Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2019 May 12;46(8):765–775. doi: 10.1111/joor.12807

Associations between tooth wear and dental sleep disorders: A narrative overview

Peter Wetselaar 1,, Daniele Manfredini 2, Jari Ahlberg 3, Anders Johansson 4, Ghizlane Aarab 1, Chryssa E Papagianni 1, Marisol Reyes Sevilla 1, Michail Koutris 1, Frank Lobbezoo 1
PMCID: PMC6852513  PMID: 31038764

Abstract

Objectives

Tooth wear is a common finding in adult patients with dental sleep disorders. The aim of this paper was to review the literature on the possible associations between tooth wear and the following dental sleep disorders: sleep‐related oro‐facial pain, oral moistening disorders, gastroesophageal reflux disease (GERD), obstructive sleep apnoea syndrome (OSAS) and sleep bruxism.

Methods

A PubMed search was performed on 1 June 2018 using MeSH terms in the following query: Tooth Wear AND (Facial Pain OR Temporomandibular Joint Disorders OR Xerostomia OR Sialorrhea OR Gastroesophageal Reflux OR Sleep Apnea Syndrome OR Sleep Bruxism).

Results

The query yielded 706 reports on tooth wear and the mentioned dental sleep disorders. Several associations between tooth wear and the dental sleep disorders were suggested in the literature. It could be concluded that: (a) tooth wear is associated with dental pain and/or hypersensitivity; (b) oral dryness is associated with tooth wear, oro‐facial pain and sleep bruxism; (c) GERD is associated with tooth wear, oro‐facial pain, oral dryness, OSAS and sleep bruxism; (d) OSAS is associated with oral dryness, GERD and sleep bruxism; and (e) sleep bruxism is associated with tooth wear.

Conclusions

Tooth wear is associated with the dental sleep disorders oro‐facial pain, oral dryness, GERD and sleep bruxism. The dental sleep disorders are interlinked with each other, which leads to indirect associations as well, and makes the consequences of each single condition difficult to disentangle. Knowledge of these associations is clinically relevant, but more research is needed to confirm their validity.

Keywords: adult, gastroesophageal reflux disease, hypersalivation, hyposalivation, oral moistening disorders, oro‐facial pain, ptyalism, sialorrhea, sleep apnoea, sleep bruxism, tooth wear, xerostomia

1. INTRODUCTION

Tooth wear is a multifactorial condition, leading to the loss of dental hard tissues, viz., enamel, dentine and cementum.1 Based on the purported aetiology, tooth wear can be mechanical or chemical (both intrinsic and extrinsic). Intrinsic mechanical wear (known as attrition) is a result of chewing and/or bruxism (eg, grinding), due to tooth‐to‐tooth contact, whilst extrinsic mechanical wear (known as abrasion) is a result of other factors than chewing and/or bruxism, for example, oral hygiene procedures and habits like nail‐ or pen‐biting. Intrinsic and extrinsic chemical wear, both known as dental erosion, are the result of gastric acid and an acidic diet or environments containing airborne acid, respectively.2 Intrinsic mechanical tooth wear is a physiological process, as the dentition is “designed” for function (chewing). Additionally, when the other wear mechanisms are involved, it can become pathological. It should be noted that single wear mechanisms rarely act alone, but interact with each other.1 There is evidence that an acidic diet plays an increasingly important role in the multifactorial condition tooth wear.3 This is also a common believe amongst dental clinicians, nevertheless, having knowledge of the whole etiological spectrum is of utmost importance.

Regarding the diagnosis of tooth wear, a comprehensive approach is necessary due to its multifactorial origin and manifestation. Recently, the Tooth Wear Evaluation System was described to implement a systematic approach to the diagnosis (qualification and quantification) and management of the condition 2. The diagnosis tooth wear is not difficult, being simply the loss of dental hard tissues that is easy to differentiate from dental caries or trauma. However, to distinguish between the different sub‐forms (ie, qualification) is very difficult. Regarding the qualification of tooth wear, there is no consensus at this time, although several proposals exist.2, 4, 5 No difference in reliability between setting the diagnosis of chemical or mechanical tooth wear can be hypothesised. In all the studies mentioned in this overview, it was not always clear how the diagnosis was set. Regarding the quantification of tooth wear, the existing situation is even worse: more than one hundred different evaluation systems exist 6. Comparison of the most commonly used systems nevertheless reveals that a universally accepted modular evaluation system is a possibility and a necessity.6 Taking these considerations into account, it is clear that comparison of tooth wear research findings is difficult. It will take time before the dental community will reach consensus on this topic (see also Table 2).

Table 2.

Description of used tools to diagnose tooth wear and the various dental sleep disorders

Condition Assessment tool
Tooth wear To assess tooth wear, qualification and quantification are necessary. Qualification (recognise and distinguish between the different sub‐forms of tooth wear) is difficult and in the majority of the studies not performed. Regarding the qualification of tooth wear, there is no consensus at this time, although several proposals exists (Wetselaar & Lobbezoo2; Gandara & Truelove4; Ganss & Lussi 5). Quantification (grading the severity of tooth wear) is performed in more than a hundred different ways, with an equal number of different indices or evaluation systems, also here no consensus (Wetselaar & Lobbezoo2; Wetselaar et al6; Margaritis & Nunn81; Schlueter & Luka82)
Oro‐facial pain In this narrative overview dental pain or hypersensitivity and TMD pain were eventually associated with tooth wear. Since pain is a subjective experience, dental pain or hypersensitivity were assessed by oral history taking, questionnaires, several dental tests and the use of an index, the Cumulative Hypersensitivity Index (CHI) (West et al17; Burnett et al18; Wazani et al19; Olley et al20; Macfarlane et al21)
  TMD pain was assessed using the Research Diagnostic Criteria for Temporomandibular Disorders (Dworkin & LeResche 83; Schierz et al22; Seligman & Pullinger 23)
Oral dryness Hyposalivation can be determined by quantifying the unstimulated or stimulated whole saliva (sialometry). Since there is a great variability in individual salivary flow rates and a wide range of flow rate is accepted, the accurate assessment of dysfunction can be difficult; with this in mind it can be argued if measurement of salivary flow rates can be used as a discriminating tool (Löfgren et al27). In addition a wide variety of tests are available, like secretion tests (sialometry, sialochemistry, oral Schirmer's test, and so on), mucosal/surface test, functional tests, glandular morphology (scintigraphy or sialography), and questionnaires or interviews (Löfgren et al27; Thomson et al84)
Gastroesophageal reflux disease (GERD) Gastroesophageal reflux disease is a complex disease with a heterogenous symptom profile. Assessment is performed by clinical history taking, questionnaires, and response to antisecretory therapy, and different tools, like endoscopy, pH monitoring (wire or wireless 24, 48, and 96 h), and/or multichannel intraluminal impedance‐pH (Gyawali et al85). All the assessment tools have their limitations because there are no universal cut‐off criteria (Vakil et al80; Gyawali et al85). Additional signs and symptoms must be present, like heartburn, regurgitation, chest pain, chronic cough and hoarseness as mentioned in the Montreal definition (Vakil et al80)
Obstructive sleep apnoea syndrome (OSAS) The diagnosis of OSAS requires the combined assessment of the objective demonstration of abnormal breathing during sleep and relevant clinical features (signs and symptoms). The golden standard for diagnosing the objective abnormal sleep is a polysomnography (at home or in a sleep laboratory), after which the severity is determined by calculating the Apnoea‐Hypopnea index. It is possible to distinguish between Positional (POSAS) and non‐positional OSAS, some determine the amount of Respiratory Effort Related Arousals, some determine the Upper Airway Resistance Syndrome. Additional by a drug‐induced sleep/sedation endoscopy, the obstruction sites can be determinate
  Relevant clinical features (signs and symptoms) during sleep are snoring, witnessed apnoea by the bedpartner, choking or gasping, recurrent awakenings and insomnia. During wakefulness these are daytime sleepiness, unrefreshing sleep, fatigue, memory/concentration impairment, personality changes, morning nausea, and morning headaches. Structured interviewing and/or questionnaires can reveal these clinical features (American Academy of Sleep Medicine Task Force, Sleep 45)
Sleepbruxism Sleepbruxism can be assessed non‐instrumental or instrumental. Non‐instrumental means@Non‐instrumental approaches includes self‐report (questionnaires, oral history) and clinical inspection. No consensus is present regarding these approach. Instrumental approaches are electromyographic recordings (including other measures used in somnography or polysomnography; audio and/or video recordings can supplement EMG data)@No consensus is present regarding cut‐off points of the findings@The grading system is as follows: (a) possible sleep bruxism is based on a positive self‐report only; (b) probable sleep bruxism is based on a positive clinical inspection, with or without a positive self‐report; (c) definite sleep bruxism is based on a positive instrumental assessment, with or without a positive self‐report and/or a positive clinical inspection (Lobbezoo et al56)

According to literature, the prevalence of severe tooth wear in adults increases from 3% at the age of 20 years to 17% at the age of 70 years.7 The prevalence of tooth wear is increasing, although data are scarce and contradictory.8, 9 Physiological tooth wear is a slow process that does normally not lead to any subjective symptoms, but when it becomes pathological, dental hypersensitivity and/or dental pain (being a form of oro‐facial pain) may occur.10 Additionally, pathological tooth wear can result in difficulties with chewing/eating; impaired oro‐facial aesthetics because of loss of dental hard tissue; crumbling off dental hard tissue; and deterioration of dental restorations.2, 10

Tooth wear is irreversible, which may require repeated and increasingly complex and expensive restorations.10 Therefore, it is important that the diagnosis of tooth wear is made early, and adequate preventive measures are undertaken in order to prevent as much as possible the loss of dental hard tissue.10, 11

Not only tooth wear is becoming increasingly significant in the management of the long‐term health of the dentition,11 but dentists are also becoming more involved with patients requesting information or needing management of oral and dental conditions in relation to dental sleep disorders.12 At this moment, dental sleep medicine is yet not recognised in the general medical literature nor recognised in the dental literature, although these terms were introduced already two decades ago.12 We do think, however, that we are at a turning point, as was mentioned in a recent review, in which a new definition of dental sleep medicine was proposed 13: “dental sleep medicine is the discipline concerned with the study of the oral and maxillofacial causes and consequences of sleep‐related problems.” In our opinion, the term dental sleep medicine is an appropriate one, although debate continues. We do realise that other choices regarding definitions and terminology are possible. Importantly, however, the dental profession ultimately must make a definitive choice, in order to enable speaking the same language, using identically definitions and terms. The sleep‐related problems, to which the proposed definition of dental sleep medicine refers, are as follows: oro‐facial pain; oral moistening disorders (both oral dryness and oral wetness; in this narrative overview, we focus on oral dryness); gastroesophageal reflux disorder (GERD); sleep‐related breathing disorders (including snoring and obstructive sleep apnoea, OSAS; in this narrative overview, we focus on OSAS); and mandibular movement disorders (including dyskinesia, dystonia, and sleep bruxism; in this narrative overview, we focus on sleep bruxism). Some peer‐reviewed journals in the field allowed us to introduce the above concepts.14, 15 For descriptions/definitions of these conditions, see Table 1.

Table 1.

Definitions of dental sleep disorders as distinguished by Lobbezoo et al13

Condition Definition
Oro‐facial pain (OFP) Oro‐facial pain refers to pain associated with the hard and soft tissues of the head, face and neck. These tissues, whether skin, blood vessels, teeth, glands or muscles, send impulses through the trigeminal nerve to be interpreted as pain by the brain circuits that are primarily responsible for the processing that controls complex behaviour. The complaint of OFP encompasses a diagnostic range from neurogenic, musculoskeletal, and psychophysiological pathology to headaches, cancer, autoimmune phenomenon, and tissue trauma (de Leeuw & Klasser16)
Oral moistening disorders
Oral moistening disorders can be divided in having too little or too much saliva, respectively, yielding oral dryness and oral wetness
  • Hyposalivation is an objective reduction of the salivary flow; salivary gland hypofunction has been defined as any objectively demonstrable reduction in whole and/or individual gland flow rates
  • Xerostomia is defined as the subjective sensation of oral dryness; although it is most commonly associated with salivary gland dysfunction, it may also occur with normal gland activity. The terms hyposalivation and xerostomia are often incorrectly used interchangeably
  • Hypersalivation (or sialorrhea or ptyalism) is the condition of increased salivary flow

(Lobbezoo et al13; Wolff et al25; Löfgren et al27; Moore & Guggenheimer78; Hopcraft & Tan26; Boyce & Bakheet79)

Gastroesophageal reflux disease (GERD)

Gastroesophageal reflux disease is defined, in the so‐called Montreal definition and classification, as a condition that develops when the reflux of stomach contents causes troublesome symptoms and/or complications The disease was subclassified into esophageal and extra‐esophageal syndromes, and the recognition of laryngitis, cough, asthma, and chemical intrinsic tooth wear as possible GERD syndromes

(Vakil et al80)

Sleep‐related breathing disorders
Sleep‐related breathing disorders include snoring and obstructive sleep apnoea syndrome (OSAS)
  • Snoring is a familiar condition that is characterised by loud breathing sounds produced in the upper airway during sleep; loud snoring is considered as the most important alarm symptom for OSAS
  • OSAS is the most common type of sleep apnoea and is caused by obstruction of the upper airway. It is characterised by repetitive pauses in breathing during sleep, despite the effort to breathe, and is usually associated with a reduction in blood oxygen saturation

(Deary et al46; American Academy of Sleep Medicine Task Force, Sleep45)

Mandibular movement disorders
Mandibular movement disorders include oromandibular dystonias, oro‐facial dyskinesias, sleep bruxism, and awake bruxism
  • Sleep bruxism is a masticatory muscle activity during sleep that is characterised as rhythmic (phasic) or non‐rhythmic (tonic) and is not a movement disorder or a sleep disorder in otherwise healthy individuals
  • Awake bruxism is a masticatory muscle activity during wakefulness that is characterised by repetitive or sustained tooth contact and/or by bracing or thrusting of the mandible and is not a movement disorder in otherwise healthy individuals

(Lobbezoo et al56)

As in the case of the evaluation of tooth wear, also regarding the assessment of the dental sleep disorders, a wide variety of tools are used (see Table 2). For these reasons, it is hard to organise the available material into a qualitative systematic literature review. A narrative overview was instead performed in the attempt to summarise the available knowledge.

The aim of this paper was to review the literature on the possible associations between tooth wear (both mechanical and chemical) and dental sleep disorders (viz., oro‐facial pain, oral dryness, GERD, OSAS and sleep bruxism), as well as the mutual associations between these disorders themselves. There is evidence that the mentioned dental sleep disorders do have an association with tooth wear, whilst at the same time it is clear that tooth wear is not the only sign or symptom of these disorders. By searching the available literature thoroughly, we will update the existing knowledge and can probably set future research questions. The results can support dental clinicians to have a better comprehension of the possible aetiological factors of tooth wear in their patients, and thus improve the provided dental care.

2. METHODS

On 1 June 2018, the biomedical literature was searched in PubMed (US National Library of Medicine), using Mesh‐Terms in the following query: Tooth Wear AND (Facial Pain OR Temporomandibular Joint Disorders OR Xerostomia OR Sialorrhea OR Gastroesophageal Reflux OR Sleep Apnea Syndrome OR Sleep Bruxism). The MeSH‐term Tooth Wear includes Tooth Attrition, Tooth Abrasion and Tooth Erosion; The MeSH‐term Facial Pain includes Toothache (dental pain and/or hypersensitivity); the MeSH‐term Temporomandibular Joint Disorders includes Temporomandibular Joint Dysfunction Syndrome; the MeSH‐term Sleep Apnea Syndrome includes OSAS. We have chosen to use MeSH‐terms in order to select only those articles that focus on our research aim. The titles and (when available) the abstracts of the publications were screened to establish whether the publications could shed light on the research aim. In addition, it was examined if a direct association and/or an indirect association (meaning through another dental sleep disorder) was present between tooth wear and a sleep disorder. For all studies, the main inclusion criterion for retrieval of the full text was that the study related to the research question about associations between tooth wear, oro‐facial pain, oral dryness, GERD, OSAS and/or sleep bruxism. To be included, the study had to describe the results of an original research in adults, had an appropriate study design or included a review of one of the subtopics of this study. In order to avoid missing relevant literature, as a search expansion strategy, the reference lists of the full‐text articles were hand‐searched for additional studies. Publications were excluded for reasons like describing single cases, rare disorders, syndromes, subgroups of patients, restorative treatment procedures or articles written in languages other than English or Dutch. The search resulted in 706 publications, of which 101 were included in this narrative review. Because of the heterogeneity in the design and quality of the studies, only a narrative approach was possible (see also Table 2).

2.1. Associations between tooth wear and dental sleep disorders

The possible associations (both direct and indirect) between tooth wear and oro‐facial pain, oral dryness, GERD, OSAS and sleep bruxism are presented in Table 3.

Table 3.

Possible direct and indirect associations between tooth wear and dental sleep disorders

Direct Indirect
TW → OFP Table 4    
OD → TW Table 4 OD → TW → OFP Table 4
OD → OFP Table 4    
OD → SB Table 4 OD → SB → TW Table 4
    OD → SB → TW → OFP Table 4
    OD → SB → OFP Table 4
GERD → TW Table 5 GERD → TW → OFP Table 5
GERD → OFP Table 5    
GERD → OD Table 5 GERD → OD → TW Table 5
    GERD → OD → TW → OFP Table 5
GERD → OSAS Table 5 GERD → OSAS Table 5
    GERD → OSAS → OD Table 5
    GERD → OSAS → OD → TW Table 5
GERD → SB Table 5 GERD → SB → TW Table 5
    GERD → SB → TW → OFP Table 5
OSAS → OD Table 5 OSAS → OD → TW → OFP Table 5
OSAS → GERD Table 5 OSAS → GERD → TW Table 5
OSAS → SB Table 5 OSAS → SB → TW Table 5
SB → TW Table 6    
SB → OFP Table 6    
    SB → GERD → TW Table 6

Abbreviations: →, association; GERD, gastroesophageal reflux disease; OD, oral dryness; OFP, oro‐facial pain; OSAS, obstructive sleep apnoea syndrome; SB, sleepbruxism; TW, tooth wear.

2.1.1. Oro‐facial pain and tooth wear

Oro‐facial pain is a multifactorial condition, with a prevalence of around 5.3%‐22%.16 Amongst the 706 publications, only seven described the association between tooth wear and oro‐facial pain.17, 18, 19, 20, 21, 22, 23 The publications did not distinguish oro‐facial pain during wakefulness or sleep. Concerning the association between tooth wear and dental pain/hypersensitivity, at first sight, contradictory findings were reported (see Table 4). When looking into detail, one can conclude that the conflicting reports can be explained by the fact that tooth wear is used as an umbrella term. When tooth wear is differentiated between chemical wear and mechanical wear, one can conclude that chemical wear can cause oro‐facial pain (dental pain/hypersensitivity), whilst mechanical wear does not cause oro‐facial pain (dental pain/hypersensitivity). Regarding tooth wear and TMD pain, Schierz et al22 demonstrated an odds ratio of 1.11, concluding that there was no statistically significant or clinically relevant relationship between tooth wear and the risk of TMD pain. Although others 23 stated that multifactorial models using mechanical tooth wear severity and rates may differentiate masticatory muscle pain patients from asymptomatic controls, they commented that these models cannot determine causation or whether any of the differentiating mechanical tooth wear is secondary to TMD pain.23 Based on this available evidence, one may conclude that chemical tooth wear is directly associated with dental pain and/or hypersensitivity (most probably in young patients, when the tooth wear process develops fast) and not with TMD pain. No publications were found in relation to other oro‐facial pains, like neuropathic pain or headache.

Table 4.

Possible direct associations between tooth wear and OFP; possible direct and indirect associations between OD and tooth wear, OFP and SB

Direct Indirect
Tooth wear  
  Reference Association  
cTW → DP/HY 17, 20 Yes  
TW → HY 18, 19 Yes  
mTW → DP/HY 21 No  
mTW → TMDP 22, 23 No  
Conclusions: Chemical tooth wear can directly be associated with dental pain and/or hypersensitivity; there is no association between tooth wear and TMD pain  
Oral dryness      
  Reference Association   Reference Association
OD → mTW + cTW 30, 31 Yes OD → TW → DP/HY 17, 18, 19, 20 Yes
OD → OFP 32 Yes      
OD → SB 32 Yes OD → SB → TW → DP/HY 17, 18, 19, 20 Yes
      OD → SB → TW 34 No
      OD → SB → TW 35 Yes
      OD → SB → TMDP 34 No
      OD → SB → TMDP 35 Yes
Conclusions: Oral dryness can directly be associated with mechanical tooth wear (when less saliva causes less lubrication), chemical tooth wear (when less saliva results in less buffer capacity), oro‐facial pain (irritation of the soft tissues of the oral cavity), and sleep bruxism (compensating the oral dryness) Conclusions: Oral dryness can indirectly be associated with oro‐facial pain (dental pain/hypersensitivity due to tooth wear, with or without sleep bruxism); oral dryness might be indirectly associated with tooth wear (due to sleep bruxism) or TMD pain (due to sleep bruxism); opposite findings are revealed

Abbreviations: →, association; cTW, chemical tooth wear; DP, dental pain; HY, hypersensitivity; mTW, mechanical tooth wear; OD, oral dryness; OFP, oro‐facial pain; SB, sleep bruxism; TMDP, TMD pain; TW, tooth wear.

2.1.2. Oral Moistening Disorders and tooth wear

With the umbrella term oral moistening disorders, we cover all the disorders that have to do with an abnormal quantity or composition of the saliva, so both oral dryness (with the already longer existing terms hyposalivation and xerostomia) and oral wetness (with the already longer existing terms hypersalivation, sialorrhea and ptyalism). It should be stressed that is not our intention to replace these terms with the umbrella term. Nevertheless, the umbrella term is in our opinion a useful one and will only exist in addition to the well‐established familiar terms. Saliva is of paramount importance for the maintenance of oral health, and therefore, in‐depth knowledge amongst healthcare professionals is of great importance. Oral dryness is a multifactorial condition, with a prevalence that varies from 10% to 80%.24 Oral dryness can be physiological and is related to age, gender, body weight and the time of the day.24 Oral dryness can be caused by salivary gland hypofunction, thus an objectively measured decrease in salivation, hyposalivation.24, 25, 26, 27 Oral dryness can also be the subjective “feeling” of a dry mouth, xerostomia 26 or the subjective “sensation” of dry mouth, which is often (but not always) associated with hypofunction of the salivary glands”.25 In general, the pathological condition that most frequently causes oral dryness is the use of certain medications: more than a thousand drugs are denoted as xerogenic in the medical literature.25 Other pathological factors resulting in oral dryness are radiotherapy to the head and neck, and systematic disorders, like autoimmune diseases (eg, Sjögren's syndrome), diabetes, depression, anxiety, stress or malnutrition.24, 26 Oral dryness upon awakening is considered a possible symptom of OSAS,28 a lower salivary secretion is seen in patients with GERD.29 Oral wetness is also a multifactorial condition, for which prevalence rates at the general population level are not available. It can be physiological during tooth eruption, during the first half of pregnancy, during menstruation, as well as in association with smell and mechanical stimuli (such as mastication) and taste stimuli.24 The pathological causes of hypersalivation include those of: oral origin, such as the first stages of wearing dentures, dental pain or any irritation or inflammatory process in the oral‐pharyngeal or digestive regions (eg, GERD); neurological disorders, such as Parkinson's disease, epilepsy, encephalitis or certain tumours; exogenous poisoning; several medications; and several serious infectious diseases.24 Amongst the included papers, none of them reported an association between oral wetness and tooth wear. Two reviews revealed a possible direct association between oral dryness and tooth wear, namely with mechanical tooth wear (when less saliva causes less lubrication) and chemical tooth wear (when less saliva results in less buffer capacity) 30, 31 (Table 4). Other direct associations were oral dryness with oro‐facial pain (causing irritation of the soft tissues of the oral cavity32, 33;) and sleep bruxism (compensating the oral dryness; 32). Oral dryness is indirectly associated with oro‐facial pain (dental pain/hypersensitivity through tooth wear, see above; regarding the indirect association between oral dryness and temporomandibular pain (through sleep bruxism), and tooth wear (through sleep bruxism), opposite findings revealed.34, 35

2.1.3. Gastroesophageal reflux disease (GERD) and tooth wear

The prevalence of GERD is high in the Western world, ranging from 10% to 40%.36 The prevalence increases with age and BMI, and men are more frequently affected than women.36 GERD can be considered physiological when occurring after a meal without further complaints and during pregnancy. It becomes pathological when a mechanical impairment of the esophagogastric junction is present and complaints develop.36 GERD is considered as a multifactorial disease; instigating factors are obesity, age and trauma.

Amongst the included papers, 65 publications described the direct association between GERD and tooth wear and oro‐facial pain (irritation of the soft tissues), including five recent reviews (Table 5). In a systematic review from the gastroenterological community,37 it was concluded that there is a strong association between GERD and intrinsic chemical tooth wear, and that the severity of the tooth wear seems to be correlated with the severity of GERD symptoms. Recently, this was concluded again by four reviews from the dental community 38, 39, 40, 41 (Table 5). It is suggested that inspection of the oral cavity in search for intrinsic chemical tooth wear should become a routine manoeuvre in patients with GERD, and cooperation between physicians and dentists is strongly advocated to prevent or ameliorate possible oral effects of GERD.41

Table 5.

Possible direct associations between GERD and tooth wear, OFP, OD, OSAS and SB; possible indirect associations between GERD and tooth wear, OFP, OD and SB; possible direct associations between OSAS and OD, GERD and SB; possible indirect associations between OSAS and tooth wear, and OFP

Direct Indirect
  Reference Association   Reference Association
GERD
GERD → cTW 37, 38, 39, 40, 41 Yes      
GERD → OFP 37, 38, 39, 40 Yes GERD → TW → OFP 37, 38, 39, 40, 41 Yes
GERD → OD 29 Yes GERD → OD → TW 42, 43 Yes
GERD → OD → TW 44 No
GERD → OD → OFP 29 Yes
GERD → OSAS 51, 52, 53 Yes      
GERD → SB 65, 66, 67, 68 Yes GERD → SB → TW 34 No
GERD → SB → TW 35 Yes
GERD → SB → OFP 34 No
GERD → SB → OFP 35 Yes
Conclusions: GERD can be directly associated with chemical tooth wear, oro‐facial pain (irritation of the soft tissues of the oral cavity), oral dryness, OSAS, and sleep bruxism Conclusions: GERD can be indirectly associated with tooth wear (through oral dryness and sleep bruxism) and oro‐facial pain (due to tooth wear, oral dryness, and sleep bruxism); opposite findings are revealed
OSAS
OSAS → OD 28 Yes OSAS → OD → TW 30, 31 Yes
      OSAS → OD → TW → DP/HY 17, 18, 19, 20 yes
OSAS → GERD 51, 52, 54, 55 Yes OSAS → GERD → cTW 51, 52, 54, 55 yes
OSAS → SB 69, 70, 71, 72, 73, 74, 75, 86 Yes OSAS → SB → mTW 49 yes
OSAS → SB 76 No      
Conclusions: OSAS can be directly associated with oral dryness, GERD, and sleepbruxism Conclusions: OSAS can be indirectly associated with tooth wear (through oral dryness), with chemical tooth wear (through GERD) with mechanical tooth wear (through sleep bruxism), and with oro‐facial pain (dental pain/hypersensitivity, through tooth wear)

Abbreviations: →, association; cTW, chemical tooth wear; DP, dental pain; HY, hypersensitivity; mTW, mechanical tooth wear; OD, oral dryness; OFP, oro‐facial pain; SB, sleepbruxism; TW, tooth wear.

Three other studies described the possible indirect association between GERD and tooth wear through oral dryness.42, 43, 44 On the one hand, it was revealed that patients with GERD had an impaired salivary flow rate as compared to controls 42, 43 and additionally a poorer salivary buffering capacity.43 However, on the other hand, Saksena et al44 reported no difference in salivary flow or buffer capacity between patients with GERD and controls (see Table 5). Based on the available evidence, one may conclude that GERD is directly associated with intrinsic chemical tooth wear, oro‐facial pain (irritation of the soft tissues), OMD (see above), OSAS (see below) and sleep bruxism (see below). GERD is indirectly associated with chemical and mechanical tooth wear (due to OMD and sleep bruxism; see above, and below) and oro‐facial pain (due to tooth wear, oral dryness, and sleep bruxism; see above, and below; see Table 5).

2.1.4. Tooth wear and obstructive sleep apnoea syndrome

Obstructive sleep apnoea syndrome (OSAS) is the most common type of a sleep‐related breathing disorders that is caused by transient obstruction of the upper airway and is a multifactorial condition as well. It is characterised by repetitive interruptions in breathing during sleep, despite the effort to breathe, and is usually associated with a reduction in blood oxygen saturation.45 Snoring is a familiar condition that is characterised by loud breathing sounds, produced in the upper airway during sleep. Although these sounds give rise to social embarrassment, it still can be considered as physiological, whilst OSAS is considered as a pathological condition.46

The prevalence of OSAS, according to general population‐based studies, is approximately 3%‐7% for adult men and 2%‐5% for adult women 47 but higher figures have been reported. In this regard, a recent systematic review highlighted that the prevalence depends on the severity of the condition, with estimated ranges between 9% and 38% for mild OSAS, and 6% to 17% for moderate OSAS, men more affected than women.48 Factors that increase vulnerability for the disorder include higher age, male sex, obesity, family history, menopause, craniofacial abnormalities and certain health behaviours like cigarette smoking and alcohol usage.47

A direct association between tooth wear and OSAS cannot be hypothesised. Amongst the included papers, only one publication described a possible indirect association between tooth wear and OSAS 49 (Table 5). These authors concluded that patients with tooth wear had a high frequency of OSAS, and they found a positive association between tooth wear severity and the severity of the OSAS. Although they did not differentiate between chemical and mechanical tooth wear, the authors suggest that tooth wear assessment can be a tool to identify patients at risk for having OSAS.49 An explanation given by the authors is the possible association between OSAS and sleep bruxism. The patients in the study were treated with an oral appliance, and in that context, it is worth noting that evidence exists that the use of an occlusal splint can worsen the sleep apnoea.50

The possible association between GERD and tooth wear was already described, concluding a strong association between GERD and chemical intrinsic tooth wear. The possible associations between OSAS and GERD themselves are described as well. There is an association because of common risk factors, like gender and obesity.51, 52 GERD can proceed OSAS because an inflammation that results from reflux into the hypopharynx causes weakening and oedema in these tissues, thus resulting in worsening an upper airway obstruction.53 The opposite namely that an apnoea event precedes an GERD event is also described; the reflux is then probably due to the generation of negative intrathoracic pressures during obstructive apnoeas and arousals 54, 55 (Table 5). Independent of the temporal relationship, one can hypothesise that, because of the coexistence of GERD and OSA, patients with OSA show more (intrinsic chemical) tooth wear in comparison with healthy individuals, because the associated GERD activities cause more chemical tooth wear.

2.1.5. Sleep bruxism and tooth wear

According to a recent consensus paper, sleep bruxism and awake bruxism are considered different behaviours observed during wakefulness and during sleep. Both are multifactorial conditions as well.56 This means that a single definition for bruxism is no longer recommended, so that two separate definitions are proposed. Within this framework, sleep bruxism is a masticatory muscle activity during sleep that is characterised as rhythmic (phasic) or non‐rhythmic (tonic) and is not a movement disorder or a sleep disorder in otherwise healthy individuals, whilst awake bruxism is a masticatory muscle activity during wakefulness that is characterised by repetitive or sustained tooth contact and/or by bracing or thrusting of the mandible and is not a movement disorder in otherwise healthy individuals.56 In otherwise healthy individuals, bruxism should not be considered as a disorder, but rather as a behaviour, a physiological phenomenon, that can be a risk (and/or protective) factor for certain clinical consequences. Bruxism will be considered as pathological when a person experiences the possible negative consequences, like oro‐facial pain (eg, meaning pain in the masticatory system).56 The prevalence of bruxism varies from 8% to 31.4%, that of sleep bruxism from 9.7% to 15.9%, depending on the diagnostic methods used. Bruxism activities were found to be unrelated to gender, and a decrease with age was described in older people.57 Considering the possible association between bruxism and tooth wear, three possible interactions are described in the literature: tooth wear causes bruxism; tooth wear is a valid clinical diagnostic tool for bruxism; and tooth wear is a consequence of bruxism, meaning directly or indirectly associated with bruxism.

Considering the first interaction, viz., that tooth wear causes bruxism, it was concluded that there is no evidence available that occlusal interferences (worn dentitions) are involved in the aetiology of bruxism.35, 58 Considering tooth wear possibly being a valid diagnostic tool for bruxism, five studies concluded that this is not the case,59, 60, 61, 62, 63 whilst only one study concluded the opposite.64 This can be explained by the fact that tooth wear is a multifactorial condition, and therefore always a combination of mechanical and chemical wear. Furthermore, tooth wear is irreversible; hence, assessing tooth wear does provide information regarding the actual amount of tooth surface loss, but does not provide information regarding the timing of the tooth surface loss, in other words: whether the process is ongoing or a result from earlier loss.

Considering the third interaction, sleep bruxism is (directly) associated with tooth wear, amongst the included papers and the additional relevant literature, one review concluded that bruxism is not directly associated with tooth wear and with oro‐facial pain 34 (Table 6), whilst another conclude that the direct association exist 35 (Table 6). The different conclusions are possible due to the fact that if sleep bruxism has been diagnosed more robustly, no consistent relationship has been found between sleep bruxism and tooth wear.34

Table 6.

Possible direct and indirect associations between SB and tooth wear, OFP and GERD

Direct Indirect
Sleep bruxism      
  Reference Association      
SB → mTW 34 No      
SB → mTW 35 Yes      
SB → OFP (TMDP) 34 No      
SB → OFP (TMDP) 35 Yes      
      SB [→] GERD [→] cTW 65, 66, 67, 68 Yes
Conclusions: Sleep bruxism might be directly associated with mechanical tooth wear and oro‐facial pain (TMD pain); opposite findings are revealed Conclusions: Sleep bruxism can be indirectly associated with intrinsic chemical tooth wear (through GERD)

Abbreviations: →, association; cTW, chemical tooth wear; DP, dental pain; HY, hypersensitivity; mTW, mechanical tooth wear; OD, oral dryness; OFP, oro‐facial pain; SB, sleepbruxism; TW, tooth wear.

Above, the association between GERD and tooth wear was outlined. Interestingly, also evidence exists that sleep bruxism and GERD are associated with each other 65, 66, 67, 68 (Table 6). Hypothetically, when the onset of a GERD event precedes the onset of a sleep bruxism event, more tooth wear can be caused by the fact that grinding on the acid stomach contents covering the teeth can accelerate the amount of hard tissue loss.

Another interesting finding is the existing evidence of the possible association between sleep bruxism and OSA, in order to find out the possible implications for tooth wear. Two studies showed this association based on self‐report 69, 70 (Table 6). Six studies showed the association based on polysomnography 71, 72, 73, 74, 75, 76 (Table 6). One study opposed regarding the possible association between sleep bruxism and OSAS 76 (Table 6). A review discussed the possible theories regarding the associations between sleep bruxism and OSAS 77 (Table 6). Hypothetically, when sleep bruxism and OSA are related, it is possible that patients with OSA show more tooth wear in comparison with healthy individuals, because the associated sleep bruxism activities cause more mechanical tooth wear. The temporal relationship between sleep bruxism and OSA is not important regarding their influence on tooth wear, since only the SB activities cause mechanical tooth wear. The temporal relationship between sleep bruxism and GERD is important regarding their influence on tooth wear, because when GERD precedes sleep bruxism, the softening of the hard dental tissues by the stomach acid can accelerate the tooth surface loos by the sleep bruxism activities.

3. CONCLUSIONS

Dental sleep disorders and tooth wear are associated with each other, and all are common multifactorial conditions. For some disorders, this association can be direct, whilst for others the association can be indirect or both. The multifactorial nature of these conditions leads to a variety of assessment tools, which makes comparison of the findings in the literature difficult. Therefore, the below‐mentioned conclusions are drawn with caution and must be used in a restraint way. We would like to stress out that further research is a necessity to better substantiate the conclusions in the future. The results of this narrative overview, however, can nevertheless serve as a starting point for further research.

For chemical tooth wear, a direct association with dental pain and/or hypersensitivity can exist. OMD can directly be associated with mechanical tooth wear (when less saliva causes less lubrication), chemical tooth wear (when less saliva results in less buffer capacity), oro‐facial pain (irritation of the soft tissues of the oral cavity and sleep bruxism (compensating the oral dryness). Oral dryness can indirectly be associated with tooth wear, oro‐facial pain (dental pain/hypersensitivity due to tooth wear and TMD pain through sleep bruxism). GERD can directly be associated with chemical tooth wear, oro‐facial pain (irritation of the soft tissues of the oral cavity), oral dryness, OSAS and sleep bruxism. GERD can indirectly be associated with tooth wear (through oral dryness and sleep bruxism) and oro‐facial pain (due to tooth wear, oral dryness and sleep bruxism). OSAS can directly be associated with oral dryness, GERD and sleep bruxism, and can indirectly be associated with chemical tooth wear (through GERD) and mechanical tooth wear (through sleep bruxism), and oro‐facial pain (dental pain/hypersensitivity through tooth wear). Sleep bruxism seems to be directly associated with mechanical tooth wear and oro‐facial pain (TMD pain). Sleep bruxism is indirectly associated with chemical tooth wear (through GERD).

Since the dental sleep disorders are interlinked with each other, the consequences are difficult to disentangle. When several sleep disorders are present at the same time, several scenarios are possible. The sleep disorders can have a synergetic effect to accelerate the tooth wear process. For example when during sleep a reflux event is followed by a bruxing event (the stomach acid will soften the hard dental tissues, which will wear away more easily by the followed grinding), or counteract and slow down the tooth wear process (for example when a bruxing event is followed by an increase of salivary flow, the risk of mechanical tooth wear is neutralised by the improved lubrication). Although more research is needed to confirm the validity of the assumed associations between the dental sleep disorders, improving knowledge is clinically relevant, because avoiding damage to the hard dental tissues during a lifespan is key. The results can support dental clinicians in finding all the aetiological factors of the assessed tooth wear in their patients, and thus improve the provided dental care. Furthermore, there is a strong need for an interdisciplinary clinical team to manage oral health‐related sleep disorders.87 Such a team ideally should consist of dentists specialised in TMD/oro‐facial pain, dentists specialised in dental sleep medicine, and dentist specialised in restorative/prosthetic dentistry, particularly in diagnosing and managing tooth wear. Only a comprehensive approach can result in a state of the art diagnostic process and thereby resulting in optimal care.

CONFLICT OF INTEREST

For this document, The authors declare no conflict of interest.

Wetselaar P, Manfredini D, Ahlberg J, et al. Associations between tooth wear and dental sleep disorders: A narrative overview. J Oral Rehabil. 2019;46:765–775. 10.1111/joor.12807

REFERENCES

  • 1. Shellis RP, Addy M. The interactions between attrition, abrasion and erosion in tooth wear. Monogr Oral Sci. 2014;25:32‐45. [DOI] [PubMed] [Google Scholar]
  • 2. Wetselaar P, Lobbezoo F. The Tooth Wear Evaluation System (TWES): a modular clinical guideline for the diagnosis and management planning of worn dentitions. J Oral Rehabil. 2016;43:69‐80. [DOI] [PubMed] [Google Scholar]
  • 3. Johansson AK, Omar R, Carlsson GE, Johansson A. Dental erosion and its growing importance in clinical practice: from past to present. Int J Dent. 2012;2012:765‐17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Gandara BK, Truelove EL. Diagnosis and management of dental erosion. J Contemp Dent Pract. 1999;1:16‐23. [PubMed] [Google Scholar]
  • 5. Ganss C, Lussi A. Diagnosis of erosive tooth wear. Monogr Oral Sci. 2014;25:22‐31. [DOI] [PubMed] [Google Scholar]
  • 6. Wetselaar P, Faris A, Lobbezoo F. A plea for the development of an universally accepted modular tooth wear evaluation system. BMC Oral Health. 2016;16:115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Van’t Spijker A, Rodriguez JM, Kreulen CM, Bronkhorst EM, Bartlett DW, Creugers NH. Prevalence of tooth wear in adults. Int J Prosthodont. 2009;22:35‐42. [PubMed] [Google Scholar]
  • 8. Jaeggi T, Lussi A. Prevalence, incidence and distribution of erosion. Monogr Oral Sci. 2014;25:55‐73. [DOI] [PubMed] [Google Scholar]
  • 9. Wetselaar P, Vermaire JH, Visscher CM, Lobbezoo F, Schuller AA. The prevalence of tooth wear in the Dutch adult population. Caries Res. 2016;50:543‐550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Loomans B, Opdam N, Attin T, et al. Severe tooth wear: European Consensus Statement on Management Guidelines. J Adhes Dent. 2017;19:111‐119. [DOI] [PubMed] [Google Scholar]
  • 11. Lussi A, Carvalho TS. Erosive tooth wear: a multifactorial condition of growing concern and increasing knowledge. Monogr Oral Sci. 2014;25:765‐15. [DOI] [PubMed] [Google Scholar]
  • 12. Lavigne GJ, Goulet JP, Zuconni M, Morrison F, Lobbezoo F. Sleep disorders and the dental patient: an overview. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;88:257‐272. [DOI] [PubMed] [Google Scholar]
  • 13. Lobbezoo F, Aarab G, Wetselaar P, Hoekema A, de Lange J, de Vries N. A new definition of dental sleep medicine. J Oral Rehabil. 2016;430:786‐790. [DOI] [PubMed] [Google Scholar]
  • 14. Aarab G, Lobbezoo F. Dental sleep medicine redefined. Sleep Breath. 2018;22:1233. [DOI] [PubMed] [Google Scholar]
  • 15. Lobbezoo F, Aarab G. Increasing the visibility of dental sleep disorders. J Clin Sleep Med. 2018;14:1827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. de Leeuw R, Klasser GD (eds). Orofacial pain. Guidelines for assessment, diagnosis, and management. Sixth Edition. The American Academy of Orofacial Pain. Chicago, IL: Quintessence Publishing Co, Inc; 2018. [Google Scholar]
  • 17. West NX, Sanz M, Lussi A, Bartlett D, Bouchard P, Bourgeois D. Prevalence of dentine hypersensitivity and study of associated factors: a European population‐based cross‐sectional study. J Dent. 2013;41:841‐851. [DOI] [PubMed] [Google Scholar]
  • 18. Burnett CA, Hussey DL, Clifford TJ. Presentation, diagnosis and initial management of patients referred to a hospital tooth wear clinic. Eur J Prosthodont Restor Dent. 2001;9:5‐7. [PubMed] [Google Scholar]
  • 19. Wazani BE, Dodd MN, Milosevic A. The signs and symptoms of tooth wear in a referred group of patients. Br Dent J. 2012;213:E10. [DOI] [PubMed] [Google Scholar]
  • 20. Olley RC, Moazzez R, Bartlett D. The relationship between incisal/occlusal wear, dentine hypersensitivity and time after the last acid exposure in vivo. J Dent. 2015;43:248‐252. [DOI] [PubMed] [Google Scholar]
  • 21. Macfarlane TV, Kenealy P, Kingdon HA, et al. Orofacial pain in young adults and associated childhood and adulthood factors: results of the population study, Wales, United Kingdom. Community Dent Oral Epidemiol. 2009;37:438‐450. [DOI] [PubMed] [Google Scholar]
  • 22. Schierz O, John MT, Schroeder E, Lobbezoo F. Association between anterior tooth wear and temporomandibular disorder pain in a German population. J Prosthet Dent. 2007;97:305‐309. [DOI] [PubMed] [Google Scholar]
  • 23. Seligman DA, Pullinger AG. Dental attrition models predicting temporomandibular joint disease or masticatory muscle pain versus asymptomatic controls. J Oral Rehabil. 2006;33:789‐799. [DOI] [PubMed] [Google Scholar]
  • 24. Llena‐Puy C. The rôle of saliva in maintaining oral health and as an aid to diagnosis. Med Oral Patol Oral Cir Bucal. 2006;11:E449‐E455. [PubMed] [Google Scholar]
  • 25. Wolff A, Joshi RK, Ekström J, et al. A guide to medications inducing salivary gland dysfunction, xerostomia, and subjective sialorrhea: a systematic review sponsored by the World Workshop on Oral Medicine VI. Drugs R D. 2017;17:765‐28. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Hopcraft MS, Tan C. Xerostomia: an update for clinicians. Aust Dent J. 2010;553:238‐244. [DOI] [PubMed] [Google Scholar]
  • 27. Löfgren CD, Wickström C, Sonesson M, Lagunas PT, Christersson C. A systematic review of methods to diagnose oral dryness and salivary gland function. BMC Oral Health. 2012;12:29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Oksenberg A, Froom P, Melamed S. Dry mouth upon awakening in obstructive sleep apnea. J Sleep Res. 2006;15:317‐320. [DOI] [PubMed] [Google Scholar]
  • 29. Campisi G, Lo Russo L, Di Liberto C, et al. Saliva variations in gastro‐oesophageal reflux disease. J Dent. 2008;36:268‐271. [DOI] [PubMed] [Google Scholar]
  • 30. Hara AT, Zero DT. The potential of saliva in protecting against dental erosion. Monogr Oral Sci. 2014;25:197‐205. [DOI] [PubMed] [Google Scholar]
  • 31. Young WG. The oral medicine of tooth wear. Aust Dent J. 2001;46:236‐250. [DOI] [PubMed] [Google Scholar]
  • 32. Thie NM, Kato T, Bader G, Montplaisir JY, Lavigne GJ. The significance of saliva during sleep and the relevance of oromotor movements. Sleep Med Rev. 2002;6:213‐227. [DOI] [PubMed] [Google Scholar]
  • 33. Huynh NT, Emami E, Helman JI, Chervin RD. Interactions between sleep disorders and oral diseases. Oral Dis. 2014;20:236‐245. [DOI] [PubMed] [Google Scholar]
  • 34. Johansson A, Omar R, Carlsson GE. Bruxism and prosthetic treatment: a critical review. J Prosthodont Res. 2011;55:127‐136. [DOI] [PubMed] [Google Scholar]
  • 35. Lobbezoo F, Ahlberg J, Manfredini D, Winocur E. Are bruxism and the bite causally related? J Oral Rehabil. 2012;39:489‐501. [DOI] [PubMed] [Google Scholar]
  • 36. Boeckxstaens G, El‐Serag HB, Smout AJ, Kahrilas PJ. Symptomatic reflux disease: the present, the past and the future. Gut. 2014;63:1185‐1193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Pace F, Pallotta S, Tonini M, Vakil N, Bianchi PG. Systematic review: gastro‐oesophageal reflux disease and dental lesions. Aliment Pharmacol Ther. 2008;27:1179‐1186. [DOI] [PubMed] [Google Scholar]
  • 38. Moazzez R, Bartlett D. Intrinsic causes of erosion. Monogr Oral Sci. 2014;25:180‐196. [DOI] [PubMed] [Google Scholar]
  • 39. Schlueter N, Tveit AB. Prevalence of erosive tooth wear in risk groups. Monogr Oral Sci. 2014;25:74‐98. [DOI] [PubMed] [Google Scholar]
  • 40. Marsicano JA, de Moura‐Grec PG, Bonato R, Sales‐Peres M, Sales‐Peres A, Sales‐Peres SHdC. Gastroesophageal reflux, dental erosion, and halitosis in epidemiological surveys: a systematic review. Eur J Gastroenterol Hepatol. 2013;25:135–141. [DOI] [PubMed] [Google Scholar]
  • 41. Ranjitkar S, Smales RJ, Kaidonis JA. Oral manifestations of gastroesophageal reflux disease. J Gastroenterol Hepatol. 2012;27:21–27. [DOI] [PubMed] [Google Scholar]
  • 42. Moazzez R, Bartlett D, Anggiansah A. Dental erosion, gastro‐oesophageal reflux disease and saliva: how are they related? J Dent. 2004;32:489–494. [DOI] [PubMed] [Google Scholar]
  • 43. Yoshikawa H, Furuta K, Ueno M, et al. Oral symptoms including dental erosion in gastroesophageal reflux disease are associated with decreased salivary flow volume and swallowing function. J Gastroenterol. 2012;47:412–420. [DOI] [PubMed] [Google Scholar]
  • 44. Saksena R, Bartlett DW, Smith BG. The role of saliva in regurgitation erosion. Eur J Prosthodont Restor Dent. 1999;7:121–124. [PubMed] [Google Scholar]
  • 45. Sleep‐related breathing disorders in adults: recommendations for syndrome definition and measurement techniques in clinical research. The Report of an American Academy of Sleep Medicine Task Force. Sleep 1999;22:667–689. [PubMed] [Google Scholar]
  • 46. Deary V, Ellis JG, Wilson JA, Coulter C, Barclay NL. Simple snoring: not quite so simple after all? Sleep Med Rev. 2014;18:453–462. [DOI] [PubMed] [Google Scholar]
  • 47. Punjabi NM. The epidemiology of adult obstructive sleep apnea. Proc Am Thorac Soc. 2008;5:136–143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48. Senaratna CV, Perret JL, Lodge CJ, et al. Prevalence of obstructive sleep apnea in the general population: a systematic review. Sleep Med Rev. 2017;34:70–81. [DOI] [PubMed] [Google Scholar]
  • 49. Durán‐Cantolla J, Alkhraisat MH, Martínez‐Null C, Aguirre JJ, Guinea ER, Anitua E. Frequency of obstructive sleep apnea syndrome in dental patients with tooth wear. J Clin Sleep Med. 2015;11:445–450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Nikolopoulou M, Naeije M, Aarab G, Hamburger HL, Visscher CM, Lobbezoo F. The effect of raising the bite without mandibular protrusion on obstructive sleep apnea. J Oral Rehabil. 2011;38:643–647. [DOI] [PubMed] [Google Scholar]
  • 51. Zanation AM, Senior BA. The relationship between extraesophageal reflux (EER) and obstructive sleep apnea (OSA). Sleep Med Rev. 2005;9:453–458. [DOI] [PubMed] [Google Scholar]
  • 52. Basoglu OK, Vardar R, Tasbakan MS, et al. Obstructive sleep apnea syndrome and gastroesophageal reflux disease: the importance of obesity and gender. Sleep Breath. 2015;19:585–592. [DOI] [PubMed] [Google Scholar]
  • 53. Emilsson ÖI, Bengtsson A, Franklin KA, et al. Nocturnal gastro‐oesophageal reflux, asthma and symptoms of OSA: a longitudinal, general population study. Eur Respir J. 2013;41:1347–1354. [DOI] [PubMed] [Google Scholar]
  • 54. Foresman BH. Sleep‐related gastroesophageal reflux. J Am Osteopath Assoc. 2000;100 (12 Suppl Pt 2):S7–10. [PubMed] [Google Scholar]
  • 55. Yang YX, Spencer G, Schutte‐Rodin S, Brensinger C, Metz DC. Gastroesophageal reflux and sleep events in obstructive sleep apnea. Eur J Gastroenterol Hepatol. 2013;25:1017–1023. [DOI] [PubMed] [Google Scholar]
  • 56. Lobbezoo F, Ahlberg J, Raphael KG, et al. Assessment of bruxism: the international consensus revisited. J Oral Rehabil. 2018;45:837–844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. Manfredini D, Winocur E, Guarda‐Nardini L, Paesani D, Lobbezoo F. Epidemiology of bruxism in adults: a systematic review of the literature. J Orofac Pain. 2013;27:99–110. [DOI] [PubMed] [Google Scholar]
  • 58. Lobbezoo F, Naeije M. Bruxism is mainly regulated centrally, not peripherally. J Oral Rehabil. 2001;28:1085–1091. [DOI] [PubMed] [Google Scholar]
  • 59. Abe S, Yamaguchi T, Rompré PH, De Grandmont P, Chen YJ, Lavigne GJ. Tooth wear in young subjects: a discriminator between sleep bruxers and controls? Int J Prosthodont. 2009;22:342–350. [PubMed] [Google Scholar]
  • 60. Palinkas M, De Luca CG, Rodrigues LA, et al. Comparative capabilities of clinical assessment, diagnostic criteria, and polysomnography in detecting sleep bruxism. J Clin Sleep Med. 2015;11:1319–1325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61. Castroflorio T, Bargellini A, Rossini G, Cugliari G, Deregibus A, Manfredini D. Agreement between clinical and portable EMG/ECG diagnosis of sleep bruxism. J Oral Rehabil. 2015;42:759–764. [DOI] [PubMed] [Google Scholar]
  • 62. Jonsgar C, Hordvik PA, Berge ME, Johansson AK, Svensson P, Johansson A. Sleep bruxism in individuals with and without attrition‐type tooth wear: an exploratory matched case‐control electromyographic study. J Dent. 2015;43:1504–1510. [DOI] [PubMed] [Google Scholar]
  • 63. Casett E, Réus JC, Stuginski‐Barbosa J, et al. Validity of different tools to assess sleep bruxism: a meta‐analysis. J Oral Rehabil. 2017;44:722–734. [DOI] [PubMed] [Google Scholar]
  • 64. Yoshizawa S, Suganuma T, Takaba M, et al. Phasic jaw motor episodes in healthy subjects with or without clinical signs and symptoms of sleep bruxism: a pilot study. Sleep Breath. 2014;18:187–193. [DOI] [PubMed] [Google Scholar]
  • 65. Miyawaki S, Tanimoto Y, Araki Y, Katayama A, Fujii A, Takano‐Yamamoto T. Association between nocturnal bruxism and gastroesophageal reflux. Sleep. 2003;26:888–892. [DOI] [PubMed] [Google Scholar]
  • 66. Miyawaki S, Tanimoto Y, Araki Y, Katayama A, Imai M, Takano‐Yamamoto T. Relationships among nocturnal jaw muscle activities, decreased esophageal pH, and sleep positions. Am J Orthod Dentofacial Orthop. 2004;126:615–619. [DOI] [PubMed] [Google Scholar]
  • 67. Ohmure H, Oikawa K, Kanematsu K, et al. Influence of experimental esophageal acidification on sleep bruxism: a randomized trial. J Dent Res. 2011;90:665–671. [DOI] [PubMed] [Google Scholar]
  • 68. Mengatto CM, da Dalberto S, Scheeren B, Barros SG. Association between sleep bruxism and gastroesophageal reflux disease. J Prosthet Dent. 2013;110:349–355. [DOI] [PubMed] [Google Scholar]
  • 69. Ohayon MM, Li KK, Guilleminault C. Risk factors for sleep bruxism in the general population. Chest. 2001;119:53–61. [DOI] [PubMed] [Google Scholar]
  • 70. Hesselbacher S, Subramanian S, Rao S, Casturi L, Surani S. Self‐reported sleep bruxism and nocturnal gastroesophageal reflux disease in patients with obstructive sleep apnea: relationship to gender and ethnicity. Open Respir Med J. 2014;8:34–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71. Phillips BA, Okeson J, Paesani D, Gilmore R. Effect of sleep position on sleep apnea and parafunctional activity. Chest. 1986;90:424–429. [DOI] [PubMed] [Google Scholar]
  • 72. Okeson JP, Phillips BA, Berry D, Cook YR, Cabelka JF. Nocturnal bruxism events in subjects with sleep‐disordered breathing and control subjects. J Craniomandib Dis Facial Oral Pain. 1991;5:258–264. [PubMed] [Google Scholar]
  • 73. Sjoholm TT, Lowe AA, Miyamoto K, Fleetham JA, Ryan CF. Sleep bruxism in sleep‐disordered breathing. Arch Oral Biol. 2000;45:889–896. [DOI] [PubMed] [Google Scholar]
  • 74. Oksenberg A, Arons E. Sleep bruxism related to obstructive sleep apnea: the effect of continuous positive airway pressure. Sleep Med. 2002;3:513–515. [DOI] [PubMed] [Google Scholar]
  • 75. Hosoya H, Kitaura H, Hashimoto T, et al. Relationship between sleep bruxism and sleep respiratory events in patients with obstructive sleep apnea syndrome. Sleep Breath. 2014;18:837–844. [DOI] [PubMed] [Google Scholar]
  • 76. Saito M, Yamaguchi T, Mikami S, et al. Weak association between sleep bruxism and obstructive sleep apnea. A sleep laboratory study. Sleep Breath. 2016;20:703–709. [DOI] [PubMed] [Google Scholar]
  • 77. Manfredini D, Guarda‐Nardini L, Marchese‐Ragona R, Lobbezoo F. Theories on possible temporal relationships between sleep bruxism and obstructive sleep apnea events. An expert opinion. Sleep and Breathing. 2015;19(4):1459–1465. [DOI] [PubMed] [Google Scholar]
  • 78. Moore PA, Guggenheimer J. Medication‐induced hyposalivation: etiology, diagnosis, and treatment. Compend Contin Educ Dent. 2008;29:50–55. [PubMed] [Google Scholar]
  • 79. Boyce HW, Bakheet MR. Sialorrhea: a review of a vexing, often unrecognized sign of oropharyngeal and esophageal disease. J Clin Gastroenterol. 2005;39:89–97. [PubMed] [Google Scholar]
  • 80. Vakil N, van Zanten SV, Kahrilas P, Dent J, Jones R. Global Consensus Group. The Montreal definition and classification of gastroesophageal reflux disease: a global evidence‐based consensus. Am J Gastroenterol. 2006;101:1900–1920. [DOI] [PubMed] [Google Scholar]
  • 81. Margaritis V, Nunn J. Challenges in assessing erosive tooth wear. Monogr Oral Sci. 2014;25:46–54. [DOI] [PubMed] [Google Scholar]
  • 82. Schlueter N, Luka B. Erosive tooth wear – a review on global prevalence and on its prevalence in risk groups. Br Dent J. 2018;224:364–370. [DOI] [PubMed] [Google Scholar]
  • 83. Dworkin SF, LeResche L. Research diagnostic criteria for temporomandibular disorders: review, criteria, examinations and specifications, critique. J Craniomandib Disord. 1992;6:301–355. [PubMed] [Google Scholar]
  • 84. Thomson WM, Chalmers JM, Spencer AJ, Williams SM. The Xerostomia Inventory: a multi‐item approach to measuring dry mouth. Community Dent Health. 1999;16:12–17. [PubMed] [Google Scholar]
  • 85. Gyawali CP, Kahrilas PJ, Savarino E, et al. Modern diagnosis of GERD: the Lyon Consensus. Gut. 2018;67:1351–1362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86. Saito M, Yamaguchi T, Mikami S, et al. Temporal association between sleep apnea‐hypopnea and sleep bruxism events. J Sleep Res. 2014;23:196–203. [DOI] [PubMed] [Google Scholar]
  • 87. Lobbezoo F, van der Zaag J, Visscher CM, Naeije M. Oral kinesiology. A new postgraduate programme in the Netherlands. J Oral Rehabil. 2004;31:192–198. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Oral Rehabilitation are provided here courtesy of Wiley

RESOURCES