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Ciurea, A.; Rednic, N.V.; Soancă, A.; Micu, I.C.; Stanomir, A.; Oneț, D.; Șurlin, P.; Filipescu, I.; Roman, A.; Stratul, �.I.; et al. Periodontitis in Systemic Sclerosis. Encyclopedia. Available online: https://encyclopedia.pub/entry/41966 (accessed on 14 April 2024).
Ciurea A, Rednic NV, Soancă A, Micu IC, Stanomir A, Oneț D, et al. Periodontitis in Systemic Sclerosis. Encyclopedia. Available at: https://encyclopedia.pub/entry/41966. Accessed April 14, 2024.
Ciurea, Andreea, Nicolae Voicu Rednic, Andrada Soancă, Iulia Cristina Micu, Alina Stanomir, Diana Oneț, Petra Șurlin, Ileana Filipescu, Alexandra Roman, Ștefan Ioan Stratul, et al. "Periodontitis in Systemic Sclerosis" Encyclopedia, https://encyclopedia.pub/entry/41966 (accessed April 14, 2024).
Ciurea, A., Rednic, N.V., Soancă, A., Micu, I.C., Stanomir, A., Oneț, D., Șurlin, P., Filipescu, I., Roman, A., Stratul, �.I., & Pamfil, C. (2023, March 08). Periodontitis in Systemic Sclerosis. In Encyclopedia. https://encyclopedia.pub/entry/41966
Ciurea, Andreea, et al. "Periodontitis in Systemic Sclerosis." Encyclopedia. Web. 08 March, 2023.
Periodontitis in Systemic Sclerosis
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Systemic sclerosis (SSc) is a chronic, autoimmune, multisystemic disease characterized by aberrant extracellular matrix protein deposition and extreme progressive microvasculopathy. These processes lead to damage within the skin, lungs, or gastrointestinal tract, but also to facial changes with physiognomic and functional alterations, and dental and periodontal lesions. Orofacial manifestations are common in SSc but are frequently overshadowed by systemic complications. In clinical practice, oral manifestations of SSc are suboptimally addressed, while their management is not included in the general treatment recommendations. Periodontitis is associated with autoimmune-mediated systemic diseases, including systemic sclerosis. In periodontitis, the microbial subgingival biofilm induces host-mediated inflammation with subsequent tissue damage, periodontal attachment, and bone loss. When these diseases coexist, patients experience additive damage, increasing malnutrition, and morbidity. 

periodontitis systemic sclerosis pathogenesis

1. Introduction

Systemic sclerosis (SSc), or scleroderma, is a chronic, autoimmune, multisystemic disease characterized by aberrant extracellular matrix protein deposition and extreme progressive microvasculopathy [1]. These processes lead to severe organ damage within the skin, lungs, or gastrointestinal tract, but also to facial changes with physiognomic, and functional alterations and dental and periodontal lesions [2][3][4].
Orofacial manifestations are common in SSc (up to 80%) but are frequently overshadowed by systemic complications [2]. In SSc, the oral involvement initiates and maintains a vicious circle leading to malnutrition: fibrosis with secondary xerostomia favors tooth decay and periodontitis, leading to impaired mastication, dysphagia, and poor nutritional status. These features, in addition to gastroesophageal reflux and malabsorption, contribute to significant morbidity and gastrointestinal-associated mortality in SSc [5].
The limitation in mouth opening induced by fibrosis is associated with difficulties in performing examinations (manometry, fibroscopy) or intubations, which hampers the assessment and treatment of SSc patients [6].
In clinical practice, oral manifestations of SSc are infrequently addressed, and their management is not included in the general treatment recommendations [7][8]. Increased awareness of oral manifestations, including periodontitis, and further research, are essential to improving patient outcomes.
Periodontitis is a chronic, complex, multi-factorial infectious disease in which subgingival dysbiotic biofilm triggers a local, usually excessive, non-resolved inflammation that leads to the destruction of periodontal tooth-surrounding tissues. Periodontitis is a highly prevalent disease affecting around 50% of the population [9][10][11][12][13], with its severe forms affecting globally 11% of the population [14]. The continuous loss of periodontal attachment and alveolar bone results in some clinical signs such as gingival recessions, increasing clinical crowns, secondary tooth migrations, tooth mobility, furcation lesions, and finally to tooth loss and severe oral dysfunction.

Although some pathogenic links between rheumatic diseases and periodontitis are specified in the literature, the pathogenic intersections between SSc and periodontitis are less obvious and less organized [15][16], requiring a systematization of data on this topic. In addition, the therapeutic approaches of periodontitis in patients with SSc are relatively vaguely specified and there is no published exhaustive therapeutic plan that logically addresses the entire oral pathology of these patients [17][18][19]. Patients with SSc and periodontitis need individualized, gradual therapy based on the latest recommendations of the literature [20][21].

2. Oral Manifestations in Systemic Sclerosis

Orofacial involvement in SSc is associated with significant morbidity and reduced quality of life [22]. The fibrosis of the salivary glands determines reduced salivary flow, negatively impacting mastication and nutrition. Xerostomia aggravates dysphagia and impairs natural oral self-cleaning, thus raising the incidence of tooth decay, erosions, periodontitis [23], and Candida albicans infections [24].
Tongue rigidity is among the first acknowledged clinical manifestations in SSc and hinders speaking and swallowing [25]; facial fibrosis leads to a classic mask-like face, with loss of wrinkles, thin white lips, and microstomia [25].
Telangiectasia of facial skin and oral mucous membranes is the result of an aberrant attempt at increasing blood perfusion to hypoxic tissues secondary to capillary loss and failed vascular repair [26].
Mandibular bone resorption is described as resorptive lesions of the mandibular angles, coronoid processes, and zygomatic arches at the sites of muscle attachment [27]. Mandibular bone resorption has been reported in 20–33% of radiographically examined patients [28] and occurs predominantly in diffuse SSc [28]. Incriminated factors include muscle contractures secondary to fibrotic changes, microvasculopathy, and pressure ischemia due to thickened skin and muscle atrophy [29]. Atrophic and fibrotic alterations of the synovia may also induce temporomandibular joint disease [29]. In time, these muscular, osseous, and synovial changes hinder mandibular movements, limit the mouth opening, and decrease the interincisal distance in SSc patients [30].
Microstomia occurs due to sclerosis of perioral soft tissues; it impairs mastication, proper oral hygiene, and social relationships. Importantly, reduced oral aperture rends dental treatments more difficult or sometimes impracticable [30]. Different proposed regimens of oral aperture augmentation and stretching exercise programs were associated with contradictory results related to the improvement in orofacial functions. Several variables related to the type of exercises, duration, number of repetitions, teaching method, and patient compliance could explain the reported inconsistencies [31][32].
The Mouth Handicap in Systemic Sclerosis (MHISS) allows a homogeneous and adequate identification, and evaluation of the limitations in mouth functioning. This short, easy-to-fill-out questionnaire evaluates the degree of mouth disability according to three domains: mouth-opening restriction, mouth dryness, and aesthetic concerns [33]. Studies that employed MHISS as a measure of the quality of life showed that oral features are associated with global disability and negative perception of health status [34].
SSc is associated with a higher incidence of periodontitis. Characteristic periodontitis-related signs identified at oral examination should prompt a specialized assessment [35]. Notably, fibrosis, especially when it involves the frenum, can promote gingival recessions unrelated to periodontitis [25]. Malocclusion has also been described in some SSc patients [36].

3. Oral Hygiene in SSc Patients

SSc disease-related factors, such as xerostomia, diminished oral aperture, and manual dexterity impairments, have been reported to impact oral hygiene behavior in these patients. The handling difficulties of interdental cleaning devices were associated with less than daily interdental hygiene. Conversely, evening dental flossing reduced gingival inflammation in SSc [37]. Beyond the factors mentioned above, depressive symptoms common in SSc patients [38] are associated with disinterest in performing oral hygiene, less likelihood to brush teeth at least twice daily, and high values of plaque indices [35]. Neglected oral hygiene should alert dentists of possible underlying depression, and prompt patient referral for evaluation and specialized care [38].
In SSc, adapted oral hygiene devices are recommended to accommodate microstomia and reduced manual dexterity [37]. An electric toothbrush with a small head can facilitate oral hygiene, improve plaque control, and mitigate gingival inflammation [39]. The round, small-sized head of electric brushes (working in an oscillating-rotating action and associated with vibrating movements) is smaller than the head of manual brushes, can facilitate overall access, and individualizes hygiene according to the level of gingival margins. Dentists should recommend at least twice daily tooth brushing to prevent oral diseases.
SSc patients should be educated on the importance of daily flossing [37]. Adapted flosser over finger flossing is preferred in patients with reduced manual dexterity, as it facilitates patient compliance and long-term regular interdental cleaning habits [40]. The choice of an adapted flossing device or interdental brushes could increase easiness to use and daily interdental hygiene adherence [37].

4. Association between SSc and Periodontitis Supported by Clinical Observational Studies

Although orofacial manifestations in SSc have long been acknowledged, only a scarce number of observational studies assessed the periodontal status in SSc.
Many case-control studies reported that SSc was associated with impaired periodontal health defined based on pathological parameters of periodontitis (periodontal pockets, clinical attachment loss, percentage of deep pockets, local inflammation, gingival recessions, widening of periodontal space) or on various periodontitis case definitions [41][42][43][44][45][46][47][48][49] valid at the time of reports. In view of the various employed definitions of periodontitis in clinical studies, or the use of surrogate parameters, the epidemiological data supporting the association between SSc and periodontitis is hard to compare or to draw conclusions.
There is a group of clinical studies that have observed the associative relationship between SSc and periodontitis by analyzing only some surrogate parameters related to periodontal destruction. A higher prevalence of periodontal pockets and periodontal attachment loss in SSc than in healthy individuals was reported, indicating a possible relationship between SSc and periodontitis [41]. The increased loss of periodontal attachment in SSc remained significant after adjustment for known risk factors and indicators of periodontitis, such as age, gender, education, smoking status, alcohol consumption, and plaque index. The reduced periodontal bleeding on probing and gingival inflammation in SSc likely reflects the underlying fibrosis and capillary loss in SSc [41]. Conversely, other studies highlighted significantly higher bleeding on probing indices, witnessing more local inflammation in SSc patients than in controls; however, the cohorts included fewer and younger SSc patients and excluded patients with xerostomia, edentulous patients, and smokers. Significantly higher mean full-mouth probing depth dimensions [42][44], and percentage of sites with probing depths of 4 to 5 mm [42] were also reported in SSc patients than in controls.
SSc patients exhibited higher odds of increased probing depth compared with controls, even after adjustment for age, sex, and the presence of major organ involvement, as well as a higher prevalence of clinical attachment loss [46]. This is in accordance with other data concluding that high indices of periodontitis were associated with autoimmune disease [43].
Periodontitis occurs primarily in diffuse SSc [47]. In SSc, periodontitis was characterized by low bleeding on probing values, normal probing depths, and a higher prevalence of gingival recessions [47].
The periodontal ligament space widening on panoramic radiographs is considered by some authors a measure of periodontal damage in SSc [50][51]. Generalized periodontal ligament space widening, as assessed by cone beam computer tomography, is reported in up to half of the patients with SSc [48]. More comprehensive analyses [52] suggest that periodontal ligament widening is the second most frequent oral manifestation in patients with SSc.
Several studies reported a higher prevalence of periodontitis in SSc [41][53], defined according to a well known case definition system [9][54].
A very recent meta-analysis of case-control studies assessing oral manifestations in SSc included 11 studies evaluating periodontal damage and demonstrated a higher prevalence of periodontitis in SSc (Odds Ratio 7.007; 95%CI [3.529, 13.915]), a higher periodontal parameters such as probing depth (Standard Mean Difference SMD 3.101; 95%CI [1.374, 4.829]), and clinical attachment loss (SMD 2.584; 95%CI [0.321, 4.846]) [2]. No statistical significance was found regarding local inflammation quantified as gingival bleeding index (SMD, 1.054; 95%CI [−0.973, 3.081]). This meta-analysis is the first more exhaustive analysis that quantitively evaluated the association between SSc and periodontitis and periodontitis-related signs. Although this meta-analysis [2] included high-quality studies, their number was small, and their case-control design prevented elucidating the cause-effect relationship between SSc and periodontitis [2].
A report not included in the above-mentioned systematic review highlighted lower serum vitamin D levels in patients with SSc and periodontitis (defined based on 2018 Control of Disease Control/American Academy of Periodontology case definition) compared with controls [55]. The number of teeth and the levels of periodontal indices were significantly dependent on serum vitamin D in SSc patients [55].
In some observational studies, the relationships between SSc and periodontitis was analyzed based on some debilitating signs as the expression of SSc. An association between periodontitis and reduced mouth opening was presumed [25], but not confirmed by other reports [56]. Other authors showed that gingivitis is associated with diffuse SSc and impaired manual dexterity [37].
The epidemiological data provided by case-control studies should be interpreted with caution, given their small number and the lack of homogeneity concerning patient characteristics and periodontal parameters. Moreover, the variability in the periodontitis case definition influences the reported prevalence of periodontitis in the SSc cohorts, and the appreciation of epidemiological associative links between periodontitis and SSc. These associative relationships should be viewed from the perspective of all pathophysiologic sequelae that accompany both diseases and are likely to contribute toward and against their evolution; they should not be evaluated in the context of a causal effect [57]. Both SSc and periodontitis are complex diseases resulting from interactions of a complex make-up of factors, external and host-derived, detrimental and protective, each accounting for different fractions in the expression of the disease.
Further well-designed studies are needed to explore the relationship between SSc and periodontitis.

5. Diagnosis and Evolution of Periodontitis in SSc

The current classification of periodontal and peri-implant diseases and conditions considers that SSc belongs to the group of systemic disorders that can result in loss of periodontal tissue independent of periodontitis; periodontitis developing in SSc was not discussed as a manifestation of systemic diseases [58].
However, periodontitis has been largely described in SSc as mentioned in the previous sections. As for other periodontitis phenotypes belonging to “PERIODONTITIS” category of diseases, a “periodontitis case” in a SSc patient is based on the diagnostic criteria provided by 2018 classification system [59]: (1) the presence of the interdental clinical attachment loss at ≥2 non-adjacent teeth, or of the buccal/oral interdental clinical attachment loss ≥ 3 mm with pocketing ≥ 3 mm at ≥2 non-adjacent teeth, (2) the clinical attachment loss cannot be ascribed to non-periodontitis causes.
A spectrum of attachment level changes following different destruction patterns have been described in periodontitis, such as: a slow, continuous tissue loss, bursts of relatively rapid periodontal destruction in certain teeth (random burst pattern), and frequent bursts of periodontal destruction during certain periods (multiple burst pattern). Presently, no differentiation between periodontitis forms based upon progression rate of destruction is possible [60]. Recent data indicated a rate of progression in a general population of 0.1 mm per year, with increased values in developing countries than in developed ones, and with a little effect of age or gender on attachment level changes [60].

6. A Brief Overview of the Pathogenesis of Periodontitis

In periodontitis, the microbial subgingival biofilm induces host-mediated inflammation with subsequent tissue damage, periodontal attachment, and bone loss [61].
Periodontitis is a typical biofilm-associated infection [61] in which periodontal biological reactions are modulated by a complex make-up of general factors. More than 700 different species with distinct subspecies are present in the oral microbiome; many colonize the subgingival areas [62] and deliver essential benefits to general health [62]. Some of these bacteria have been identified as drivers in the pathogenic processes of periodontitis [61].
The ‘red complex’ model is one of the periodontitis pathogenic theories that supports the concept that periodontitis is a multimicrobial disease and acknowledges Porphyromonas gingivalis, Tannerella forsythia, and Treponema denticola as major subgingival pathogens responsible for the development and progression of periodontitis [63]. However, less virulent bacteria have also been linked to periodontitis.
The current polymicrobial synergy and dysbiosis models of periodontitis [61] indicate that the pathogenic driver is a synergistic polymicrobial community in which different members fulfill distinct roles in generating subgingival microbial dysbiosis and host immune disruption [64]. The accumulation of subgingival biofilm induces an inflammatory response where the increased gingival flow and subgingival accumulation of host molecules act as substrates for proteolytic bacteria. These changes in the oral environment cause alterations in microbial proportions and dysbiosis [62], enhancing the risk for periodontitis [64]. ‘Keystone pathogens’ such as Porphyromonas gingivalis modulate the immune response to impair host immune surveillance and tip the balance from homeostasis to dysbiosis [65].
The dysbiotic biofilm releases large amounts of bacterial products, including lipopolysaccharides, which induce the recruitment of immune cells, osteoclast activation, the synthesis of pro-inflammatory cytokines and chemokines, and eventually the destruction of bone and soft tissues [66]. The interleukin-1 (IL-1) and IL-6 family members and tumor necrosis factor (TNF) are pro-inflammatory cytokines with key roles in the progression of periodontitis [67]. IL-1 family members bind to their corresponding receptors, mediate lymphocyte activation, and enhance pro-inflammatory and metalloproteinase (MMP) production destroying periodontal components [67].
The binding between TNF family members and their specific receptors induces a large variety of cell fates, such as death (apoptosis) or life (secretion of pro-inflammatory and osteoclastogenic factors); both drive the destruction of periodontal tissues [66]. TNF-α is locally synthesized by neutrophils, macrophages, and Th1 lymphocytes. TNF-α induces an independent action on receptor activator of nuclear factor kappa-Β ligand, (RANKL) [68] and inhibits osteoblast differentiation and bone nodule formation. In periodontitis, inflammatory cells provide the most abundant expression of RANKL in response to bacterial stimulation [69]. A downregulated expression of osteoprotegerin (OPG)—the soluble decoy receptor that blocks RANKL—has been reported in periodontitis, which increases the RANKL/OPG ratio and, thus, osteoclastogenesis [68].
During periodontal inflammation, the increased oxygen consumption and consecutive local hypoxia induce up-regulation of the transcription of vascular endothelial growth factor (VEGF) within the human periodontal ligament and gingival fibroblast cells. VEGF-A and -C contribute to angiogenesis and lymphangiogenesis in periodontitis [70], but may also accentuate fibrotic changes in SSc.

7. Periodontal Therapy in SSc

Three main issues should be considered for the care of SSc patients: oral mucosa involvement, the limitations in mouth opening, and the treatment of related diseases [17]. Prevention of tooth caries and periodontitis is a major objective of oral care in SSc patients. The screening of periodontitis and its detailed diagnosis in the overall picture of oral pathology ensure the development of a comprehensive treatment plan.

Preventive therapy

  • The management of hyposialia should be carried out by prescribing saliva substitutes and stimulators (pilocarpine hydrochloride if Sjogren’s syndrome is associated) to diminish the risk of periodontitis, oral ulcers, and caries. Daily baking soda mouthwash should also be prescribed.
  • Prevention and management of microstomia. In patients with microstomia, mouth-opening exercises can improve the inter-incisor distance with severe limitations and the ability to chew, phonation, and dental hygiene [17]. Two times per day, five repetitions of each orofacial physical exercise, holding each for 10 s, should be included in the rehabilitation program of SSc patients: stretching lips with fingers, inflating checks, maximal mouth opening, biting a wood stick with left and right molars, pushing chins to left and right sides with the hand [31].
    • Personal oral hygiene or “patient package”. The “patient package” can be used to implement a tailored-oral hygiene protocol for efficiently removing tooth biofilm. The “patient package” represents a complex repetitive approach that implies information, motivation, and teaching the use of personalized oral devices (toothbrush and interdental cleaning aids -dental floss and interdental brushes). The oral-cleaning devices are prescribed to accommodate microstomia and decreased manual dexterity. A small-head oscillating-rotating electric toothbrush or a manual toothbrush with a child-sized brush head, used twice daily, are suitable options for SSc patients [37].

Adapted handle-flossing devices or individualized interdental brushes should be used once daily.

  • Management of risk factors. Cessation of smoking is mandatory.
  • Prevention of tooth caries. A complex prophylactic package must be implemented to interfere with the cariogenic risk. The package consists of alimentary advice addressing pH modifications, proper specialist-supervised dental hygiene for combating microbial aggression, and systematic fluoridation through fluoride-containing toothpaste associated with fluoride-carrying devices or professional applications of fluoride varnishes [17]
  • Bi-annual dental visits for screening of oral lesions (complete periodontal, dental, and oral mucosal examination) and maintenance by providing professional hygienic care and, eventually, treatments.

Specific oral treatments

  • Tooth caries should be treated according to current clinical guidelines.
  • If diagnosed, periodontitis treatment should follow current clinical guides [20][21]. Briefly, the first phase of therapy is supragingival hygiene and the control of risk factors; the second phase involves subgingival instrumentation and reevaluation. Surgical approaches, orthodontic treatment, and prosthetic rehabilitation drive patients to the end of active therapy and inclusion in the maintenance phase.
    • The use of dental implants is case-dependent, according to the ability to perform oral hygiene, the degree of microstomia, and the insertion of posterior implants [17]. Ideally, anterior implants are recommended, particularly at the canine levels of the jaw, to stabilize a removable metal prosthesis [17]. The implant treatment plan should be tailored with regard to disease severity, the presence of sicca syndrome, limitations in performing oral hygiene, and/or the treatment of an oral cancer. Marked gingival fibrosis and severe microvascular impairment contraindicate dental implants. However, the risk-benefit ratio of implant rehabilitation should be appraised.
    • Oral ulcers should be combated by local applications of topical antiseptics and anesthetics (such as chlorhexidine and lidocaine 2%) between meals to limit the risk of aspiration.
    • Soft resins may be used to manufacture the base of the removable prostheses to overcome oral lesions induced by rigid materials and microstomia.
    • Anaesthetics without vasoconstrictors should be used in these patients.

References

  1. Denton, C.P.; Khanna, D. Systemic sclerosis. Lancet 2017, 390, 1685–1699.
  2. Zhang, S.; Zhu, J.; Zhu, Y.; Zhang, X.; Wu, R.; Li, S.; Su, Y. Oral manifestations of patients with systemic sclerosis: A meta-analysis for case-controlled studies. BMC Oral Health 2021, 21, 250.
  3. Perelas, A.; Silver, R.M.; Arrossi, A.V.; Highland, K.B. Systemic sclerosis-associated interstitial lung disease. Lancet Respir. Med. 2020, 8, 304–320.
  4. Di Battista, M.; Barsotti, S.; Orlandi, M.; Lepri, G.; Codullo, V.; Della Rossa, A.; Guiducci, S.; Del Galdo, F. One year in review 2021: Systemic sclerosis. Clin. Exp. Rheumatol. 2021, 39, 3–12.
  5. Østbø, N.; Jimenez, E.Y.; Harb, S.; Bourgeault, A.; Carrier, M.; Thombs, B.D.; the Scleroderma Patient-Centered Intervention Network (SPIN) Diet and Nutrition Education Patient Advisory Team. Nutrition Information Resources Used by People with Systemic Sclerosis and Perceived Advantages and Disadvantages: A Nominal Group Technique Study. ACR Open Rheumatol. 2021, 3, 540–549.
  6. Shionoya, D.Y.; Kamiga, D.H.; Tsujimoto, D.G.; Nakamura, E.; Nakamura, K.; Sunada, D.K. Anesthetic Management of a Patient With Systemic Sclerosis and Microstomia. Anesthesia Prog. 2020, 67, 28–34.
  7. Denton, C.P.; Hughes, M.; Gak, N.; Vila, J.; Buch, M.; Chakravarty, K.; Fligelstone, K.; Gompels, L.L.; Griffiths, B.; Herrick, A.L.; et al. BSR and BHPR guideline for the treatment of systemic sclerosis. Rheumatology 2016, 55, 1906–1910.
  8. De Vries-Bouwstra, J.K.; Allanore, Y.; Matucci-Cerinic, M.; Balbir-Gurman, A. Worldwide Expert Agreement on Updated Recommendations for the Treatment of Systemic Sclerosis. J. Rheumatol. 2019, 47, 249–254.
  9. Eke, P.I.; Page, R.C.; Wei, L.; Thornton-Evans, G.; Genco, R.J. Update of the Case Definitions for Population-Based Surveillance of Periodontitis. J. Periodontol. 2012, 83, 1449–1454.
  10. Nazir, M.; Al-Ansari, A.; Al-Khalifa, K.; Alhareky, M.; Gaffar, B.; Almas, K. Global Prevalence of Periodontal Disease and Lack of Its Surveillance. Sci. World J. 2020, 2020, 2146160.
  11. Eke, P.I.; Thornton-Evans, G.O.; Wei, L.; Borgnakke, W.S.; Dye, B.A.; Genco, R.J. Periodontitis in US Adults. J. Am. Dent. Assoc. 2018, 149, 576–588.e6.
  12. Stødle, I.H.; Verket, A.; Høvik, H.; Sen, A.; Koldsland, O.C. Prevalence of periodontitis based on the 2017 classification in a Norwegian population: The HUNT study. J. Clin. Periodontol. 2021, 48, 1189–1199.
  13. Sødal, A.T.T.; Hove, L.H.; Diep, M.T.; Skudutyte-Rysstad, R.; Koldsland, O.C. Periodontal conditions in a 65-year-old population and prevalence of periodontitis according to three different bone level thresholds. BMC Oral Health 2022, 22, 246.
  14. GBD 2017 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 354 diseases and injuries for 195 countries and territories, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet 2018, 392, 1789–1858.
  15. De Molon, R.S.; Rossa, C., Jr.; Thurlings, R.M.; Cirelli, J.A.; Koenders, M.I. Linkage of Periodontitis and Rheumatoid Arthritis: Current Evidence and Potential Biological Interactions. Int. J. Mol. Sci. 2019, 20, 4541.
  16. Möller, B.; Kollert, F.; Sculean, A.; Villiger, P.M. Infectious Triggers in Periodontitis and the Gut in Rheumatoid Arthritis (RA): A Complex Story about Association and Causality. Front. Immunol. 2020, 11, 1108.
  17. Alantar, A.; Cabane, J.; Hachulla, E.; Princ, G.; Ginisty, D.; Hassin, M.; Sorel, M.; Maman, L.; Pilat, A.; Mouthon, L. Recommendations for the care of oral involvement in patients with systemic sclerosis. Arthritis Care Res. 2011, 63, 1126–1133.
  18. Laforgia, A.; Corsalini, M.; Stefanachi, G.; Tafuri, S.; Ballini, A.; Pettini, F.; Di Venere, D. Non-surgical periodontal management in scleroderma disease patients. J. Biol. Regul. Homeost. Agents 2016, 30, 847–851.
  19. Poole, J.; Conte, C.; Brewer, C.; Good, C.C.; Perella, D.; Rossie, K.M.; Steen, V. Oral hygiene in scleroderma: The effectiveness of a multi-disciplinary intervention program. Disabil. Rehabil. 2009, 32, 379–384.
  20. Sanz, M.; Herrera, D.; Kebschull, M.; Chapple, I.; Jepsen, S.; Berglundh, T.; Sculean, A.; Tonetti, M.S.; Aass, A.M.; Aimetti, M.; et al. Treatment of stage I–III periodontitis—The EFP S3 level clinical practice guideline. J. Clin. Periodontol. 2020, 47, 4–60.
  21. Herrera, D.; Sanz, M.; Kebschull, M.; Jepsen, S.; Sculean, A.; Berglundh, T.; Papapanou, P.N.; Chapple, I.; Tonetti, M.S.; Aimetti, M.; et al. Treatment of stage IV periodontitis: The EFP S3 level clinical practice guideline. J. Clin. Periodontol. 2022, 49, 4–71.
  22. Smirani, R.; Truchetet, M.; Poursac, N.; Naveau, A.; Schaeverbeke, T.; Devillard, R. Impact of systemic sclerosis oral manifestations on patients’ health-related quality of life: A systematic review. J. Oral Pathol. Med. 2018, 47, 808–815.
  23. Parat, K.; Radić, M.; Perković, D.; Lukenda, D.B.; Kaliterna, D.M. Reduced salivary flow and caries status are correlated with disease activity and severity in patients with diffuse cutaneous systemic sclerosis. J. Int. Med. Res. 2020, 48, 030006052094137.
  24. Mohamed, A.A.; Lu, X.-L.; Mounmin, F.A. Diagnosis and Treatment of Esophageal Candidiasis: Current Updates. Can. J. Gastroenterol. Hepatol. 2019, 2019, 3585136.
  25. Jagadish, R.; Mehta, D.S.; Jagadish, P. Oral and periodontal manifestations associated with systemic sclerosis: A case series and review. J. Indian Soc. Periodontol. 2012, 16, 271–274.
  26. Balanescu, P.; Balanescu, E.; Baicus, C.; Balanescu, A. S100A6, Calumenin and Cytohesin 2 as Biomarkers for Cutaneous Involvement in Systemic Sclerosis Patients: A Case Control Study. J. Pers. Med. 2021, 11, 368.
  27. Taveras, J.M. The interpretation of radiographs. In Disorders of the Temporomandibular Joint; Schwartz, L., Ed.; W.B. Saunders: Philadelphia, PA, USA, 1959; pp. 154–162.
  28. Haers, P.; Sailer, H. Mandibular resorption due to systemic sclerosis. Case Report of Surgical Correction of a Secondary Open Bite Deformity. Int. J. Oral Maxillofac. Surg. 1995, 24, 261–267.
  29. Aliko, A.; Ciancaglini, R.; Alushi, A.; Tafaj, A.; Ruci, D. Temporomandibular joint involvement in rheumatoid arthritis, systemic lupus erythematosus and systemic sclerosis. Int. J. Oral Maxillofac. Surg. 2011, 40, 704–709.
  30. Ferreira, E.L.A.; Christmann, R.B.; Borba, E.F.; Borges, C.T.L.; Siqueira, J.T.T.; Bonfa, E. Mandibular function is severely impaired in systemic sclerosis patients. J. Orofac. Pain 2010, 24, 197–202.
  31. Cüzdan, N.; Türk, I.; Çiftçi, V.; Arslan, D.; Doğan, M.C.; Ünal, I. The effect of a home-based orofacial exercise program on oral aperture of patients with systemic sclerosis: A single-blind prospective randomized controlled trial. Arch. Rheumatol. 2021, 36, 176–184.
  32. Sydow, E.; Van der Elst, K.; Verschueren, P.; Lenaerts, J.; Westhovens, R.; De Langhe, E. A mixed method study exploring patient satisfaction and feasibility of two exercise programmes in systemic sclerosis-associated microstomia. Rheumatol. Adv. Pract. 2021, 5, rkab017.
  33. Mouthon, L.; Rannou, F.; Berezne, A.; Pagnoux, C.; Arene, J.; Fois, E.; Cabane, J.; Guillevin, L.; Revel, M.; Fermanian, J.; et al. Development and validation of a scale for mouth handicap in systemic sclerosis: The Mouth Handicap in Systemic Sclerosis scale. Ann. Rheum. Dis. 2007, 66, 1651–1655.
  34. Maddali-Bongi, S.; Del Rosso, A.; Mikhaylova, S.; Francini, B.; Branchi, A.; Baccini, M.; Matucci-Cerinic, M. Impact of hand and face disabilities on global disability and quality of life in systemic sclerosis patients. Clin. Exp. Rheumatol. 2014, 32, 15–20.
  35. Klasser, G.D.; Balasubramaniam, R.; Epstein, J. Topical review-connective tissue diseases: Orofacial manifestations including pain. J. Orofac. Pain 2007, 21, 171–184.
  36. Matarese, G.; Isola, G.; Alibrandi, A.; Gullo, A.L.; Bagnato, G.; Cordasco, G.; Perillo, L. Occlusal and MRI characterizations in systemic sclerosis patients: A prospective study from Southern Italian cohort. Jt. Bone Spine 2016, 83, 57–62.
  37. Yuen, H.; Hant, F.; Hatfield, C.; Summerlin, L.; Smith, E.; Silver, R. Factors associated with oral hygiene practices among adults with systemic sclerosis. Int. J. Dent. Hyg. 2013, 12, 180–186.
  38. Garaiman, A.; Mihai, C.; Dobrota, R.; Jordan, S.; Maurer, B.; Flemming, J.; Distler, O.; Becker, M.O. The Hospital Anxiety and Depression Scale in patients with systemic sclerosis: A psychometric and factor analysis in a monocentric cohort. Clin. Exp. Rheumatol. 2021, 39, 34–42.
  39. Yuen, H.K.; Weng, Y.; Bandyopadhyay, D.; Reed, S.G.; Leite, R.S.; Silver, R.M. Effect of a multi-faceted intervention on gingival health among adults with systemic sclerosis. Clin. Exp. Rheumatol. 2011, 29, S26–S32.
  40. Kleber, C.J.; Putt, M.S. Formation of flossing habit using a floss-holding device. J. Dent. Hyg. JDH 1990, 64, 140–143.
  41. Pischon, N.; Hoedke, D.; Kurth, S.; Lee, P.; Dommisch, H.; Steinbrecher, A.; Pischon, T.; Burmester, G.R.; Buttgereit, F.; Detert, J.; et al. Increased Periodontal Attachment Loss in Systemic Sclerosis Patients. J. Periodontol. 2016, 87, 763–771.
  42. Leung, W.K.; Chu, C.H.; Mok, M.Y.; Yeung, K.S.; Ng, S.K. Periodontal Status of Adults With Systemic Sclerosis: Case-Control Study. J. Periodontol. 2011, 82, 1140–1145.
  43. Mayer, Y.; Elimelech, R.; Balbir-Gurman, A.; Braun-Moscovici, Y.; Machtei, E.E. Periodontal condition of patients with autoimmune diseases and the effect of anti-tumor necrosis factor—A therapy. J. Periodontol. 2013, 84, 136–142.
  44. Elimelech, R.; Mayer, Y.; Braun-Moscovici, Y.; Machtei, E.E.; Balbir-Gurman, A. Periodontal Conditions and Tumor Necrosis Factor-Alpha Level in Gingival Crevicular Fluid of Scleroderma Patients. Isr. Med. Assoc. J. IMAJ 2015, 17, 549–553.
  45. Baron, M.; Hudson, M.; Tatibouet, S.; Steele, R.; Lo, E.; Gravel, S.; Gyger, G.; Sayegh, T.E.; Pope, J.; Fontaine, A.; et al. The Canadian systemic sclerosis oral health study: Orofacial manifestations and oral health-related quality of life in systemic sclerosis compared with the general population. Rheumatology 2014, 53, 1386–1394.
  46. Isola, G.; Williams, R.C.; Gullo, A.L.; Ramaglia, L.; Matarese, M.; Iorio-Siciliano, V.; Cosio, C.; Matarese, G. Risk association between scleroderma disease characteristics, periodontitis, and tooth loss. Clin. Rheumatol. 2017, 36, 2733–2741.
  47. Da Silva, G.S.G.; de Melo, M.L.M.; Leão, J.C.; Carvalho, A.T.; Porter, S.; Duarte, A.L.B.P.; Dantas, A.T.; Gueiros, L.A. Oral features of systemic sclerosis: A case–control study. Oral Dis. 2019, 25, 1995–2002.
  48. Iordache, C.; Antohe, M.-E.; Chirieac, R.; Ancuța, E.; Țănculescu, O.; Ancuța, C. Volumetric Cone Beam Computed Tomography for the Assessment of Oral Manifestations in Systemic Sclerosis: Data from an EUSTAR Cohort. J. Clin. Med. 2019, 8, 1620.
  49. Geurs, N.; Iacono, V.; Krayer, J.; Mealey, B.L.; Paquette, D.; Pearson, B.; Schweinebraten, M. American Academy of Periodontology Task Force Report on the Update to the 1999 Classification of Periodontal Diseases and Conditions. J. Periodontol. 2015, 86, 835–838.
  50. Dagenais, M.; MacDonald, D.; Baron, M.; Hudson, M.; Tatibouet, S.; Steele, R.; Gravel, S.; Mohit, S.; El Sayegh, T.; Pope, J.; et al. The Canadian Systemic Sclerosis Oral Health Study IV: Oral radiographic manifestations in systemic sclerosis compared with the general population. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2015, 120, 104–111.
  51. White, S.C.; Frey, N.W.; Blaschke, D.D.; Ross, M.D.; Clements, P.J.; Furst, D.E.; Paulus, H.E. Oral radiographic changes in patients with progressive systemic sclerosis (scleroderma). J. Am. Dent. Assoc. 1977, 94, 1178–1182.
  52. Said, M.H.; Foletti, J.; Graillon, N.; Guyot, L.; Chossegros, C. Orofacial manifestations of scleroderma. A literature review. Rev. Stomatol. Chir. Maxillofac. Chir. Orale 2016, 117, 322–326.
  53. Baron, M.; Hudson, M.; Tatibouet, S.; Steele, R.; Lo, E.; Gravel, S.; Gyger, G.; El Sayegh, T.; Pope, J.; Fontaine, A.; et al. The Canadian Systemic Sclerosis Oral Health Study III: Relationship between disease characteristics and oro-facial manifestations in systemic sclerosis. Arthritis Care Res. 2014, 12, 180–186.
  54. Page, R.C.; Eke, P.I. Case Definitions for Use in Population-Based Surveillance of Periodontitis. J. Periodontol. 2007, 78, 1387–1399.
  55. Isola, G.; Palazzo, G.; Polizzi, A.; Murabito, P.; Giuffrida, C.; Gullo, A.L. Association of Systemic Sclerosis and Periodontitis with Vitamin D Levels. Nutrients 2021, 13, 705.
  56. Chu, C.H.; Yeung, C.M.K.; Lai, I.A.; Leung, W.K.; Mok, M.Y. Oral health of Chinese people with systemic sclerosis. Clin. Oral Investig. 2010, 15, 931–939.
  57. Papapanou, P.N. Systemic effects of periodontitis: Lessons learned from research on atherosclerotic vascular disease and adverse pregnancy outcomes. Int. Dent. J. 2015, 65, 283–291.
  58. Jepsen, S.; Caton, J.G.; Albandar, J.M.; Bissada, N.F.; Bouchard, P.; Cortellini, P.; Demirel, K.; de Sanctis, M.; Ercoli, C.; Fan, J.; et al. Periodontal Manifestations of Systemic Diseases and Developmental and Acquired Conditions: Consensus Report of Workgroup 3 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions: Classification and Case Definitions for Periodontal Manifestations of Systemic Diseases and Developmental and Acquired Conditions. J. Periodontol. 2018, 89, S237–S248.
  59. Papapanou, P.N.; Sanz, M.; Buduneli, N.; Dietrich, T.; Feres, M.; Fine, D.H.; Flemmig, T.F.; Garcia, R.; Giannobile, W.V.; Graziani, F.; et al. Periodontitis: Consensus Report of Workgroup 2 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions: Classification and Case Definitions for Periodontitis. J. Periodontol. 2018, 89, S173–S182.
  60. Needleman, I.; Garcia, R.; Gkranias, N.; Kirkwood, K.L.; Kocher, T.; Di Iorio, A.; Moreno, F.; Petrie, A. Mean annual attachment, bone level, and tooth loss: A systematic review. J. Periodontol. 2018, 89, S120–S139.
  61. Lamont, R.J.; Koo, H.; Hajishengallis, G. The oral microbiota: Dynamic communities and host interactions. Nat. Rev. Microbiol. 2018, 16, 745–759.
  62. Abusleme, L.; Hoare, A.; Hong, B.; Diaz, P.I. Microbial signatures of health, gingivitis, and periodontitis. Periodontology 2000 2021, 86, 57–78.
  63. Socransky, S.S.; Haffajee, A.D.; Cugini, M.A.; Smith, C.; Kent, R.L., Jr. Microbial complexes in subgingival plaque. J. Clin. Periodontol. 1998, 25, 134–144.
  64. Abusleme, L.; Dupuy, A.K.; Dutzan, N.; Silva, N.; Burleson, J.A.; Strausbaugh, L.D.; Gamonal, J.; Diaz, P.I. The subgingival microbiome in health and periodontitis and its relationship with community biomass and inflammation. ISME J. 2013, 7, 1016–1025.
  65. Hajishengallis, G. Immunomicrobial pathogenesis of periodontitis: Keystones, pathobionts, and host response. Trends Immunol. 2013, 35, 3–11.
  66. Plemmenos, G.; Evangeliou, E.; Polizogopoulos, N.; Chalazias, A.; Deligianni, M.; Piperi, C. Central Regulatory Role of Cytokines in Periodontitis and Targeting Options. Curr. Med. Chem. 2021, 28, 3032–3058.
  67. Pan, W.; Wang, Q.; Chen, Q. The cytokine network involved in the host immune response to periodontitis. Int. J. Oral Sci. 2019, 11, 30.
  68. Tsukasaki, M. RANKL and osteoimmunology in periodontitis. J. Bone Miner. Metab. 2020, 39, 82–90.
  69. Di Benedetto, A.; Gigante, I.; Colucci, S.; Grano, M. Periodontal Disease: Linking the Primary Inflammation to Bone Loss. Clin. Dev. Immunol. 2013, 2013, 503754.
  70. Niklander, S.; Bordagaray, M.; Fernández, A.; Hernández, M. Vascular Endothelial Growth Factor: A Translational View in Oral Non-Communicable Diseases. Biomolecules 2021, 11, 85.
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