Abstract
This review summarizes the literature on association between gastroesophageal reflux disease (GERD) and bruxism. A systematic search was performed in June 2024 and updated in October 2025 across electronic databases (MedLine/PubMed, LILACS/BBO, SciELO, EMBASE, Scopus, and Web of Science) and grey literature (OpenGrey, ProQuest, and LIVIVO). Case reports, clinical trials, and observational studies addressing the GERD-bruxism association in individuals of any age without systemic diseases, syndromes, or neuromotor disorders were included. Study selection and data extraction were independently conducted by two reviewers. Twenty-two articles met inclusion: six case reports, six cross-sectional studies, four case-control studies, and six clinical trials, totaling 15,889 participants (73.4% women; mean age 44.5 years). All but three cross-sectional studies reported an association between GERD and bruxism. Clinical studies have consistently demonstrated that esophageal acidification, whether experimentally induced or present in patients with GERD, increases the hourly frequency of rhythmic masticatory muscle activity (RMMA), short bursts and RMMA with grinding. Two clinical trials that tested proton pump inhibitors observed a reduced RMMA frequency. One clinical study assessed awake bruxism, and two observational studies assessed sleep bruxism. Bibliometric analysis identified 9 author clusters and 17 collaboration networks, with research concentrated in Japan but showing marked global growth from 2018 to 2025. Bruxism and GERD showed a positive association. However, methodological heterogeneity and numerous confounders prevented robust evidence and limited the clinical inference. Bibliometric analysis shows that research remains centered in Japan but is expanding globally, reflecting growing interdisciplinary interest and the need for greater international and methodological integration.
Descriptors: Bruxism, Gastroesophageal Reflux
Introduction
Gastroesophageal reflux disease (GERD) and bruxism have considerable global prevalence, varying from 2.5 to 51.2% and around 10 to 20% in Europe and the USA. 1 Sleep bruxism (SB) prevalence ranges across 9.7 to 15.9%, 2 while possible awake bruxism (AB) varies between 16 to 32 %, 3 based on the employed diagnostic method. 4
The latest international bruxism consensus redefined the terms SB and AB. SB is masticatory muscle activity during sleep, characterized by rhythmic (phasic) or nonrhythmic (tonic) and is not a movement disorder or a sleep disorder. AB is a “masticatory muscle activity during wakefulness, characterized by repetitive or sustained tooth contact and/or by bracing or thrusting of the mandible and is not a movement disorder. 5 Bruxism and GERD may share common factors such as sleep quality, obstructive sleep apnea, and psychological disorders such as stress, anxiety, and depression. 6,7 Furthermore, bruxism has been hypothesized to exert a protective effect by activation mechanism of the salivary glands through masticatory muscle movements. 8 Thereby, acts as a resource to neutralize intraoral pH during gastroesophageal reflux events. However, the hypothesis remains uncertain. 9
Although GERD is not an exclusive sleep disorder, it is more frequent and intense during sleep. 6 Thus, it has been associated with sleep fragmentation, mainly due to conscious awakening caused by reflux symptoms or amnestic arousal. One study reported that reflux events occurred most often immediately after microarousal. The authors hypothesized that the lower esophageal sphincter transiently relaxes after arousal, which might explain the increase in acid reflux events. 10 SB presents a complex pathophysiology modulated by serial events before rhythmic masticatory muscle activity (RMMA), such as autonomic cardiac activation (four to eight minutes before RMMA), increased electroencephalographic activity (four seconds before RMMA), tachycardia (one second before RMMA), altered respiratory activity, and microarousals. 6 Arousals from sleep may represent a permissive window for the onset of RMMA episodes. 6
A systematic review with a meta-analysis of observational studies confirmed a strong association between reflux and SB and between SB and GERD/reflux. 11 However, observational studies have examined this association by administering proton pump inhibitors (PPIs) in GERD patients 12 and the association between GERD and AB and SB through experimental acidification of the gastroesophageal tract in healthy individuals. 13,14 These studies could be integrated and analyzed together with those included in the aforementioned systematic review. 11 Thereby, providing additional insights into the association between GERD and bruxism.
To fill this gap, this study aimed to explore the potential association between GERD and bruxism to improve the diagnosis and treatment based on all types of evidence available in the literature. It has two specific objectives: 1) to conduct a scoping review to identify and analyze existing literature, and 2) to verify these findings through bibliometric analysis assessing characteristics and trends in published scientific research on this topic.
Methodology
Protocol and registration
This scoping review was based on the Joanna Briggs Institute (JBI) manual recommendations 15 and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR). 16 The review protocol was registered in the Open Science Framework database (https://doi.10.17605/OSF.IO/E2VYD).
The bibliometric analysis followed BIBLIO checklist for reporting bibliometric reviews of the biomedical literature. 17
Eligibility criteria
This scoping review was based on the following question: What is known about the association between gastroesophageal reflux/acidification and bruxism in adults? The questions followed the PCC acronym: Population – children, adolescents, and adult patients with SB or AB; Concept - the association of gastroesophageal reflux/acidification with bruxism; and Context - any healthcare or community setting.
The inclusion criteria were studies reporting animal, laboratory, case report, case series, clinical, and observational studies with human individuals of any age, and investigations establishing the association between acidification of the gastroesophageal tract and SB and AB. This study considered both objective (upper digestive endoscopy, polysomnography, pH monitoring, actigraphy, EMG devices for bruxism, and dental wear indices) and subjective (survey) methods. There were no restrictions on the language or publication year. Exclusion criteria were studies involving participants with other systemic diseases, syndromes, or neuromotor problems, or pregnant women.
Search and information sources
Electronic searches were conducted up to June 2024 and updated in October 2025 in MedLine (via PubMed), Scopus, Web of Science, EMBASE, LILACS/BBO, and SciELO databases. OpenGrey, ProQuest (for theses and dissertations), and LIVIVO platforms partially captured the grey literature. The references of the eligible articles were carefully analyzed. This search model aimed to minimize selection bias. The MeSH (Medical Subject Headings), Embase Subject Headings (Emtree), and DeCS (Health Science Descriptors) provided search descriptors. Boolean operators “AND” and “OR” were combined keywords, respecting the syntax rules of each database (Table 1).
Table 1. Strategies for database searches.
| Database | Search strategy June 2024 - (updated in October 2025) |
|---|---|
| Main Databases | |
| MedLine (via PubMed) | #1 “sleep bruxism”[Mesh Term] OR “bruxism” [Mesh Term] OR “nocturnal bruxism”[tw] OR “sleep-related bruxism”[tw] OR “awake bruxism”[tw] OR “bruxer*”[tw] OR “tooth grinding”[tw] OR “tooth clenching”[tw] OR “teeth grinding”[tw] OR “teeth clenching”[tw] OR “teeth grinding disorder[tw] OR “jaw clenching”[tw] |
| http://www.ncbi.nlm.nih.gov/pubmed/ | #2 “gastroesophageal reflux”[Mesh Term] OR “gastro oesophageal reflux”[tw] OR “GERD”[tw] OR “GORD”[tw] OR “oesophageal reflux”[tw] OR “gastro-oesophageal reflux disease”[tw] OR “acid reflux”[tw] OR “esophageal acid perfusion”[tw] OR “gastric acid reflux”[tw] OR “gastric acid reflux disease”[tw] OR “stomach ulcer”[tw] OR “gastric ulcer”[tw] OR “stomach damage”[tw] OR “stomach lesion”[tw] OR “erosive esophagitis”[tw] OR “reflux esophagitis”[tw] |
| #1 AND #2 | |
| Scopus | #1 TITLE-ABS-KEY (“sleep bruxism” OR “bruxism” OR “nocturnal bruxism” OR “sleep-related bruxism” OR “awake bruxism” OR “bruxer” OR “bruxers” OR “tooth grinding” OR “tooth clenching” OR “teeth grinding” OR “teeth clenching” OR “jaw clenching” OR “mandibular parafunction”) |
| http://www.scopus.com/ | #2 TITLE-ABS-KEY (gastroesophageal reflux disease” OR “gastro oesophageal reflux” OR “GERD” OR “GORD” OR “oesophageal reflux” OR “gastro-oesophageal reflux disease” OR “acid reflux” OR “esophageal acid perfusion” OR “gastric acid reflux” OR “gastric acid reflux disease” OR “stomach ulcer” OR “gastric ulcer” OR “stomach damage” OR “stomach lesion” OR “erosive esophagitis” OR “reflux esophagitis”) |
| #1 AND #2 | |
| Web of Science | #1TS =(sleep bruxism) OR TS =(bruxism) OR TS =(nocturnal bruxism) OR TS =(sleep-related bruxism) OR TS =(bruxer) OR TS =(bruxers) OR TS =(tooth grinding) OR TS =(tooth clenching) OR TS =(teeth grinding) OR TS =(teeth clenching) OR TS =(jaw clenching) OR TS =(mandibular parafunction) |
| http://apps.webofknowledge.com/ | #2TS =(gastroesophageal reflux disease) OR TS =(Gastro oesophageal Reflux) OR TS =(GERD) OR TS =(GORD) OR OR TS =(oesophageal reflux) OR TS =(gastro-oesophageal reflux disease) OR TS =(acid reflux) OR TS =(esophageal acid perfusion) OR TS =(gastric acid reflux) OR TS =(gastric acid reflux disease) OR TS =(stomach ulcer) OR TS =(gastric ulcer) OR TS =(stomach damage) OR TS =(stomach lesion) OR TS =(erosive esophagitis) OR TS =(reflux esophagitis) |
| #1 AND #2 | |
| Embase | #1 (‘sleep bruxism’/exp OR ‘sleep bruxism’ OR ‘bruxism’/exp OR ‘bruxism’ OR ‘nocturnal bruxism’/exp OR ‘nocturnal bruxism’ OR ‘sleep-related bruxism’/exp OR ‘sleep-related bruxism’ OR ‘awake bruxism’/exp OR ‘awake bruxism’ OR ‘bruxer’ OR ‘bruxers’ OR ‘tooth grinding’/exp OR ‘tooth grinding’ OR ‘tooth clenching’/exp OR ‘tooth clenching’ OR ‘teeth grinding’/exp OR ‘teeth grinding’ OR ‘teeth clenching’/exp OR ‘teeth clenching’ OR ‘jaw clenching’ OR ‘mandibular parafunction’) |
| http://www.embase.com/ | #2 (‘gastroesophageal reflux disease’ OR ‘gastro oesophageal reflux’ OR ‘gerd’ OR ‘gord’ OR ‘oesophageal reflux’ OR ‘gastro-oesophageal reflux disease’ OR ‘acid reflux’ OR ‘esophageal acid perfusion’ OR ‘gastric acid reflux’ OR ‘gastric acid reflux disease’ OR ‘stomach ulcer’ OR ‘gastric ulcer’ OR ‘stomach damage’ OR ‘stomach lesion’ OR ‘erosive esophagitis’ OR ‘reflux esophagitis’) |
| #1 AND #2 | |
| LILACS / BBO | ((“sleep bruxism” OR “bruxism” OR “nocturnal bruxism” OR “sleep-related bruxism” OR “awake bruxism OR “bruxer” OR “bruxers” OR “tooth grinding” OR “tooth clenching” OR “teeth grinding” OR “teeth clenching” OR “jaw clenching” OR “mandibular parafunction”) AND (“gastroesophageal reflux disease” OR “gastro oesophageal Reflux” OR “GERD” OR “GORD” OR “oesophageal reflux” OR “gastro-oesophageal reflux disease” OR “acid reflux” OR “esophageal acid perfusion” OR “gastric acid reflux” OR “gastric acid reflux disease” OR “stomach ulcer” OR “gastric ulcer” OR “stomach damage” OR “stomach lesion” OR “erosive esophagitis” OR “reflux esophagitis”)) |
| http://lilacs.bvsalud.org/ | |
Data charting process
The findings from the primary databases were exported to EndNote Web™ software (Clarivate™ Analytics, Philadelphia, USA). The program automatically excluded duplicates and the remaining duplicates were manually removed. Other results were exported to Rayyan QCRI (Qatar Computing Research Institute, Doha, Qatar) 18 to select and evaluate titles and abstracts. Grey literature studies were analyzed manually, first removing duplicates and then reading the titles and abstracts on Microsoft Word™ 2010 (Microsoft™ Ltd., Washington, USA). Two reviewers firstly discussed the inclusion and exclusion criteria, subsequently performed a calibration exercise by assessing 20% of articles to determine inter-rater agreement. Selection was initiated after reaching an adequate level of agreement (Kappa ≥ 0.81).
In the first stage of the review, two examiners (V.L.G.F. and D.T.S.) independently evaluated titles according to the eligibility criteria. Titles that were unrelated to the review proposal were discarded. The reviewers evaluated the abstracts and read those that were considered eligible. A third reviewer (L.R.P.) helped to evaluate and resolve disagreements between the reviewers. Potentially eligible studies were retrieved and analyzed. Furthermore, the reference lists of all the retrieved studies were read to search for eligible studies.
Data collection
The reviewers performed a calibration exercise by analyzing 20% of the retrieved articles to ensure consistency, coherence, and agreement during data extraction prior to data collection. Two reviewers (V.L.G.F. and D.T.S.) independently extracted the data from the eligible studies, and a third reviewer (L.R.P.) analyzed the conflicts.
General data extracted from the articles included study identification (author, year, country, and study type) and sample characteristics (number, distribution by sex, average age, body mass index (BMI), alcoholism, and sleep and psychological disorders). Specific information included diagnostic methodologies for GERD and bruxism, experimental and gastroesophageal pH assessment methods, and primary and secondary study outcomes.
Studies that provided participants’ weight and height but did not report BMI were calculated as stipulated by the World Health Organization (WHO) by dividing body weight (kilograms) by height (square meters). 19
In cases of unavailable data, the authors were contacted via e-mail. Regarding missing or incomplete data and the absence of further clarification from the study authors, a ‘no information’ annotation was applied.
Data synthesis and analysis
The included articles were divided into two categories to standardize the outcome comparisons: a) observational studies and b) experimental clinical studies. Bruxism was analyzed and divided into two domains: sleep and awake bruxism. Microsoft Excel™ 2019 (Microsoft™ Ltd., Washington, USA) spreadsheets organized the data collected from the eligible studies. Descriptive and qualitative analyses were used to report the study characteristics, frequency of outcomes, and assessment methods for bruxism and gastroesophageal reflux. The summarized mean and 95% confidence interval were calculated for the average age of the sample participants.
Bibliometric analysis
The eligible studies were imported into EndNote X9 and exported as an RIS file for analysis in VOSviewer 1.6.15 (Centre for Science and Technology Studies, Leiden University, Netherlands) and Power BI (Microsoft, Redmond, WA, USA). Each article provided the following data: publication year, authors, country, journal, and impact factor, supplied by the Journal Citation Reports (JCR, Clarivate Analytics, https://jcr.clarivate.com/jcr/). Co-authorship connections were grouped into clusters and country data were based on author affiliations to assess international collaborations. GraphPad Prism 9.5.1 (Boston, MA, USA) was used to visualize the journals and countries with the most publications on this topic.
Results
Evidence source selection
The first phase of study selection identified 468 records distributed across nine electronic databases, including grey literature. After removal of duplicates, 255 results remained for title and abstract screening. After review, 40 studies were selected for a full-text reading. Subsequently, unrelated articles not as per the inclusion criteria were excluded, resulting in a final inclusion of 22 studies. Figure 1 illustrates the search, identification, inclusion, and exclusion of eligible studies. Table 2 lists the studies excluded after full-text readings along with the reasons for exclusion.
Figure 1. Flowchart of the selection process according to PRISMA.
Table 2. Studies excluded after full-text readings and reasons for exclusion (n = 18).
| Excluded study | Reason for exclusion | |
|---|---|---|
| 1 | Smith & Rafeek, 2008 | Does not establish an association between bruxism and GERD |
| 2 | Khois., 2009 | Presence of syndrome (OSA) |
| 3 | Sakaguchi et al., 2014 | Does not establish an association between bruxism and GERD |
| 4 | Scaramucci et al., 2014 | Does not establish an association between bruxism and GERD |
| 5 | Noble et al., 2015 | Does not clearly indicate the presence of both conditions |
| 6 | Arman et al., 2016 | Isolated prevalence of each condition |
| 7 | Peşkersoy et al. - 2016 | Does not establish an association between bruxism and GERD |
| 8 | Bernardes et al., 2019 | Does not establish an association between bruxism and GERD |
| 9 | Li et al., 2019 | Does not specify bruxism |
| 10 | Zuza et al., 2019 | Does not establish an association between bruxism and GERD |
| 11 | Blumer et al., 2022 | Does not establish an association between bruxism and GERD |
| 12 | Iqbal et al. 2022 | Does not establish an association between bruxism and GERD |
| 13 | McEloy, 2023 | Does not establish an association between bruxism and GERD |
| 14 | Mendieta-Hernández et al., 2023 | Does not establish an association between bruxism and GERD |
| 15 | Khan., 2023 | Does not establish an association between bruxism and GERD |
| 16 | Ramos, 2023 | Does not establish an association between bruxism and GERD |
| 17 | Jiménez-Núñez et al., 2024 | Does not establish an association between bruxism and GERD |
| 18 | Sun et al., 2024 | Does not establish an association between bruxism and GERD |
Characteristics of the included studies
The publication intervals of the included studies ranged from 1977 to 2025. Most selected articles were conducted in Japan, 12-14,20-24 followed by China, 6,25 Brazil, 7,26-29 Turkey, 30,31 USA, 32,33 Finland 34 and Poland 35 and one multicenter study was performed in two countries: France and Romania. 36 The included studies assessed 15.889 participants, with 26.6% (4.217) men and 73.4% (15.889) women. The participant ages varied with a mean of 44.5 years. A total of six case reports 26-29,31,32 , six cross-sectional 7,22,33-36 studies, four case-control 6,20,25,30 studies, and six clinical 12-14,21,23,24 studies were included. SB was assessed in one case report 29 , four case-control 6,20,25,30 studies, six cross-sectional 7,22,33-36 studies, and four clinical studies. 12-14,21 AB was evaluated independently in one case report 32 and two clinical 23,24 studies and simultaneously with SB in two case-control studies. 6,25 The type of bruxism was not specified in four case reports 26-28,31 . Only one case report 32 and one observational 33 study analyzed the association between SB and GERD in children without syndromes or other health conditions. Few studies have reported participants’ BMI, with a mean of 21.94, indicating normal weight for the sample, according to the WHO. 19 Alcoholism, 6,22,25,30,35 sleep disorders, 6,34 and psychological disorders, 6,7,32,34 such as anxiety, depression and stress, were the most frequent risk factors. Figure 2 provides a schematic illustration of the association between bruxism and GERD, along with their associated risk factors. Studies used different methods to evaluate bruxism, such as electromyography (EMG) of masticatory muscles 12-14,20,21,23,24 audio and video recordings, 12-14,20,21 polysomnography (PSG), 12-14,33,35 questionnaires, 7,23-25,30,36 and clinical evaluations. 6,7,22,25-33,36 Esophagogastroduodenoscopy, 12,26 endoscopy, 7,12,22,27,28 and trans nasal probe with pH sensors on a portable endoscope, 13,14,20,21,23,33 investigated acidification of the gastroesophageal tract, Other studies have reported the use of clinical assessments, 22,29,31,32,35 and questionnaires, 6,7,12,22,25,30,35,36 to diagnose GERD (Table 3).
Figure 2. Diagram of the association between bruxism and GERD and their related risk factors.

Table 3. Main characteristics of the eligible studies.
| Author | Country | Risk factors | Assessment method for GERD or gastroesophageal acidification | Assessment method for bruxism | |||||
|---|---|---|---|---|---|---|---|---|---|
| Study type | Sample/ type of bruxism investigated | Sex | Age (mean/SD or MD) | BMI (mean) | Alcohol, Caffein comsuption, Smokinga; Sleep disordersb; Psychological disordersc | ||||
| Griffin, 1977 | USA | Case Report | 1 | 1 ♂ | 7 | * | Emotional stress | History of regurgitation associated with emotional stress and abdominal pain. | History and clinical evaluation |
| Awake bruxism | |||||||||
| Stephan, 2002 | Brazil | Case Report | 1 | 1 ♂ | 29 | * | Normal acid drinks or food stuffs consumption. No drugs or alcohol use. | Esophagogastroduodenoscopy, | History and clinical evaluation |
| Bruxism* | |||||||||
| Miyawaki et al., 2003 | Japan | Case-control | G1 (cases - with bruxism) = 10 | 10 ♂ | G1 = 27 ± 7.0 | 20.9 | * | Transnasal probe with pH sensor | EMG and audio-video recordings |
| G2 (controls - without bruxism) = 10 | 10 ♀ | G2 = 26.4 ± 4.7 | |||||||
| Sleep bruxism | |||||||||
| Miyawaki et al., 2004 | Japan | Prospective clinical study | Without bruxism = 8 | 8 ♂ | 24 ± 2.1 | * | * | Transnasal probe with pH sensor | EMG and audio-video recordings |
| With bruxism = 4 | 4 ♀ | ||||||||
| Sleep bruxism | |||||||||
| Herrera et al., 2006 | USA | Cross-sectional | 20 | 10 ♂ | 5 – 15 (9.2 ± 3.2) | * | * | pH-probe testing | PSG; Clinical evaluation |
| Without bruxism = 10 | 10 ♀ | ||||||||
| With bruxism = 10 | |||||||||
| Sleep bruxism | |||||||||
| Machado et al., 2007 | Brazil | Case Report | 1 | 1♀ | 42 | * | Smoker | Endoscopy | Clinical evaluation |
| Bruxism* | |||||||||
| Broliato et al., 2008 | Brazil | Case Report | 1 | 1 ♂ | 22 | * | * | Endoscopy | Clinical evaluation |
| Bruxism* | |||||||||
| Cengiz et al., 2009 | Turkey | Case Report | 1 | 1 ♂ | 54 | * | * | Clinical history | Clinical evaluation |
| Bruxism* | |||||||||
| Fernandes et al., 2011 | Brazil | Case Report | 1 Sleep bruxism | 1 ♂/ | 37/ | * | * | Medical evaluation/ | Clinical evaluation |
| 1 Sleep bruxism | 1 ♀ | 18 | Endoscopy | Clinical evaluation | |||||
| Ohmure et al., 2011 | Japan | Cross-over | G1 (experimental night/saline infusion) = 6 | 12 ♂ | 24.2 ± 2.8 | 21.4 | * | Transnasal probe with pH sensor | PSG, EMG and audio-video recordings |
| G2 (saline infusion/experimental night) = 6 | |||||||||
| Sleep bruxism | |||||||||
| Mengatto et al., 2013 | Brazil | Cross-sectional | G1 (GERD) = 19 | 13 ♂ | 44.6 ± 14.0 | 25.1 | c: Stress: 51.1% of the sample | Questionnaire and endoscopy | Questionnaire and clinical evaluation |
| G2 (Non-GERD) = 26 | 32♀ | (63.2% GERD group; 42.3% non-Gerd group) | |||||||
| Sleep bruxism | |||||||||
| Ohmure et al., 2014 | Japan | Quasi-experimental | Healthy adult men | 15 ♂ | 23.6 ± 4.3 | 21.9 | * | Transnasal probe with pH sensor | PSG, EMG and audio-video recordings |
| Sleep bruxism | |||||||||
| Ohmure et al., 2016 | Japan | Cross-over | G1 (placebo/PPI) = 6 | 5 ♂ | 30.3 ± 7.9 | * | * | Endoscopy, Esophagogastroduodenoscopy, Questionaire | PSG, EMG and audio-video recordings |
| G2 (PPI/placebo) = 6 | 7 ♀ | ||||||||
| Sleep bruxism | |||||||||
| Watababe et al..2017 | Japan | Retrospective Cross-sectional | G1 (GERD) = 105 | 90 ♂ | G1: 66.4 ± 13.0 | G1: 22.9 ± 3.6 | a (alcohol): G1: 27.6% | Clinical evaluation and | Clinical history |
| G2 (Non-GERD) = 50 | 65 ♀ | G2: Older 63.8 ± 8.2 | G2: Older 22.8 ± 4.3 | G2: Older 24% | gastrointestinal fiberscope | ||||
| Sleep bruxism | Younger: 28.7 ± 2.6 | Younger: 22.1 ± 3.3 | Younger: 12% | ||||||
| Li et al., 2018a | China | Case-control | G1 (cases - with bruxism) = 887 | 887 ♂ | G1 = 27 (22-37) | G1 = 21.1 | a(alcohol): 17.3% | Questionnaire | Questionnaire and clinical evaluation |
| G2 (control – without bruxism) = 887 | 887 ♀ | G2 = 28 (22-37) | G2 = 20.8 | n = 308 (G1 = 158; G2 = 150) | |||||
| Sleep and awake bruxism | b: 39.5% (48.7% G1; 39.4% G2) | ||||||||
| n = 742 (423 G1; 310 G2) | |||||||||
| c: Depression: | |||||||||
| % = 14.3% (18.6% G1; 10% G2) | |||||||||
| n = 254 (165 G1; 89 G2) | |||||||||
| Anxiety: | |||||||||
| % = 8.1% (11.2% G1; 5.2% G2) n = 145 (99 G1; 46 G2) | |||||||||
| Li et al., 2018b | China | Case-Control | G1 (cases - with bruxism) = 363 | 294 ♂ | G1 = 28 (22 - 38) | G1 = 21.4 | 20.6% (21.5% G1; 19.8% G2) | Questionnaire | Clinical evaluation |
| G2 (control – without bruxism) = 363 | 432 ♀ | G2 = 29 (23 - 39) | G2 = 21.0 | n = 150 (78 G1; 72 G2) | |||||
| Sleep and awake bruxism | |||||||||
| Maeda-lino et al., 2020 | Japan | Cross-over | 12 healthy men | 12 ♂ | 24.1 ± 4.6 | 21.9 | * | Transnasal probe with pH sensor | EMG, Questionnaire |
| Awake bruxism | |||||||||
| Picos et al., 2020 | France and Romania | Cross-sectional | G1 – GERD | 100 ♂ | 43 (median age) | * | * | Questionnaire | Questionnaire and clinical evaluation |
| patients =141 | 163 ♀ | ||||||||
| G2 - non-GERD | |||||||||
| controls =122 | |||||||||
| Sleep bruxism | |||||||||
| Eninanç, 2023 | Turkey | Case-control | G1 (cases - with bruxism) = 200 | 200 ♂ | G1 = 27.17 ± 8.060 | * | a(alcohol): G1 = 21 (10.5%) | Questionnaire | Questionnaire and clinical evaluation |
| G2 (control – without bruxism) = 200 | 200 ♀ | G2 = 25.94 ± 6.945 | G2 = 14(7%) | ||||||
| Sleep bruxism | |||||||||
| Strausz et al., 2023 | Finland | Cross-sectional | 12.297 (Bruxism) | 2427 ♂ | 51 ± 15.8 | * | b(insomnia): 2.7% | International Classification of Diseases | International Classification of Diseases |
| 1370 (GERD and Bruxism) | 9821 ♀ | c(anxiety): 10.6% | |||||||
| Sleep Bruxism | c(depression): 22.3% | ||||||||
| Orzeszek et al., 2025 | Poland | Cross-sectional | 114 TMD patients | 72 ♂ | 21–71 (37.67) | * | a(alcohol): 36.84% | History | PSG |
| Sleep bruxism | 42 ♀ | a(caffein): 22.8% | |||||||
| a(smoking): 10.53% | |||||||||
| Takahashi et al., 2025 | Japan | Quasi-experimental | 10 healthy men | 8 ♂ | 18 – 49 (25.4 ± 2.8) | * | * | Transnasal probe with pH sensor | EMG, Questionnaire |
| Awake bruxism | 2 ♀ | ||||||||
♂: male; ♀: female; *Data not provided by the authors. G1 – group 1; G2 – group 2; EMG: Electromyography; PSG: Polysomnography; TMD: Temporomandibular disorders.
Study types
a) Observational studies
The remaining articles showed an association between bruxism and GERD, considering the cross-sectional and case-control studies, with the exception of Herrera et al 33 , Picos et al. 36 , and Orzeszek et al. 35 The analytical methods varied among studies, as odds ratio calculations were performed in the studies by Mengatto et al. 7 , Li et al. 6,25 , and Strausz et al.. 34 In the studies by Watanabe et al. 22 , Picos et al., 36 and EniNanç 30 bivariate association tests were conducted to compare prevalence rates. However, the association was not quantified. In a study by Orzeszek et al., 35 the authors did not find significant differences in the frequency or intensity of bruxism in relation to GERD based on group comparisons. Miyawaki et al. 21 did not apply a direct association test between SB and GERD. Instead, they performed within-group comparisons (paired t-tests or Wilcoxon tests) to examine the differences in physiological measures related to bruxism and reflux episodes. Through an analysis of the frequency of RMMA, short bursts, and teeth-clenching episodes, they reported that these were significantly higher during periods of esophageal pH drop than at other times. In contrast, Herrera et al., 33 through the analysis of RMMA alone, found no relationship between SB and GERD in a pediatric sample through the analysis of RMMA alone. SB was the most frequently investigated type, as AB was evaluated alongside SB only in the studies by Li et al.. 6,25 The case-control study by Li et al. 6 documented a statistically significant association between GERD and all types of bruxism, isolated (SB and AB) and combined (SB + AB), after adjusting for confounding variables (p < 0.001). Li et al. 25 also identified a statistically significant association between the two conditions. However, no differentiation between the bruxism types was reported, providing only an overall odds ratio (OR) (Table 4).
Table 4. Main findings of the observational studies.
| Author, year | Type of bruxism | GERD and bruxism | GERD | Bruxism | Dental tightening frequency (times/h) | Short-burst EMG frequency (times/h) | RMMA frequency (times/h) | Relationship GERD and Bruxism | Outcome |
|---|---|---|---|---|---|---|---|---|---|
| Miyawaki et al., 2004 | Sleep | * | * | n = 4 | Without pH drop = 0.1 ± 0.1 | Without pH drop = 2.0 ± 2.2 | Without pH drop = 1.3 ± 1.0 | Frequency RMMA; short-burst, and clenching episodes | Positive association (p <0.01) |
| With pH drop = 0.7 ± 1.1 | With pH drop = 8.6 ± 2.9 | With pH drop = 12.4 ± 7 | On pH decrease: 12.4(7); 8.6(2.9); 0.7(1.1) | ||||||
| Other times: 1.3(1); 2.0(2.2); 0.1(0.1) | |||||||||
| Herrera et al., 2006 | Sleep | n = 2 | * | n = 10 | * | * | 6 ± 5 | Pearson correlation | Negative correlation (p > 0.05) |
| Mengatto et al., 2013 | Sleep | n = 14 | n = 5 | n = 6 | * | * | * | SB: OR = 6.58; 95% CI [1.40-30.98] | Positive association (p = 0.017) |
| Watanabe et al., 2017 | Sleep | n = 18 | n = 87 | n = 2 | * | * | * | Prevalence SB | Positive association (p = 0.041) |
| Non-GERD: 23.1% | |||||||||
| GERD: 73.7% | |||||||||
| Li et al., 201 8 a | Sleep and awake | n = 155 | n = 23 | n = 732 | * | * | * | SB: OR = 6.71, 95% CI (4.22–10.68) | Positive association (p < 0.001) |
| AB: OR 13.06, 95% CI [5.32–32.05] | |||||||||
| SB+AB: OR = 6.48, 95% CI [3.05–13.77] | |||||||||
| Li et al., 2018b | Sleep and awake | n = 68 | * | n = 295 | * | * | * | OR = 5.30, 95% CI [2.62-10.70] | Positive association (p < 0.001) |
| Picos et al., 2020 | Sleep | n = 83 | * | n = 50 | * | * | * | Prevalence SB | Negative association (p = 0.166) |
| GERD: 58.8% | |||||||||
| Control: 41.2% | |||||||||
| Eninanç., 2023 | Sleep | n = 29 | n = 5 | n = 171 | * | * | * | BS and GERD: 14.5% | Positive association (p < 0.000) |
| BS Non-GERD: 85.5% | |||||||||
| GERD and Non-Bruxism: (2.5%) | |||||||||
| Non-GERD and Non-Bruxism (97.5%) | |||||||||
| Strausz et al., 2023 | Sleep | 1.370 | 26.184 | 12.297 | * | * | * | OR = 2.06 95% CI [1.94-2.19] | Positive association (p < 1×10-4) |
| Orzeszek et al., 2025 | Sleep | 33 | * | 90 | * | * | * | Prevalence SB | Negative association (p = 0.542) |
| GERD: 28,95% |
*information not reported; RMMA: rhythmic masticatory muscle activity; EMG: electromyography; GERD: gastroesophageal reflux disease. Odds Ratio.
The cross-sectional study by Strausz et al. 34 evaluated the association between SB and GERD in a large population-based sample (n = 377,277) drawn from the FinnGen and UK Biobank cohorts, using health records coded according to the International Classification of Diseases (ICD). Phenotypic and genetic analyses were performed, including logistic regression and LD Score Regression adjusted for age, sex, and behavioral factors. The results demonstrated significant phenotypic and genetic correlations between SB and GERD, with no evidence of a direct causal relationship or a specific genetic overlap between the conditions.
Except for Griffin Jr, 32 all the other case reports have primarily focused on the oral rehabilitation of patients with advanced tooth wear associated with bruxism and GERD.
b) Experimental studies
Among the experimental studies, crossover clinical trial 12,13,20,23 designs were observed, as well as quasi-experimental models. 14,24 Two studies 12,20 tested PPIs, and four 13,14,23,24 tested acid solution infusions in the gastroesophageal tract (0.1 N HCI, pH 1.2). Ohmure et al. 12 was the only study on SB using the esophageal acidification methodology and identified a significant increase in masseter muscle activity during acid infusion compared to the control group. Many other studies that also evaluated SB, 12,20 tested the effect of PPIs and documented statistically significant reductions in RMMA frequency. None of the studies simultaneously evaluated both types of bruxism. Two studies 23,24 evaluated AB using the esophageal acidification methodology and documented statistically significant increases in RMMA and masseter muscle activity after acid infusion compared with saline infusion. In the study by Takahashi et al., 24 the authors employed a faster infusion rate and a larger volume (10 mL/min for 10 minutes; total of 100 mL) to observe more pronounced effects and their temporal changes. Masseter muscle activity increased significantly compared with pre-infusion levels and decreased 10 and 20 min after acid infusion. This study did not provide mean and standard deviation values; instead, the results were presented graphically as medians without specific interquartile ranges for each time point. Ohmure et al. 13 and Ohmure et al. 12 measured the EMG burst frequency. The distinct experimental methodology demonstrated a significant reduction in EMG bursts on the second night after PPI administration and an increase during acid infusion (Table 5).
Table 5. Main findings of the clinical trials.
| Author, year | Bruxism type | RMMA frequency (times/h) | RMMA frequency with grinding (times/h) | Short-burst EMG frequency | RMMA frequency (times/h) | RMMA frequency with grinding (times/h) | Short-burst EMG frequency | Outcome | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PROTON PUMP INHIBITOR | ||||||||||||
| Miyawaki et al., 2003 | Sleep | Bruxism: | Control: | * | Bruxism: | Control: | * | * | Positive association (p < 0.01) | |||
|
|
-Placebo: 6.0 ± 2.2 | -Placebo: 1.9 ± 3.2 | |||||||||
| -PPI: 3.7 ± 1.9 | -PPI: 1.0 ± 0.6 | |||||||||||
| Ohmure et al., 2016 | Sleep | * | * | * | Night 1 | Night 2 | Night 1 | Night 2 | Night 1: | Night 2: | ||
| -Placebo: 6.3 ± 3.1 | -Placebo: 6.1 ± 3.3 | -Placebo: 1.6 ± 1.6 | Placebo: 3.2 ± 2.9 | -Placebo: 59.4 ± 30.5 | -Placebo: 59.7 ± 33.1 | Positive association RMMA freq. 2nd night (p = 0.012) | ||||||
| -PPI: 4.8 ± 3.8 | -PPI: 4.8 ± 2.3 | -PPI: 1.3 ± 2.2 | -PPI: 2.2 ± 2.6 | -PPI: 45.7 ± 36.5 | -PPI: 46.0 ± 21.7 | Frequency of EMG bursts 2nd night (p = 0.025) | ||||||
| Ohmure et al., 2011 | Sleep | Baseline | Baseline | Baseline | S.I. | A.I. | S.I. | A.I. | S.I. | A.I. | Positive association Frequency of RMMA (p = 0.008) | |
| 0.1 ± 0.2 | 14.6 ± 11.7 | 1.4 ± 1.1 | 1.3 ± 1.2 | 4.7 ± 4.2 | 0.2 ± 0.4 | 1.2 ± 1.1 | 12.1 ± 9.2 | 49.0 ± 33.0 | Frequency of EMG bursts (p = 0.002) Positive correlation (p=0.020) | |||
| Total masseter muscle activity (%.s) | Total masseter muscle activity (%.s) | |||||||||||
| Baseline | S.I. | A.I. | ||||||||||
| Ohmure et al., 2014 | Sleep | 2668 ± 1619 | 2778 ± 173 | 3370 ± 2148 | ||||||||
| Maeda-Lino et al., 2020 | Awake | Reading task: 4105 ± 2852 | Reading task: 4187 ± 2601 | Reading task: 5180 ± 3558 | Positive association (p = 0.019) | |||||||
| Calculation task: 4887 ± 2407 | Calculation task: 5033 ± 1784 | Calculation task: 6053 ± 2744 | Reading: (p = 0.583) Calculating: (p = 0.875) | |||||||||
| Takahashi et al., 2025 | Awake | * | * | * | Positive association (p < 0.001) | |||||||
*Data not available; RMMA: rhythmic masticatory muscle activity; EMG: electromyography; A.I.: acid infusion; S.I: saline infusion.
In the study by Miyawaki al. 20 the authors used the term “association”. However, they performed statistical comparisons using t-tests and Mann–Whitney tests. No specific tests of association between variables were conducted, indicating that the use of the term “association” was descriptive rather than statistically justified. In contrast, Ohmure et al. 13 performed a correlation analysis between masticatory muscle activity and other variables using Spearman’s correlation test. The remaining studies did not explicitly describe the relationship between bruxism and GERD.
All the studies that conducted experimental acidification of the gastroesophageal tract 13,14,23,24 included healthy individuals. Regarding blinding processes, four studies 13,14,23,24 blinded the participants, two 12,20 reported double blinding, and one 23 did not perform blinding. The follow-up time varied between studies, as three 14,23,24 occurred in a single day, one 20 in two nights (with a one-week interval in between), one 13 in four nights, and one 12 in six nights. Table 4 presents the primary outcomes of experimental clinical studies.
Bibliometric analysis
Authorship analysis identified nine clusters with 108 authors distributed across 17 clusters. The five clusters demonstrated strong internal linking (Figure 3). The most connected authors within this group were S. Miyawaki (seven articles included, nine links) and A. Ido (n = 3,27 links).
Figure 3. Co-authorship networks in the eligible studies. The image shows the grouping of five clusters forming the most solid network. Labels of different colors represent year of publication and line thickness the link-strength between co-authors.

Figure 4 summarizes the number of articles published on this topic categorized by journal, impact factor, and publication trend over time. The Journal of Oral Rehabilitation and Sleep published the most articles (n = 3 each) (Figure 4A). All journals had an impact factor of 5–25.9. Publication trends over time demonstrated that most eligible studies were published over the past ten years, with 2021-2025 being the most productive period for articles on GERD and bruxism (n = 5), followed by 2018-2020 (n = 4).
Figure 4. Graphical representation of the distribution of eligible articles by (a) journals, according to the prevalence of published articles and their corresponding impact factor in the Journal Citation Reports. Journals marked with × do not have an available impact factor in the Journal Citation Reports; and (b) publication trends over time.

Regarding the geographic distribution, Japan led with 8 publications on esophageal acidification and bruxism, followed by Brazil and the United States, with five and three publications, respectively (Figure 5A). The largest international collaboration network was between China and the United States (n = 2) (Figure 5B).
Figure 5. (a) Radar chart illustrating the prevalence of articles across countries with the eligible authors. Data points near the center represent lower article or citation counts, while those closer to the outer edge indicate higher counts. (b) The chord diagram visualizes the international collaboration among eligible studies, with thicker lines indicating higher citation weights between collaborations.

Discussion
Almost all observational studies showed an association between GERD and bruxism, except for three cross-sectional studies. 33,35,36 All clinical studies showed that esophageal acidification, either experimentally or in patients with GERD, increased the frequency (times/h) of RMMA, short bursts, and RMMA with grinding.
Several studies included in this scoping review reported an association between GERD and both forms of bruxism. However, investigations specifically addressing AB remain scarce. The pathophysiology differs between SB and AB: psychosocial factors such as stress and anxiety play a greater role in AB, while SB is more frequently associated with alcohol and caffeine consumption, smoking, psychotropic medications, and GERD itself. 30 The hypothesis is that both conditions share common risk factors and neurobiological mechanisms within the brain–gut axis that influence visceral sensitivity, gastrointestinal motility, and permeability. 37 Cytokines resulting from chronic esophageal inflammation in GERD may also affect the central nervous system, contributing to psychological disorders 37 . In turn, stress-related biomarkers such as cortisol, as well as self-reported measures, support a positive association between stress, bruxism, and GERD. 38 Li et al. 6 found that depression, anxiety, and poor sleep quality partially mediated this association, with stronger relationship in women, possibly due to estrogen-related 39 relaxation of the lower esophageal sphincter and increased reflux susceptibility.
Although smoking and alcohol use are more prevalent among men 30 , most studies did not statistically control for sex, and three studies included only male participants 13,14,23 . For example, Maeda-Iino et al., 23 For example, Maeda-Iino et al. used an all-male sample to avoid confounding effects related to hormonal and genetic variability. Lifestyle factors such as alcohol and caffeine consumption and smoking were often examined as exogenous risks. However, only Eninanç 30 reported significantly higher smoking and caffeine use among bruxism patients, whereas Li et al. 6 and Watanabe et al. 22 found no significant associations. These discrepancies may result from low alcohol intake among study participants, cross-sectional designs, small sample sizes and limited statistical power. 22 Ethanol, nicotine, and caffeine have been associated with bruxism and GERD 40-42 . These substances can disrupt sleep and mood, increase masticatory activity, and impair esophageal function, thereby promoting reflux symptoms.
BMI has also been correlated with exacerbated GERD symptoms due to greater intra-abdominal pressure and altered gastric positioning from visceral fat accumulation. 43 However, the few studies in this review that evaluated BMI 7,22,25 found no significant relationship with bruxism, likely because their samples consisted of individuals within the normal weight range.
Studies 33,35,36 with an association between bruxism and GERD may be justified by the fact that the association was not the primary research objective. In addition, GERD was not confirmed using definitive diagnostic methods, and Herrera et al. 33 employed a particularly small pediatric sample.
Previous literature supports the physiological association between the two conditions: exposure of the esophagus to gastric juice, composed of hydrochloric acid, pepsin, and enzymes active below pH 4 44 , reduces epithelial resistance 45 and triggers salivation through the esophageal–salivary reflex via vagal stimulation, inducing reflex salivation. 46 In GERD and SB, arousal and swallowing episodes increase RMMA, enhancing oral lubrication, mucosal protection, and acid neutralization 47 . The clinical studies included in this scoping review that tested experimental acidification of the gastroesophageal tract reported a significant increase in the occurrence of bruxism. Maeda-Iino et al. 23 observed that intraesophageal acid infusion heightened masseter and sympathetic activity while suppressing parasympathetic responses, whereas psychological stress alone did not affect muscle activity. These findings suggest that patients with GERD may present greater daytime masticatory activity and a higher predisposition to AB.
It is important to note that the acid infusions (0.1 N HCl, pH 1.2) used in experimental models do not fully replicate the complexity of gastric juice, which contains multiple chemical components. 44 Furthermore, these experiments were performed in healthy individuals, which limits their applicability to symptomatic GERD populations. 14,23,24 Two clinical studies 12,20 demonstrated that PPI therapy significantly reduced the frequency of RMMA compared with placebo, indicating that acid suppression not only relieved GERD symptoms and promoted mucosal healing, but also improved sleep quality by decreasing arousal frequency and prolonging the REM stage. 48
Despite the predominance of SB research, only five studies 12-14,33,35 employed PSG for diagnosis. PSG objectively records masticatory muscle activity during sleep through EMG, allows differentiation of RMMA from other orofacial or sleep-related movements. 49 Additionally, it correlates these muscle events with sleep stages and arousal patterns, ensuring diagnostic accuracy 49 . Its limited use likely reflects accessibility issues, the need for specialized training, and high operational costs 50 . Most experimental studies and one observational study 21 utilized EMG, which quantifies the RMMA, short bursts, and grinding frequency. However, diagnosing AB remains challenging because EMG recordings in awake individuals may not fully capture masticatory activity patterns 51 .
Bruxism and GERD are the potential risk factors for tooth wear 2 . Clinical history and examinations are the most common diagnostic tools for both disorders. Dental wear analysis has been frequently investigated, particularly in studies centered on tooth surface loss, where data on bruxism and GERD were collected given their shared outcomes. Most case reports have described patients presenting with both conditions requiring extensive oral rehabilitation due to generalized tooth wear, highlighting the clinical significance of their association.
Bibliometric analysis identified Japan as the epicenter of research and collaboration on the association between GERD and bruxism, with highly influential contributors such as Miyawaki and Ido leading cohesive author networks that have produced extensive experimental evidence on esophageal acidification and masticatory activity. Asian researchers appear particularly engaged in this topic, likely influenced by environmental and epidemiological factors that increased basal and stimulated gastric acid secretion in Japan between the 1970s and the 1990s, 52 along with declining Helicobacter pylori infection rates that have heightened GERD susceptibility. 53 Since 2018, there has been a marked global increase in publications, reflecting growing interdisciplinary interest across dentistry, sleep medicine, and gastroenterology, as evidenced by the diversity of high-impact journals addressing this topic. Despite Japan’s leading role, the asymmetric geographic distribution highlights emerging, yet limited, intercontinental collaborations, suggesting opportunities for broader international engagement and greater scientific representativeness in future studies.
This review identified the limitations of the studies that should be addressed. A limited number of investigations, mostly observational, and only a few clinical trials were identified, and there was a further lack of information. Regarding the available clinical studies, only Ohmure et al. 12 included patients diagnosed with GERD, while three 14,20,23 experimentally induced esophageal acidification in healthy individuals, which did not accurately reflect real clinical conditions. These studies also showed substantial methodological variability, including heterogeneous variable categorization, inconsistent data collection and analysis procedures, unclear diagnostic criteria, lack of specification of the bruxism type investigated, and inconsistent reporting of findings. Importantly, many studies failed to analyze or report relevant risk factors and most relied on questionnaires or self-reports to diagnose bruxism and GERD, limiting the reliability and scientific validity of the associations observed.
Future research should prioritize randomized controlled trials, cohort studies, and double-blind crossover designs with longer follow-up periods, including patients with GERD confirmed by digestive endoscopy and evaluated by dentists using objective diagnostic tools such as polysomnography. Regardless of the study type, the shared risk factors of GERD and bruxism should be systematically assessed using appropriate statistical models to clarify their influence. Additionally, greater attention should be given to AB, which remains underexplored compared with SB. Accurate diagnosis can be improved through ecological monitoring, as smartphone-based applications have enabled the real-time assessment of masticatory muscle activity, while advances in data analysis continue to enhance reliability 51 . Self-reports, third-party observations, and clinical examinations (e.g., tooth wear and muscle hypertrophy) can support the diagnosis; however, these indicators lack specificity and may also result from other conditions, such as GERD triggering RMMA, based on our eligible studies.
Clinical implications
Evidence suggesting a bidirectional relationship between GERD and bruxism underscores the importance of integrated diagnostic and therapeutic approaches. Dental professionals should consider screening for reflux symptoms in patients presenting with signs of bruxism, particularly in those with unexplained dental wear, muscle fatigue, or morning discomfort. Physicians managing GERD should be aware of the potential orofacial manifestations associated with this condition. Early identification and multidisciplinary management involving dental and medical teams may prevent the progression of mucosal and dental damage, improve sleep quality, and reduce symptom recurrence. Moreover, controlling acid exposure through pharmacological or behavioral measures, along with interventions aimed at stress reduction and sleep hygiene, may play a complementary role in mitigating bruxism episodes and enhancing overall patient outcomes.
Conclusion
Bruxism and GERD are positively associated, as esophageal acidification experimentally induced or present in patients with GERD increases the frequency (times/h) of RMMA, short bursts, and RMMA with grinding. Moreover, PPI appeared to reduce the RMMA frequency. However, heterogeneity and varied confounders limited clinical inferences. Bibliometric analysis remained centered to Japan but is expanding globally, underscoring growing interdisciplinary interest and the need for greater international and methodological integration.
Funding Statement
Funding: This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brazil (CAPES; Finance Code 001). We are thankful for the support of Conselho Nacional de Desenvolvimento Científico e Tecnológico - Brazil (CNPq, INCT 406840/2022-9 AND CNPq grant number 305356/2024-0) and of Fundação de Amparo à Pesquisa do Estado de Minas Gerais - Brazil (FAPEMIG - RED-00204-23).
Footnotes
Funding: This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Brazil (CAPES; Finance Code 001). We are thankful for the support of Conselho Nacional de Desenvolvimento Científico e Tecnológico - Brazil (CNPq, INCT 406840/2022-9 AND CNPq grant number 305356/2024-0) and of Fundação de Amparo à Pesquisa do Estado de Minas Gerais - Brazil (FAPEMIG - RED-00204-23).
Data availability:
The authors declare that all data generated or analyzed during this study are included in this published article.
References
- 1.Eusebi LH, Ratnakumaran R, Yuan Y, Solaymani-Dodaran M, Bazzoli F, Ford AC. Global prevalence of, and risk factors for, gastro-oesophageal reflux symptoms: a meta-analysis. Gut. 2018 Mar;67(3):430–440. doi: 10.1136/gutjnl-2016-313589. [DOI] [PubMed] [Google Scholar]
- 2.Nota A, Pittari L, Paggi M, Abati S, Tecco S. Correlation between Bruxism and gastroesophageal reflux disorder and their effects on tooth wear. a systematic review. J Clin Med. 2022 Feb;11(4):1107. doi: 10.3390/jcm11041107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Oliveira JM, Pauletto P, Massignan C, D'Souza N, Gonçalves DA, Flores-Mir C, et al. Prevalence of awake bruxism: a systematic review. 104715J Dent. 2023 Nov;138 doi: 10.1016/j.jdent.2023.104715. [DOI] [PubMed] [Google Scholar]
- 4.Bracci A, Lobbezoo F, Häggman-Henrikson B, Colonna A, Nykänen L, Pollis M, et al. Current knowledge and future perspectives on awake bruxism assessment: expert consensus recommendations. J Clin Med. 2022 Aug;11(17):5083. doi: 10.3390/jcm11175083. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Verhoeff MC, Lobbezoo F, Ahlberg J, Bender S, Bracci A, Colonna A, et al. Updating the bruxism definitions: report of an International Consensus Meeting. J Oral Rehabil. 2025 May;(4):271–277. doi: 10.1111/joor.13985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Li Y, Yu F, Niu L, Long Y, Tay FR, Chen J. Association between bruxism and symptomatic gastroesophageal reflux disease: a case-control study. J Dent. 2018 Oct;77:51–58. doi: 10.1016/j.jdent.2018.07.005. [DOI] [PubMed] [Google Scholar]
- 7.Mengatto CM, Dalberto CS, Scheeren B, Barros SG. Association between sleep bruxism and gastroesophageal reflux disease. J Prosthet Dent. 2013 Nov;110(5):349–355. doi: 10.1016/j.prosdent.2013.05.002. [DOI] [PubMed] [Google Scholar]
- 8.Lavigne GJ, Kato T, Kolta A, Sessle BJ. Neurobiological mechanisms involved in sleep bruxism. Crit Rev Oral Biol Med. 2003;14(1):30–46. doi: 10.1177/154411130301400104. [DOI] [PubMed] [Google Scholar]
- 9.Bechir F, Pacurar M, Tohati A, Bataga SM. Comparative study of salivary pH, buffer capacity, and flow in patients with and without gastroesophageal reflux disease. 201Int J Environ Res Public Health. 2021 Dec;19(1) doi: 10.3390/ijerph19010201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Shepherd K, Ockelford J, Ganasan V, Holloway R, Hillman D, Eastwood P. Temporal relationship between night-time gastroesophageal reflux events and arousals from sleep. Am J Gastroenterol. 2020 May;115(5):697–705. doi: 10.14309/ajg.0000000000000627. [DOI] [PubMed] [Google Scholar]
- 11.Khazaie S, Farhadian N, Zereshki E, Khazaie H. Association between sleep bruxism and gastroesophageal reflux disease in healthy adults: a systematic review and meta-analysis. Scand J Sleep Med. 2022 Jan;2(1):71–79. https://doi,org/10.1016/j.prosdent.2013.05.002 [Google Scholar]
- 12.Ohmure H, Kanematsu-Hashimoto K, Nagayama K, Taguchi H, Ido A, Tominaga K, et al. Evaluation of a proton pump inhibitor for sleep bruxism: a randomized clinical trial. J Dent Res. 2016 Dec;95(13):1479–1486. doi: 10.1177/0022034516662245. [DOI] [PubMed] [Google Scholar]
- 13.Ohmure H, Oikawa K, Kanematsu K, Saito Y, Yamamoto T, Nagahama H, et al. Influence of experimental esophageal acidification on sleep bruxism: a randomized trial. J Dent Res. 2011 May;90(5):665–671. doi: 10.1177/0022034510393516. [DOI] [PubMed] [Google Scholar]
- 14.Ohmure H, Sakoguchi Y, Nagayama K, Numata M, Tsubouchi H, Miyawaki S. Influence of experimental oesophageal acidification on masseter muscle activity, cervicofacial behaviour and autonomic nervous activity in wakefulness. J Oral Rehabil. 2014 Jun;41(6):423–431. doi: 10.1111/joor.12159. [DOI] [PubMed] [Google Scholar]
- 15.Moola SZ, Munn Z, Tufanaru C, Aromataris E, Sears K, Sfetcu R. JBI Manual for evidence synthesis. Adelaide: JBI; 2020. [cited 2024 March 30]. https://jbi-global-wiki.refined.site/space/MANUAL [Google Scholar]
- 16.Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. Int J Surg. 2021 Apr;88:105906. doi: 10.1016/j.ijsu.2021.105906. [DOI] [PubMed] [Google Scholar]
- 17.Montazeri A, Mohammadi S, M Hesari P, Ghaemi M, Riazi H, Sheikhi-Mobarakeh Z. Preliminary guideline for reporting bibliometric reviews of the biomedical literature (BIBLIO): a minimum requirements. 239Syst Rev. 2023 Dec;12(1) doi: 10.1186/s13643-023-02410-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Ouzzani M, Hammady H, Fedorowicz Z, Elmagarmid A. Rayyan-a web and mobile app for systematic reviews. 210Syst Rev. 2016 Dec;5(1) doi: 10.1186/s13643-016-0384-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.World Health Organization . WHO AnthroPlus for personal computers manual: software for assessing growth of the world's children and adolescentes. Geneva: World Health Organization; 2009. [Google Scholar]
- 20.Miyawaki S, Tanimoto Y, Araki Y, Katayama A, Fujii A, Takano-Yamamoto T. Association between nocturnal bruxism and gastroesophageal reflux. Sleep. 2003 Nov;26(7):888–892. doi: 10.1093/sleep/26.7.888. [DOI] [PubMed] [Google Scholar]
- 21.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 Nov;126(5):615–619. doi: 10.1016/j.ajodo.2004.02.007. [DOI] [PubMed] [Google Scholar]
- 22.Watanabe M, Nakatani E, Yoshikawa H, Kanno T, Nariai Y, Yoshino A, et al. Oral soft tissue disorders are associated with gastroesophageal reflux disease: retrospective study. 92BMC Gastroenterol. 2017 Aug;17(1) doi: 10.1186/s12876-017-0650-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Maeda-Iino A, Fukushima M, Sakoguchi Y, Omure H, Oishi A, Oga Y, et al. Effects of intra-oesophageal acid infusion and a stress task on masseter muscle activity and autonomic nervous activity in wakefulness. J Oral Rehabil. 2020 May;47(5):567–576. doi: 10.1111/joor.12947. [DOI] [PubMed] [Google Scholar]
- 24.Takahashi K, Maeda-Iino A, Oga Y, Osako Y, Fukushima M, Harada M, et al. Changes over time in masseter muscle activity, symptoms of discomfort, stress sevel and salivary flow rate following intra-oesophageal acid infusion. J Oral Rehabil. 2025 Mar;52(3):332–342. doi: 10.1111/joor.13905. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Li Y, Yu F, Niu L, Hu W, Long Y, Tay FR, et al. Associations among bruxism, gastroesophageal reflux disease, and tooth wear. J Clin Med. 2018 Nov;7(11):417. doi: 10.3390/jcm7110417. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Stephan AD. Diagnosis and dental treatment of a young adult patient with gastroesophageal reflux: a case report with 2-year follow-up. Quintessence Int. 2002 Sep;33(8):619–626. [PubMed] [Google Scholar]
- 27.Machado NA, Fonseca RB, Branco CA, Barbosa GA, Fernandes AJ, Neto, Soares CJ. Dental wear caused by association between bruxism and gastroesophageal reflux disease: a rehabilitation report. J Appl Oral Sci. 2007 Aug;15(4):327–333. doi: 10.1590/S1678-77572007000400016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Broliato GA, Volcato DB, Reston EG, Kramer PF, Marquezan M, Ruzzarin F, et al. Esthetic and functional dental rehabilitation in a patient with gastroesophageal reflux. Quintessence Int. 2008 Feb;39(2):131–137. [PubMed] [Google Scholar]
- 29.Fernandes G, Castanharo SM, Franco AL. Clinical features of the sleep bruxism and gastroesophageal reflux association deserve professional attention. Rev Odontol UNESP. 2011 Nov;40(6):344–348. [Google Scholar]
- 30.Eni?nanç I. Evaluation of risk factors associated with bruxism in adult turkish population. Cumhur Dent J. 2023 Jun;26(2):188–193. doi: 10.7126/cumudj.1304333. [DOI] [Google Scholar]
- 31.Cengiz S, Cengiz MI, Saraç YS. Dental erosion caused by gastroesophageal reflux disease: a case report. 8018Cases J. 2009 Jul;2(1) doi: 10.4076/1757-1626-2-8018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Griffin JB., Jr Rumination in a 7-year-old child. South Med J. 1977 Feb;70(2):243–245. doi: 10.1097/00007611-197702000-00040. [DOI] [PubMed] [Google Scholar]
- 33.Herrera M, Valencia I, Grant M, Metroka D, Chialastri A, Kothare SV. Bruxism in children: effect on sleep architecture and daytime cognitive performance and behavior. Sleep. 2006 Sep;29(9):1143–1148. doi: 10.1093/sleep/29.9.1143. [DOI] [PubMed] [Google Scholar]
- 34.Strausz T, Strausz S, Palotie T, Ahlberg J, Ollila HM, FinnGen Genetic analysis of probable sleep bruxism and its associations with clinical and behavioral traits. Sleep. 2023 Oct;46(10):zsad107. doi: 10.1093/sleep/zsad107. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Orzeszek S, Martynowicz H, Smardz J, Kresse-Walczak K, Wojakowska A, Bombala W, et al. Assessment of the relationship between sleep bruxism, reported pain and headache, selected health factors, and general health conditions among temporomandibular disorder patients: a preliminary report. Dent Med Probl. 2025;62(2):393–399. doi: 10.17219/dmp/192824. [DOI] [PubMed] [Google Scholar]
- 36.Picos A, Lasserre JF, Chisnoiu AM, Berar AM, D'Incau E, Picos AM, et al. Factors associated with dental erosions in gastroesophageal reflux disease: a cross-sectional study in patients with heartburn. Med Pharm Rep. 2019 Dec;92(4):354–360. doi: 10.15386/mpr-1332. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.He M, Wang Q, Yao D, Li J, Bai G. Association between psychosocial disorders and gastroesophageal reflux disease: a systematic review and meta-analysis. J Neurogastroenterol Motil. Apr;28(2):212–221. doi: 10.5056/jnm21044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Polmann H, Réus JC, Massignan C, Serra-Negra JM, Dick BD, Flores-Mir C, et al. Association between sleep bruxism and stress symptoms in adults: a systematic review and meta-analysis. J Oral Rehabil. 2021 May;48(5):621–631. doi: 10.1111/joor.13142. [DOI] [PubMed] [Google Scholar]
- 39.Kang A, Khokale R, Awolumate OJ, Fayyaz H, Cancarevic I. Is estrogen a curse or a blessing in disguise? Role of estrogen in gastroesophageal reflux disease. Cureus. 2020 Oct;12(10):e11180. doi: 10.7759/cureus.11180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Bertazzo-Silveira E, Kruger CM, Porto De Toledo I, Porporatti AL, Dick B, Flores-Mir C, et al. Association between sleep bruxism and alcohol, caffeine, tobacco, and drug abuse: A systematic review. J Am Dent Assoc. 2016 Nov;147(11):859–866.:e4. doi: 10.1016/j.adaj.2016.06.014. [DOI] [PubMed] [Google Scholar]
- 41.Pan J, Cen L, Chen W, Yu C, Li Y, Shen Z. Alcohol consumption and the risk of gastroesophageal reflux disease: a systematic review and meta-analysis. Alcohol Alcohol. 2019 Jan;54(1):62–69. doi: 10.1093/alcalc/agy063. [DOI] [PubMed] [Google Scholar]
- 42.Mahatma G, Septiana VT, Triansyah I, Abdullah D, Vani AT. Analysis of the relationship between gastroesophageal reflux disease (gerd) and patients'smoking patterns and coffee consumption. Community Dev J J Pengabdi Masy. 2023 Jun;4(2):3322–3325. doi: 10.31004/cdj.v4i2.15204. [DOI] [Google Scholar]
- 43.Tong MH, Zhang MJ, Wang LX, Zhang ZF, Duan ZJ. Incorporating body mass index into esophageal manometry metrics and mean nocturnal baseline impedance for the evaluation of gastro-esophageal reflux disease. 18269Sci Rep. 2024 Aug;14(1) doi: 10.1038/s41598-024-69253-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Nguyen SP, Do TC, Tran TT, Pham TK, De Tran V, Nguyen KT. Characteristics of basal gastric juice in Helicobacter pylori-associated gastritis before and after eradication therapy. Trop J Pharm Res. 2022 Nov;21(10):2241–2246. doi: 10.4314/tjpr.v21i10.27. [DOI] [Google Scholar]
- 45.Lee SW, Chang CS. Impact of overlapping functional gastrointestinal disorders on the quality of life in patients with gastroesophageal reflux disease. J Neurogastroenterol Motil. 2021 Apr;27(2):176–184. doi: 10.5056/jnm19006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Frazzoni M, Frazzoni L, Ribolsi M, De Bortoli N, Tolone S, Conigliaro R, et al. Esophageal pH increments associated with post-reflux swallow-induced peristaltic waves show the occurrence and relevance of esophago-salivary reflex in clinical setting. Neurogastroenterol Motil. 2021 Jul;33(7):e14085. doi: 10.1111/nmo.14085. [DOI] [PubMed] [Google Scholar]
- 47.Lavigne GJ, Khoury S, Abe S, Yamaguchi T, Raphael K. Bruxism physiology and pathology: an overview for clinicians. J Oral Rehabil. 2008 Jul;35(7):476–494. doi: 10.1111/j.1365-2842.2008.01881.x. [DOI] [PubMed] [Google Scholar]
- 48.Kim JS, Seo SI, Kang SH, Lee SK, Kim AR, Park HW, et al. Effects of tegoprazan versus esomeprazole on nighttime heartburn and sleep quality in gastroesophageal reflux disease: a multicenter double-blind randomized controlled trial. J Neurogastroenterol Motil. 2023 Jan;29(1):58–64. doi: 10.5056/jnm22104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Lobbezoo F, Ahlberg J, Raphael KG, Wetselaar P, Glaros AG, Kato T, et al. International consensus on the assessment of bruxism: report of a work in progress. J Oral Rehabil. 2018 Nov;45(11):837–844. doi: 10.1111/joor.12663. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Holanda TA, Castagno CD, Barbon FJ, Costa YM, Goettems ML, Boscato N. Sleep architecture and factors associated with sleep bruxism diagnosis scored by polysomnography recordings: a case-control study. Arch Oral Biol. 2020 Apr;112:104685. doi: 10.1016/j.archoralbio.2020.104685. [DOI] [PubMed] [Google Scholar]
- 51.Emodi-Perlman A, Manfredini D, Shalev T, Bracci A, Frideman-Rubin P, Eli I. Psychosocial and behavioral factors in awake bruxism: Self-Report versus Ecological momentary assessment. J Clin Med. 2021 Sep;10(19):4447. doi: 10.3390/jcm10194447. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Kinoshita Y, Adachi K, Fujishiro H. Therapeutic approaches to reflux disease, focusing on acid secretion. J Gastroenterol. 2003 Mar;38(Suppl 15):13–19. doi: 10.1007/s00535-003-1181-4. [DOI] [PubMed] [Google Scholar]
- 53.Sugimoto M, Uotani T, Ichikawa H, Andoh A, Furuta T. Gastroesophageal reflux disease in time covering eradication for all patients infected with Helicobacter pylori in Japan. Digestion. 2016;93(1):24–31. doi: 10.1159/000441741. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The authors declare that all data generated or analyzed during this study are included in this published article.

