies supporting local release of mediators IL-1β, TNF-α, and expression of chemokines that ultimately promotes leukocyte adhesion and migration . IL-1β (N = 21) and TNF-α (N = 10) are the most researched cytokines, supporting their role in the inflammatory changes associated with orthodontic tooth movement (OTM). Variation in mediator levels with type of force and force reactivations has also been evaluated to study their clinical implications with IL-1β, PGE2, or TNF-α levels showing an initial increase, both in continuous and interrupted force ,. However, timely reactivations in interrupted force led to an upregulation of these mediators, indicative of greater inflammation than on continuous force application ,. This finding is in accordance with other studies that support association of light continuous forces for OTM with minimal inflammation, root resorption, and hyalinization of the periodontal ligament -. More recent techniques for accelerated orthodontics like micro-osteoperforations have also conducted studies at cellular level that led to increase in GCF levels of cytokines ( IL-1α, IL-1β, IL-6, TNF-α) and chemokines at 24 h, giving evidence of underlying inflammatory process associated with inducing perforations in cortical bone . An animal study further supports the release of proinflammatory cytokines with micro-osteoperforations, known to recruit osteoclast precursors and hence increase OTM by influencing the bone remodeling process .
Results of the review showed that compression side witnessed a decrease in bone-formative OPG by 24 h  and increase in bone-resorptive RANK and TGF-β1 after 7 days ,. Other mediators showing temporal variation on compression side were IL-1β that increased as early as 1 min  or after 4 h , RANKL after 42 days  or after 24 h both in juveniles and adults , and IL-8 after 4 h  or after 10 days . In contrast, the tension site showed an appreciable increase in TNF-α  and other bone-resorbing mediators like IL-1β, PGE2, and IL-8. But the rise occurred earlier than compression and at all observation points with levels higher than at the compression site ,. This difference is hard to understand as the concept of compression on one side and tension on the other side of the tooth undergoing movement is hypothetical. It has been logically contradicted since the anatomical shape and surface morphology of the tooth root cannot be considered confined to definite geometry. Thus, forces when applied lead to biological response in whole of the periodontal apparatus that cannot be differentiated for release of inflammatory mediators in GCF which is a freely circulating fluid in gingival sulcus. Therefore, mediator levels in GCF collected from mesial or distal sites of the tooth may not be indicative solely of compression or tension zone activity.
Synopsis of the studies included in the review also revealed that age and growth status were factors influencing the level of cytokines in GCF that is shown to have an effect on the rate and amount of tooth movement. Mediator levels were seen to vary with growth status of individuals as evaluated in adolescents and adults  or compared in juveniles and adults ,. In one study, different mediators were found to increase in different age groups with IL-6, GM-CSF increasing only in juveniles while PGE2 increasing both in juveniles and adults . In addition, activity index (AI) that is the ratio of IL-1β/IL-1RA in GCF, was found to influence velocity (Vt) of OTM both in growers and non-growers . Mean Vt of growers was 0.050 mm/day and of non-growers was 0.024 mm/day for the same amount of applied stress that was correlated with higher levels of IL-1β and an increased AI in growers . A greater Vt and amount of OTM in juveniles as compared to adults could be explained on the basis of a higher RANKL/OPG ratio in GCF in juveniles . Other studies also support the variation in Vt according to varying mediator levels and AI in GCF ,,,. It was found that association between AI and Vt was stronger from distal than from mesial of retracted teeth, thus emphasizing greater values of IL-1β on the distal . Thus, evidence from this literature review emphasizes the role of RANKL/OPG ratio in OTM in either of the age groups owing to its significance in osteoclastogenesis and bone resorption that ultimately alters the amount and velocity of OTM.
Secondary outcome of this review was the association of intensity of pain with different force levels. The level of IL-1β was seen to increase at 1 day  that correlated with increased pain intensity and subsequently, there was a decrease seen in 7 days. Another study suggested pain was less with 50-g force as compared to 150-g force that was correlated with greater levels of IL-1β with application of 150-g force . It can be concluded that 150-g force is marked by higher levels of IL-1β in GCF compared to 50-g force and high pain intensity.
This systematic review is focused on association of cytokine and receptor levels or activity index in GCF with velocity of tooth movement, nature of force applied, pain intensity, and growth status/age of the subjects, leading to following conclusions:
Application of orthodontic forces causes an immediate release of inflammatory bone-resorptive mediators (IL-1β, TNF-α) in 1 h that reach peak in 24 h, thus supporting the role of inflammation in initial OTM.
Bone-forming mediators like OPG witnessed a fall in levels immediately after orthodontic force application indicating bone resorption to be the key process in initiating tooth movement.
The levels of cytokines decrease after attaining peak values, mostly at 24 h in continuous forces but repeated activations in interrupted force upregulate their secretion.
A rise in GCF levels of IL-1β with higher force levels (150 vs 50 g) has been linked to increased pain intensity during OTM.
Juveniles exhibiting greater RANKL/OPG ratio and activity index (AI) (IL-1β/IL-1RA) in GCF displayed faster rate of OTM than adults or non-growers.
Increased velocity of tooth movement (Vt) has been correlated with a greater activity index (AI) in GCF.
The literature search and critical review have also provided a lead to lacunae of the research in this field. There is lack of uniformity of study design with respect to sample size, age, sex ratio, observation intervals, duration of observations, mechanism employed to initiate OTM and ethnic/nutritional barriers. These are potential confounders which can influence the outcome . A major drawback identified in the current review was the lack of consideration of sex on mediator levels that are known to be sensitive to estrous cycle. Animal studies have evaluated correlation between ovarian activity and PGE2, IL-1β levels in GCF of female cats during OTM. Results revealed that mediator levels of estrous groups were lower than anestrous and ovariectomized groups on 6 and 12 days, indicating that ovarian activity can affect OTM . The threshold levels of the inflammatory mediators for initiation for OTM also remain unexplored. Besides GCF, peri-implant fluid may also be a potential medium to study these markers noninvasively in future studies . Search of pain killers having least effect on bone-resorbing mediator levels as a drug of choice may be a potential area of future research . Research related to the role of mediators in external apical root resorption (EARR) and relapse has also received little attention and are important research areas requiring further exploration.
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The authors are grateful to Dr Sushma Chaurasia who provided valuable inputs for the study.
The authors declare that they have no competing interests.
PK and NM retrieved the articles for the study and compiled them into manuscript form. OPK gave the concept of this descriptive review, crosschecked the studies, and was actively involved in writing and reviewing the manuscript. RM and SK formulated the preparation of the manuscript. All authors read and approved the final manuscript.
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Kapoor, P., Kharbanda, O.P., Monga, N. et al. Effect of orthodontic forces on cytokine and receptor levels in gingival crevicular fluid: a systematic review. Prog Orthod. 15, 65 (2014). https://doi.org/10.1186/s40510-014-0065-6