Skip to main content
World Journal of Gastrointestinal Pharmacology and Therapeutics logoLink to World Journal of Gastrointestinal Pharmacology and Therapeutics
. 2025 Mar 5;16(1):97918. doi: 10.4292/wjgpt.v16.i1.97918

Insight into global burden of gastroesophageal reflux disease: Understanding its reach and impact

Nilanka Wickramasinghe 1, Niranga Manjuri Devanarayana 2
PMCID: PMC11907340  PMID: 40094147

Abstract

The exact worldwide prevalence of gastroesophageal reflux disease (GERD) remains uncertain, despite its recognition as a common condition. This conundrum arises primarily from the lack of a standardized definition for GERD. The gold standard diagnostic tests for GERD, such as pH impedance testing and endoscopy, are cumbersome and impractical for assessing community prevalence. Consequently, most epidemiological studies rely on symptom-based screening tools. GERD symptoms can be both esophageal and extraesophageal, varying widely among individuals. This variability has led to multiple symptom-based definitions of GERD, with no consensus, resulting in prevalence estimates ranging from 5% to 25% worldwide. Most systematic reviews define GERD as experiencing heartburn and/or regurgitation at least once weekly, yielding a calculated prevalence of 13.98%. In 2017, the global age-standardized prevalence of GERD was estimated at 8819 per 100000 people (95% confidence interval: 7781-9863), a figure that has remained stable from 1990 to 2017. Prevalence increases with age, leading to more years lived with disability. GERD significantly impairs quality of life and can lead to multiple complications. Additionally, it imposes a severe economic burden, with the United States alone estimated to spend around 10 billion dollars annually on diagnosis and treatment. In summary, GERD prevalence varies greatly by region and even within different areas of the same province. Determining the exact prevalence is challenging due to inconsistent diagnostic criteria. However, it is well-documented that GERD poses a significant global burden, affecting the quality of life of individuals and creating a substantial healthcare cost.

Keywords: Gastroesophageal reflux disease, Global, Prevalence, Heartburn, Screening


Core Tip: Globally, the prevalence of gastroesophageal reflux disease (GERD) and GERD symptoms vary depending from country to country and region to region. Defining GERD and pinpointing its prevalence are problematic due to its diagnostic issues. However, understanding the differences in prevalence will help us identify the differences in associated risk factors, such as genetics and diet, that lead to an individual’s susceptibility to suffering from GERD and its symptoms.

INTRODUCTION

Effortless reflux of gastric contents into the esophagus is a normal physiological process termed gastroesophageal reflux. However, when such reflux occurs frequently and for a prolonged duration, it can lead to symptoms such as heartburn and regurgitation. Gastroesophageal reflux can lead to complications such as esophagitis or strictures. This is termed gastroesophageal reflux disease (GERD)[1,2]. GERD is a multifactorial disease with a complex pathophysiology, usually simplified to a malfunctioning lower esophageal sphincter[3]. It is linked with many genetic and behavioral risk factors such as diet, obesity, mental stress, and medications[4-9]. It is discussed extensively as a common condition[10]. However, its exact worldwide prevalence is not estimated, despite many attempts. The main reasons are the lack of uniform diagnostic criteria and the diversity of underlying symptoms. This article attempts to shed light on the epidemiology of GERD, its impact, and related issues.

Clinical features of GERD

GERD gives rise to a wide range of unpleasant symptoms, both gastrointestinal and extraintestinal. The most common symptoms of GERD are listed in Table 1. Of them, heartburn is recognized as the commonest symptom and the strongest indicator of GERD[11,12]. While heartburn is defined in the Montreal consensus as “a burning sensation in the retrosternal area”[13], the interpretation of “heartburn” and its perception vary in each culture, country, and language, as there are no direct translations of the term “heartburn” in many languages[14]. This issue can confound research[15]. Some non-English speaking populations and Asian cultures like Chinese do not have a term equivalent to heartburn, and dyspeptic symptoms can be counted as part of the diagnosis. Heartburn can also be due to several disorders other than GERD, such as heart disease, gallstones, and eosinophilic esophagitis[16-18]. Despite such issues, heartburn is said to have a 78% sensitivity and 60% specificity[19]. The second commonly described symptom is regurgitation[20], which is defined as the “perception of the flow of refluxed gastric content to the mouth or hypopharynx” or can simply be described as the feeling of a sour taste inside the mouth or fluid moving up in the chest[13,20]. This symptom can also be present in other disorders such as achalasia cardia and rumination syndrome[13,21,22].

Table 1.

Common symptoms of gastroesophageal reflux disease

Ref.
Symptom
[97] Non cardiac chest pain
[11] Heartburn
[20] Regurgitation
[98] Dysphagia
[99] Globus sensation
[13] Epigastric pain
[100] Dyspepsia
[101] Belching
[102] Gall bladder disease
[33] Nausea
[103] Headache
[104] Disturbance of sleep
[13] Dental erosions
[105] Increased salivation
[106] Temporomandibular dysfunction
[107] Chronic cough
[108] Laryngitis
[109] Asthma
[110] Chronic otitis media
[111] Chronic sinusitis
[112,113] Taste and smell changes
[114] Asymptomatic

GERD classification

GERD can be classified as erosive reflux disease (ERD) and non-ERD (NERD)[23]. When reflux-induced esophageal inflammation/ulceration is noted on endoscopy, it is diagnosed as esophagitis[23]. Esophagitis is graded based on the Los Angeles classifications A, B, C, and D[24], with only Grades C and D considered ERD (Table 2)[25]. Patients with NERD have no endoscopic changes but still show abnormal acid exposure time (AET) in 24-hour multichannel intraluminal impedance and pH monitoring (MII-pH). Approximately 50%-85% of all GERD cases are said to be classified as NERD[26].

Table 2.

Los Angeles classification of reflux esophagitis

Grade
Criteria
A One or more mucosal breaks < 5 mm that do not extend between the tops of two mucosal folds
B One or more mucosal breaks > 5 mm that do not extend between the tops of two mucosal folds
C One or more mucosal breaks that are continuous between the tops of two or more mucosal folds but that involve < 75% of the circumference

Differential diagnoses of GERD

Many diseases can mimic GERD. Some of these conditions are listed in Table 3. Two important differential diagnoses of GERD presenting with symptoms of heartburn and regurgitation are reflux hypersensitivity (RH), where normal physiological refluxes elicit symptoms and functional heartburn (FH), where there is no evidence either on the ambulatory pH monitoring or endoscopy, but the patient still complains of heartburn[27,28]. A further problem is that RH and FH can overlap with GERD, as patients can continue to suffer from symptoms despite improvement of reflux and esophagitis[29].

Table 3.

Diseases with symptoms overlapping with gastroesophageal reflux disease

Ref.
Diseases with overlapping symptoms
[115] Eosinophilic esophagitis
[116] Infectious esophagitis
Esophageal candidiasis
Herpes and cytomegalovirus esophagitis
[117] Drug-induced esophagitis
[118] Achalasia and esophageal motility disorders
[119] Pharyngeal and esophageal diverticula, rings, and webs
[120] Disorders of gastric motility/ gastroparesis
[121] Gastritis & peptic ulcer disease
[122] Gluten-related disorders
[123] Functional gastrointestinal disorders: Functional chest pain, functional heartburn, reflux hypersensitivity, globus sensation, functional dysphagia, functional dyspepsia, postprandial distress syndrome, epigastric pain syndrome, belching disorders, and rumination syndrome
[124] Functional abdominal bloating/distension and esophageal and gastric carcinoma
[125] Cardiac disease
[126] Gall bladder and pancreatic diseases

DIAGNOSIS OF GERD

The initial diagnosis of GERD is usually symptom-based but can be confirmed by upper gastrointestinal endoscopy or combined multichannel intraluminal impedance and pH monitoring (MII-pH)[30].

Symptom-based diagnosis of GERD

Clinical history plays a large part in the first-time diagnosis of GERD and is also the main tool used in epidemiological studies[13]. Since investigations used to confirm GERD are invasive and uncomfortable, the symptom criteria play a very significant role in the diagnosis of this condition. From the vast array of symptoms, heartburn and/or regurgitation have a somewhat higher sensitivity and specificity for the diagnosis of GERD and are considered “typical” symptoms[13]. However, diagnosing GERD by clinical history alone is inaccurate since some patients with GERD are asymptomatic or have atypical symptoms other than typical symptoms such as heartburn and regurgitation[31,32]. The Diamond Study findings showed that even a history taken by an expert (e.g., a gastroenterologist) has a sensitivity and specificity of just 70% and 67%, respectively, compared with pH impedance testing or endoscopy[33].

The lack of universally recognized criteria to grade the severity of GERD is another major issue in assessing the burden of this condition. Vakil et al[13], in the Montreal classification with 44 content experts, defined patients with GERD as those who have mild symptoms occurring on ≥ 2 days of the week or those having moderate to severe symptoms occurring on ≥ 1 day of the week. However, according to a review by Nirwan et al[34] in 2020, only 10 studies have used this definition when studying GERD. Many tools and questionnaires are developed and used for GERD screening (Table 4), but the majority, including questionnaires such as the GERD Questionnaire (GerdQ) and Reflux Disease Questionnaire, do not have the sensitivity and specificity of pH impedance studies[33]. The systematic review by Nirwan et al[34] identified 14 different definitions of GERD being used together with 12 different tools and questionnaires (Table 4). These can measure different or similar dimensions, including symptoms, frequency, and severity, and are used in various regions and countries of the world in various languages. These cultural changes lead to issues regarding interpretation as well[15]. Furthermore, some studies, despite using the same tool, had used different cut-offs, leading to further confusion[34]. The screening tools can also give different results based on the duration questioned, with the highest and lowest GERD prevalence found in those tools that collected data for the past 12 months and 1 month, respectively[34].

Table 4.

Tools and questionnaires developed and used for gastroesophageal reflux disease screening

Tool or questionnaire
Abbreviation
Gastroesophageal reflux disease questionnaire GerdQ
Reflux Disease Questionnaire RDQ
Carlsson-Dent Questionnaire CDQ
Bowel Disease Questionnaire BDQ
Frequency Scale for the Symptoms of GERD FSSG
General Health Questionnaire-28 GHQ-28
Gastrointestinal Symptom Rating Scale GSRS
Domestic/International Gastroenterology Surveillance Study DIGEST
Subjective Symptom Assessment Profile SSA-P
GERD Symptom and Medication Questionnaire GERD-SMQ
Chest Pain Questionnaire CPQ
Quality of Life and Utility Evaluation Survey Technology QUEST
Infant Gastro-Esophageal Reflux Questionnaire I-GERQ
GERD Activity Index GRACI
Esophageal Symptom Questionnaire
Standardized Esophageal Symptom Questionnaire
Ulcer Esophagitis Subjective Symptoms Scale UESS
GERD Activity Index GRACI
Digestive Health Status Instrument DHSI
Modified Bowel Disease Questionnaire BDQ
GERD Symptom Assessment Scale GSAS
GERD Screener

GERD: Gastroesophageal reflux disease.

One of the most used questionnaires worldwide is the GerdQ[35]. This is utilized worldwide and has been translated into many languages[36]. It questions the frequency of heartburn and regurgitation as well as sleep disturbance and use of medication for those two symptoms for the past week and gives positive marks, while non-cardiac chest pain and nausea give negative points. GERD is diagnosed if the marks are equal or more than 8[36]. One of the eight questions in GerdQ is “How often does a patient use medication for heartburn or reflux other than what the doctor prescribed?” In countries where the prescribing is not streamlined, self-medication is common, and the ability to buy “prescription drugs” over the counter without a doctor’s prescription is rampant, this question might not be relevant. Despite all the criticisms of decreased sensitivity and specificity, diagnosis of GERD based on usual symptoms is practical and affordable, and many international guidelines support it[1].

Confirmatory tests for GERD

Endoscopy: Endoscopy can identify erosive esophagitis and its complications[23]. Erosive esophagitis is the most common endoscopic manifestation seen in GERD and is reported in 3%-16% of patients, with most having mild esophagitis[37]. However, most GERD patients do not have visible mucosal lesions. Patients with a negative result on endoscopy are recommended to undergo pH impedance testing to confirm the diagnosis of NERD.

24-hour pH impedance: MII-pH can identify the retrograde bolus movement, number of reflux events, total reflux time, the association between symptoms and reflux episodes, and acidic, weakly acidic, and alkaline refluxes[38]. Thus, it is the most sensitive and specific investigation in diagnosing GERD[38]. It can also differentiate GERD from FH and RH. There are many controversies in using 24-hour pH impedance in diagnosing GERD. The Lyon consensus in 2018 proposed that an AET of less than 4% for 24 hours be considered normal and that those above 6% are definitively abnormal and considered GERD. Those within 4% to 6% are recommended to have an adjunctive measure to prove GERD. The consensus also proposes that more than 80 reflux episodes lasting 24 hours are considered abnormal, while less than 40 is normal[25]. However, there are many limitations regarding diagnosis via AET, as cut-off values have been rebutted or contradicted by research done worldwide with high variability in studies that calculated normal values for AET[39,40].

MII-pH also had many regional differences which were further complicated by the different analytic systems and software used in different countries[41]. Cut-offs and normal values for MII-pH are further controversial due to other reasons as well. One is that their values rely on very small cohorts of healthy volunteers from only a few countries[42,43]. Another reason is that there is significant inter-reviewer variability due to technical issues related to analysis such as artifacts and subjective identification of reflux events[44]. Thus, it is problematic that despite all these differences related to different systems and regional differences, the GERD categorization is still related to the Lyon consensus with a fixed cut-off[25]. Furthermore, different systems were used to detect MII-pH metrics, and a significant number of false-positive refluxes in automated analyses of these systems were identified[45,46]. Some experts now recommend lower AET values to diagnose GERD than the Lyon consensus, going as low as 3.2%[47].

High-resolution manometry of the esophagus: High-resolution manometry (HRM) is not a diagnostic test for GERD and most GERD patients have a normal manometric study. However, there can be abnormalities in the LES or the esophageal body that can be detected by HRM[25]. It is recommended in patients with treatment-resistant GERD as it can identify conditions such as achalasia, hiatal hernia, abnormal LES pressures, and esophageal dysmotility that can give rise to GERD symptoms[48]. Manometry also helps identify the exact location of the LES, which helps with the accurate placement of pH sensors[48]. Combined impedance and HRM can also differentiate GERD from rumination[49].

Updates to consensus in diagnosis of GERD

Figure 1 summarizes the currently accepted GERD diagnostic guidelines published by leading authorities in gastroenterology, including the Lyon consensus, Porto consensus, British society, and American College of Gastroenterology guidelines[1,25,50,51].

Figure 1.

Figure 1

Pathway for diagnosing gastroesophageal reflux disease. GERD: Gastroesophageal reflux disease; GI: Gastrointestinal; PPI: Proton pump inhibitor; AET: Acid exposure time.

GLOBAL PREVALENCE OF GERD

Conundrum in obtaining global prevalences

The global prevalence of GERD remains unclear, despite its frequent mention as a common condition. This uncertainty primarily arises from the absence of a universally accepted definition of GERD. A key issue is that the gold standard for diagnosing GERD, the combined pH impedance testing (MII-pH), is underutilized. This limitation is due to both the invasive nature of the procedure and the limited availability of facilities equipped to perform it. MII-pH as well as endoscopy is cumbersome and cannot be carried out in a practical setup to identify the community prevalence of a country or region. Furthermore, despite endoscopy being more widely utilized than ambulatory pH studies, with its inability to identify NERD[53], it cannot be utilized to identify community prevalence, especially in pediatric age groups. Thus, most of the studies on the epidemiology of GERD used various questionnaires as screening tools to assess the symptoms of GERD. The symptoms of GERD can be both esophageal and extraesophageal with much variation, with also an added component of asymptomatic patients[54].

These account for the wide variety of prevalence estimates presented, ranging from 5% to 25% worldwide[6]. Some systematic reviews by experts have used heartburn and or regurgitation at least once weekly as their cut-off for GERD when going through studies worldwide[55]. The latest comprehensive systematic review and meta-analysis on GERD was conducted by Nirwan et al[34] in 2020. The definition was “having heartburn and/or regurgitation at least once weekly”. However, this does not represent the other multitude of GERD patients who might be asymptomatic or have other symptoms other than heartburn or regurgitation as well as those who fit into other differential diagnoses of GERD such as RH and FH.

Prevalences of GERD global, regional, and country-wise

The recent systematic review conducted by Nirwan et al[34], reported a global prevalence of 13.98%, using 102 studies. The highest pooled prevalence of GERD is reported in Turkey (22.4%). The lowest GERD prevalence has been reported in China (4.16%). The prevalence of GERD in North America and Europe is 19.55% and 14.12%, respectively[34]. Pooled prevalence was not calculated in some regions such as Asia in this systematic review. Even though several few South Asian studies (from Bangladeshi and India) were cited in this systematic review, the pooled prevalence was not calculated for this region[34]. When the definition of heartburn and/or regurgitation at least once a week was used, the prevalence of GERD in Bangladeshi was 5.25%[56] and in Indian studies it was 7.6%[57] and 23.6%[58], respectively. A recent study from Sri Lanka in 2024[59], using the same definition as that used by Nirwan et al[34], reported a country-wide prevalence of 25.3%, which is higher than that of Turkey, the country with the highest pooled prevalence reported by Nirwan et al[34]. Table 5 shows the data on regional and country GERD prevalences around the world updated with the latest data using the definition used by Nirwan et al[34].

Table 5.

Pooled prevalence of gastroesophageal reflux disease according to geographical location

Geographical location
Number of studies used for calculation by Nirwan et al[34], 2020
Number of participants
GERD prevalence, %
Global
Overall 102 469899 13.98
Male 50 122849 15.69
Female 50 138435 17.17
Hemisphere
Western 10-20[6,55]
Eastern 2-7[6,127]
Continents
Asia 54 240451 12.92
Europe 29 90057 14.12
North America 9 20525 19.55
Latin America and the Caribbean 4 12756 12.88
Oceania 4 3760 13.78
Africa 2 2350 NA
Countries
China 10 36887 4.16
Japan 7 27912 13.81
South Korea 7 43897 5.84
Taiwan 1 1238 NA
Indonesia 1 278 NA
Bangladesh 1 2000 5.25[56]
India 3 6296 NA
Iran 16 102295 18.43
Turkey 4 13332 22.4
Israel 2 3008 NA
Saudi Arabia 2 3308 NA
Poland 1 850 NA
Romania 1 184 NA
Russia 2 8877 NA
Albania 1 845 NA
Italy 2 2032 NA
Greece 1 700 NA
Spain 3 5365 NA
Switzerland 2 7736 NA
Netherlands 1 502 NA
France 2 46377 NA
Germany 1 268 NA
Sweden 4 8120 16.15
Finland 1 1700 NA
Norway 1 44997 NA
United Kingdom 4 12467 14.53
Denmark 1 48027 NA
United States 8 19489 21.04
Canada 1 1036 NA
Argentina 1 839 NA
Brazil 1 3934 NA
Uruguay 1 1141 NA
Colombia 1 6842 NA
Australia 3 2982 12[62], 9.2[63]
New Zealand 1 778 NA
Nigeria 1 410 NA
Côte d’Ivoire 1 1940 NA
Sri Lanka 1 1200 23.5[59]

GERD: Gastroesophageal reflux disease; NA: Not available.

When one moves away from the definition of GERD as heartburn and/or regurgitation once a week and analyzes the studies done with other questionnaires, the prevalence is even more variable. The Western hemisphere has a higher prevalence of GERD, with prevalence rates of 27.8% in North America, 25.9% in Europe, and 23% in South America given as examples[6,60]. A prevalence of 19.55% was noted in the North American region[34], with at least 30% of the United States population having GERD symptoms at least one time in their life[61]. An Australian study reported a prevalence of GERD symptoms of 12% in their subjects[62], while another estimated it at 9.2%[63]. Studies done in Latin America have shown that GERD prevalence is around 11.9% and 31.3%[64].

GERD was reported traditionally as being less common in Asian countries, with the prevalence ranging around 2% to 7%[6,37,65,66]. But over the last decades, it has been noted to be increasing in Asia, most probably due to the westernization of diets[14,67]. In Eastern Asian countries, the prevalence, which was around 2.5% to 4.8% in 2005 increased to 5.2% and 8.5% in 2010. This rise is seen higher in Southeast and Western Asian countries where in 2010 the prevalence was noted to be around 6.3% to 18.3%[65]. This rise is also noted by many studies done in China where the current estimate is pooled at 4.16%[34,68]. While the above-quoted number is quite small, surprisingly studies done in neighboring Taiwan meanwhile showed a prevalence of around 25%[69]. Far Eastern countries such as China, Japan, and South Korea had a prevalence that was very much lower, while in the Middle Eastern region, the quoted prevalence rates are quite higher[6]. A study done in Saudi Arabia showed the prevalence of GERD at 45.4%[70], while a study done in Iran quoted 43.07% as the percentage of the population having GERD symptoms[71]. The prevalence studies done in India show varying percentages ranging from 10%[72] to 19%[73], and even 22.2% in South India[74].

Prevalences of different GERD symptoms

Except for heartburn or regurgitation, which are the typical GERD symptoms, the others are considered atypical GERD symptoms[13]. We compared various aspects of the symptom profile of studies done around the world using the same GERD definition used by Nirwan et al[34]. The prevalence of symptoms other than heartburn and regurgitation in those with GERD was wide and varied among studies worldwide[75]. For instance, a study from Sri Lanka found that bloating, affecting 55.6% of GERD patients, was the most troublesome symptom after heartburn and regurgitation[59]. This finding contrasts with a Korean study, where only 15.2% of GERD patients reported bloating[76]. In Turkey, dysphagia affected 11.9% of those with GERD[77], whereas a study from China reported a significantly higher dysphagia rate of 35.7% among GERD patients[78].

Even the prevalence of those who suffer from daily heartburn and regurgitation differs from country to country. In a study in Turkey, which has a similar sample size (n = 1345) and a similar GERD prevalence (19.3%) as the study conducted in Sri Lanka, the prevalence of daily symptoms of heartburn and regurgitation was 1.2% and 1.2%, respectively, which is lower than reported from Sri Lanka (25.3% and 15.8%, respectively)[59,77]. Studies show conflicting results on whether heartburn or regurgitation is the most common typical symptom in patients with GERD. Some researchers have suggested that heartburn is more frequent than regurgitation[56], while others have reported regurgitation to be more frequent[79].

Prevalence of confirmed GERD

Due to the unavailability of conducting endoscopy and pH-impedance testing to diagnose and identify GERD in the general population, the prevalence of confirmed GERD is still not available as of now. The global age-standardized prevalence of GERD in 2017 was calculated to be 8819 cases per 100000 population (95% confidence interval: 7781-9863). This prevalence has been stabled from 1990 to 2017, but with increased prevalence in older age groups and increased years lived with disability[80]. The Global Burden of Diseases Study 2019 calculated that from 1990 to 2019, the total number of prevalent cases and incident cases increased by 77.53% (from 441.57 million in 1990 to 783.95 million in 2019) and 74.79%, respectively[81].

FACTORS ASSOCIATED WITH GERD

GERD has many associated factors as well as risk factors[5]. These are summarized in Table 6. These factors, especially diet, could be the reason for the wide variations of prevalence in countries worldwide.

Table 6.

Factors associated with gastroesophageal reflux disease symptoms

Factor
Evidence
Age With increasing age, the elasticity of the pharyngoesophageal membrane reduces, progressively leading to hiatal hernias, predisposing to GERD[128]; the prevalence of GERD symptoms is highest in those aged 40 to 59 years in the systematic review by Nirwan et al[34]
Gender Females had a slightly higher prevalence of GERD than males in systematic reviews by Nirwan et al[34] and Friedland et al[128]
Education level Those with the lowest education level had the highest GERD prevalence, whilst those with the highest level of education had the lowest GERD prevalence[34,129]
Ethnicities Ethnicities can play a role in development of GERD even in the same country[14], though some studies did not find any significant difference[59]
Economic strata Lower-income groups are reported to have a significantly higher prevalence of GERD[34,128]
Urban or rural GERD is reported to be higher in urban populations[34,74,130]
Obesity Obesity is an identified risk factor for GERD[34,131,132]
Mental stress Mental stress is shown to increase GERD symptoms[9,133]
Diet Common food items associated with GERD are: Spices[10], carbonated beverages[134], wheat products[135], tea[136], coffee[137], sour and acidic food[138], alcohol[78], chocolate[139], dietary sugar[140]
Habits Habits associated with GERD include: Large meals[141], sleeping after eating a meal[142], eating a meal fast[135], habit of midnight snacks[143], skipping meals[143], inadequate sleep[134], exercise[142,144], smoking[145]
Diseases and treatments Some diseases such as asthma[146], diabetes mellitus[147], and different medications[148-151] are known to be associated with GERD symptoms

GERD: Gastroesophageal reflux disease.

IMPACTS OF GERD

Economic burden on healthcare cost

The United States is estimated to spend more than 10 billion dollars per year on the diagnosis and treatment of GERD[25], with an estimated number of up to 4663644 annual hospital visits made for GERD and reflux esophagitis just for the year 2016[82]. A mean ± SD of dollars 6955 ± 35880 was estimated to be the annual disease-related cost per patient for GERD in the United States for the year 2020[83]. Another study in the United States noted that a mean incremental cost of 3355 dollars per employee was associated with GERD, with 17% of it accounting for prescription drug costs and 19% for indirect costs[84]. Increasing severity and complications of the GERD spectrum towards dysplasia and carcinoma result in further expenses as well[83]. The average monthly medical costs for proton pump medications were estimated to be approximately 163 dollars in South Korea[85].

Quality of life

GERD affects the quality of life (QoL) of its sufferers. The Global Burden of Diseases Study 2019 has calculated that between the years 1990 and 2019, the estimated years lived in disability has increased by 77.19%[81]. Patients with GERD have lower physical and mental health scores, increased work absenteeism, reduced percent productivity, increased healthcare utilization, and more concomitant diseases. The QoL parameters invariably deteriorate if the severity of GERD increases[86]. Due to its effect on daily life, several QoL questionnaires have been developed alongside screening tools and diagnostic questionnaires[87,88]. Studies using these questionnaires have shown that the QoL of GERD sufferers become worse with increasing age and obesity[89].

Complications

GERD leads to many complications such as reflux esophagitis, Barret’s esophagus, and strictures[90,91]. The damage to the esophagus that leads to esophagitis and dysplasia was initially thought to be due to the chemical injury caused by refluxed stomach acid, bile salts, and other erosive and noxious materials in gastric secretions[92]. But now the school of thought is more toward acid-mediated inflammation through cytokines than direct injury[93]. Receptors mediating nociception such as protease-activated receptor-2, also cause inflammation of the mucosa through cytokines such as interleukin-8 (IL-8)[94]. Its levels increase with the progression of the disease, while they decrease with treatment[95]. IL-1β and IL-6 are other cytokines noted to be expressed at high levels in the esophageal mucosa of GERD patients[96]. This inflammatory process of the mucosa of the esophagus is what causes reflux esophagitis or ERD[24].

Continuous inflammation can sometimes change the normal esophageal stratified squamous epithelium into a metaplastic columnar epithelium, leading to Barrett’s esophagus (BE). BE is diagnosed if the columnar epithelium is more than 1 cm proximal to the gastroesophageal junction, together with confirmation from biopsies. BE is a concerning situation, as there could be a progression from metaplastic to dysplastic epithelium and even to carcinoma[91]. Mucosal damage and chronic inflammatory changes can also cause fibrosis, scarring, and loss of esophageal distensibility, leading to an esophageal stricture with dysphagia as a symptom[90].

CONCLUSION

GERD is a common disorder with high worldwide prevalence. Its burden on some regions of the world is still not clear due to a lack of research and variations in screening tools and diagnostic criteria. When studied, the prevalence is estimated using GERD symptoms, and the exact prevalence of confirmed GERD (using endoscopy and gastrointestinal physiology investigations) is unknown. Accurate knowledge on GERD prevalence is crucial for allocating resources effectively. This includes ensuring access to gastroenterology specialists and diagnostic tools such as endoscopy, pH impedance testing, and esophageal manometry, as well as medications and facilities for surgical treatment options like fundoplication. GERD is a lifelong debilitating disorder with poor QoL, high health care costs, and multiple complications. Early diagnosis and effective treatment are essential to reduce the burden of this disease on the healthcare system and to improve the QoL. A global consensus must be reached to develop highly sensitive symptomatic diagnostic criteria for screening GERD patients as well as for effective management of this cumbersome and complicated disease.

Footnotes

Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.

Provenance and peer review: Invited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Gastroenterology and hepatology

Country of origin: Sri Lanka

Peer-review report’s classification

Scientific Quality: Grade C

Novelty: Grade C

Creativity or Innovation: Grade C

Scientific Significance: Grade C

P-Reviewer: Liu J S-Editor: Wei YF L-Editor: Wang TQ P-Editor: Zheng XM

Contributor Information

Nilanka Wickramasinghe, Department of Physiology, Faculty of Medicine, University of Colombo, Colombo 00800, Western Province, Sri Lanka.

Niranga Manjuri Devanarayana, Department of Physiology, Faculty of Medicine, University of Kelaniya, Ragama 11010, Western Province, Sri Lanka. niranga@kln.ac.lk.

References

  • 1.Katz PO, Dunbar KB, Schnoll-Sussman FH, Greer KB, Yadlapati R, Spechler SJ. ACG Clinical Guideline for the Diagnosis and Management of Gastroesophageal Reflux Disease. Am J Gastroenterol. 2022;117:27–56. doi: 10.14309/ajg.0000000000001538. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Sontag SJ. Defining GERD. Yale J Biol Med. 1999;72:69–80. [PMC free article] [PubMed] [Google Scholar]
  • 3.Belhocine K, Galmiche JP. Epidemiology of the complications of gastroesophageal reflux disease. Dig Dis. 2009;27:7–13. doi: 10.1159/000210097. [DOI] [PubMed] [Google Scholar]
  • 4.Ayazi S, Hagen JA, Chan LS, DeMeester SR, Lin MW, Ayazi A, Leers JM, Oezcelik A, Banki F, Lipham JC, DeMeester TR, Crookes PF. Obesity and gastroesophageal reflux: quantifying the association between body mass index, esophageal acid exposure, and lower esophageal sphincter status in a large series of patients with reflux symptoms. J Gastrointest Surg. 2009;13:1440–1447. doi: 10.1007/s11605-009-0930-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Argyrou A, Legaki E, Koutserimpas C, Gazouli M, Papaconstantinou I, Gkiokas G, Karamanolis G. Risk factors for gastroesophageal reflux disease and analysis of genetic contributors. World J Clin Cases. 2018;6:176–182. doi: 10.12998/wjcc.v6.i8.176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Dent J, El-Serag HB, Wallander MA, Johansson S. Epidemiology of gastro-oesophageal reflux disease: a systematic review. Gut. 2005;54:710–717. doi: 10.1136/gut.2004.051821. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Moraes-Filho JP, Chinzon D, Eisig JN, Hashimoto CL, Zaterka S. Prevalence of heartburn and gastroesophageal reflux disease in the urban Brazilian population. Arq Gastroenterol. 2005;42:122–127. doi: 10.1590/s0004-28032005000200011. [DOI] [PubMed] [Google Scholar]
  • 8.Sontag SJ. Rolling review: gastro-oesophageal reflux disease. Aliment Pharmacol Ther. 1993;7:293–312. doi: 10.1111/j.1365-2036.1993.tb00101.x. [DOI] [PubMed] [Google Scholar]
  • 9.Wickramasinghe N, Thuraisingham A, Jayalath A, Wickramasinghe D, Samarasekara N, Yazaki E, Devanarayana NM. The association between symptoms of gastroesophageal reflux disease and perceived stress: A countrywide study of Sri Lanka. PLoS One. 2023;18:e0294135. doi: 10.1371/journal.pone.0294135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Nebel OT, Fornes MF, Castell DO. Symptomatic gastroesophageal reflux: incidence and precipitating factors. Am J Dig Dis. 1976;21:953–956. doi: 10.1007/BF01071906. [DOI] [PubMed] [Google Scholar]
  • 11.Rothman M, Farup C, Stewart W, Helbers L, Zeldis J. Symptoms associated with gastroesophageal reflux disease: development of a questionnaire for use in clinical trials. Dig Dis Sci. 2001;46:1540–1549. doi: 10.1023/a:1010660425522. [DOI] [PubMed] [Google Scholar]
  • 12.Dent J, Brun J, Fendrick A, Fennerty M, Janssens J, Kahrilas P, Lauritsen K, Reynolds J, Shaw M, Talley N. An evidence-based appraisal of reflux disease management--the Genval Workshop Report. Gut. 1999;44 Suppl 2:S1–16. doi: 10.1136/gut.44.2008.s1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.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;101:1900–20; quiz 1943. doi: 10.1111/j.1572-0241.2006.00630.x. [DOI] [PubMed] [Google Scholar]
  • 14.Sharma P, Wani S, Romero Y, Johnson D, Hamilton F. Racial and geographic issues in gastroesophageal reflux disease. Am J Gastroenterol. 2008;103:2669–2680. doi: 10.1111/j.1572-0241.2008.02089.x. [DOI] [PubMed] [Google Scholar]
  • 15.Spechler SJ, Jain SK, Tendler DA, Parker RA. Racial differences in the frequency of symptoms and complications of gastro-oesophageal reflux disease. Aliment Pharmacol Ther. 2002;16:1795–1800. doi: 10.1046/j.1365-2036.2002.01351.x. [DOI] [PubMed] [Google Scholar]
  • 16.Kia L, Hirano I. Distinguishing GERD from eosinophilic oesophagitis: concepts and controversies. Nat Rev Gastroenterol Hepatol. 2015;12:379–386. doi: 10.1038/nrgastro.2015.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Diehl AK. Symptoms of gallstone disease. Baillieres Clin Gastroenterol. 1992;6:635–657. doi: 10.1016/0950-3528(92)90044-f. [DOI] [PubMed] [Google Scholar]
  • 18.Simpson FG, Kay J, Aber CP. Chest pain--indigestion or impending heart attack? Postgrad Med J. 1984;60:338–340. doi: 10.1136/pgmj.60.703.338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Klauser AG, Schindlbeck NE, Müller-Lissner SA. Symptoms in gastro-oesophageal reflux disease. Lancet. 1990;335:205–208. doi: 10.1016/0140-6736(90)90287-f. [DOI] [PubMed] [Google Scholar]
  • 20.Kahrilas PJ. Regurgitation in patients with gastroesophageal reflux disease. Gastroenterol Hepatol (N Y) 2013;9:37–39. [PMC free article] [PubMed] [Google Scholar]
  • 21.Jung DH, Park H. Is Gastroesophageal Reflux Disease and Achalasia Coincident or Not? J Neurogastroenterol Motil. 2017;23:5–8. doi: 10.5056/jnm16121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Talley NJ. Rumination syndrome. Gastroenterol Hepatol (N Y) 2011;7:117–118. [PMC free article] [PubMed] [Google Scholar]
  • 23.Martínek J, Benes M, Hucl T, Drastich P, Stirand P, Spicák J. Non-erosive and erosive gastroesophageal reflux diseases: No difference with regard to reflux pattern and motility abnormalities. Scand J Gastroenterol. 2008;43:794–800. doi: 10.1080/00365520801908928. [DOI] [PubMed] [Google Scholar]
  • 24.Lundell LR, Dent J, Bennett JR, Blum AL, Armstrong D, Galmiche JP, Johnson F, Hongo M, Richter JE, Spechler SJ, Tytgat GN, Wallin L. Endoscopic assessment of oesophagitis: clinical and functional correlates and further validation of the Los Angeles classification. Gut. 1999;45:172–180. doi: 10.1136/gut.45.2.172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Gyawali CP, Kahrilas PJ, Savarino E, Zerbib F, Mion F, Smout AJPM, Vaezi M, Sifrim D, Fox MR, Vela MF, Tutuian R, Tack J, Bredenoord AJ, Pandolfino J, Roman S. Modern diagnosis of GERD: the Lyon Consensus. Gut. 2018;67:1351–1362. doi: 10.1136/gutjnl-2017-314722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.El-Serag HB. Epidemiology of non-erosive reflux disease. Digestion. 2008;78 Suppl 1:6–10. doi: 10.1159/000151249. [DOI] [PubMed] [Google Scholar]
  • 27.Sawada A, Sifrim D, Fujiwara Y. Esophageal Reflux Hypersensitivity: A Comprehensive Review. Gut Liver. 2023;17:831–842. doi: 10.5009/gnl220373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Fass R, Tougas G. Functional heartburn: the stimulus, the pain, and the brain. Gut. 2002;51:885–892. doi: 10.1136/gut.51.6.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Aziz Q, Fass R, Gyawali CP, Miwa H, Pandolfino JE, Zerbib F. Functional Esophageal Disorders. Gastroenterology. 2016;150:1368–1379. doi: 10.1053/j.gastro.2016.02.012. [DOI] [PubMed] [Google Scholar]
  • 30.Katz PO, Gerson LB, Vela MF. Guidelines for the diagnosis and management of gastroesophageal reflux disease. Am J Gastroenterol. 2013;108:308–28; quiz 329. doi: 10.1038/ajg.2012.444. [DOI] [PubMed] [Google Scholar]
  • 31.Fass R, Dickman R. Clinical consequences of silent gastroesophageal reflux disease. Curr Gastroenterol Rep. 2006;8:195–201. doi: 10.1007/s11894-006-0075-8. [DOI] [PubMed] [Google Scholar]
  • 32.Fass R. Symptom assessment tools for gastroesophageal reflux disease (GERD) treatment. J Clin Gastroenterol. 2007;41:437–444. doi: 10.1097/MCG.0b013e31802e849f. [DOI] [PubMed] [Google Scholar]
  • 33.Dent J, Vakil N, Jones R, Bytzer P, Schöning U, Halling K, Junghard O, Lind T. Accuracy of the diagnosis of GORD by questionnaire, physicians and a trial of proton pump inhibitor treatment: the Diamond Study. Gut. 2010;59:714–721. doi: 10.1136/gut.2009.200063. [DOI] [PubMed] [Google Scholar]
  • 34.Nirwan JS, Hasan SS, Babar ZU, Conway BR, Ghori MU. Global Prevalence and Risk Factors of Gastro-oesophageal Reflux Disease (GORD): Systematic Review with Meta-analysis. Sci Rep. 2020;10:5814. doi: 10.1038/s41598-020-62795-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Bolier EA, Kessing BF, Smout AJ, Bredenoord AJ. Systematic review: questionnaires for assessment of gastroesophageal reflux disease. Dis Esophagus. 2015;28:105–120. doi: 10.1111/dote.12163. [DOI] [PubMed] [Google Scholar]
  • 36.Bai Y, Du Y, Zou D, Jin Z, Zhan X, Li ZS, Yang Y, Liu Y, Zhang S, Qian J, Zhou L, Hao J, Chen D, Fang D, Fan D, Yu X, Sha W, Nie Y, Zhang X, Xu H, Lv N, Jiang B, Zou X, Fang J, Fan J, Li Y, Chen W, Wang B, Zou Y, Li Y, Sun M, Chen Q, Chen M, Zhao X Chinese GerdQ Research Group. Gastroesophageal Reflux Disease Questionnaire (GerdQ) in real-world practice: a national multicenter survey on 8065 patients. J Gastroenterol Hepatol. 2013;28:626–631. doi: 10.1111/jgh.12125. [DOI] [PubMed] [Google Scholar]
  • 37.Goh KL. Changing epidemiology of gastroesophageal reflux disease in the Asian-Pacific region: an overview. J Gastroenterol Hepatol. 2004;19 Suppl 3:S22–S25. doi: 10.1111/j.1440-1746.2004.03591.x. [DOI] [PubMed] [Google Scholar]
  • 38.Bredenoord AJ, Weusten BL, Timmer R, Conchillo JM, Smout AJ. Addition of esophageal impedance monitoring to pH monitoring increases the yield of symptom association analysis in patients off PPI therapy. Am J Gastroenterol. 2006;101:453–459. doi: 10.1111/j.1572-0241.2006.00427.x. [DOI] [PubMed] [Google Scholar]
  • 39.Kahrilas PJ, Quigley EM. Clinical esophageal pH recording: a technical review for practice guideline development. Gastroenterology. 1996;110:1982–1996. doi: 10.1053/gast.1996.1101982. [DOI] [PubMed] [Google Scholar]
  • 40.Savarino E, Tutuian R, Zentilin P, Dulbecco P, Pohl D, Marabotto E, Parodi A, Sammito G, Gemignani L, Bodini G, Savarino V. Characteristics of reflux episodes and symptom association in patients with erosive esophagitis and nonerosive reflux disease: study using combined impedance-pH off therapy. Am J Gastroenterol. 2010;105:1053–1061. doi: 10.1038/ajg.2009.670. [DOI] [PubMed] [Google Scholar]
  • 41.Sifrim D, Roman S, Savarino E, Bor S, Bredenoord AJ, Castell D, Cicala M, de Bortoli N, Frazzoni M, Gonlachanvit S, Iwakiri K, Kawamura O, Krarup A, Lee YY, Soon Ngiu C, Ndebia E, Patcharatraku T, Pauwels A, Pérez de la Serna J, Ramos R, Remes-Troche JM, Ribolsi M, Sammon A, Simren M, Tack J, Tutuian R, Valdovinos M, Xiao Y, Zerbib F, Gyawali CP. Normal values and regional differences in oesophageal impedance-pH metrics: a consensus analysis of impedance-pH studies from around the world. Gut. 2020;70:1441–1449. doi: 10.1136/gutjnl-2020-322627. [DOI] [PubMed] [Google Scholar]
  • 42.Sifrim D, Castell D, Dent J, Kahrilas PJ. Gastro-oesophageal reflux monitoring: review and consensus report on detection and definitions of acid, non-acid, and gas reflux. Gut. 2004;53:1024–1031. doi: 10.1136/gut.2003.033290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Zerbib F, Roman S, Bruley Des Varannes S, Gourcerol G, Coffin B, Ropert A, Lepicard P, Mion F Groupe Français De Neuro-Gastroentérologie. Normal values of pharyngeal and esophageal 24-hour pH impedance in individuals on and off therapy and interobserver reproducibility. Clin Gastroenterol Hepatol. 2013;11:366–372. doi: 10.1016/j.cgh.2012.10.041. [DOI] [PubMed] [Google Scholar]
  • 44.Tenca A, Campagnola P, Bravi I, Benini L, Sifrim D, Penagini R. Impedance pH Monitoring: Intra-observer and Inter-observer Agreement and Usefulness of a Rapid Analysis of Symptom Reflux Association. J Neurogastroenterol Motil. 2014;20:205–211. doi: 10.5056/jnm.2014.20.2.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Koop AH, Francis DL, DeVault KR. Visual and Automated Computer Analysis Differ Substantially in Detection of Acidic Reflux in Multichannel Intraluminal Impedance-pH Monitoring. Clin Gastroenterol Hepatol. 2018;16:979–980. doi: 10.1016/j.cgh.2017.10.039. [DOI] [PubMed] [Google Scholar]
  • 46.Hemmink GJ, Bredenoord AJ, Aanen MC, Weusten BL, Timmer R, Smout AJ. Computer analysis of 24-h esophageal impedance signals. Scand J Gastroenterol. 2011;46:271–276. doi: 10.3109/00365521.2010.531483. [DOI] [PubMed] [Google Scholar]
  • 47.Frazzoni L, Frazzoni M, de Bortoli N, Tolone S, Martinucci I, Fuccio L, Savarino V, Savarino E. Critical appraisal of Rome IV criteria: hypersensitive esophagus does belong to gastroesophageal reflux disease spectrum. Ann Gastroenterol. 2018;31:1–7. doi: 10.20524/aog.2017.0199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Chen X, Wang F. Refractory Gastroesophageal Reflux Disease (GERD) Symptoms. In: Gastroesophageal Reflux Disease - Theory and Research. London: IntechOpen, 2019. [Google Scholar]
  • 49.Martos Vizcaino E, Canga Rodriguez-Valcárcel F, Ciriza de Los Ríos C. Rumination Syndrome: Unknown Pathology Easy to Diagnose With High-resolution Impedance Manometry. J Neurogastroenterol Motil. 2018;24:503–505. doi: 10.5056/jnm18048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Savarino E, Bredenoord AJ, Fox M, Pandolfino JE, Roman S, Gyawali CP International Working Group for Disorders of Gastrointestinal Motility and Function. Expert consensus document: Advances in the physiological assessment and diagnosis of GERD. Nat Rev Gastroenterol Hepatol. 2017;14:665–676. doi: 10.1038/nrgastro.2017.130. [DOI] [PubMed] [Google Scholar]
  • 51.Trudgill NJ, Sifrim D, Sweis R, Fullard M, Basu K, McCord M, Booth M, Hayman J, Boeckxstaens G, Johnston BT, Ager N, De Caestecker J. British Society of Gastroenterology guidelines for oesophageal manometry and oesophageal reflux monitoring. Gut. 2019;68:1731–1750. doi: 10.1136/gutjnl-2018-318115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Rossi P, Isoldi S, Mallardo S, Papoff P, Rossetti D, Dilillo A, Oliva S. Combined multichannel intraluminal impedance and pH monitoring is helpful in managing children with suspected gastro-oesophageal reflux disease. Dig Liver Dis. 2018;50:910–915. doi: 10.1016/j.dld.2018.03.031. [DOI] [PubMed] [Google Scholar]
  • 53.Hershcovici T, Fass R. Nonerosive Reflux Disease (NERD) - An Update. J Neurogastroenterol Motil. 2010;16:8–21. doi: 10.5056/jnm.2010.16.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Schneider H. Gastro-oesophageal reflux disease: The Montreal definition and classification. S Afr Fam Pract. 2007;49:19–26. [Google Scholar]
  • 55.El-Serag HB. Time trends of gastroesophageal reflux disease: a systematic review. Clin Gastroenterol Hepatol. 2007;5:17–26. doi: 10.1016/j.cgh.2006.09.016. [DOI] [PubMed] [Google Scholar]
  • 56.Shaha M, Perveen I, Alamgir MJ, Masud MH, Rahman MH. Prevalence and risk factors for gastro-esophageal reflux disease in the North-Eastern part of Bangladesh. Bangladesh Med Res Counc Bull. 2012;38:108–113. doi: 10.3329/bmrcb.v38i3.14338. [DOI] [PubMed] [Google Scholar]
  • 57.Bhatia SJ, Reddy DN, Ghoshal UC, Jayanthi V, Abraham P, Choudhuri G, Broor SL, Ahuja V, Augustine P, Balakrishnan V, Bhasin DK, Bhat N, Chacko A, Dadhich S, Dhali GK, Dhawan PS, Dwivedi M, Goenka MK, Koshy A, Kumar A, Misra SP, Mukewar S, Raju EP, Shenoy KT, Singh SP, Sood A, Srinivasan R. Epidemiology and symptom profile of gastroesophageal reflux in the Indian population: report of the Indian Society of Gastroenterology Task Force. Indian J Gastroenterol. 2011;30:118–127. doi: 10.1007/s12664-011-0112-x. [DOI] [PubMed] [Google Scholar]
  • 58.Kumar S, Shivalli S. Prevalence, Perceptions and Profile of Gastroesophageal Reflux Disease in A Rural Population of North Bihar. Natl J Community Med. 2014;5:214–218. [Google Scholar]
  • 59.Wickramasinghe N, Thuraisingham A, Jayalath A, Wickramasinghe D, Samarasekera DN, Yazaki E, Devanarayana NM. Gastroesophageal reflux disease in Sri Lanka: An island-wide epidemiological survey assessing the prevalence and associated factors. PLOS Glob Public Health. 2024;4:e0003162. doi: 10.1371/journal.pgph.0003162. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.El-Serag HB, Sweet S, Winchester CC, Dent J. Update on the epidemiology of gastro-oesophageal reflux disease: a systematic review. Gut. 2014;63:871–880. doi: 10.1136/gutjnl-2012-304269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Katz PO. Lessons learned from intragastric pH monitoring. J Clin Gastroenterol. 2001;33:107–113. doi: 10.1097/00004836-200108000-00003. [DOI] [PubMed] [Google Scholar]
  • 62.Watson DI, Lally CJ. Prevalence of symptoms and use of medication for gastroesophageal reflux in an Australian community. World J Surg. 2009;33:88–94. doi: 10.1007/s00268-008-9780-9. [DOI] [PubMed] [Google Scholar]
  • 63.Knox SA, Harrison CM, Britt HC, Henderson JV. Estimating prevalence of common chronic morbidities in Australia. Med J Aust. 2008;189:66–70. doi: 10.5694/j.1326-5377.2008.tb01918.x. [DOI] [PubMed] [Google Scholar]
  • 64.Salis G. [Systematic review: Epidemiology of gastroesophageal reflux disease in Latin America] Acta Gastroenterol Latinoam. 2011;41:60–69. [PubMed] [Google Scholar]
  • 65.Jung HK. Epidemiology of gastroesophageal reflux disease in Asia: a systematic review. J Neurogastroenterol Motil. 2011;17:14–27. doi: 10.5056/jnm.2011.17.1.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Wu JC. Gastroesophageal reflux disease: an Asian perspective. J Gastroenterol Hepatol. 2008;23:1785–1793. doi: 10.1111/j.1440-1746.2008.05684.x. [DOI] [PubMed] [Google Scholar]
  • 67.Song HJ, Shim KN, Yoon SJ, Kim SE, Oh HJ, Ryu KH, Ha CY, Yeom HJ, Song JH, Jung SA, Yoo K. The prevalence and clinical characteristics of reflux esophagitis in koreans and its possible relation to metabolic syndrome. J Korean Med Sci. 2009;24:197–202. doi: 10.3346/jkms.2009.24.2.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.He J, Ma X, Zhao Y, Wang R, Yan X, Yan H, Yin P, Kang X, Fang J, Hao Y, Li Q, Dent J, Sung JJ, Zou D, Wallander MA, Johansson S, Liu W, Li Z. A population-based survey of the epidemiology of symptom-defined gastroesophageal reflux disease: the Systematic Investigation of Gastrointestinal Diseases in China. BMC Gastroenterol. 2010;10:94. doi: 10.1186/1471-230X-10-94. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Hung LJ, Hsu PI, Yang CY, Wang EM, Lai KH. Prevalence of gastroesophageal reflux disease in a general population in Taiwan. J Gastroenterol Hepatol. 2011;26:1164–1168. doi: 10.1111/j.1440-1746.2011.06750.x. [DOI] [PubMed] [Google Scholar]
  • 70.Almadi MA, Almousa MA, Althwainy AF, Altamimi AM, Alamoudi HO, Alshamrani HS, Alharbi OR, Azzam NA, Sadaf N, Aljebreen AM. Prevalence of symptoms of gastroesopahgeal reflux in a cohort of Saudi Arabians: a study of 1265 subjects. Saudi J Gastroenterol. 2014;20:248–254. doi: 10.4103/1319-3767.136982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Karimian M, Nourmohammadi H, Salamati M, Hafezi Ahmadi MR, Kazemi F, Azami M. Epidemiology of gastroesophageal reflux disease in Iran: a systematic review and meta-analysis. BMC Gastroenterol. 2020;20:297. doi: 10.1186/s12876-020-01417-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Bhatia S, Gupta DK, Vennalaganti P. Epidemiology of Gastroesophageal Reflux in Asia. In: Sharma P, Bhatia S, Goh K. The Rise of Acid Reflux in Asia. New Delhi: Springer, 2018. [Google Scholar]
  • 73.Kumar S, Sharma S, Norboo T, Dolma D, Norboo A, Stobdan T, Rohatgi S, Munot K, Ahuja V, Saraya A. Population based study to assess prevalence and risk factors of gastroesophageal reflux disease in a high altitude area. Indian J Gastroenterol. 2011;30:135–143. doi: 10.1007/s12664-010-0066-4. [DOI] [PubMed] [Google Scholar]
  • 74.Wang HY, Leena KB, Plymoth A, Hergens MP, Yin L, Shenoy KT, Ye W. Prevalence of gastro-esophageal reflux disease and its risk factors in a community-based population in southern India. BMC Gastroenterol. 2016;16:36. doi: 10.1186/s12876-016-0452-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Pourhoseingholi A, Pourhoseingholi MA, Moghimi-Dehkordi B, Barzegar F, Safaee A, Vahedi M, Dulaimi DA, Prabhakaran S. Epidemiological features of gastro-esophageal reflux disease in Iran based on general population. Gastroenterol Hepatol Bed Bench. 2012;5:54–59. [PMC free article] [PubMed] [Google Scholar]
  • 76.Min BH, Huh KC, Jung HK, Yoon YH, Choi KD, Song KH, Keum B, Kim JW Functional Dyspepsia Study Group of Korean Society of Neurogastroenterology and Motility. Prevalence of uninvestigated dyspepsia and gastroesophageal reflux disease in Korea: a population-based study using the Rome III criteria. Dig Dis Sci. 2014;59:2721–2729. doi: 10.1007/s10620-014-3243-y. [DOI] [PubMed] [Google Scholar]
  • 77.Yönem Ö, Sivri B, Özdemir L, Nadir I, Yüksel S, Uygun Y. Gastroesophageal reflux disease prevalence in the city of Sivas. Turk J Gastroenterol. 2013;24:303–310. doi: 10.4318/tjg.2013.0256. [DOI] [PubMed] [Google Scholar]
  • 78.Wang JH, Luo JY, Dong L, Gong J, Tong M. Epidemiology of gastroesophageal reflux disease: a general population-based study in Xi'an of Northwest China. World J Gastroenterol. 2004;10:1647–1651. doi: 10.3748/wjg.v10.i11.1647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Ma XQ, Cao Y, Wang R, Yan X, Zhao Y, Zou D, Wallander MA, Johansson S, Liu W, Gu Z, Zhao J, He J. Prevalence of, and factors associated with, gastroesophageal reflux disease: a population-based study in Shanghai, China. Dis Esophagus. 2009;22:317–322. doi: 10.1111/j.1442-2050.2008.00904.x. [DOI] [PubMed] [Google Scholar]
  • 80.GBD 2017 Gastro-oesophageal Reflux Disease Collaborators. The global, regional, and national burden of gastro-oesophageal reflux disease in 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5:561–581. doi: 10.1016/S2468-1253(19)30408-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Zhang D, Liu S, Li Z, Wang R. Global, regional and national burden of gastroesophageal reflux disease, 1990-2019: update from the GBD 2019 study. Ann Med. 2022;54:1372–1384. doi: 10.1080/07853890.2022.2074535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Peery AF, Crockett SD, Murphy CC, Jensen ET, Kim HP, Egberg MD, Lund JL, Moon AM, Pate V, Barnes EL, Schlusser CL, Baron TH, Shaheen NJ, Sandler RS. Burden and Cost of Gastrointestinal, Liver, and Pancreatic Diseases in the United States: Update 2021. Gastroenterology. 2022;162:621–644. doi: 10.1053/j.gastro.2021.10.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Sharma P, Falk GW, Bhor M, Ozbay AB, Latremouille-Viau D, Guerin A, Shi S, Elvekrog MM, Limburg P. Healthcare Resource Utilization and Costs Among Patients With Gastroesophageal Reflux Disease, Barrett's Esophagus, and Barrett's Esophagus-Related Neoplasia in the United States. J Health Econ Outcomes Res. 2023;10:51–58. doi: 10.36469/001c.68191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Brook RA, Wahlqvist P, Kleinman NL, Wallander MA, Campbell SM, Smeeding JE. Cost of gastro-oesophageal reflux disease to the employer: a perspective from the United States. Aliment Pharmacol Ther. 2007;26:889–898. doi: 10.1111/j.1365-2036.2007.03428.x. [DOI] [PubMed] [Google Scholar]
  • 85.Park S, Kwon JW, Park JM, Park S, Seo KW. Treatment Pattern and Economic Burden of Refractory Gastroesophageal Reflux Disease Patients in Korea. J Neurogastroenterol Motil. 2020;26:281–288. doi: 10.5056/jnm19050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Wahlqvist P, Karlsson M, Johnson D, Carlsson J, Bolge SC, Wallander MA. Relationship between symptom load of gastro-oesophageal reflux disease and health-related quality of life, work productivity, resource utilization and concomitant diseases: survey of a US cohort. Aliment Pharmacol Ther. 2008;27:960–970. doi: 10.1111/j.1365-2036.2008.03671.x. [DOI] [PubMed] [Google Scholar]
  • 87.Jurkowska G, Świdnicka-siergiejko A, Łagoda K, Sierżantowicz R, Dąbrowski A. Quality of life in patients with gastroesophageal reflux disease following pharmacotherapeutic, endoscopic, and surgical treatment. Studia Medyczne. 2016;4:299–306. [Google Scholar]
  • 88.Kleinman L, Nelson S, Kothari-Talwar S, Roberts L, Orenstein SR, Mody RR, Hassall E, Gold B, Revicki DA, Dabbous O. Development and psychometric evaluation of 2 age-stratified versions of the Pediatric GERD Symptom and Quality of Life Questionnaire. J Pediatr Gastroenterol Nutr. 2011;52:514–522. doi: 10.1097/MPG.0b013e318205970e. [DOI] [PubMed] [Google Scholar]
  • 89.Alshammari SA, Alabdulkareem AM, Aloqeely KM, Alhumud MI, Alghufaily SA, Al-Dossare YI, Alrashdan NO. The Determinants of the Quality of Life of Gastroesophageal Reflux Disease Patients Attending King Saud University Medical City. Cureus. 2020;12:e9505. doi: 10.7759/cureus.9505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Triggs JR, Pandolfino JE. Esophageal Strictures. 2nd ed. In: Kuipers EJ. Encyclopedia of Gastroenterology. Elsevier, 2020. [Google Scholar]
  • 91.Eluri S, Shaheen NJ. Barrett's esophagus: diagnosis and management. Gastrointest Endosc. 2017;85:889–903. doi: 10.1016/j.gie.2017.01.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Spechler SJ. Carcinogenesis at the gastroesophageal junction: free radicals at the frontier. Gastroenterology. 2002;122:1518–1520. doi: 10.1053/gast.2002.33368. [DOI] [PubMed] [Google Scholar]
  • 93.Dunbar KB, Agoston AT, Odze RD, Huo X, Pham TH, Cipher DJ, Castell DO, Genta RM, Souza RF, Spechler SJ. Association of Acute Gastroesophageal Reflux Disease With Esophageal Histologic Changes. JAMA. 2016;315:2104–2112. doi: 10.1001/jama.2016.5657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Vergnolle N, Bunnett NW, Sharkey KA, Brussee V, Compton SJ, Grady EF, Cirino G, Gerard N, Basbaum AI, Andrade-Gordon P, Hollenberg MD, Wallace JL. Proteinase-activated receptor-2 and hyperalgesia: A novel pain pathway. Nat Med. 2001;7:821–826. doi: 10.1038/89945. [DOI] [PubMed] [Google Scholar]
  • 95.Yoshida N, Imamura Y, Baba Y, Baba H. Pathogenesis of acute gastroesophageal reflux disease might be changing. Transl Cancer Res. 2016;5:S645–S647. [Google Scholar]
  • 96.Rieder F, Cheng L, Harnett KM, Chak A, Cooper GS, Isenberg G, Ray M, Katz JA, Catanzaro A, O'Shea R, Post AB, Wong R, Sivak MV, McCormick T, Phillips M, West GA, Willis JE, Biancani P, Fiocchi C. Gastroesophageal reflux disease-associated esophagitis induces endogenous cytokine production leading to motor abnormalities. Gastroenterology. 2007;132:154–165. doi: 10.1053/j.gastro.2006.10.009. [DOI] [PubMed] [Google Scholar]
  • 97.Shim KN, Hong SJ, Sung JK, Park KS, Kim SE, Park HS, Kim YS, Lim SH, Kim CH, Park MJ, Yim JY, Cho KR, Kim D, Park SJ, Jee SR, Kim JI, Park JY, Song GA, Jung HY, Lee YC, Kim JG, Kim JJ, Kim N, Park SH, Jung HC, Chung IS H. pylori and GERD Study Group of Korean College of Helicobacter and Upper Gastrointestinal Research. Clinical spectrum of reflux esophagitis among 25,536 Koreans who underwent a health check-up: a nationwide multicenter prospective, endoscopy-based study. J Clin Gastroenterol. 2009;43:632–638. doi: 10.1097/MCG.0b013e3181855055. [DOI] [PubMed] [Google Scholar]
  • 98.Kidambi T, Toto E, Ho N, Taft T, Hirano I. Temporal trends in the relative prevalence of dysphagia etiologies from 1999-2009. World J Gastroenterol. 2012;18:4335–4341. doi: 10.3748/wjg.v18.i32.4335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Jones D, Prowse S. Globus pharyngeus: an update for general practice. Br J Gen Pract. 2015;65:554–555. doi: 10.3399/bjgp15X687193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Gerson LB, Kahrilas PJ, Fass R. Insights into gastroesophageal reflux disease-associated dyspeptic symptoms. Clin Gastroenterol Hepatol. 2011;9:824–833. doi: 10.1016/j.cgh.2011.05.015. [DOI] [PubMed] [Google Scholar]
  • 101.Bredenoord AJ, Weusten BL, Timmer R, Smout AJ. Air swallowing, belching, and reflux in patients with gastroesophageal reflux disease. Am J Gastroenterol. 2006;101:1721–1726. doi: 10.1111/j.1572-0241.2006.00687.x. [DOI] [PubMed] [Google Scholar]
  • 102.Morton JM, Bowers SP, Lucktong TA, Mattar S, Bradshaw WA, Behrns KE, Koruda MJ, Herbst CA, McCartney W, Halkar RK, Smith CD, Farrell TM. Gallbladder function before and after fundoplication. J Gastrointest Surg. 2002;6:806–10; discussion 810. doi: 10.1016/s1091-255x(02)00087-2. [DOI] [PubMed] [Google Scholar]
  • 103.Aamodt AH, Stovner LJ, Hagen K, Zwart JA. Comorbidity of headache and gastrointestinal complaints. The Head-HUNT Study. Cephalalgia. 2008;28:144–151. doi: 10.1111/j.1468-2982.2007.01486.x. [DOI] [PubMed] [Google Scholar]
  • 104.Jung HK, Choung RS, Talley NJ. Gastroesophageal reflux disease and sleep disorders: evidence for a causal link and therapeutic implications. J Neurogastroenterol Motil. 2010;16:22–29. doi: 10.5056/jnm.2010.16.1.22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Yandrapu H, Marcinkiewicz M, Poplawski C, Han K, Zbroch T, Goldin G, Sarosiek I, Namiot Z, Sarosiek J. Role of saliva in esophageal defense: implications in patients with nonerosive reflux disease. Am J Med Sci. 2015;349:385–391. doi: 10.1097/MAJ.0000000000000443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Gharaibeh TM, Jadallah K, Jadayel FA. Prevalence of temporomandibular disorders in patients with gastroesophageal reflux disease: a case-controlled study. J Oral Maxillofac Surg. 2010;68:1560–1564. doi: 10.1016/j.joms.2009.06.027. [DOI] [PubMed] [Google Scholar]
  • 107.Irwin RS, Corrao WM, Pratter MR. Chronic persistent cough in the adult: the spectrum and frequency of causes and successful outcome of specific therapy. Am Rev Respir Dis. 1981;123:413–417. doi: 10.1164/arrd.1981.123.4.413. [DOI] [PubMed] [Google Scholar]
  • 108.Fraser AG. Review article: gastro-oesophageal reflux and laryngeal symptoms. Aliment Pharmacol Ther. 1994;8:265–272. doi: 10.1111/j.1365-2036.1994.tb00287.x. [DOI] [PubMed] [Google Scholar]
  • 109.Mallah N, Turner JM, González-Barcala FJ, Takkouche B. Gastroesophageal reflux disease and asthma exacerbation: A systematic review and meta-analysis. Pediatr Allergy Immunol. 2022;33:e13655. doi: 10.1111/pai.13655. [DOI] [PubMed] [Google Scholar]
  • 110.Miura MS, Mascaro M, Rosenfeld RM. Association between otitis media and gastroesophageal reflux: a systematic review. Otolaryngol Head Neck Surg. 2012;146:345–352. doi: 10.1177/0194599811430809. [DOI] [PubMed] [Google Scholar]
  • 111.Lin YH, Chang TS, Yao YC, Li YC. Increased Risk of Chronic Sinusitis in Adults With Gastroesophgeal Reflux Disease: A Nationwide Population-Based Cohort Study. Medicine (Baltimore) 2015;94:e1642. doi: 10.1097/MD.0000000000001642. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Liu J, Wang W, Wang Y, Wu D, Sun C, Lv C, Wu D, Yu Y. Subjective Changes of Taste and Smell in Conjunction With Anxiety and Depression Are Associated With Symptoms in Globus Patients Without Evidence of Pathologic Acid Reflux. J Clin Gastroenterol. 2022;56:505–511. doi: 10.1097/MCG.0000000000001603. [DOI] [PubMed] [Google Scholar]
  • 113.Kabadi A, Saadi M, Schey R, Parkman HP. Taste and Smell Disturbances in Patients with Gastroparesis and Gastroesophageal Reflux Disease. J Neurogastroenterol Motil. 2017;23:370–377. doi: 10.5056/jnm16132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.Wang FW, Tu MS, Chuang HY, Yu HC, Cheng LC, Hsu PI. Erosive esophagitis in asymptomatic subjects: risk factors. Dig Dis Sci. 2010;55:1320–1324. doi: 10.1007/s10620-009-0888-z. [DOI] [PubMed] [Google Scholar]
  • 115.Spechler SJ, Genta RM, Souza RF. Thoughts on the complex relationship between gastroesophageal reflux disease and eosinophilic esophagitis. Am J Gastroenterol. 2007;102:1301–1306. doi: 10.1111/j.1572-0241.2007.01179.x. [DOI] [PubMed] [Google Scholar]
  • 116.Rosołowski M, Kierzkiewicz M. Etiology, diagnosis and treatment of infectious esophagitis. Prz Gastroenterol. 2013;8:333–337. doi: 10.5114/pg.2013.39914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Zografos GN, Georgiadou D, Thomas D, Kaltsas G, Digalakis M. Drug-induced esophagitis. Dis Esophagus. 2009;22:633–637. doi: 10.1111/j.1442-2050.2009.00972.x. [DOI] [PubMed] [Google Scholar]
  • 118.Spechler SJ, Souza RF, Rosenberg SJ, Ruben RA, Goyal RK. Heartburn in patients with achalasia. Gut. 1995;37:305–308. doi: 10.1136/gut.37.3.305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119.Liu JJ, Kahrilas PJ. Pharyngeal and esophageal diverticula, rings, and webs. GI Motility Online. 2006 [Google Scholar]
  • 120.Jehangir A, Parkman HP. Reflux Symptoms in Gastroparesis: Correlation With Gastroparesis Symptoms, Gastric Emptying, and Esophageal Function Testing. J Clin Gastroenterol. 2020;54:428–438. doi: 10.1097/MCG.0000000000001190. [DOI] [PubMed] [Google Scholar]
  • 121.Najm WI. Peptic ulcer disease. Prim Care. 2011;38:383–394, vii. doi: 10.1016/j.pop.2011.05.001. [DOI] [PubMed] [Google Scholar]
  • 122.Sapone A, Bai JC, Ciacci C, Dolinsek J, Green PH, Hadjivassiliou M, Kaukinen K, Rostami K, Sanders DS, Schumann M, Ullrich R, Villalta D, Volta U, Catassi C, Fasano A. Spectrum of gluten-related disorders: consensus on new nomenclature and classification. BMC Med. 2012;10:13. doi: 10.1186/1741-7015-10-13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Drossman DA. Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features and Rome IV. Gastroenterology. 2016;150:1262–1279.e2. doi: 10.1053/j.gastro.2016.02.032. [DOI] [PubMed] [Google Scholar]
  • 124.Abbas G, Krasna M. Overview of esophageal cancer. Ann Cardiothorac Surg. 2017;6:131–136. doi: 10.21037/acs.2017.03.03. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Tougas G, Spaziani R, Hollerbach S, Djuric V, Pang C, Upton AR, Fallen EL, Kamath MV. Cardiac autonomic function and oesophageal acid sensitivity in patients with non-cardiac chest pain. Gut. 2001;49:706–712. doi: 10.1136/gut.49.5.706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Pera M, Trastek VF, Carpenter HA, Fernandez PL, Cardesa A, Mohr U, Pairolero PC. Influence of pancreatic and biliary reflux on the development of esophageal carcinoma. Ann Thorac Surg. 1993;55:1386–92; discussion 1392. doi: 10.1016/0003-4975(93)91077-z. [DOI] [PubMed] [Google Scholar]
  • 127.Goh KL, Chang CS, Fock KM, Ke M, Park HJ, Lam SK. Gastro-oesophageal reflux disease in Asia. J Gastroenterol Hepatol. 2000;15:230–238. doi: 10.1046/j.1440-1746.2000.02148.x. [DOI] [PubMed] [Google Scholar]
  • 128.Friedland GW. Progress in radiology: historical review of the changing concepts of lower esophageal anatomy: 430 B.C.--1977. AJR Am J Roentgenol. 1978;131:373–378. doi: 10.2214/ajr.131.3.373. [DOI] [PubMed] [Google Scholar]
  • 129.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;67:430–440. doi: 10.1136/gutjnl-2016-313589. [DOI] [PubMed] [Google Scholar]
  • 130.Seto KC, Fragkias M, Güneralp B, Reilly MK. A meta-analysis of global urban land expansion. PLoS One. 2011;6:e23777. doi: 10.1371/journal.pone.0023777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Hampel H, Abraham NS, El-Serag HB. Meta-analysis: obesity and the risk for gastroesophageal reflux disease and its complications. Ann Intern Med. 2005;143:199–211. doi: 10.7326/0003-4819-143-3-200508020-00006. [DOI] [PubMed] [Google Scholar]
  • 132.Corley DA, Kubo A. Body mass index and gastroesophageal reflux disease: a systematic review and meta-analysis. Am J Gastroenterol. 2006;101:2619–2628. doi: 10.1111/j.1572-0241.2006.00849.x. [DOI] [PubMed] [Google Scholar]
  • 133.Söderholm JD. Stress-related changes in oesophageal permeability: filling the gaps of GORD? Gut. 2007;56:1177–1180. doi: 10.1136/gut.2007.120691. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.Fass R, Quan SF, O'Connor GT, Ervin A, Iber C. Predictors of heartburn during sleep in a large prospective cohort study. Chest. 2005;127:1658–1666. doi: 10.1378/chest.127.5.1658. [DOI] [PubMed] [Google Scholar]
  • 135.Song JH, Chung SJ, Lee JH, Kim YH, Chang DK, Son HJ, Kim JJ, Rhee JC, Rhee PL. Relationship between gastroesophageal reflux symptoms and dietary factors in Korea. J Neurogastroenterol Motil. 2011;17:54–60. doi: 10.5056/jnm.2011.17.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136.Gudjonsson H, McAuliffe TL, Kaye MD. [The effect of coffee and tea upon lower esophageal sphincteric function] Laeknabladid. 1995;81:484–488. [PubMed] [Google Scholar]
  • 137.Thomas FB, Steinbaugh JT, Fromkes JJ, Mekhjian HS, Caldwell JH. Inhibitory effect of coffee on lower esophageal sphincter pressure. Gastroenterology. 1980;79:1262–1266. [PubMed] [Google Scholar]
  • 138.Price SF, Smithson KW, Castell DO. Food sensitivity in reflux esophagitis. Gastroenterology. 1978;75:240–243. [PubMed] [Google Scholar]
  • 139.Murphy DW, Castell DO. Chocolate and heartburn: evidence of increased esophageal acid exposure after chocolate ingestion. Am J Gastroenterol. 1988;83:633–636. [PubMed] [Google Scholar]
  • 140.Riegler M, Kristo I, Asari R, Rieder E, Schoppmann SF. Dietary sugar and Barrett's esophagus. Eur Surg. 2017;49:279–281. doi: 10.1007/s10353-017-0494-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 141.Iwakiri K, Kobayashi M, Kotoyori M, Yamada H, Sugiura T, Nakagawa Y. Relationship between postprandial esophageal acid exposure and meal volume and fat content. Dig Dis Sci. 1996;41:926–930. doi: 10.1007/BF02091532. [DOI] [PubMed] [Google Scholar]
  • 142.Parasher A, Ranjan K. The prevalence of gastroesophageal reflux disease and its association with various risk factors in a tertiary care centre in West Bengal. Int J Res Med Sci. 2021;9:780. [Google Scholar]
  • 143.Yamamichi N, Mochizuki S, Asada-Hirayama I, Mikami-Matsuda R, Shimamoto T, Konno-Shimizu M, Takahashi Y, Takeuchi C, Niimi K, Ono S, Kodashima S, Minatsuki C, Fujishiro M, Mitsushima T, Koike K. Lifestyle factors affecting gastroesophageal reflux disease symptoms: a cross-sectional study of healthy 19864 adults using FSSG scores. BMC Med. 2012;10:45. doi: 10.1186/1741-7015-10-45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Pandeya N, Green AC, Whiteman DC Australian Cancer Study. Prevalence and determinants of frequent gastroesophageal reflux symptoms in the Australian community. Dis Esophagus. 2012;25:573–583. doi: 10.1111/j.1442-2050.2011.01287.x. [DOI] [PubMed] [Google Scholar]
  • 145.Nilsson M, Johnsen R, Ye W, Hveem K, Lagergren J. Lifestyle related risk factors in the aetiology of gastro-oesophageal reflux. Gut. 2004;53:1730–1735. doi: 10.1136/gut.2004.043265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 146.Avidan B, Sonnenberg A, Schnell TG, Sontag SJ. Temporal associations between coughing or wheezing and acid reflux in asthmatics. Gut. 2001;49:767–772. doi: 10.1136/gut.49.6.767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 147.Sun XM, Tan JC, Zhu Y, Lin L. Association between diabetes mellitus and gastroesophageal reflux disease: A meta-analysis. World J Gastroenterol. 2015;21:3085–3092. doi: 10.3748/wjg.v21.i10.3085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 148.Spence AD, Busby J, Murchie P, Kunzmann AT, McMenamin ÚC, Coleman HG, Johnston BT, O'Rorke MA, Murray LJ, Iversen L, Lee AJ, Cardwell CR. Medications that relax the lower oesophageal sphincter and risk of oesophageal cancer: An analysis of two independent population-based databases. Int J Cancer. 2018;143:22–31. doi: 10.1002/ijc.31293. [DOI] [PubMed] [Google Scholar]
  • 149.DiMarino AJ, Cohen S. The adrenergic control of lower esophageal sphincter function. An experimental model of denervation supersensitivity. J Clin Invest. 1973;52:2264–2271. doi: 10.1172/JCI107413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 150.Berquist WE, Rachelefsky GS, Kadden M, Siegel SC, Katz RM, Mickey MR, Ament ME. Effect of theophylline on gastroesophageal reflux in normal adults. J Allergy Clin Immunol. 1981;67:407–411. doi: 10.1016/0091-6749(81)90087-7. [DOI] [PubMed] [Google Scholar]
  • 151.Farrell RL, Roling GT, Castell DO. Stimulation of the incompetent lower esophageal sphincter. A possible advance in therapy of heartburn. Am J Dig Dis. 1973;18:646–650. doi: 10.1007/BF01072035. [DOI] [PubMed] [Google Scholar]

Articles from World Journal of Gastrointestinal Pharmacology and Therapeutics are provided here courtesy of Baishideng Publishing Group Inc

RESOURCES