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Journal of Neurogastroenterology and Motility logoLink to Journal of Neurogastroenterology and Motility
. 2016 Jan 30;22(1):86–93. doi: 10.5056/jnm15124

Recurrence and Its Impact on the Health-related Quality of Life in Patients with Gastroesophageal Reflux Disease: A Prospective Follow-up Analysis

Yang Won Min 1, Yong Woon Shin 2, Gab Jin Cheon 3, Kyung Sik Park 4, Hyun Soo Kim 5, Chong-Il Sohn 6, Tae Nyeun Kim 7, Hyeung Cheol Moon 8, Poong-Lyul Rhee 1,*
PMCID: PMC4699725  PMID: 26486229

Abstract

Background/Aims

Limited data exist on the outcome of gastroesophageal reflux disease (GERD) treatment and its impact on the health-related quality of life (HRQoL) in the Asian population. This study aims to evaluate the treatment outcomes, to investigate the factors associated with recurrence, and to evaluate the impact of the treatment outcome on the HRQoL in a Korean GERD population.

Methods

This was a prospective, multicenter study involving a total of 824 GERD patients. The response to treatment was assessed at week 4 (or week 8 for the patients who did not achieve complete resolution [CR] at week 4). The EQ-5D questionnaire was used at baseline, end of treatment, and first recurrence to assess the HRQoL. To assess GERD symptoms, contact of patients by phone at 1, 6, and 12 months following treatment was carried out.

Results

CR was achieved in 65.6% and recurrence was observed in 47.8% following treatment. CR and recurrence rates did not differ by the presence of esophagitis. Multivariate analysis revealed that acid regurgitation (odds ratio 2.249; 95% confidence interval 1.293–3.912; P = 0.004) and both acid regurgitation and heartburn (odds ratio 2.330; 95% confidence interval 1.392–3.901; P = 0.001) were independent risk factors for GERD recurrence. EQ-5D scores were more improved in patients with CR than in those without CR, and worsened more during follow-up in patients with recurrence than in those without recurrence.

Conclusions

We should achieve complete symptom relief and attempt to prevent recurrence in GERD patients to improve their HRQoL.

Keywords: Gastroesophageal reflux, Quality of life, Recurrence, Therapy

Introduction

Although proton pump inhibitor (PPI) therapy is effective for patients with gastroesophageal reflux disease (GERD), many patients will relapse over time when they are no longer taking PPIs.13 Thus, maintenance PPI therapy is recommended for patients who continue to have symptoms after discontinuing PPIs, and for patients with complications including erosive esophagitis and Barrett’s esophagus. In Eastern Asia, the lifestyle and dietary habits have changed towards a more Western style, and the prevalence of GERD is likely to have increased as a result.49 However, limited data exist on the response to PPI therapy and the recurrence of GERD in East Asian countries, including Korea.1013

Patients with GERD have a decreased health-related quality of life (HRQoL).12,14,15 Although HRQoL improves with treatment, persistent symptoms after PPI therapy are associated with a reduced HRQoL.14,16,17 However it is unclear how the recurrence of GERD symptoms impacts patients’ HRQoL. Furthermore, there have been no reports regarding the difference in the impact of relapsed GERD symptoms on HRQoL between patients with erosive reflux disease (ERD) and non-erosive reflux disease (NERD).

The aim of the current study is to evaluate the response rate to PPI therapy and the post-treatment recurrence rate in a Korean GERD population. In addition, we investigated the factors associated with recurrence and assess HRQoL in patients with GERD.

Materials and Methods

Study Design and Population

This was a prospective, multicenter, observational study involving a total of 857 GERD patients among 23 hospitals in South Korea. Patients aged between 20 and 80 years, who complained of typical reflux symptoms of heartburn and/or regurgitation were consecutively enrolled into this study. The study subjects underwent an upper endoscopy within the preceding 12 months and were supposed to take no acid suppressing agents at least 4 weeks before enrollment. The first subject was enrolled on the 7th of July 2011 and the last visit of all subjects was on the 21st of September 2013. Subjects who fell under any of the following criteria were excluded: (1) any previous gastrointestinal surgery; (2) any malignancies; (3) significant medical comorbidity including ischemic heart disease, chronic renal disease, congestive heart failure, chronic obstructive pulmonary disease, liver cirrhosis, and acute or chronic pancreatitis; (4) pregnant or nursing women; (5) subjects who participated in another clinical study within 30 days or are currently enrolled in; and (6) other conditions likely to interfere with study procedures, as judged by the investigator. Of the participating subjects, 33 were excluded from the study: 13 used acid suppressing agents during the 4 week period preceding enrollment, 10 had histories of malignancy, 7 had significant ischemic heart disease or chronic renal disease, and 5 had no typical reflux symptoms. Finally, a total of 824 consecutive patients were included in the current study (Fig. 1). This study protocol was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board at the Samsung Medical Center, Seoul, Korea (No. 2011-08-109). All subjects provided written informed consent before inclusion in the study.

Figure 1.

Figure 1

Patients flow.

Data Collection and Questionnaire

At baseline, data including age, gender, weight, height, waist circumference, hip circumference, smoking history, drinking history, concomitant medications, previous medical history, and previous GERD treatment history were collected. The response to treatment was assessed by interview with an attending physician at week 4 (or week 8 for the patients who did not achieve complete resolution [CR] at week 4).

The EuroQol-5D-3L18 (EQ-5D-3L) questionnaire was used at baseline, end of treatment (week 4 or week 8), and first recurrence (if applicable) to assess the impact of GERD on HRQoL. The EQ-5D-3L questionnaire consisted of a descriptive system and visual analogue scale (VAS). The EQ descriptive system comprises the following 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has 3 levels: no problems, some problems, and extreme problems. The EQ VAS records the respondent’s self-rated health on a vertical, visual analogue scale (from 0 to 100), where the endpoints are labelled “best imaginable health state” and “worst imaginable health state.” Higher scores represent a better health status.

To assess GERD symptoms, phone contact at 1, 6, and 12 months following the end of treatment was conducted on the subjects without recurring disease. This survey was conducted by the contract research company Gallup using structured questions. If a subject visited after a recurrence, a phone contact was only carried out at month 12.

Definitions and Assessments

Subjects were divided into ERD or NERD based on the endoscopic findings, according to the Los Angeles (LA) classification system.19 Subjects with at least grade LA-A esophagitis were included in the ERD group. Response to treatment was categorized into 4 grades (CR, ≥ 80% of the symptoms resolved; satisfactory resolution, ≤ 50% of the symptoms remained; partial response, ≥ 50% of the symptoms remained; and refractory response, no response to the 8-week PPI treatment). Recurrence was defined as the recurrence of typical symptoms of reflux after complete resolution of GERD symptoms.

The primary outcomes were the response rate to PPI treatment and the post-treatment recurrence rate. The secondary outcomes were the factors associated with the recurrence of GERD following PPI treatment and the difference between ERD and NERD in terms of the rate of CR with the treatment, the rate of recurrence, and HRQoL.

Statistical Methods

The current study is an observatory, descriptive study based on routine medical practice without any intervention except the measurement of HRQoL using verified questionnaires. Therefore, the estimation of the required number of subjects based on the estimation of statistical power could not be applied to this study. Considering the number of patients who visited 30 representative study sites during a 6 month period, our intended study period, we planned to recruit 2000 subjects. The full analysis set (n = 824) defined as the subject group without serious violation at enrollment was used for analysis, and the response to PPI treatment and recurrence could be confirmed in 611 subjects.

Continuous variables were compared parametrically using a Student’s t test or non-parametrically using the Mann-Whitney U-test. Categorical variables were compared using the χ2-test or Fisher’s exact test as appropriate. Multivariate analysis was performed on variables that were associated with recurrence based on univariate analysis (P < 0.2). Odds ratios (ORs) were presented together with 95% confidence intervals (CI). Statistical results are presented as the mean ± SD, median (minimum and maximum), or number of patients (%). Two-sided P-values < 0.05 were taken as statistically significant. Statistical analyses were conducted using SAS version 9.2 (SAS Institute Inc, Cary, North Carolina, USA).

Results

Subject Characteristics

Baseline characteristics of subjects are summarized in Table 1. The mean age was 53.7 ± 12.3 years and 361 patients (43.8%) were male. The mean height, weight, and body mass index (BMI) were 162.5 ± 8.3 cm, 62.1 ± 11.1 kg, and 23.4 ± 3.1 kg/m2, respectively. The mean waist circumference, hip circumference, and waist/hip (W/H) ratio were 84.4 ± 10.4 cm, 96.6 ± 9.0 cm, and 0.9 ± 0.1, respectively. A total of 150 subjects (18.2%) had hypertension. Regarding smoking, 589 subjects (71.5%) were non-smokers, 135 (16.4%) current smokers (mean 20.8 ± 12.3 pack-years), and 100 (12.1%) ex-smokers (mean 22.4 ± 13.8 pack-years). The number of times alcohol was drunk per week was 0.8 ± 1.6 times. Normal or minimal change lesion on endoscopy in the lower esophagus (NERD) was shown in 341 subjects (41.4%), while 483 (58.6%) had reflux esophagitis (ERD). Of the 824 subjects who participated in the current study, 281 (34.1%) complained of heartburn, 203 (24.6%) experienced regurgitation, and 340 (41.3%) had both. Atypical esophageal symptoms were also observed in 711 subjects (86.2%). The most prevalent symptom was epigastric burning in 542 subjects (76.2%), followed by globus sensation in 389 (54.7%), chest pain in 303 (42.6%), a cough in 250 (35.2%), hoarseness in 155 (21.8%), and wheezing in 78 (11.0%). The most common PPI used was esomeprazole (82.9%). The characteristics of all study participants are similar to that of subjects included in the response assessment.

Table 1.

Baseline Characteristics of Subjects

Variables All subjects (n = 824) Subjects included in response assessment (n = 611)
Age (yr) 53.7 ± 12.3 54.2 ± 12.2
Gender (male) 361 (43.8) 266 (43.5)
Height (cm) 162.5 ± 8.3 162.3 ± 8.3
Weight (kg) 62.1 ± 11.1 62.2 ± 11.2
Body mass index (kg/m2) 23.4 ± 3.1 23.5 ± 3.2
Waist circumference (cm) 84.4 ± 10.4 84.6 ± 10.5
Hip circumference (cm) 96.6 ± 9.0 96.8 ± 9.2
Waist/hip ratio 0.9 ± 0.1 0.9 ± 0.1
Hypertension 150 (18.2) 133 (18.5)
Smoking
 Non-smoker 589 (71.5) 449 (73.5)
 Ex-smoker 100 (12.1) 68 (11.1)
 Current smoker 135 (16.4) 94 (15.4)
Days of drinking per week 0.8 ± 1.6 0.8 ± 1.6
ERD:NERD 483 (58.6):341 (41.4) 358 (58.6):253 (41.4)
Typical reflux symptom
 Acid regurgitation 203 (24.6) 153 (25.0)
 Heartburn 281 (34.1) 212 (34.7)
 Both symptoms 340 (41.3) 246 (40.3)
Atypical esophageal symptom 711 (86.2) 530 (86.7)
Type of PPIa
 Esomeprazole 682 (82.9) 518 (84.8)
 Others 164 (20.0) 116 (18.9)
a

There were multiple counts.

ERD, erosive reflux disease; NERD, non-erosive reflux disease.

Data are shown as the mean ± SD or number (%) of patients.

Treatment Response and Recurrence Rate

Figure 2 shows the similar treatment responses between patients with ERD and NERD (P = 0.835). Among the 611 subjects assessed at the end of the treatment, a CR was present in 401 (65.6%), a satisfactory resolution in 132 (21.6%), a partial response in 70 (11.5%), and a refractory response in 8 (1.3%). The CR rate did not differ between patients with ERD and NERD (64.5% vs 67.2%, P = 0.494). Among the subjects with CR, recurrence was able to be assessed in 343, and of these, 164 subjects (47.8%) experienced recurrent symptoms following treatment, and the recurrence rate did not differ between patients with ERD and NERD (45.1% vs 51.3%, P = 0.250).

Figure 2.

Figure 2

Response at the end of the treatment. Among the 611 subjects assessed, a complete resolution was present in 401 (65.6%), a satisfactory resolution in 132 (21.6%), a partial response in 70 (11.5%) and a refractory response in 8 (1.3%). The treatment response did not differ between patients with erosive reflux disease (ERD) and non-erosive reflux disease (NERD).

Among the 329 subjects without CR at week 4, 111 achieved CR at week 8 and 218 did not. However, response at week 4 did not differ between the subjects with and without CR at week 8.

Factors Associated with Gastroesophageal Reflux Disease Recurrence

Factors associated with recurrence after complete resolution of GERD were investigated. There were no significant differences between patients with and without recurrence with respect to age, gender, BMI, W/H ratio, smoking, alcohol consumption, presence of reflux esophagitis, and atypical esophageal symptoms (Table 2). However, patients with acid regurgitation, and both acid regurgitation and heartburn, were more likely to recur than those with heartburn alone (31.1% and 43.3% vs 25.6%, respectively; P = 0.001). In addition, patients who achieved CR at week 4 showed a tendency to recur less often than those who achieved CR at week 8, with marginal statistical significance (44.6% vs 56.4%, P = 0.051).

Table 2.

Factors Associated with the Recurrence of Gastroesophageal Reflux Disease

Variables Recurrence (n = 164) No recurrence (n = 179) P-value
Age (yr) 54.3 ± 11.7 55.2 ± 11.8 0.476
Gender (male) 74 (45.1) 83 (46.4) 0.817
Body mass index (kg/m2) 23.6 ± 3.0 23.9 ± 3.2 0.520
Waist/hip ratio 0.9 ± 0.1 0.9 ± 0.1 0.285
Hypertension 32 (19.5) 34 (19.0) 0.903
Smoking 0.999
 Non-smoker 117 (71.3) 128 (71.5)
 Ex-smoker 21 (12.8) 23 (12.9)
 Current smoker 26 (15.9) 28 (15.6)
Days of drinking per week 1.7 ± 2.2 1.4 ± 1.8 0.224
ERD:NERD 87 (53.1):77 (46.9) 106 (59.2):73 (40.8) 0.250
Typical reflux symptom 0.001
 Heartburn 42 (25.6) 80 (44.7)
 Acid regurgitation 51 (31.1) 43 (24.0)
 Both symptoms 71 (43.3) 56 (31.3)
Atypical esophageal symptom 142 (86.6) 150 (83.8) 0.469
Complete remission 0.051
 At week 4 111 (44.6) 138 (55.4)
 At week 8 53 (56.4) 41 (43.6)

ERD, erosive reflux disease; NERD, non-erosive reflux disease

Data are shown as the mean ± SD or number (%) of patients.

Multivariate analysis using the two significant factors from univariate analysis revealed that acid regurgitation and both acid regurgitation and heartburn were independent risk factors associated with GERD recurrence (Table 3). Compared with heartburn, the ORs of acid regurgitation and both acid regurgitation and heartburn were 2.249 (95% CI, 1.293–3.912, P = 0.004) and 2.330 (95% CI, 1.392–3.901, P = 0.001), respectively.

Table 3.

Multivariate Analysis of Factors Associated with the Recurrence of Gastroesophageal Reflux Disease

Variables Multivariate analysis

OR (95% CI) P-value
Typical reflux symptom
 Heartburn 1.000
 Acid regurgitation 2.249 (1.293–3.912) 0.004
 Both symptoms 2.330 (1.392–3.901) 0.001
Complete remission
 At week 4 1.000
 At week 8 1.526 (0.937–2.488) 0.090

OR, odds ratio; CI, confidence interval.

Health-related Quality of Life

Figure 3 shows the change in HRQoL after treatment, according to the outcome. The EQ descriptive score showed a marked improvement in subjects with CR compared with those without CR (change from baseline of 0.06 ± 0.10 vs 0.03 ± 0.08, P < 0.001). The EQ VAS score also showed greater improvement in subjects with CR than in those without CR (change from baseline of 14.3 ± 17.9 vs 9.4 ± 16.4, P = 0.001).

Figure 3.

Figure 3

Change in health-related quality of life after the end of treatment according to the presence of recurrence. The EQ descriptive score and the visual analogue scale (VAS) score shows a greater improvement in subjects with complete resolution compared with those without complete resolution.

Figure 4 shows the change in HRQoL according to the presence of recurrence after CR. Among the subjects with CR, the EQ descriptive score at the end of the treatment did not differ between subjects with and without recurrence (0.92 ± 0.05 vs 0.93 ± 0.04, P = 0.732), but worsened more during follow-up in subjects with recurrence compared with those without recurrence (change from the end of treatment at recurrence vs. at month 12, −0.02 ± 0.08 vs 0.00 ± 0.06, P = 0.003). However, the EQ VAS score at the end of the treatment was lower in subjects with recurrence than in those without recurrence (79.6 ± 12.9 vs 82.5 ± 12.8, P = 0.042), but the change in EQ VAS during follow-up did not differ between subjects with and without recurrence (change from the end of treatment at recurrence vs. at month 12, −6.3 ± 17.3 vs −3.4 ± 16.3, P = 0.131).

Figure 4.

Figure 4

Change of health-related quality of life after the end of treatment according to the presence of recurrence. EQ descriptive score worsened during follow-up in subjects with recurrence compared with those without recurrence, while EQ visual analogue scale (VAS) score did not differ between subjects with and without recurrence.

The EQ descriptive score at baseline and its changes after treatment and recurrence did not differ between subjects with ERD and NERD (0.87 ± 0.10 vs 0.86 ± 0.10, P = 0.179; 0.04 ± 0.10 vs 0.05 ± 0.09, P = 0.260; and −0.01 ± 0.07 vs −0.01 ± 0.08, P = 0.919, respectively). However, the EQ VAS score at baseline was higher in subjects with ERD than in those with NERD (66.2 ± 17.3 vs 62.7 ± 18.4, P = 0.005). Its changes after treatment and recurrence did not differ between subjects with ERD and NERD (11.4 ± 16.0 vs 14.4 ± 19.4, P = 0.051 and −5.3 ± 15.8 vs −4.0 ± 18.1, P = 0.498, respectively).

Discussion

Considering the increasing prevalence of GERD in Asia, efforts to establish optimal treatment strategies are necessary. However, data regarding the outcomes of PPI therapy in GERD from Asian countries, including Korea, are limited.1012 Furthermore, the impact of GERD on the QoL according to the treatment response and recurrence following the treatment has yet to be evaluated. Thus the present study sought to evaluate the treatment outcome of PPI therapy in a Korean GERD population, to further investigate its prognostic factors, and to assess its impact on QoL. In this study population, CR was achieved in 65.6% after PPI therapy, however almost half of them experienced recurred symptoms following treatment. Patients with acid regurgitation at baseline were more likely to recur than those without. HRQoL was markedly improved in patients with CR compared with those without, and worsened more during follow-up in patients with recurrence compared with those without.

In our results, complete relief on PPI therapy was similarly observed between the patients with ERD and NERD, however, this is in contrast to data from other studies. PPI therapy has been associated with a greater rate of relief in patients with ERD compared with those with NERD.2022 In an Asian study, PPI response rates at 8 weeks were also different between the patients with ERD and NERD (72.4% vs 66.6%, P = 0.02).11 Other recent Asian studies also show lower similar findings.12,23,24 In the present study, ERD was determined according to the LA classification system.19 Despite the exclusion of minimal changes constituting a grade of reflux esophagitis in this system, uncertainty remains in the detection of mucosal breaks, leading to an inconsistency among endoscopists.25,26 Thus, there may be a small possibility that patients without a true mucosal break were erroneously included into the ERD group. In fact, subjects with ERD were more prevalent (58.6%) than those with NERD in the present study.

After achieving CR, almost half of the subjects experienced recurrent symptoms within 12 months. The recurrence rate did not differ between patients with ERD and NERD. Maintenance PPI therapy was administered according to the attending physicians’ judgement. The proportion of subjects with maintenance, on-demand or continuous medication, was not included in the present study. However, our results are consistent with a prior Asian study.11 In that study, 44.3% of the subjects in the erosive esophagitis group and 43.2% in the NERD group had symptomatic relapses without a difference between the two groups. In addition, it is well known that recurrence of esophagitis symptoms is frequent.3,27 Thus, we explored the clinical factors associated with recurrence after CR of GERD. As a result, the presence of regurgitation at baseline was revealed as an independent prognostic factor for recurrence. Patients complaining of regurgitation were more than twice as likely to recur than those without regurgitation. This observation is supported in part by previous findings.28,29 According to the data from the clinical trials, regurgitation is less responsive to acid suppression than heartburn in patients with GERD. Thus our results indicate that regurgitation is not only a risk factor for an incomplete treatment response but also for recurrence in patients with GERD.

The impact of recurrence of GERD on HRQoL has not been previously studied. To our knowledge, this is the first study showing that the improved HRQoL on achievement of CR worsens more during follow-up in patients with recurrence compared with those without. In addition, the impact of GERD on HRQoL did not differ according to the presence of esophagitis. From our results, we suggest that complete symptom relief should be achieved and that recurrence needs to be prevented, in order to improve QoL in patients with GERD.

The prevalence of GERD is relatively low in Eastern countries.49 Obesity may be the important cause of discrepancy in the prevalence of GERD between Eastern and Western countries.30 Obesity was associated with frequent GERD symptoms in a dose-dependent manner.31 Besides symptoms, increased esophageal acid and non-acid exposure was observed in obese patients with GERD.32,33 These observations could explain a decreased response to PPI therapy in obese patients with GERD.34 Although no definite data exist regarding the role of diet in GERD,35,36 high-fat diet is frequent in the obese patients and appears to induce GER by itself.37 Thus, the different lifestyle, in particular diet, may cause ethnic and geographic differences in GERD. In addition, the higher prevalence of Helicobacter pylori and atrophic gastritis in East Asian countries may be another factor in the lower prevalence of GERD. Gastric acid secretion is a pathophysiological factor for GERD.38 The atrophic pan-gastritis causes a marked suppression of acid secretion in H. pylori infected population.39 However, data are conflicting in the association between H. pylori infection and GERD. The present study has some limitations. The treatment response could only be assessed in 74% of the enrolled subjects due to follow-up loss, despite regular phone calls. In addition, information regarding maintenance therapy is not included in this study. Conversely, the present study also has several strengths. The first important strength is that this study was conducted nationwide with a relatively large GERD population. Secondly, this is the first study to show that QoL worsens due to recurrence of GERD. Lastly, we reveal that regurgitation is a risk factor for recurrence in patients with GERD. In conclusion, we should achieve complete symptom relief and attempt to prevent relapse in patients with GERD, which would result in an improvement of QoL. After CR, we need to give increased attention to patients complaining of regurgitation.

Acknowlegements

We are indebted to collaborators: Hyung Seok Park, Sun Moon Kim, Sung Kook Kim, Young-Tae Bak, Bora Keum, Jin Tae Jung, Gwang Ha Kim, Dong Ho Lee, Kook Lae Lee, Hwoon-Yong Jung, Kwang Jae Lee, Seong Hwan Kim, Soo Teik Lee, Hyun Yong Jeong, and Tae Oh Kim.

Footnotes

Financial support: This study was sponsored by AstraZeneca Korea (PHO3112185).

Conflicts of interest: None.

Author contributions: Yang Won Min contributed to data analysis and interpretation, and drafted the manuscript; Yong Woon Shin, Gab Jin Cheon, Kyung Sik Park, Hyun Soo Kim, Chong-Il Sohn, Tae Nyeun Kim, and Hyeung Cheol Moon recruited subjects and performed critical revision of the manuscript; and Poong-Lyul Rhee designed and coordinated the study, contributed to data interpretation, and edited the manuscript.

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