Journal of Neurogastroenterology and Motility 2017; 23(1): 41-48
The Role of Microaspiration in the Pathogenesis of Gastroesophageal Reflux-related Chronic Cough
Pelin Özdemir1,2,*, Münevver Erdinç2,3, Rukiye Vardar2,4, Ali Veral5, Serdar Akyıldız2,6, Özer Özdemir7, and Serhat Bor2,4
1Department of Chest Diseases, Su Hospital, İzmir, Turkey, 2Ege Reflux Study Group, Ege University School of Medicine, Izmir, Turkey, 3Department of Chest Diseases, Ege University School of Medicine, İzmir, Turkey, 4Department of Gastroenterology, Ege University School of Medicine, İzmir, Turkey, 5Department of Pathology, Ege University School of Medicine, İzmir, Turkey, 6Department of Otolaryngology, Ege University School of Medicine, İzmir, Turkey, 7Department of Chest Diseases, Egepol Hospital, İzmir, Turkey
Correspondence to: Pelin Özdemir, MD, Department of Chest Diseases, Su Hospital, Güneşli District, 526/4 Str. No:7 Bulvar Apt. No:19 Konak, İZMİR 35270, Turkey, Tel: +90-505-494-8336, Fax: +90-232-262-8270, E-mail:
Received: April 6, 2016; Revised: June 24, 2016; Accepted: August 15, 2016; Published online: January 1, 2017.
© The Korean Society of Neurogastroenterology and Motility. All rights reserved.

cc This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Gastroesophageal reflux disease (GERD) is one of the main causes of chronic cough. We evaluated the role of microaspiration in the pathogenesis of reflux-related cough by determining the amount of lipid-laden macrophages (LLMs) in bronchoalveolar lavage (BAL) specimens.


A total of 161 cases of chronic cough were evaluated, and 36 patients (average age 48.2 years) were recruited for this single center prospective study. Patients with a history of smoking, angiotensin converting enzyme inhibitor usage, any abnormality on pulmonary function tests, abnormal chest X-rays, occupational or environmental exposures, or upper airway cough syndrome were excluded. GERD was evaluated by 24-hour esophageal impedance-pH monitoring. BAL specimens for LLM determination were obtained from 34 patients by flexible bronchoscopy.


Patients with pathological intra-esophageal reflux according to multichannel intraluminal impedance and pH monitoring had higher LLM positivity in BAL specimens than patients without pathological reflux (8/14 in reflux positive group vs 1/22 in reflux negative group; P = 0.004). The BAL cell distribution was not different between the 2 groups (P = 0.574 for macrophages, P = 0.348 for lymphocytes, P = 0.873 for neutrophils and P = 0.450 for eosinophils).


Our results confirm the role of the microaspiration of refluxate in the pathogenetic mechanism of chronic cough. While bronchoscopy is indicated in patients with chronic cough, in addition to the routine airway evaluation, BAL and LLM detection should be performed. LLM can be used to diagnose aspiration in reflux-related chronic cough. Future studies are needed to evaluate the response to anti-reflux medications or surgery in patients with LLM positivity.

Keywords: Cough, Gastroesophageal reflux, Macrophages, alveolar

Chronic cough is a common medical complaint. The most common causes of chronic cough (cough lasting over 8 weeks) in non-smoking adults with a normal chest radiograph include upper airway cough syndrome, gastroesophageal reflux disease, asthma and non-asthmatic eosinophilic bronchitis.

Gastroesophageal reflux disease (GERD) is one of the most common diseases in modern populations. An increased prevalence of GERD is associated with numerous factors, including lifestyle changes, such as nutritional habits, and obesity.1 The prevalence of the disease in Turkey is similar to that in Western countries, and 3 studies in Turkey showed similar prevalences ranging from 19.3% to 23%.24

GERD is considered to be one of the 3 main causes of chronic cough following the exclusion of parenchymal lung diseases, tobacco usage, environmental exposures and angiotensin converting enzyme inhibitor (ACEI) side effects.5 The association between GERD and chronic cough was initially based on observational studies and small treatment trials and is supported by epidemiological data.6,7 However, acid suppression with proton pump inhibitors failed to show superiority over placebo for the relief of reflux-related cough.8,9 Whether a causal relationship between these 2 conditions exists or their simultaneous occurrence is coincidental remains controversial.

Multiple mechanisms have been claimed to play a role in GERD-related cough, and cough may be provoked by the effect of refluxate on the esophagus, larynx or bronchi. There are 2 main mechanisms in the pathogenesis of reflux-related cough.10 One is named the “esophagobronchial reflex,” and it is based on shared vagal innervations of the distal esophagus and airways.11 According to this theory, distal esophageal sensory nerve terminals stimulated by refluxate activate a reflex arc resulting in cough. The other mechanism is microaspiration, in which refluxate reaches the airways through the proximal esophagus and larynx directly resulting in cough. The risk of microaspiration is thought to be increased by decreased sensitivity of the protective laryngeal and pharyngeal reflexes, impaired coordination of swallowing and esophageal dys-motility.12

Different techniques, such as simultaneous measurement of esophageal and tracheal pH, scintigraphic scans of the lungs, detection of pepsin in BAL or saliva, and detection of bile acids and lipid-laden macrophages (LLMs) in airway specimens, have been used to identify microaspiration of refluxate into airways.1315 Studies on those measurement techniques have mostly been conducted in paediatric populations. Studies in adult populations focusing on reflux, bronchoalveolar lavage (BAL) and LLMs are limited. Clinically it would be highly advantageous to have a diagnostic test that could discriminate between respiratory symptoms and diseases caused by GERD from those with other causes.

The primary aim of our study was to evaluate the role of micro-aspiration in patients with chronic cough due to gastroesophageal reflux disease diagnosed by multichannel intraluminal impedance and pH (MII-pH) monitoring. Microaspiration was indicated by the presence of LLMs in BAL specimens. The secondary aim of this study was to assess the bronchoalveolar cell distribution in patients with gastroesophageal reflux-related chronic cough.

Materials and Methods

Study Population

Patients admitted to the out-patient department of Ege University Medical Faculty Chest Disease between January 2010 and May 2011 complaining of cough lasting for 8 weeks or more were enrolled and evaluated by pulmonary and ear-nose-throat (ENT) specialists. Patients with concomitant symptoms of GERD (once a week or common heartburn and/or acid regurgitation) and pathologic reflux detected by 24-hour MII-pH monitoring were included in our study. All patients were older than 18 years of age. Written informed consent was obtained from all patients. This study was approved by the Ege University Research Ethics Committee.

The exclusion criteria were as follows: history of smoking, use of angiotensin converting enzyme inhibitors, abnormal chest X-rays, presence of ENT pathologies, abnormal pulmonary function tests with reversibility and bronchial provocation tests, occupational or environmental exposures that could lead to pulmonary problems, immunosuppression, any treatment that can cause lipid aspiration, any other disease that can lead to aspiration, and findings compatible with upper airway cough syndrome. None of the included patients had a lipid storage disease or had ever received nutritional supplementation with lipid emulsions.

A total of 161 consecutive chronic cough patients were prospectively evaluated for this study: 36 patients were included, and 125 patients were excluded for the following reasons (Figure): 65 patients due to abnormal chest X-rays, 32 patients due to abnormal pulmonary function test with reversibility or bronchoprovocation test, 24 patients due to findings compatible with upper airway cough syndrome, 3 patients due to ACEI usage and 1 patient due to environmental exposure.

Pulmonary Function Tests

Spirometry (Sensormedics 2400; Sensormedics, Yorba Linda, CA, USA) was applied to all patients. At least 3 reproducible values were obtained, and the highest value was accepted. Patients with a FEV1 value above 80% and a FEV1/FVC value above 75% were considered to have normal pulmonary function. A bronchoprovocation test with methacholine was performed if the spirometric measures were normal and was evaluated using the Cockroft concentration method with a threshold of positivity of a PC20 of 16 mg/mL.

Combined Multichannel Intraluminal Impedance and pH Monitoring

All patients were examined for pathological reflux by 24-hour MII-pH monitoring. Patients were asked to stop proton pump inhibitors and H2 receptor blocking drugs for 7 days and to stop drugs affecting the lower esophageal sphincter for 48 hours prior to the procedure. After detection of lower esophageal sphincter localization by high-resolution manometric examination, a MII catheter (2–4–6–8–10–14–16th cm impedance rings and 5th cm pH electrode) was placed to provide a pH probe at 5 cm above the LES transnasally that was connected to a portable data recorder (Ohmega; MMS, Enschede, The Netherlands). Twenty-four-hour monitoring was carried out, and the patients were instructed to have a usual day with a regular diet and to push the symptom button whenever they had symptoms of reflux. pH changes were recorded, and the data were analysed after the test was completed. Only liquid refluxes, defined as a retrograde drop in impedance of 50% or more from the baseline, were evaluated. A pH of < 4 was defined as acidic reflux, whereas a pH of 4–7 was defined as weak acid reflux and a pH of > 7 was defined as nonacidic reflux. Normal values of total distal reflux were total reflux events ≤ 73, acid reflux events ≤ 55, weakly acid reflux events ≤ 26 and weakly alkaline reflux ≤ 1 based on the 95th percentile as the upper limit of the normal. Normal values for impedance pH monitoring were % bolus exposure (impedance parameter) and % acid exposure (pH parameter): total 1.4%; 6.3%; upright: 2.1%, 9.7%; and recumbent: 0.7%, 2.1%.16,17

Bronchoscopy and Bronchoalveolar Lavage

Except for 4 patients who declined to give informed consent, transnasal or transoral bronchoscopic examination was performed in all patients with a fiberoptic bronchoscope (Olympus BF-2T10; Olympus Co, Tokyo, Japan). Local anaesthesia (2% lidocaine HCl, topical, maximum 10 mL) and premedication with midazolam were applied before the procedure. The bronchial branches on both sides were assessed for macroscopic abnormality. The middle lobe medial segment bronchus was wedged, and 120–150 mL saline was instilled for BAL. The lavage material was filtered before cytological examination.

BAL specimens were examined by liquid-based cytology and slides prepared on a Thinprep device were stained with Sudan Black to detect LLM positivity. The cells with cytoplasmic orangered granules was counted as positive. The pathologist who evaluated the BAL specimens was blinded to the patients’ GERD status.

Examination for Upper Airway Cough Syndrome

All patients underwent an examination by an ENT specialist before the reflux work-up. A reflux finding score was obtained to evaluate laryngopharyngeal reflux, as described in the literature.18 A score greater than 7 was considered positive for laryngopharyngeal reflux, whereas a score greater than 11 was considered strongly suggestive of laryngopharyngeal reflux.

Statistical Methods

Statistical analyses were performed using SPSS v16 (SPSS for Windows; SPSS Inc, Chicago, IL, USA). Fisher’s exact test and χ2 test were used to compare the MII-pH monitoring data and BAL LLM positivity. Reflux index, impedance pH-metry parameters and BAL cell distribution were evaluated by nonparametric statistical analysis, as data were not normally distributed. The Mann Whitney U test was used to compare the reflux positive group to the control group. P levels below 0.05 were considered statistically significant.


A total of 161 patients were screened, and 36 patients were included in this study; 78% of the included patients were female, and the mean age of the patients was 48.2 ± 12.9 years. The average cough time of the patients was 35.1 ± 35.6 months (3–180 months). Thirty-four patients had never smoked, one patient had a smoking history of 3 pack-years and one had a smoking history of 4 pack-years. All patients included in this study had normal pulmonary function test values and normal bronchoprovocation test results with methacholine.

Fourteen patients (38.9%) had pathological reflux detected by MII-pH monitoring (pathological reflux [+] group). The control group was composed of 22 patients (61.1%) whose MII-pH monitoring results were considered normal (pathological reflux [−] group). In the pathological reflux group, the average incidences of different levels of reflux were as follows: total reflux, 90.4 ± 38.7; acidic reflux, 56.4 ± 27.4; weak acidic reflux, 33.7 ± 23.3; and nonacidic reflux, 0.2 ± 0.6.

A total of 25.0% (n = 9) of all patients had BAL LLM positivity. While 8 out of 14 patients (57.1%) in the pathological reflux group had LLM positivity, only one patient (4.5%) in the control group had LLM positivity. Compared with the control group, patients with pathological reflux had significantly higher BAL LLM positivity (P = 0.004).

Reflux finding scores, which were evaluated by an ENT specialist, were significantly higher in the pathological reflux group: in the pathological reflux group median was 14 with an interquartile range (IQR) of 4; whereas in the control group median was 6 with an IQR of 8 (P < 0.001). The comparison of the pathological reflux group and control group is presented in Table 1.

When LLM-positive and LLM-negative groups were compared, the reflux finding scores were significantly higher in the LLM-positive group (median 14, IQR 4 vs median 6, IQR 8; P < 0.001). The incidence of total reflux and the acidic reflux numbers were higher in the LLM-positive group than the LLM-negative group (respectively, for total reflux median 76, IQR 57 vs median 43, IQR 32; P = 0.032 and for acidic reflux median 53.5, IQR 49 vs median 18, IQR 57; P = 0.003). The comparison of LLM-positive and LLM-negative groups is shown in Table 2. LLM positivity according to GERD status is shown in Table 3.

Considering all patients, on average, the BAL cell distribution was 87.9% for macrophages, 8.8% for lymphocytes, and 3% for neutrophils. There were no significant differences between the pathological reflux group and the control group in regard to BAL macrophage, lymphocyte, neutrophil or eosinophil distributions (P = 0.574, 0.348, 0.873, and 0.450, respectively). Similarly, there were no significant differences in BAL macrophage, lymphocyte, neutrophil or eosinophil distributions between the LLM-positive and LLM-negative groups (P = 0.472, 0.443, 0.743, and 0.775, respectively).


Main mechanisms of reflux associated chronic cough are the esophagobronchial vagal reflex mechanism and microaspiration. In this study we investigated the role of microaspiration in patients with gastroesophageal reflux-associated chronic cough by measuring LLM positivity in BAL specimens. Patients with pathological reflux according to MII/pH monitoring findings had significantly higher BAL LLM positivity compared to patients without pathological reflux, suggesting the importance of microaspiration. On the other hand, patients with LLM positivity had a higher incidence of total and acidic reflux compared to patients who were negative for LLM. BAL cell distributions were not different between the groups. The reflux finding scores at the pharynx and larynx scored by an ENT specialist supported the BAL findings, with a significantly high score in the pathological reflux group compared to that in the reflux-negative group. The difference in the reflux finding scores between the LLM-positive and LLM-negative patients was also statistically significant (P < 0.001).

Early studies have mostly focused on the shared vagal innervations of the esophagus and airways as the main mechanism of chronic cough because cough episodes were temporally associated with distal esophageal acidification in patients with normal chest X-ray, bronchoscopy or laryngeal examination.19 Additionally, reflux-related cough was suppressed with esophageal lidocaine instillation or tracheal ipratropium inhalation.11 Javorkova et al20 showed that the acidification of the distal esophagus increased cough sensitivity in patients with GERD and chronic cough in comparison to healthy volunteers and patients with GERD only. This effect was also observed in asthma patients without cough or GERD.21 These findings support the concept that this reflex may not be the sole mechanism of reflux cough and that some airway disease may be needed for cough sensitivity to occur. Although in chronic cough patients, proximal esophageal reflux episodes do not seem to be different than in healthy volunteers,22 microaspiration of gastric content into the airways is considered to be one of the causes of cough. Dysfunction of the upper esophageal sphincter and insufficiency of protective laryngeal and pharyngeal reflexes may predispose patients to microaspiration.23 Simultaneous esophageal and tracheal pH drops during reflux episodes in asthma patients supports this hypothesis.13

The presence of pepsin, bile acids or LLMs in BAL specimens has been proposed as an index to establish the degree of gastric aspiration. The LLM index is mostly used to detect aspiration-induced chronic lung diseases in pediatric patients, especially in cases that are due to chronic aspiration.24 The value of that index has also been confirmed in an adult patient population with aspiration pneumonia.25 The importance of LLM positivity in assessing GERD was shown in cystic fibrosis patients with lung transplantation by Hayes et al.26 In that study, some patients underwent laparoscopic Nissen fundoplication and others underwent anti-reflux medical therapy. The LLM index was significantly lower in the surgical group. Opposing the reliability of LLM index as a marker of microaspiration, Kitz et al27 conducted a study in children with GERD related respiratory symptoms and found no association between reflux events and LLM counts. But MII was not used in this study, and also underlying pulmonary disease of the selected patient population may cause more reduction in sensitivity and specificity of LLM index.

However, LLM presence in BAL may not differentiate direct aspiration to the airways from secondary aspiration of reflux. Additionally, lipids in macrophages may include endogenous lipids as well as exogenous lipids, as observed in reflux material. Any disorder leading to pulmonary inflammation may cause LLM positivity. In our study, the patient population was carefully chosen to avoid these problems by excluding patients with any airway or lung disease, radiographic abnormality or any environmental exposure that can cause airway inflammation. Patients with bronchial obstruction, malignancy, and organic dust exposure were also excluded, as those conditions may result in endogenous lipid phagocytosis of macrophages. It must be kept in mind that in the opinion of some researchers, LLM presence in BAL may not be an adequate test for aspiration because of the absence of reference values in healthy volunteers and the probable discrepancy between observers, as it is scored visually.

In our study 6 out of 14 patients with GERD showed LLM negativity, and 1 control patient showed LLM positivity. Regarding the sensitivity and specificity of LLM positivity, there may be false negative or false positive results. Maybe these are the results of other causes of LLM positivity that are mentioned above. Also it should be kept in mind that there is no gold standard test for GERD diagnosis. Other markers, like pepsin and bile acids are also used as markers of microaspiration. In a study by Stovold et al,28 BAL pepsin levels were found to be elevated in lung transplant recipients, with the highest levels in subjects with acute vascular rejection. BAL pepsin levels of GERD patients with and without chronic cough were found to be similar and lower. In a study of Grabowski et al29 pepsin and bile acids in induced sputum of chronic cough patients were not different between GERD patients and the control group. In a study of Decalmer et al,30 BAL pepsin levels were found to be lower in chronic cough patients compared with controls, and they found no correlation between proximal and distal reflux events and BAL pepsin concentration. The results of these studies conflicts with our findings. This confliction may have some several probable methodological reasons. In the study of Grabowski et al29 GERD diagnosis was based on gastroscopy findings and treatment response, multichannel impedance, and pH-metry was not used and also pepsin levels were detected in sputum samples, not in BAL. In the study of Decalmer et al,30 selection of the study population was different, mainly considering unexplained chronic cough patients with various respiratory diagnoses or GERD including ex-smokers. It should also be kept in mind that pepsin measurement is also not validated as a marker of aspiration because of some significant methodological issues, like cross reaction of the immunologic assay with pepsinogen.31 For aspiration to occur, the refluxate should traverse the length of the esophagus and reach the larynx and pharynx. Although pharyngeal reflux is not prominent in chronic cough patients, our findings indicate that it may occur more often in these patients.32 Because of the technical difficulties of placement of 2 catheters or placement of an impedance catheter with 2 pH probes, proximal reflux events were not evaluated in our study. However, the reflux finding score was positive in 20 (55.6%) patients, although the accuracy of evaluating proximal esophageal reflux with this score is arguable, as it depends on a subjective visual scoring system. Limited data exist about the value of proximal pH probe monitoring in patients with chronic cough and GERD; however, many studies have shown the inefficiency of this technique for the diagnosis of laryngopharyngeal reflux.33

MII-pH monitoring for the diagnosis of GERD allowed for the detection of gaseous and weak-nonacidic reflux in addition to acidic and liquid reflux. Proximal reflux episodes and nonacidic reflux associated with cough episodes have been observed in a small portion of the patient population, and an increase in reflux episodes in patients with chronic cough compared to healthy volunteers is seldom observed. This finding indicates the possibility that even physiological reflux can provoke cough in these patients.

There was no significant difference in the BAL cell distribution between the pathological reflux group and control group or between the LLM (+) and LLM (−) groups. In a study by Chang et al,34 GERD patients without any pulmonary disease showed no difference in BAL cell distribution or LLM positivity compared with controls. According to these limited data, BAL cell distribution changes may be attributed to pulmonary diseases, not GERD itself. This study of Chang et al,34 differs from our results regarding LLM positivity. This difference may be due to difference of selected populations, as children with gastrointestinal symptoms with indication of gastroendoscopy was included in that study. Also GERD diagnosis methods and BAL were different.

Our study has some limitations. We tried to recruit patients with isolated true reflux cough: patients with any sign of airway or parenchymal disease, upper airway cough syndrome, or any other condition that can result in cough were excluded. This choice caused the patient population to be small, although it was one of the largest groups used to study this topic in the literature. Acidic and nonacidic reflux episodes were identified by MII/pH monitoring, but proximal reflux episodes were not evaluated with a proximal pH probe.

As a result, based on the hypothesis that esophagobronchial reflex and microaspiration are the 2 main mechanisms of reflux cough, our results confirm the role of refluxate microaspiration in the pathogenetic mechanism of chronic cough. In patients with chronic cough, who represents a challenging patient group in pulmonary medicine, LLM in BAL specimens may indicate the presence of microaspiration due to GERD; however, larger controlled trials are necessary to determine the reference values for this evaluation. It should be taken into consideration that although bronchoscopy is indicated in patients with chronic cough, routine airway evaluation, BAL and LLM staining should also be performed. Future studies are needed to evaluate the response to anti-reflux medications and surgery in patients with LLM positivity.

Fig. 1. Diagram of patient recruitment. PFT, pulmonary function test; BPT, bronchoprovocation test; ACEI, angiotensin converting enzyme inhibitor; ENT, ear-nose-throat; MII, multichannel intraluminal impedance.

Comparison of Pathological Reflux Group and Control Group

Pathological reflux (+)Pathological reflux (−)P-value
(n = 14)(n = 22)
Age (median ± SD, yr)46.1 ± 12.549.5 ± 13.20.445
Duration of cough (median ± SD, mo)34.1 ± 16.635.8 ± 44.00.876
LLM (n [%])8 (57.1)1 (4.5)0.004
BAL cell distribution (median [IQR])
 Macrophages91.5 (7)90.0 (6)0.574
 Lymphocytes6.0 (4)8.0 (4)0.348
 Neutrophils3.0 (4)3.0 (3)0.873
 Eosinophils0.0 (1)0.0 (1)0.450
 Reflux finding score14.0 (4)6.0 (8)< 0.001

LLM, lipid-laden macrophage; BAL, bronchoalveolar lavage; IQR, interquartile range.

Comparison of Lipid-laden Macrophage Positive and Lipid-laden Macrophage Negative Patients

LLM (+)LLM (−)P-value
(n = 9)(n = 27)
Age (median ± SD, yr)49.0 ± 12.546.7 ± 13.20.646
Duration of cough (median ± SD, mo)38.1 ± 16.735.0 ± 42.30.842
Reflux finding score (median [IQR])14.0 (4)6.0 (8)< 0.001
Total reflux number (median [IQR])76.0 (57)43.0 (32)0.032
Acidic reflux (median [IQR])53.5 (49)18.0 (18)0.003
Weak acidic reflux (median [IQR])20.2 (25)26.0 (19)0.968
Nonacidic reflux (median [IQR])0.0 (0)1.0 (4)0.030
BAL cell distribution (median [IQR])
 Macrophages92.0 (6)88.0 (6)0.472
 Lymphocytes5.5 (5)8.0 (3)0.443
 Neutrophils2.5 (2)3.0 (4)0.743
 Eosinophils0.0 (1)0.0 (1)0.775

LLM, lipid-laden macrophages; IQR, interquartile range; BAL, bronchoalveolar lavage.

Lipid-laden Macrophage Positivity According to Gastro-esophageal Reflux Disease Status

GERD (+)GERD (−)
LLM (+)81
LLM (−)621

GERD, gastroesophageal reflux disease; LLM, lipid-laden macrophages. Data are presented as number of patients.

  1. Bonatti, H, Achem, SR, and Hinder, RA (2008). Impact of changing epidemiology of gastroesophageal reflux disease on its diagnosis and treatment. J Gastro-intest Surg. 12, 373-381.
  2. Bor, S, Mandiracioglu, A, Kitapcioglu, G, Caymaz-Bor, C, and Gilbert, RJ (2005). Gastroesophageal reflux disease in a low-income region in Turkey. Am J Gastroenterol. 100, 759-765.
    Pubmed CrossRef
  3. Bor, S, Kitapcioglu, G, Kasap, E, and Ilter, T (2006). The prevalence of gastroesophageal reflux disease in Turkey: lessons from a high Helicobacter pylori prevalent country. J Clin Gastroenterol. 40, S182-S183.
  4. Mungan, Z (2012). Prevalence and demographic determinants of gastroesophageal reflux disease (GERD) in the Turkish general population. population: a population-based cross-sectional study. Turk J Gastroenterol. 23, 323-332.
    Pubmed CrossRef
  5. Palombini, BC, Villanova, CA, and Araújo, E (1999). A pathogenic triad in chronic cough: asthma, postnasal drip syndrome, and gastroesophageal reflux disease. Chest. 116, 279-284.
    Pubmed CrossRef
  6. Irwin, RS, Curley, FJ, and French, CL (1990). Chronic cough: the spectrum and frequency of causes, key components of the diagnostic evaluation, and outcome of specific therapy. Am Rev Respir Dis. 141, 640-647.
    Pubmed CrossRef
  7. Ing, AJ, Ngu, MC, and Breslin, AB (1994). Pathogenesis of chronic persistent cough associated with gastroesophageal reflux. Am J Respir Crit Care Med. 149, 160-167.
    Pubmed CrossRef
  8. Shaheen, NJ, Crockett, SD, and Bright, SD (2011). Randomised clinical trial: high-dose acid suppression for chronic cough - a double-blind, placebo-controlled study. Aliment Pharmachol Ther. 33, 225-234.
  9. Faruqi, S, Molyneux, ID, Fathi, D, Wright, C, Thompson, R, and Morice, AH (2011). Chronic cough and esomeprazole: a double-blind placebo-controlled parallel study. Respirology. 16, 1150-1156.
    Pubmed CrossRef
  10. Smith, JA, Abdulqawi, R, and Houghton, LA (2011). GERD-related cough: pathophysiology and diagnostic approach. Curr Gastroenterol Rep. 13, 247-256.
    Pubmed CrossRef
  11. Ing, AJ, Ngu, MC, and Breslin, ABX (1991). Chronic persistent cough and gastro-esophageal reflux. Thorax. 46, 479-483.
    Pubmed KoreaMed CrossRef
  12. Phua, SY, McGarvey, LP, Ngu, MC, and Ing, AJ (2005). Patients with gastro-oesophageal reflux disease and cough have impaired laryngopharyngeal mechanosensitivity. Thorax. 60, 488-491.
    Pubmed KoreaMed CrossRef
  13. Jack, CI, Calverley, PM, and Donnelly, RJ (1995). Simultaneous tracheal and oesophageal pH measurements in asthmatic patients with gastro-oesophageal reflux. Thorax. 50, 201-204.
    Pubmed KoreaMed CrossRef
  14. Stein, MR (2003). Possible mechanisms of influence of esophageal acid on airway hyperresponsiveness. Am J Med. 115, 55S-59S.
    Pubmed CrossRef
  15. Grabowski, M, Kasran, A, and Seys, S (2011). Pepsin and bile acids in induced sputum of chronic cough patients. Respir Med. 105, 1257-1261.
    Pubmed CrossRef
  16. Shay, S, Tutuian, R, and Sifrim, D (2004). Twenty-four hour ambulatory simultaneous impedance and pH monitoring: a multicenter report of normal values from 60 healthy volunteers. Am J Gastroenterol. 99, 1037-1043.
    Pubmed CrossRef
  17. Zentilin, P, Iiritano, E, and Dulbecco, P (2006). Normal values of 24-h ambulatory intraluminal impedance combined with pH-metry in subjects eating a Mediterranean diet. Dig Liver Dis. 38, 226-232.
    Pubmed CrossRef
  18. Belafsky, PC, Postma, GN, and Koufman, JA (2001). The validity and reliability of the reflux finding score (RFS). Laryngoscope. 111, 1313-1317.
    Pubmed CrossRef
  19. Irwin, RS, French, CL, Curley, FJ, Zawacki, JK, and Bennett, FM (1993). Chronic cough due to gastroesophageal reflux. Clinical, diagnostic, and pathogenetic aspects. Chest. 104, 1511-1517.
    Pubmed CrossRef
  20. Javorkova, N, Varechova, S, and Pecova, R (2008). Acidification of the oesophagus acutely increases the cough sensitivity in patients with gastro-oesophageal reflux and chronic cough. Neurogastroenterol Motil. 20, 119-124.
  21. Wu, DN, Yamauchi, K, and Kobayashi, H (2002). Effects of esophageal acid perfusion on cough responsiveness in patients with bronchial asthma. Chest. 122, 505-509.
    Pubmed CrossRef
  22. Blondeau, K, Dupont, LJ, Mertens, V, Tack, J, and Sifrim, D (2007). Improved diagnosis of gastro-oesophageal reflux in patients with unexplained chronic cough. Aliment Pharmacol Ther. 25, 723-732.
    Pubmed CrossRef
  23. Smith, JA, and Houghton, LA (2013). The oesophagus and cough: laryngo-pharyngeal reflux, microaspiration and vagal reflexes. Cough. 9, 12.
    Pubmed KoreaMed CrossRef
  24. Corwin, RW, and Irwin, RS (1985). The lipid-laden alveolar macrophage as a marker of aspiration in parenchymal lung disease. Am Rev Respir Dis. 132, 576-581.
  25. Adams, R, Ruffin, R, and Campbell, D (1997). The value of the lipid-laden macrophage index in the assessment of aspiration pneumonia. Aust N Z J Med. 27, 550-553.
    Pubmed CrossRef
  26. Hayes, D, Kirkby, S, and McCoy, KS (2013). Reduction of lipid-laden macrophage index after laparoscopic Nissen fundoplication in cystic fibrosis patients after lung transplantation. Clin Transplant. 27, 121-125.
  27. Kitz, R, Boehles, HJ, Rosewich, M, and Rose, MA (2012). Lipid-laden alveolar macrophages and pH monitoring in gastroesophageal reflux-related respiratory symptoms. Pulm Med. 2012, 673637.
    Pubmed KoreaMed CrossRef
  28. Stovold, R, Forrest, IA, and Corris, PA (2007). Pepsin, a biomarker of gastric aspiration in lung allografts: a putative association with rejection. Am J Respir Crit Care Med. 175, 1298-1303.
    Pubmed CrossRef
  29. Grabowski, M, Kasran, A, and Seys, S (2011). Pepsin and bile acids in induced sputum of chronic cough patients. Respir Med. 105, 1257-1261.
    Pubmed CrossRef
  30. Decalmer, S, Stovold, R, and Houghton, LA (2012). Chronic cough: relationship between microaspiration, gastroesophageal reflux, and cough frequency. Chest. 142, 958-964.
    Pubmed CrossRef
  31. Trinick, R, Johnston, N, Dalzell, AM, and McNamara, PS (2012). Reflux aspiration in children with neurodisability--a significant problem, but can we measure it?. J Pediatr Surg. 47, 291-298.
    Pubmed CrossRef
  32. Sifrim, D, Dupont, L, Blondeau, K, Zhang, X, Tack, J, and Janssens, J (2005). Weakly acidic reflux in patients with chronic unexplained cough during 24 hour pressure, pH, and impedance monitoring. Gut. 54, 449-454.
    Pubmed KoreaMed CrossRef
  33. Bilgen, C, Ogüt, F, Kesimli-Dinç, H, Kirazli, T, and Bor, S (2003). The comparison of an empiric proton pump inhibitor trial vs. 24-hour double-probe pH monitoring in laryngopharyngeal reflux. J Laryngol Otol. 117, 386-390.
    Pubmed CrossRef
  34. Chang, AB, Cox, NC, and Purcell, J (2005). Airway cellularity, lipid laden macrophages and microbiology of gastric juice and airways in children with reflux oesophagitis. Respir Res. 6, 72.
    Pubmed KoreaMed CrossRef

This Article



Aims and Scope