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neuropeptides, systematic review, periodontal disease, periodontitis, neurogenic inflammation
Smrithi V. Varma , Sheeja Varghese, Vijayashree J. Priyadharsini, Jayakrishnan Radhakrishnan, Sajan V. Nair
Published: July 15, 2022 (see history)
DOI: 10.7759/cureus.26889
Cite this article as: Varma S V, Varghese S, Priyadharsini V J, et al. (July 15, 2022) Establishing the Role of Neurogenic Inflammation in the Pathogenesis of Periodontitis: A Systematic Review. Cureus 14(7): e26889. doi:10.7759/cureus.26889
The role of neurogenic inflammation in various systemic diseases has been well established, but there is a dearth of studies and evidence regarding its role in periodontitis. This study aimed to systematically review the evidence in establishing the role of neurogenic inflammation in chronic periodontitis. Databases such as PubMed, Scopus, and Google Scholar were reviewed. We analyzed studies of any design that compared and evaluated the presence of neuropeptides such as substance P, calcitonin gene-related peptide, neurokinin A, neuropeptide Y, and vasoactive intestinal polypeptide in systemically healthy patients with and without periodontitis. We screened 2,495 articles and abstracts electronically and manually, which yielded 191 articles relevant to our study. Full-text examination of these 191 articles led to the final inclusion of 14 publications. Most studies here confirmed an association between various neuropeptides and periodontitis, but there is a high heterogeneity between the studies, making it necessary to clarify the mechanism between these two. Although most studies included in this review found a positive association between neurogenic inflammation and periodontitis, the evidence is of moderate to low quality.
Chronic periodontitis is a disease of inflammatory origin caused predominantly by bacteria present in the dental plaque. Although bacteria are a well-established cause of periodontitis, their presence alone is not enough to produce advanced periodontal tissue destruction. Apart from being one of the reasons for tooth loss, periodontal diseases are associated with many systemic diseases in developing and developed nations. A neurogenic component is integral to periodontitis [1]. The role of neurogenic inflammation in various systemic diseases has been well established. Many inflammatory diseases, including periodontitis, have been implied to have a neurogenic component. Jancso and Szolcsany, in 1967, introduced the term neurogenic inflammation [2]. Neurogenic inflammation is a protective mechanism; however, severe or prolonged stimulation might result in injury rather than repair. When a chemical combines with chemical irritant receptors on sensory nerves, it can release Substance P (SP) and other inflammatory neuropeptides resulting in neurogenic inflammation [3]. Neurons generate biologically active peptides known as neuropeptides (i.e., peptide neurotransmitters) [4]. A neuropeptide is a peptide synthesized and released from neurons, and its actions are biologically mediated through extracellular receptors on the target cells [4]. A brief outline of the various neuropeptides and their mode of action are given in Table 1 [2,5-17]. We conducted this study to systematically review the evidence in establishing the role of neurogenic inflammation in chronic periodontitis.
SP, substance P; CGRP, calcitonin gene-related peptide; NKA, neurokinin A; NPY, neuropeptide Y; VIP, vasoactive intestinal polypeptide
We followed the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines to conduct this systematic review [18]. We sought to determine the weight of evidence existing to establish the link between neurogenic inflammation and periodontitis. Our review included studies of any design (e.g., randomized controlled trials, cohort studies, case-control studies, cross-sectional studies) that compared and evaluated the presence of any one of the neuropeptides such as SP, calcitonin gene-related peptide (CGRP), neurokinin A (NKA), neuropeptide Y (NPY), and vasoactive intestinal polypeptide (VIP) in systemically healthy patients with and without periodontitis. The studies included defined periodontal disease according to any clinical periodontal indexes. Our search strategy used a combination of Medical Subject Headings (MeSH) terms as in Table 2. Our review excluded review articles, articles published in languages other than English, studies that lacked baseline data, and animal studies.
MeSH, Medical Subject Heading
We reviewed databases such as PubMed, Scopus, and Google Scholar. An independent reviewer searched the reference lists of the original and review articles using the MeSH terms. No year restrictions were applied while searching for articles. Screening 2,495 articles and abstracts both electronically and manually yielded 191 relevant articles. Full-text examination of the 191 eligible articles led to a final inclusion of 14 publications. We assessed the quality and main study characteristics of each article. The variables included adequately defined periodontal disease criteria and whether the article assessed one or more of the neuropeptides. Data from 14 selected articles were obtained and appraised by an independent reviewer. Figure 1 presents a structural outline of the search strategy.
PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analysis
Studies involved in this systematic review needed to present confounding factors controlled through randomization, matching, stratification, restriction, or statistical modeling to impede the course of periodontal disease. We included studies where confounding factors have been controlled through randomization, matching, and restriction. Studies included had to also state adequate criteria by which periodontal disease is defined (e.g., clinical attachment loss, probing depth, alveolar bone loss, bleeding on probing, gingival recession, and missing teeth). The studies had to have adequate criteria for establishing neurogenic inflammation.
Study Characteristics
Of the 14 studies included, seven were case-control studies, three were longitudinal, two were in vitro, and two were cross-sectional studies. All studies were published in English between 1989 and 2019. The studies were conducted in eight different countries (six in Ireland, one in India, Sweden, Australia, Japan, England, and China, and two in Turkey). The patient sample ranged from eight to 179 patients. Nine studies included healthy subjects and periodontitis patients, three assessed pre- and post-periodontitis treatment, one consisted of only a periodontitis group, and one contained patients with chronic migraine with or without periodontitis.
Study Outcomes and Parameters Assessed
The data were extracted and organized from the included articles by heading, author’s name, type of study, study location, sample size, study groups and characteristics, the statistical method used, outcome parameters, employed diagnostic method, results, and the sample collected in each study and conclusions. Tabular columns were created and rechecked to confirm the accuracy of the extracted information. We could not perform a meta-analysis due to the heterogeneity of the studies.
Outlines of the available studies are presented in Table 3 [19-25], Table 4 [26-28], Table 5 [29-30], and Table 6 [31-32]. Several studies analyzed the relationship between periodontal disease and more than one neuropeptide. In all, 11 of 14 studies suggested that periodontal disease is a risk factor for neurogenic inflammation. Five neuropeptides (SP, CGRP, VIP, NKA, and NPY) were assessed to evaluate their role in the pathogenesis of periodontitis. Nine of 14 studies evaluated SP while eight used gingival crevicular fluid (GCF) as the sample.
ANOVA, analysis of variance; M, male; F, female; CI, confidence interval; NA, not applicable; GCF, gingival crevicular fluid; SP, substance P; CGRP, calcitonin gene-related peptide; NKA, neurokinin A; NPY, neuropeptide Y (NPY)
GCF, gingival crevicular fluid; SP, substance P; NKA, neurokinin A; VIP, vasoactive intestinal polypeptide; NKA-LI, neurokinin A-like immunoreactivity; SP-LI, Substance P-like immunoreactivity
ANOVA, analysis of variance; SP, substance P; CGRP, calcitonin gene-related peptide; NPY, neuropeptide Y; VIP, vasoactive intestinal polypeptide
ANOVA, analysis of variance; SP, substance P; GCF, gingival crevicular fluid; NKA, neurokinin A; NKA-LI, neurokinin A-like immunoreactivity; PPD, periodontal probing depth
In Pradeep et al.’s study, the mean concentration of SP was highest among periodontitis patients (GCF: 45.13± 13.99 pg/mL, plasma: 67.80 ± 11.01 pg/mL) and decreases after treatment (GCF: 7.58 ± 3.25 pg/mL, plasma: 39.7 ± 3.83 pg/mL) [27]. This trend was supported by similar studies where pretreatment levels of SP decrease after treatment [19]. However, Luthman et al. found that despite immunoreactivity for SP, CGRP, NPY, and VIP, no discernable differences were observed between healthy and diseased sites [29]. Studies have shown that smokers with periodontitis had higher SP in the gingival biopsy sample than smokers with periodontally healthy teeth, nonsmokers with periodontitis, and nonsmokers with periodontally healthy teeth [23]. Sert et al. had seen similar findings where SP levels were higher in the diseased state than in healthy periodontium [25]. In a cross-sectional study, Hanioka et al. found that SP was significantly correlated to probing pocket depth (r=0.637, p≤.001), therefore, SP could be a key element in GCF [31]. According to Linden et al., a significant increase in SP-like immunoreactivity was seen in subjects with periodontitis (42.4 pg) than in control groups (2.0 pg) [32].
CGRP is a potent vasodilator [5] and is often co-localized with SP. Compared to healthy patients, there was extensive degradation of CGRP in periodontitis patients [19]. A notable increase in CGRP immunoreactivity was detected in periodontally healthy patients compared to those with gingivitis and periodontitis-affected sites [21]. Sert et al. demonstrated that CGRP levels decreased in diseased states [25]. CGRP levels in healthy periodontal tissues were 48.99 ± 0.78 pg/µL 30 s, whereas, in diseased states, they decreased to 23.93 ± 1.80 pg/µL 30s. Some studies revealed higher SP and CGRP levels in smokers with periodontitis than smokers with periodontally healthy teeth or nonsmokers. Leira et al. demonstrated that increased periodontal inflammation was associated with higher circulating levels of CGRP in chronic migraine patients compared to healthy patients [24].
VIP is a ubiquitous peptide with a well-established role as an immunomodulatory peptide capable of regulating both pro- and anti-inflammatory mediators. Linden et al. suggested that the amount of VIP decreased significantly after periodontal treatment [26]. VIP levels were 302.0 pg at the diseased site before treatment and 78.0 pg after treatment.
Lundy et al. demonstrated that the pretreatment levels of NKA (30.5 pg) decreased after treatment (10.6 pg) [20]. Linden et al. showed a significant increase in NKA in periodontitis-affected subjects compared to healthy controls [31]. However, Sert et al. reported that NKA levels decreased in diseased states [25]. NKA levels in healthy periodontal tissues were 583.11 ± 13.58 pg/µL 30 s but decreased to 108.33 ± 18.31 pg/µL 30s in disease states.
NPY is widespread throughout the central and peripheral nervous systems. It is a potent vasoconstrictor and is predominantly anti-inflammatory, as supported by Lundy et al.’s results [20]. Elevated NPY levels are present in the GCF of healthy tissues (161 ng) compared to periodontitis-affected tissues (39.8 ng). Sert et al. found that NPY levels decreased in diseased states [25].
This study was an attempt to systematically review the existing data from selected studies on the influence of neurogenic inflammation on periodontitis. This study is the first to systematically review the link between various neuropeptides and periodontitis. Specific neuropeptides could systemically modulate inflammatory disorders such as periodontitis and other orofacial conditions. Tissue samples from gingivitis and periodontitis-affected sites revealed the presence of neurochemical markers, indicating the appearance of neuropeptide in the etiopathogenesis of periodontitis [29-30]. The initiation and progression of periodontal disease are multifactorial, and variations in neuropeptide levels are only part of the neurogenic aspect of the etiology, making it challenging to understand the development of the disease.
Most of the studies included in the present review suggest that periodontitis is associated with neurogenic inflammation. This relationship was derived mainly from case-control, longitudinal, in vitro, and cross-sectional studies. Case-control, longitudinal, and cross-sectional studies supply compelling evidence for this correlation.
Four of the seven studies with CGRP as an outcome parameter showed greater CGRP levels in periodontally healthy sites than in periodontally affected sites [19,21,23,25]. This could be because CGRP inhibits lymphocytic proliferation [33] and interleukin (IL)-2 production [34], inhibiting osteoclastic bone resorption and stimulating osteogenesis. Another explanation could be the rapid breakdown of CGRP due to carboxypeptidase activity in the gingival crevicular fluid obtained from periodontitis sites. This is significant because this neuropeptide can inhibit osteoclastic bone resorption and stimulate osteogenesis [19]. On the contrary, however, two studies reported no discernable differences between the levels of CGRP and SP in periodontitis-affected sites and clinically healthy sites [22,29]. A significant body of evidence studying the relation of SP to periodontitis has been included in this review. SP was higher in periodontitis sites than in clinically healthy sites [19,23,25,27-28,32]. Pro-inflammatory neuropeptides, such as SP, stimulate lymphocyte proliferation [35] and potentiate IL-2 production [36]. SP and NKA are not susceptible to carboxypeptidase activity, so they remain elevated in periodontitis [19]. Many studies have shown a positive association between SP and NKA clinical measurement, demonstrating their effects on periodontal disease severity. However, anti-inflammatory neuropeptides, such as NPY, have an important role in maintaining periodontal health [25].
The cause of increased SP in periodontitis is multifactorial, but one reason is that SP increases the activity of osteoclasts, thus stimulating bone resorption [37]. SP-like immunoreactivity prior to the presence of neutrophil ingress suggests its involvement in the early stages of the inflammatory response [38]. SP could influence leukocyte infiltration through several mechanisms, which is an essential feature of the inflammatory process [28]. Clinical studies showed a significant reduction in pro-inflammatory neuropeptides, such as SP, after periodontal treatment [28-27].
Several studies reported a notable reduction in VIP after periodontal therapy. However, increased VIP levels (as seen in clinically healthy sites) could be due to its anti-inflammatory role. VIP is a macrophage deactivating factor that prevents excessive production of pro-inflammatory factors [26] and inhibits lipopolysaccharide (LPS)-induced tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-12 production in activated macrophages [39-40]. Down-modulation of CD14 stimulates the production of IL-10, a potent anti-inflammatory cytokine [41]. A significant increase in VIP in periodontitis sites could be because LPS is a potent stimulus for inducing VIP production and secretion in vitro [42]. This shows that SP and VIP have antagonistic roles in periodontal inflammation. An integral part of the host immune response is the maintenance of equilibrium between pro- and anti-inflammatory neuropeptides. Linden et al. found a significant increase in SP-like immunoreactivity and NKA-like immunoreactivity in gingivitis and periodontitis sites as compared to healthy sites [32].
Most studies here confirmed an association between various neuropeptides and periodontitis, but there is a high heterogeneity between the studies, making it necessary to clarify the mechanism between these two. The pathophysiological mechanisms are still unclear, and further studies that use a standardized periodontitis assessment are needed in this regard. Since periodontitis is a multifactorial disease, multiple factors could have influenced the initiation and progression of the disease such as systemic disease, obesity, smoking, poor oral hygiene, stress, and genetics. These factors could have increased the host’s susceptibility to periodontitis. Therefore, ignoring these factors could have influenced the results of this review. All the studies included in this review used different methodological aspects, such as selection guidelines for patients in each group, methods used to evaluate periodontal disease, external variables, such as the population studied, and demographics; this heterogeneity is evident given the difference in the clinical parameters analyzed in each study.
The inconsistencies in how periodontal disease was defined across these studies indicate the presence of potential biases. Clinical attachment level and probing pocket depth are the most used methods of assessing periodontal disease as established in 1959 [43]. Different criteria have been used to define periodontal disease, which could lead to different results given that there are no universally accepted standards for periodontal disease diagnosis. For the studies to be standardized and comparable, there needs to be a universal definition for periodontal disease. Secondly, the insufficient sample size was one concern, increasing the probability of an association observed either by chance or by lack of statistical power. Larger sample sizes can minimize the effect of such bias.
Further limitations of the study would be a lack of information regarding comorbidities, missing data, a limited number of studies, inadequate methodology, and heterogeneity of the underlying condition. Controlling the confounding factors could be challenging, especially for highly prevalent conditions such as periodontitis. The methodical strategy used in these 14 studies is quite different; these differences may account for the conflicting results between studies.
Emerging evidence suggests a strong relationship between the extent and severity of periodontitis and neurogenic inflammation, but this relationship is unlikely to be causal. There is enough evidence to support that both these conditions could have resulted from an imbalance in the pro-inflammatory and anti-inflammatory cytokines.
Periodontitis is pathophysiologically complex and multifactorial. Many factors are responsible for the initiation and progression of the disease, one of which is neuropeptides. Although most of the studies included in this review found a positive association between neurogenic inflammation and periodontitis, the supporting evidence is moderate to low quality. There are limited numbers of studies on this topic. Therefore, more studies are needed in the future to assess the definitive role of the neurogenic mechanism in the pathophysiology of periodontitis. Future investigations should be directed toward research studies with long-term follow-up periods and better control of confounders; these parameters could further our understanding of the role of neuropeptides in periodontitis.
Department of Periodontology, Saveetha Dental College, Chennai, IND
Department of Periodontology, Saveetha Dental College, Chennai, IND
Clinical Genetics, Saveetha Dental College, Chennai, IND
Department of Community Oncology, Regional Cancer Center, Kerala, IND
Department of Orthodontics, Sri Sankara Dental College, Kerala, IND
Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
10.7759/cureus.26889
Varma S V, Varghese S, Priyadharsini V J, et al. (July 15, 2022) Establishing the Role of Neurogenic Inflammation in the Pathogenesis of Periodontitis: A Systematic Review. Cureus 14(7): e26889. doi:10.7759/cureus.26889
Peer review began: July 12, 2022
Peer review concluded: July 13, 2022
Published: July 15, 2022
© Copyright 2022
Varma et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 4.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analysis
SP, substance P; CGRP, calcitonin gene-related peptide; NKA, neurokinin A; NPY, neuropeptide Y; VIP, vasoactive intestinal polypeptide
MeSH, Medical Subject Heading
ANOVA, analysis of variance; M, male; F, female; CI, confidence interval; NA, not applicable; GCF, gingival crevicular fluid; SP, substance P; CGRP, calcitonin gene-related peptide; NKA, neurokinin A; NPY, neuropeptide Y (NPY)
GCF, gingival crevicular fluid; SP, substance P; NKA, neurokinin A; VIP, vasoactive intestinal polypeptide; NKA-LI, neurokinin A-like immunoreactivity; SP-LI, Substance P-like immunoreactivity
ANOVA, analysis of variance; SP, substance P; CGRP, calcitonin gene-related peptide; NPY, neuropeptide Y; VIP, vasoactive intestinal polypeptide
ANOVA, analysis of variance; SP, substance P; GCF, gingival crevicular fluid; NKA, neurokinin A; NKA-LI, neurokinin A-like immunoreactivity; PPD, periodontal probing depth
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