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Prevalence of non-obstructive dysphagia in patients with heartburn and regurgitation

Abstract

OBJECTIVE:

Heartburn and regurgitation are the most common gastroesophageal reflux symptoms, and dysphagia could be a possible symptom. This investigation aimed to evaluate the prevalence of non-obstructive dysphagia in patients with heartburn and regurgitation.

METHODS:

A total of 147 patients (age, 20-70 years; women, 72%) complaining of heartburn and regurgitation, without esophageal stricture, previous esophageal surgery, or other diseases, were evaluated. Twenty-seven patients had esophagitis. The Eating Assessment Tool (EAT-10) was employed to screen for dysphagia; EAT-10 is composed of 10 items, and the patients rate each item from 0 to 4 (0, no problems; 4, most severe symptom). Results of the 147 patients were compared with those of 417 healthy volunteers (women, 62%; control group) aged 20-68 years.

RESULTS:

In the control group, only two (0.5%) had an EAT-10 score ≥5, which was chosen as the threshold to define dysphagia. EAT-10 scores ≥5 were found in 71 (48.3%) patients and in 55% of the patients with esophagitis and 47% of the patients without esophagitis. This finding indicates a relatively higher prevalence of perceived dysphagia in patients with heartburn and regurgitation and in patients with esophagitis. We also found a positive correlation between EAT-10 scores and the severity of gastroesophageal reflux symptoms based on the Velanovich scale.

CONCLUSION:

In patients with heartburn and regurgitation symptoms, the prevalence of dysphagia was at least 48%, and has a positive correlation with the overall symptoms of gastroesophageal reflux.

Dysphagia; Gastroesophageal Reflux; Deglutition; Deglutition Disorders; Heartburn; Esophagitis


INTRODUCTION

Gastroesophageal reflux disease (GERD) is prevalent worldwide (11. Yamasaki T, Hemond C, Eisa M, Ganocy S, Fass R. The Changing Epidemiology of Gastroesophageal Reflux Disease: Are Patients Getting Younger? J Neurogastroenterol Motil. 2018;24(4):559-69. https://doi.org/10.5056/jnm18140.
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,22. Vaezi MF, Sifrim D. Assessing Old and New Diagnostic Test for Gastroesophageal Reflux Disease. Gastroenterology. 2018;154(2):289-301. https://doi.org/10.1053/j.gastro.2017.07.040.
https://doi.org/10.1053/j.gastro.2017.07...
), and its incidence among young individuals has been increasing (11. Yamasaki T, Hemond C, Eisa M, Ganocy S, Fass R. The Changing Epidemiology of Gastroesophageal Reflux Disease: Are Patients Getting Younger? J Neurogastroenterol Motil. 2018;24(4):559-69. https://doi.org/10.5056/jnm18140.
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). Although the most frequent symptoms are heartburn and regurgitation, other symptoms, such as dysphagia, odynophagia, globus sensation, chest pain, belching, chronic cough, laryngitis, hoarseness, and asthma, may be present (33. Chen J, Brady P. Gastroesophageal Reflux Disease: Pathophysiology, Diagnosis, and Treatment. Gastroenterol Nurs. 2019;42(1):20-8. https://doi.org/10.1097/SGA.0000000000000359.
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,44. Fisichella PM, Schlottmann F, Patti MG. Evaluation of gastroesophageal reflux disease. Updates Surg. 2018;70(3):309-13. https://doi.org/10.1007/s13304-018-0563-z.
https://doi.org/10.1007/s13304-018-0563-...
).

Dysphagia means difficulty in swallowing that may occur in the oral, pharyngeal, or esophageal phases of swallowing (55. Clavé P, Shaker R. Dysphagia: current reality and scope of the problem. Nat Rev Gastroenterol Hepatol. 2015;12(5):259-70. https://doi.org/10.1038/nrgastro.2015.49.
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). Non-obstructive GERD is the most common identifiable cause of esophageal dysphagia (66. 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(32):4335-41. https://doi.org/10.3748/wjg.v18.i32.4335.
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,77. Cho SY, Choung RS, Saito YA, Schleck CD, Zinsmeister AR, Locke GR 3rd, et al. Prevalence and risk factors for dysphagia: a USA community study. Neurogastroenterol Motil. 2015;27(2):212-9. https://doi.org/10.1111/nmo.12467.
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) and the major cause in younger individuals. A previous study reported that non-obstructive GERD was observed in approximately 24% of the patients who sought treatment for dysphagia (66. 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(32):4335-41. https://doi.org/10.3748/wjg.v18.i32.4335.
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). Intermittent dysphagia is independently associated with GERD (88. Eslick GD, Talley NJ. Dysphagia: epidemiology, risk factors and impact on quality of life - a population-based study. Aliment Pharmacol Ther. 2008;27(10):971-9. https://doi.org/10.1111/j.1365-2036.2008.03664.x.
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), and 31.6% and 18% of patients with GERD have frequent and infrequent dysphagia, respectively (77. Cho SY, Choung RS, Saito YA, Schleck CD, Zinsmeister AR, Locke GR 3rd, et al. Prevalence and risk factors for dysphagia: a USA community study. Neurogastroenterol Motil. 2015;27(2):212-9. https://doi.org/10.1111/nmo.12467.
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). Moreover, 37-46.8% of patients with esophagitis reported dysphagia in previous studies (99. Vakil NB, Traxler B, Levine D. Dysphagia in patients with erosive esophagitis: prevalence, severity, and response to proton pump inhibitor treatment. Clin Gastroenterol Hepatol. 2004;2(8):665-8. https://doi.org/10.1016/S1542-3565(04)00289-7.
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,1010. Triadafilopoulos G. Nonobstructive dysphagia in reflux esophagitis. Am J Gastroenterol. 1989;84(6):614-8.).

Symptom descriptions based on self-reports with dichotomized answers, i.e., yes or no, are not always precise (1111. Heading RC, Thomas EC, Sandy P, Smith G, Fass R, Hungin PS. Discrepancies between upper GI symptoms described by those who have them and their identification by conventional medical terminology: a survey of sufferers in four countries. Eur J Gastroenterol Hepatol. 2016;28(4):455-62. https://doi.org/10.1097/MEG.0000000000000565.
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) and may be influenced by culture, beliefs, and ethnicity (1212. Fang X, Francisconi CF, Fukudo S, Gerson MJ, Kang JY, Schmulson WMJ, et al. Multicultural Aspects in Functional Gastrointestinal Disorders (FGIDs). Gastroenterology. 2016. pii: S0016-5085(16)00179-7.). Thus, we used the validated instrument Eating Assessment Tool (EAT-10), which evaluates dysphagia based on an individual’s perception, to determine the prevalence of dysphagia in patients with heartburn and regurgitation in Brazil.

EAT-10 is a quick, easy-to-complete, non-invasive, inexpensive, and self-administered screening tool, which is based on patient’s self-perception, to detect possible swallowing impairment before performing a more specific examination (1313. Belafsky PC, Mouadeb DA, Rees CJ, Pryor JC, Postma GN, Allen J, et al. Validity and reliability of the Eating Assessment Tool (EAT-10). Ann Otol Rhinol Laryngol. 2008;117(12):919-24. https://doi.org/10.1177/000348940811701210.
https://doi.org/10.1177/0003489408117012...
). This instrument has good internal consistency and test-retest reproducibility and validity (1313. Belafsky PC, Mouadeb DA, Rees CJ, Pryor JC, Postma GN, Allen J, et al. Validity and reliability of the Eating Assessment Tool (EAT-10). Ann Otol Rhinol Laryngol. 2008;117(12):919-24. https://doi.org/10.1177/000348940811701210.
https://doi.org/10.1177/0003489408117012...
,1414. Shapira-Galitz Y, Yousovich R, Halperin D, Wolf M, Lahav Y, Drendel M. Does the Hebrew Eating Assessment Tool-10 Correlate with Pharyngeal Residue, Penetration and Aspiration on Fiberoptic Endoscopic Examination of Swallowing? Dysphagia. 2019;34(3):372-81. https://doi.org/10.1007/s00455-018-9964-x.
https://doi.org/10.1007/s00455-018-9964-...
), with a sensitivity of 0.85 and specificity of 0.82 to detect dysphagia (1515. Rofes L, Arreola V, Mukherjee R, Clave P. Sensitivity and specificity of the Eating Assessment Tool and the Volume-Viscosity Swallow Test for clinical evaluation of oropharyngeal dysphagia. Neurogastroenterol Motil. 2014;26(9):1256-65. https://doi.org/10.1111/nmo.12382.
https://doi.org/10.1111/nmo.12382...
); moreover, it has the ability to predict aspiration (1616. Plowman EK, Tabor LC, Robison R, Gaziano J, Dion C, Watts SA, et al. Discriminant ability of the Eating Assessment Tool-10 to detect aspiration in individuals with amyotrophic lateral sclerosis. Neurogastroenterol Motil. 2016;28(1):85-90. https://doi.org/10.1111/nmo.12700.
https://doi.org/10.1111/nmo.12700...

17. Cheney DM, Siddiqui MT, Litts JK, Kuhn MA, Belafski PC. The Ability of the 10-Item Eating Assessment Tool (EAT-10) to Predict Aspiration Risk in Persons With Dysphagia. Ann Otol Rhinol Laryngol. 2015;124(5):351-4. https://doi.org/10.1177/0003489414558107.
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18. Regan J, Lawson S, De Aguiar V. The Eating Assessment Tool-10 Predicts Aspiration in Adults with Stable Chronic Obstructive Pulmonary Disease. Dysphagia. 2017;32(5):714-20. https://doi.org/10.1007/s00455-017-9822-2.
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19. Arslan SS, Demir N, Kilinç HE, Karaduman AA. The Ability of the Eating Assessment Tool-10 to Detect Aspiration in Patients With Neurological Disorders. J Neurogastroenterol Motil. 2017;23(4):550-4. https://doi.org/10.5056/jnm16165.
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-2020. Zuniga SA, Ebersole B, Jamal N. Utility of Eating Assessment Tool-10 in Predicting Aspiration in Patients with Unilateral Vocal Fold Paralysis. Otolaryngol Head Neck Surg. 2018;159(1):92-6. https://doi.org/10.1177/0194599818762328.
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). EAT-10 is recommended as the first-line screening tool for at-risk patients (1515. Rofes L, Arreola V, Mukherjee R, Clave P. Sensitivity and specificity of the Eating Assessment Tool and the Volume-Viscosity Swallow Test for clinical evaluation of oropharyngeal dysphagia. Neurogastroenterol Motil. 2014;26(9):1256-65. https://doi.org/10.1111/nmo.12382.
https://doi.org/10.1111/nmo.12382...
), has been validated in different languages, and is currently used for dysphagia evaluation in different populations (1414. Shapira-Galitz Y, Yousovich R, Halperin D, Wolf M, Lahav Y, Drendel M. Does the Hebrew Eating Assessment Tool-10 Correlate with Pharyngeal Residue, Penetration and Aspiration on Fiberoptic Endoscopic Examination of Swallowing? Dysphagia. 2019;34(3):372-81. https://doi.org/10.1007/s00455-018-9964-x.
https://doi.org/10.1007/s00455-018-9964-...
,2121. Gonçalves MI, Remaili CB, Behlau M. Cross-cultural adaptation of the Brazilian version of the Eating Assessment Tool - EAT-10. Codas. 2013;25(6):601-4. https://doi.org/10.1590/S2317-17822013.05000012.
https://doi.org/10.1590/S2317-17822013.0...

22. Demir N, Serel Arslan S, Inal O, Karaduman AA. Reliability and Validity of the Turkish Eating Assessment Tool (T-EAT-10). Dysphagia. 2016;31(5):644-9. https://doi.org/10.1007/s00455-016-9723-9.
https://doi.org/10.1007/s00455-016-9723-...

23. Nogueira DS, Ferreira PL, Reis EA, Lopes IS. Measuring Outcomes for Dysphagia: Validity and Reliability of the European Portuguese Eating Assessment Tool (P-EAT-10). Dysphagia. 2015;30(5):511-20. https://doi.org/10.1007/s00455-015-9630-5.
https://doi.org/10.1007/s00455-015-9630-...

24. Giraldo-Cadavid LF, Gutiérrez-Achury AM, Ruales-Suárez K, Rengifo-Varona ML, Barros C, Posada A, et al. Validation of the Spanish Version of the Eating Assessment Tool-10 (EAT-10spa) in Colombia. A Blinded Prospective Cohort Study. Dysphagia. 2016;31(3):398-406. https://doi.org/10.1007/s00455-016-9690-1.
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25. Schindler A, Mozzanica F, Monzani A, Ceriani E, Atac M, Jukic-Peladic N, et al. Reliability and validity of the Italian Eating Assessment Tool. Ann Otol Rhinol Laryngol. 2013;122(11):717-24. https://doi.org/10.1177/000348941312201109.
https://doi.org/10.1177/0003489413122011...

26. Burgos R, Sarto B, Segurola H, Romagosa A, Puiggrós C, Vázquez C, et al. [Translation and validation of the Spanish version of the EAT-10 (Eating Assessment Tool-10) for the screening of dysphagia]. Nutr Hosp. 2012;27(6):2048-54.

27. Wakabayashi H, Kayashita J. Translation, reliability, and validity of the Japanese version of the 10-item Eating Assessment Tool (EAT-10) for the screening of dysphagia. Jomyaku Keicho Eiyo. 2014;29(3):871-6.

28. Farahat M, Mesallam TA. Validation and Cultural Adaptation of the Arabic Version of the Eating Assessment Tool (EAT-10). Folia Phoniatr Logop. 2015;67(5):231-7. https://doi.org/10.1159/000442199.
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29. Printza A, Kyrgidis A, Pavlidou E, Triaridis S, Constantinidis J. Reliability and validity of the Eating Assessment Tool-10 (Greek adaptation) in neurogenic and head and neck cancer-related oropharyngeal dysphagia. Eur Arch Otorhinolaryngol. 2018;275(7):1861-8. https://doi.org/10.1007/s00405-018-5001-9.
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-3030. Kertscher B, Speyer R, Fong E, Georgiou AM, Smith M. Prevalence of oropharyngeal dysphagia in Netherlands: a telephone survey. Dysphagia. 2015;30(2):114-20. https://doi.org/10.1007/s00455-014-9584-z.
https://doi.org/10.1007/s00455-014-9584-...
). In addition, while this tool could be used for both oropharyngeal and esophageal dysphagia, it is most frequently used to detect the former (1313. Belafsky PC, Mouadeb DA, Rees CJ, Pryor JC, Postma GN, Allen J, et al. Validity and reliability of the Eating Assessment Tool (EAT-10). Ann Otol Rhinol Laryngol. 2008;117(12):919-24. https://doi.org/10.1177/000348940811701210.
https://doi.org/10.1177/0003489408117012...
). Each of the 10 questions can be rated from 0 to 4 (0, no problem; 4, severe swallowing problem). Previous investigations found that EAT-10 scores ≥3 is indicative of dysphagia (1313. Belafsky PC, Mouadeb DA, Rees CJ, Pryor JC, Postma GN, Allen J, et al. Validity and reliability of the Eating Assessment Tool (EAT-10). Ann Otol Rhinol Laryngol. 2008;117(12):919-24. https://doi.org/10.1177/000348940811701210.
https://doi.org/10.1177/0003489408117012...
,1414. Shapira-Galitz Y, Yousovich R, Halperin D, Wolf M, Lahav Y, Drendel M. Does the Hebrew Eating Assessment Tool-10 Correlate with Pharyngeal Residue, Penetration and Aspiration on Fiberoptic Endoscopic Examination of Swallowing? Dysphagia. 2019;34(3):372-81. https://doi.org/10.1007/s00455-018-9964-x.
https://doi.org/10.1007/s00455-018-9964-...
,2323. Nogueira DS, Ferreira PL, Reis EA, Lopes IS. Measuring Outcomes for Dysphagia: Validity and Reliability of the European Portuguese Eating Assessment Tool (P-EAT-10). Dysphagia. 2015;30(5):511-20. https://doi.org/10.1007/s00455-015-9630-5.
https://doi.org/10.1007/s00455-015-9630-...
,2626. Burgos R, Sarto B, Segurola H, Romagosa A, Puiggrós C, Vázquez C, et al. [Translation and validation of the Spanish version of the EAT-10 (Eating Assessment Tool-10) for the screening of dysphagia]. Nutr Hosp. 2012;27(6):2048-54.), and this cut-off value has a sensitivity of 0.76 and specificity of 0.75 (3131. Heijnen BJ, Speyer R, Bülow M, Kuijpers LM. “What About Swallowing” Diagnostic Performance of Daily Clinical Practice Compared with the Eating Assessment Tool-10. Dysphagia. 2016;31(2):214-22. https://doi.org/10.1007/s00455-015-9680-8.
https://doi.org/10.1007/s00455-015-9680-...
).

This study hypothesized that dysphagia is highly prevalent in patients with heartburn and regurgitation and is associated with the overall gastroesophageal reflux symptoms.

MATERIALS AND METHODS

In this study, EAT-10 was administered to 147 patients (106 [72%] women, 41 [28%] men) aged 20-68 years (mean 43.2 [13.2] years) who had heartburn and regurgitation (Table 1). The patients completed the instrument just before endoscopic examination in a public tertiary hospital. They also responded to the questionnaire on reflux symptoms proposed by Velanovich et al. (3232. Velanovich V, Vallance SR, Gusz JR, Tapia FV, Harkabus MA. Quality of life scale for gastroesophageal reflux disease. J Am Coll Surg. 1996;183(3):217-24.), which was translated to Portuguese (3333. Fornari F, Gruber AC, Lopes Ade B, Cecchetti D, de Barros SG. [Symptom’s questionnaire for gastroesophageal reflux disease]. Arq Gastroenterol. 2004;41(4):263-7. https://doi.org/10.1590/S0004-28032004000400012.
https://doi.org/10.1590/S0004-2803200400...
). Each of the 10 items in the questionnaire could be rated from a 0 to 5 (0, no symptom; 5, incapacitating symptom), with a possible total rating ranging from 0 to 50. None of the patients had esophageal stricture, history of previous surgery of the upper digestive tract, or other diseases, and they did not receive proton pump inhibitors regularly.

Table 1
Characteristics of the groups evaluated by the Eating Assessment Tool (EAT-10).

Endoscopic examination revealed esophagitis in 25 patients (11 Los Angeles classification (LA) grade A (3434. Lundell LR, Dent J, Bennett JR, Blum AL, Armstrong D, Galmiche JP, et al. Endoscopic assessment of oesophagitis: clinical and functional correlates and further validation of Los Angeles classification. Gut. 1999;45(2):172-80. https://doi.org/10.1136/gut.45.2.172.
https://doi.org/10.1136/gut.45.2.172...
), 11 LA grade B, two LA grade C, and one LA grade D), and two patients had Barrett’s esophagus. No endoscopic abnormality was found in the remaining 120 patients; moreover, none of the patients had pharyngeal or esophageal strictures, cancer, or eosinophilic esophagitis based on endoscopic findings. Twenty-four-hour intraesophageal pH monitoring was performed in 38 patients, with a pH probe placed 5 cm above the lower esophageal sphincter after manometry. Excessive reflux was considered when the acid exposure time (intraesophageal pH <4) was greater than 6% of the monitoring time (3535. Gyawali CP, Kahrilas PJ, Savarino E, Zerbib F, Mion F, Smout AJPM, et al. Modern diagnosis of GERD: the Lyon Consensus. Gut. 2018;67(7):1351-62. https://doi.org/10.1136/gutjnl-2017-314722.
https://doi.org/10.1136/gutjnl-2017-3147...
).

EAT-10 was also administered to 417 healthy individuals (control group). These individuals had no disease, symptoms, or previous surgery of the upper digestive tract and were not treated for any disease. This group was composed of 257 (62%) women and 160 (38%) men aged 20 to 70 years (mean 37.9 [14.3] years).

This study was approved by the Human Research Committee of the university hospital (IRB numbers 9635/2013 and 12220/2016). Written informed consent was obtained from each participant, and anonymity of all participants was guaranteed. The EAT-10 questionnaire was translated from the original version to Brazilian Portuguese and validated (2121. Gonçalves MI, Remaili CB, Behlau M. Cross-cultural adaptation of the Brazilian version of the Eating Assessment Tool - EAT-10. Codas. 2013;25(6):601-4. https://doi.org/10.1590/S2317-17822013.05000012.
https://doi.org/10.1590/S2317-17822013.0...
) (Table 2).

Table 2
Eating Assessment Tool (EAT-10) in Brazilian Portuguese.

Statistical analysis was performed by non-parametric tests, the Mann-Whitney test, Kruskal-Wallis test with pos-test of Dunn, and Spearman test of correlation. The program used was SAS 9.2 (SAS Inst., Cary NC, 2011). The results are shown in mean, standard deviation, median, correlation coefficient (rho), and percentage. A p value ≤0.05 was considered significant.

RESULTS

Figure 1 shows the EAT-10 scores in the control and study groups. The total score ranged from 0 to 8 (mean 0.59, median 0) in the control group and from 0 to 37 (mean 9.2, median 4) in the study group (Table 1). If we consider EAT-10 scores ≥3 as the threshold to define dysphagia, 29 controls (6.9%) and 95 patients (64.6%) had dysphagia. Almost all controls (99.3%) had EAT-10 scores ≤4, which we used as the threshold to define dysphagia in our study. Using this threshold, the number of patients with dysphagia was 71(48.3%). Mean EAT-10 score in patients with dysphagia (EAT-10 ≥5) was 17.5, and the median was 18 (range 5-37).

Figure 1
Eating Assessment Tool (EAT -10) scores.

Moreover, mean EAT-10 score was 10.0 (9.9) in patients with esophagitis and 9.1(10.2) in patients without esophagitis (p>0.05). EAT-10 score ≥5 was noted in 56% of the patients with esophagitis and 47% of the patients without esophagitis (p>0.05). A positive correlation between EAT-10 scores and Velanovich scores was found (p<0.01; Table 3). Mean Velanovich score was 30.3 (10.2), with a median of 31.

Table 3
Correlation of age, height, body mass index, and Velanovich score with EAT-10 scores (Spearman’s correlation coefficient [rho]).

In addition, 20% of the patients who performed the manometric examination had a diagnosis of ineffective esophageal motility, with no association with EAT-10 scores (p>0.05), which suggested that a higher EAT-10 score may be observed in patients with or without ineffective esophageal motility.

DISCUSSION

Based on the threshold of EAT-10 score ≥3, 64.6% of the patients with heartburn and regurgitation had dysphagia, and using the threshold EAT-10 score of ≥5, we found that 48.3% of the patients have dysphagia. These findings indicated a high frequency of dysphagia among the patients evaluated in Brazil.

In the patients included in this study, several conditions may have been associated with heartburn and regurgitation, including erosive GERD, non-erosive GERD, reflux hypersensitivity, and functional heartburn (3636. Katzka DA, Pandolfino JE, Kahrilas PJ. Phenotypes of Gastroesophageal Reflux Disease: Where Rome, Lyon, and Montreal Meet. Clin Gastroenterol Hepatol. 2019. pii: S1542-3565(19)30748-7.). Although heartburn and regurgitation are the most frequent symptoms of GERD, the sensitivity and specificity of these symptoms for the identification of GERD are insufficient (sensitivity, 65%; specificity, 75%) (22. Vaezi MF, Sifrim D. Assessing Old and New Diagnostic Test for Gastroesophageal Reflux Disease. Gastroenterology. 2018;154(2):289-301. https://doi.org/10.1053/j.gastro.2017.07.040.
https://doi.org/10.1053/j.gastro.2017.07...
,44. Fisichella PM, Schlottmann F, Patti MG. Evaluation of gastroesophageal reflux disease. Updates Surg. 2018;70(3):309-13. https://doi.org/10.1007/s13304-018-0563-z.
https://doi.org/10.1007/s13304-018-0563-...
).

The presence of dysphagia in patients with heartburn and regurgitation may be explained by the following:

  1. Upper esophageal sphincter (UES) dysfunction.

    Gastroesophageal reflux could influence UES function. Patients with GERD have longer UES opening during deglutition, which means a longer time for the bolus to pass through the sphincter (3737. Mendell DA, Logemman JA. A retrospective analysis of the pharyngeal swallow in patients with clinical diagnosis of GERD compared with normal controls: a pilot study. Dysphagia. 2002;17(3):220-6. https://doi.org/10.1007/s00455-002-0056-5.
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    ,3838. Cassiani RA, Mota GA, Dantas RO. Oral and pharyngeal bolus transit in gastroesophageal reflux disease. Esophagus. 2015;12(4):345-51. https://doi.org/10.1007/s10388-014-0481-1.
    https://doi.org/10.1007/s10388-014-0481-...
    ). Other UES changes have been described, such as short and hypotonic sphincter (3939. Nadaleto BF, Herbella FA, Pinna BR, Patti MG. Upper esophageal sphincter motility in gastroesophageal reflux disease in the light of the high-resolution manometry. Dis Esophagus. 2017;30(4):1-5. https://doi.org/10.1093/dote/dox001.
    https://doi.org/10.1093/dote/dox001...
    ) and increased UES pressure associated with transient lower esophageal sphincter relaxation (4040. Kim HI, Hong SJ, Han JP, Seo JY, Hwang KH, Maeng HJ, et al. Specific movement of esophagus during transient lower esophageal sphincter relaxation in gastroesophageal reflux disease. J Neurogastroenterol Motil. 2013;19(3):332-7. https://doi.org/10.5056/jnm.2013.19.3.332.
    https://doi.org/10.5056/jnm.2013.19.3.33...
    ). Reflux events cause an intraesophageal pressure increase, which evokes UES contractile response (4141. Torrico S, Kern M, Aslam M, Narayanan S, Kannappan A, Ren J, et al. Upper esophageal sphincter function during gastroesophageal reflux events revisited. Am J Physiol Gastrointest Liver Physiol. 2000;279(2):G262-7. https://doi.org/10.1152/ajpgi.2000.279.2.G262.
    https://doi.org/10.1152/ajpgi.2000.279.2...
    ). Chronic acid exposure in the esophageal body could cause hypertonicity of the UES and thus difficulty in opening (4242. Bognár L, Vereczkei A, Papp A, Jancsó G, HorváthO P. Gastroesophageal Reflux Disease Might Induce Certain-Supposedly Adaptive-Changes in Esophagus: A Hypothesis. Dig Dis Sci. 2018;63(10):2529-35. https://doi.org/10.1007/s10620-018-5184-3.
    https://doi.org/10.1007/s10620-018-5184-...
    ). The UES opening diameter during swallowing was smaller in patients with than in those without hiatal hernia (4343. Nativ-Zeltzer N, Rameau A, Kuhn MA, Kaufman M, Belafsky PC. The Relationship Between Hiatal Hernia and Cricopharyngeus Muscle Dysfunction. Dysphagia. 2019;34(3):391-6. https://doi.org/10.1007/s00455-018-9950-3.
    https://doi.org/10.1007/s00455-018-9950-...
    ). Slower passage of the bolus through the UES has been associated with dysphagia in patients with esophagitis (3838. Cassiani RA, Mota GA, Dantas RO. Oral and pharyngeal bolus transit in gastroesophageal reflux disease. Esophagus. 2015;12(4):345-51. https://doi.org/10.1007/s10388-014-0481-1.
    https://doi.org/10.1007/s10388-014-0481-...
    ), and a slower bolus transit through the pharynx has also been reported in the disease (3737. Mendell DA, Logemman JA. A retrospective analysis of the pharyngeal swallow in patients with clinical diagnosis of GERD compared with normal controls: a pilot study. Dysphagia. 2002;17(3):220-6. https://doi.org/10.1007/s00455-002-0056-5.
    https://doi.org/10.1007/s00455-002-0056-...
    ,3838. Cassiani RA, Mota GA, Dantas RO. Oral and pharyngeal bolus transit in gastroesophageal reflux disease. Esophagus. 2015;12(4):345-51. https://doi.org/10.1007/s10388-014-0481-1.
    https://doi.org/10.1007/s10388-014-0481-...
    ). A recent investigation found that patients with reflux-associated dysphagia have delayed airway closure relative to the arrival of the bolus at the UES, suggesting a delay in airway protection when the bolus is already in the pharynx (4444. Kendall KA. Airway Closure Delay: The Predominant Pathophysiology in Reflux-Associated Dysphagia. Otolaryngol Head Neck Surg. 2019;160(5):885-90. https://doi.org/10.1177/0194599818824302.
    https://doi.org/10.1177/0194599818824302...
    ).

  2. Hypersensitivity

    Some patients with heartburn may have abnormal esophageal sensitivity to acid (reflux hypersensitivity), which is characteristic of a functional esophageal disorder (4545. Yamasaki T, Fass R. Reflux Hypersensitivity: A New Functional Esophageal Disorder. J Neurogastroenterol Motil. 2017;23(4):495-503. https://doi.org/10.5056/jnm17097.
    https://doi.org/10.5056/jnm17097...
    ). These patients have increased chemo- and mechano receptor sensitivity to acid perfusion and balloon distention (4545. Yamasaki T, Fass R. Reflux Hypersensitivity: A New Functional Esophageal Disorder. J Neurogastroenterol Motil. 2017;23(4):495-503. https://doi.org/10.5056/jnm17097.
    https://doi.org/10.5056/jnm17097...
    ). They manifest GERD symptoms during reflux even in the absence of abnormal acid exposure or esophagitis (4646. Farmer AD, Ruffle JK, Aziz Q. The Role of Esophageal Hypersensitivity in Functional Esophageal Disorders. J Clin Gastroenterol. 2017;51(2):91-9. https://doi.org/10.1097/MCG.0000000000000757.
    https://doi.org/10.1097/MCG.000000000000...
    ,4747. Kondo T, Miwa H. The Role of Esophageal Hypersensitivity in Functional Heartburn. J Clin Gastroenterol. 2017;51(7):571-8. https://doi.org/10.1097/MCG.0000000000000885.
    https://doi.org/10.1097/MCG.000000000000...
    ). In functional heartburn, the symptoms are not associated with gastroesophageal reflux. Nevertheless, functional esophageal disorders are associated with peripheral sensitization, central sensitization, and viscera-visceral hyperalgesia and cause a significant reduction in the quality of life (4646. Farmer AD, Ruffle JK, Aziz Q. The Role of Esophageal Hypersensitivity in Functional Esophageal Disorders. J Clin Gastroenterol. 2017;51(2):91-9. https://doi.org/10.1097/MCG.0000000000000757.
    https://doi.org/10.1097/MCG.000000000000...
    ,4848. Aziz Q, Fass R, Gyawali CP, Miwa H, Pandolfino JE, Zerbib F. Functional Esophageal disorders. Gastroenterology. 2016. pii:S0016-5085(16)00178-5.). Such hypersensitivity related to esophageal innervations (4646. Farmer AD, Ruffle JK, Aziz Q. The Role of Esophageal Hypersensitivity in Functional Esophageal Disorders. J Clin Gastroenterol. 2017;51(2):91-9. https://doi.org/10.1097/MCG.0000000000000757.
    https://doi.org/10.1097/MCG.000000000000...
    ) may increase patients’ perception of esophageal bolus transit during swallows, and stress, anxiety, and hypervigilance may have a role in the development of esophageal hypersensitivity (4949. Ribolsi M, Biasutto D, Giordano A, Balestrieri P, Cicala M. Role of Esophageal Motility, Acid Reflux, and of Acid Suppression in Nonobstructive Dysphagia. J Clin Gastroenterol. 2018;52(7):607-13.). In addition, calcitonin gene-related positive nerves, which is a marker of nociceptive sensory innervation, are more superficial in the proximal and distal esophagus of patients with non-erosive reflux disease, which may contribute to symptoms during swallows (5050. Woodland P, Shen Ooi JL, Grassi F, Nikaki K, Lee C, Evans JA, et al. Superficial Esophageal Mucosal Afferent Nerves May Contribute to Reflux Hypersensitivity in Nonerosive Reflux Disease. Gastroenterology. 2017;153(5):1230-9. https://doi.org/10.1053/j.gastro.2017.07.017.
    https://doi.org/10.1053/j.gastro.2017.07...
    ).

  3. Esophageal dismotility

    GERD may be the cause or the consequence of esophageal dismotility (5151. Gyawali CP, Roman S, Bredenoord AJ, Fox M, Keller J, Pandolfino JE, et al. Classification of esophageal motor findings in gastro-esophageal reflux disease: Conclusions from an international consensus group. Neurogastroenterol Motil. 2017;29(12). https://doi.org/10.1111/nmo.13104.
    https://doi.org/10.1111/nmo.13104...
    ,5252. Martinucci I, de Bortoli N, Giacchino M, Bodini G, Marabotto E, Marchi S, et al. Esophageal motility abnormalities in gastroesophageal reflux disease. World J Gastrointest Pharmacol Ther. 2014;5(2):86-96. https://doi.org/10.4292/wjgpt.v5.i2.86.
    https://doi.org/10.4292/wjgpt.v5.i2.86...
    ). The frequency and intensity of esophageal motility abnormalities increase with the severity of reflux disease (5252. Martinucci I, de Bortoli N, Giacchino M, Bodini G, Marabotto E, Marchi S, et al. Esophageal motility abnormalities in gastroesophageal reflux disease. World J Gastrointest Pharmacol Ther. 2014;5(2):86-96. https://doi.org/10.4292/wjgpt.v5.i2.86.
    https://doi.org/10.4292/wjgpt.v5.i2.86...
    ). Transient lower esophageal sphincter relaxation followed by reflux, hypotensive lower esophageal sphincter, ineffective esophageal peristalsis, and bolus transit abnormalities are strongly implicated in GERD (5353. Ribolsi M, Biasutto D, Giordano A, Balestrieri P, Cicala M. High-resolution Manometry Findings During Solid Swallows Correlate With Delayed Reflux Clearance and Acid Exposure Time in Non-erosive Reflux Disease Patients. J Neurogastroenterol Motil. 2019;25(1):68-74. https://doi.org/10.5056/jnm18054.
    https://doi.org/10.5056/jnm18054...
    ). High-resolution esophageal manometry during solid swallows demonstrated motility abnormality in patients with a non-erosive disease, including ineffective swallows, large breaks, and decreased distal contractile integral, leading to a delay in acid clearance (5353. Ribolsi M, Biasutto D, Giordano A, Balestrieri P, Cicala M. High-resolution Manometry Findings During Solid Swallows Correlate With Delayed Reflux Clearance and Acid Exposure Time in Non-erosive Reflux Disease Patients. J Neurogastroenterol Motil. 2019;25(1):68-74. https://doi.org/10.5056/jnm18054.
    https://doi.org/10.5056/jnm18054...
    ). Excessive esophageal acid exposure with reduced esophageal peristaltic contractions may be seen in a high proportion of patients with dysphagia, even in those without heartburn and regurgitation (4949. Ribolsi M, Biasutto D, Giordano A, Balestrieri P, Cicala M. Role of Esophageal Motility, Acid Reflux, and of Acid Suppression in Nonobstructive Dysphagia. J Clin Gastroenterol. 2018;52(7):607-13.). These esophageal motility changes may be the cause of non-obstructive dysphagia (5454. Philpott H, Garg M, Tomic D, Balasubramanian S, Sweis R. Dysphagia: Thinking outside the box. World J Gastroenterol. 2017;23(38):6942-51. https://doi.org/10.3748/wjg.v23.i38.6942.
    https://doi.org/10.3748/wjg.v23.i38.6942...
    ).

Results of the EAT-10 were associated with the severity of gastroesophageal reflux symptoms, indicating that the intensity of overall symptoms is related to dysphagia severity. Depressive disorders are frequently comorbid with GERD (5555. Bilgi MM, Vardar R, Yildirim E, Veznedaroglu B, Bor S. Prevalence of Psychiatric Comorbidity in Symptomatic Gastroesophageal Reflux Subgroups. Dig Dis Sci. 2017;62(4):984-93. https://doi.org/10.1007/s10620-016-4273-4.
https://doi.org/10.1007/s10620-016-4273-...
) and may also be related to the intensity of the symptoms, including the perception of dysphagia.

Previous investigations found that the odds ratio for patients with heartburn to have frequent dysphagia is 5.9 and that for patients with acid regurgitation is 10.6 (77. Cho SY, Choung RS, Saito YA, Schleck CD, Zinsmeister AR, Locke GR 3rd, et al. Prevalence and risk factors for dysphagia: a USA community study. Neurogastroenterol Motil. 2015;27(2):212-9. https://doi.org/10.1111/nmo.12467.
https://doi.org/10.1111/nmo.12467...
). Among patients with dysphagia, 58% had heartburn, 67% had regurgitation, and 72% had GERD, and an association between intermittent dysphagia and GERD was observed (odds ratio, 2.96) (88. Eslick GD, Talley NJ. Dysphagia: epidemiology, risk factors and impact on quality of life - a population-based study. Aliment Pharmacol Ther. 2008;27(10):971-9. https://doi.org/10.1111/j.1365-2036.2008.03664.x.
https://doi.org/10.1111/j.1365-2036.2008...
). Functional dysphagia is not the most probable diagnosis because in the Rome IV criteria, GERD is an exclusion criterion for functional dysphagia, which is the least prevalent among functional esophageal disorders (4848. Aziz Q, Fass R, Gyawali CP, Miwa H, Pandolfino JE, Zerbib F. Functional Esophageal disorders. Gastroenterology. 2016. pii:S0016-5085(16)00178-5.). Although the definition of dysphagia and the methods of evaluation may differ and thus yield different results, the number of patients with symptomatic dysphagia is usually high, suggesting that, after endoscopy, esophageal manometry with provocation testing is an essential examination to determine the etiology of dysphagia.

This investigation has some limitations. The number of patients with an erosive disease was small; however, it still reflects the real-world situation, as only 30% of patients with heartburn have an erosive disease (3535. Gyawali CP, Kahrilas PJ, Savarino E, Zerbib F, Mion F, Smout AJPM, et al. Modern diagnosis of GERD: the Lyon Consensus. Gut. 2018;67(7):1351-62. https://doi.org/10.1136/gutjnl-2017-314722.
https://doi.org/10.1136/gutjnl-2017-3147...
). The 24-h pH monitoring was not performed in all subjects because of technical and cost limitations. The patients’ treatment for GERD with proton pump inhibitors was not regular; they were instructed to stop receiving the medications 1 week before endoscopy and pH monitoring. Adequate treatment for GERD decreases the frequency and severity of dysphagia (99. Vakil NB, Traxler B, Levine D. Dysphagia in patients with erosive esophagitis: prevalence, severity, and response to proton pump inhibitor treatment. Clin Gastroenterol Hepatol. 2004;2(8):665-8. https://doi.org/10.1016/S1542-3565(04)00289-7.
https://doi.org/10.1016/S1542-3565(04)00...
) and improves esophageal motility (4949. Ribolsi M, Biasutto D, Giordano A, Balestrieri P, Cicala M. Role of Esophageal Motility, Acid Reflux, and of Acid Suppression in Nonobstructive Dysphagia. J Clin Gastroenterol. 2018;52(7):607-13.).

Therefore, heartburn and regurgitation are associated with dysphagia, with somatization as a risk factor for non-obstructive dysphagia (57). The complaint of dysphagia in patients with no previous dysphagia may be a manifestation of a complication, such as a benign or malignant esophageal stricture. An anatomic cause of dysphagia, such as diverticula or hiatal hernias, may not be seen on endoscopy, however, it is unlikely to occur in these patients because they received medical attention and evaluations before the indication of endoscopy.

CONCLUSION

Using an EAT-10 score ≥5 as the threshold to define dysphagia, we found that 48% of patients with heartburn and regurgitation have dysphagia. This symptom has a positive correlation with the overall symptoms of gastroesophageal reflux, which suggested that the presence and intensity of dysphagia are related to the symptoms due to GERD.

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Publication Dates

  • Publication in this collection
    24 Jan 2020
  • Date of issue
    2020

History

  • Received
    26 Sept 2019
  • Accepted
    9 Dec 2019
Creative Common - by 4.0
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