<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJGas</journal-id><journal-title-group><journal-title>Open Journal of Gastroenterology</journal-title></journal-title-group><issn pub-type="epub">2163-9450</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojgas.2014.46037</article-id><article-id pub-id-type="publisher-id">OJGas-46968</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>MEDICINE &amp; HEALTHCARE</subject></subj-group></article-categories><title-group><article-title>Etiologies of Dyspepsia among a Chinese Population: One Hospital-Based Study</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shou-Wu</surname><given-names>Lee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Han-Chung</surname><given-names>Lien</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Teng-Yu</surname><given-names>Lee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sheng-Shun</surname><given-names>Yang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hong-Zen</surname><given-names>Yeh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Chi-Sen</surname><given-names>Chang</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Chinese Taipei</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ericest@vghtc.gov.tw(SL)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>19</day><month>06</month><year>2014</year></pub-date><volume>04</volume><issue>06</issue><fpage>249</fpage><lpage>254</lpage><history><date date-type="received"><day>15</day>	<month>April</month>	<year>2014</year></date><date date-type="rev-recd"><day>26</day>	<month>May</month>	<year>2014</year>	</date><date date-type="accepted"><day>10</day>	<month>June</month>	<year>2014</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>Background and Methods: Dyspepsia refers to a collection of upper gastrointestinal symptoms, and the causes may be either organic or functional. The aim of this study was to investigate the etiologies of dyspepsia among a Chinese population in Taiwan. Patients who underwent upper endoscopy for symptoms of dyspepsia were retrospectively analyzed between January and December 2008. Exclusion criteria included cirrhosis with varices, heart-burn sensation as the main symptom, gastrointestinal bleeding, hepatobiliary abnormalities, prior gastric surgery, and use of anti-acid medication for more than 2 months. Patients were classified according to the findings of upper endoscopy. Results: Data from the medical records of 2062 patients were collected and retrospectively analyzed. Normal endoscopic findings, gastritis, gastric ulcers, duodenal ulcers, reflux esophagitis and esophageal or gastric malignancy accounted for 1174 (56.9%), 215 (10.4%), 254 (12.3%), 194 (9.4%), 182 (8.8%) and 43 (2.1%) cases, respectively. The overall ratio of &lt;i&gt;H. pylori&lt;/i&gt; infection was 28.4%. The ratio was the highest in duodenal ulcers and the lowest in reflux esophagitis. A significantly higher ratio of patients with gastric ulcers had a history of aspirin or non-steroidal anti-inflammatory drugs (NSAIDs) usage. Conclusion: Patients with organic dyspepsia, compared to those with functional dyspepsia, were older, male, and had a higher &lt;i&gt;H. pylori&lt;/i&gt; infection ratio, a positive relationship with aspirin or NSAIDs usage, and more risk factors. These findings demonstrate that upper endoscopy has a high diagnostic yield in patients in this group.</p></abstract><kwd-group><kwd>Duodenal Ulcer</kwd><kwd> Dyspepsia</kwd><kwd> Gastric Ulcer</kwd><kwd> Gastritis</kwd><kwd> Malignancy</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Background</title><p>Dyspepsia refers to a collection of upper gastrointestinal symptoms that is believed to be commonly world-wide [<xref ref-type="bibr" rid="scirp.46968-ref1">1</xref>] , occurring in approximately 25 percent of the population each year [<xref ref-type="bibr" rid="scirp.46968-ref2">2</xref>] -[<xref ref-type="bibr" rid="scirp.46968-ref4">4</xref>] . However, most affected people do not seek medical care due to several factors, including the severity or frequency of symptoms, fear of underlying disease, lower social class, advancing age, anxiety and lack of adequate psychological support [<xref ref-type="bibr" rid="scirp.46968-ref5">5</xref>] . The definition of dyspepsia that is generally accepted by most clinicians is the presence of upper abdominal pain or discomfort with or without other upper gastrointestinal symptoms, such as nausea, belching and vomiting. The causes of dyspepsia may be either organic (structural or physiological) or functional (non-organic or non-ulcer). The usual identifiable causes of the organic subgroup are peptic ulcer disease, gastro-esophageal reflux, and rarely, gastric or esophageal cancer. The definition of functional dyspepsia is the presence of “chronic or recurrent pain or discomfort centered in the upper abdomen in the absence of any known structural cause and without any features of irritable bowel syndrome” [<xref ref-type="bibr" rid="scirp.46968-ref6">6</xref>] .</p><p>Several previous literature reviews have documented the rate of dyspepsia in Western countries, and functional dyspepsia accounted for the highest number of cases, whereas malignancy accounted for the lowest number.</p><p>However, to the best of our knowledge, no study of documented cases of dyspepsia among Chinese patients in Taiwan has been conducted. The aims of this study were to determine the prevalence of etiologies and to provide formal evidence of the empirical treatment and investigation to help primary care physicians combat dyspepsia in Chinese patients.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>Data from the medical records of 2062 consecutive patients who underwent open-access upper endoscopy for symptoms of dyspepsia in our hospital, a 1155-bed academic urban tertiary-care center, were retrospectively analyzed between January 2008 and December 2008. Dyspepsia was defined as pain and discomfort centered in the upper abdomen. Exclusion criteria were as follows: [<xref ref-type="bibr" rid="scirp.46968-ref1">1</xref>] cirrhosis with varices or portal hypertensive gastropathy, [<xref ref-type="bibr" rid="scirp.46968-ref2">2</xref>] heart-burn sensation as the main symptom, [<xref ref-type="bibr" rid="scirp.46968-ref3">3</xref>] overt gastrointestinal bleeding, including hematemesis, tarry stool, or melena, as the major presentation, [<xref ref-type="bibr" rid="scirp.46968-ref4">4</xref>] chronic hepatitis, chronic pancreatitis or gallstones diagnosed by blood examination or image findings, [<xref ref-type="bibr" rid="scirp.46968-ref5">5</xref>] prior gastric surgery, and [<xref ref-type="bibr" rid="scirp.46968-ref6">6</xref>] use of anti-acid medication, such as a proton pump inhibitor (PPI) or an H2-receptor antagonist (H2RB), for more than 2 months. Written informed consent for upper endoscopy was obtained from all patients before the procedure. Use of medications, including aspirin, other nonsteroidal anti-inflammatory drugs (NSAIDs) or coumadin, was recorded. Alarm symptoms included dysphagia, poor response to short-course medications, including PPI, H2RB or gastrokinetic agents, unexplained weight loss of more than 5 kilograms in 2 months, and signs of gastrointestinal bleeding such as melena, positive fecal occult blood test, or hematemesis within the preceding month. Helicobacter pylori status was determined from antral biopsy used in the rapid urease test (CLO test, Delta West, Bentley, Australia), and testing was done at the discretion of primary gastroenterologists. Patients were classified according to the findings of upper endoscopy, which were confirmed by two experienced gastroenterologists.</p><p>Data was expressed as the standard derivation of the mean for each of the measured parameters. Gender, H. pylori infection, combined medication, and risk factors were expressed as percentages of the total patient number. A p-value below 0.05 was considered statistically significant. Statistical comparisons were made using Pearson’s chi-square test to compare gender, H. pylori infection, combined medication, and risk factors; Mann-Whitney U test was used for analysis of the distribution of age among patient groups.</p></sec><sec id="s3"><title>3. Results</title><p>Data from the medical records of 2062 consecutive patients with symptoms of dyspepsia were collected between January and December 2008 and are displayed in <xref ref-type="table" rid="table1">Table 1</xref>. Among these patients, 1174 patients (56.9%) had normal endoscopic findings. The diagnosis of gastritis, gastric ulcers, duodenal ulcers, reflux esophagitis and esophageal or gastric malignancy, which was made by open-access upper endoscopy, accounted for 215 (10.4%), 254 (12.3%), 194 (9.4%), 182 (8.8%) and 43 (2.1%) cases, respectively.</p><p>The distribution of age among the patients with normal endoscopic findings was 30 - 39 years, followed by those with gastritis, duodenal ulcers and reflux esophagitis (40 - 49 years) and patients with gastric ulcers and</p><table-wrap id="table1"  position="float"><object-id pub-id-type="pii">Table 1</object-id><label>Table 1</label><caption><p>. Clinical characteristics of the patients with dyspepsia at admission.</p></caption><table><thead><tr><th align="center" valign="middle"  colspan="2"   rowspan="2"  ></th><th align="center" valign="middle"  colspan="8"  >Upper Endoscopy Finding</th></tr></thead><tbody><tr><td align="center" valign="middle" >Normal</td><td align="center" valign="middle" >Gastritis</td><td align="center" valign="middle" >GU</td><td align="center" valign="middle" >DU</td><td align="center" valign="middle" >Reflux  esophagitis</td><td align="center" valign="middle" >Malignancy</td><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >p-value</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Case numbers  (prevalence)</td><td align="center" valign="middle" >1174 (56.9%)</td><td align="center" valign="middle" >215 (10.4%)</td><td align="center" valign="middle" >254 (12.3%)</td><td align="center" valign="middle" >194 (9.4%)</td><td align="center" valign="middle" >182 (8.8%)</td><td align="center" valign="middle" >43 (2.1%)</td><td align="center" valign="middle" >2062 (100%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  colspan="2"  >Age (years)</td><td align="center" valign="middle" >47.36 &#177; 15.43</td><td align="center" valign="middle" >55.42 &#177; 14.69</td><td align="center" valign="middle" >60.44 &#177; 15.27</td><td align="center" valign="middle" >51.99 &#177; 16.24</td><td align="center" valign="middle" >51.87 &#177; 17.99</td><td align="center" valign="middle" >61.12 &#177; 14.32</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.001a</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Gender</td><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >473 (40.3%)</td><td align="center" valign="middle" >106 (49.3%)</td><td align="center" valign="middle" >142 (55.8%)</td><td align="center" valign="middle" >110 (56.7%)</td><td align="center" valign="middle" >116 (63.7%)</td><td align="center" valign="middle" >30 (69.8%)</td><td align="center" valign="middle" >977 (47.4%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >701 (59.7%)</td><td align="center" valign="middle" >109 (50.7%)</td><td align="center" valign="middle" >112 (44.1%)</td><td align="center" valign="middle" >84 (43.3%)</td><td align="center" valign="middle" >66 (36.3%)</td><td align="center" valign="middle" >13 (30.2%)</td><td align="center" valign="middle" >1085 (52.6%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  rowspan="3"  >H.P.</td><td align="center" valign="middle" >Positive</td><td align="center" valign="middle" >141 (12.0%)</td><td align="center" valign="middle" >75 (51.1%)</td><td align="center" valign="middle" >144 (56.7%)</td><td align="center" valign="middle" >111 (57.2%)</td><td align="center" valign="middle" >8 (4.4%)</td><td align="center" valign="middle" >7 (16.2%)</td><td align="center" valign="middle" >438 (21.2%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >Negative</td><td align="center" valign="middle" >632 (53.8%)</td><td align="center" valign="middle" >110 (34.9%)</td><td align="center" valign="middle" >96 (37.8%)</td><td align="center" valign="middle" >73 (37.6%)</td><td align="center" valign="middle" >111 (61%)</td><td align="center" valign="middle" >30 (69.8%)</td><td align="center" valign="middle" >1100 (53.3%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Not done</td><td align="center" valign="middle" >401 (34.2%)</td><td align="center" valign="middle" >30 (14%)</td><td align="center" valign="middle" >14 (5.5%)</td><td align="center" valign="middle" >10 (5.2%)</td><td align="center" valign="middle" >63 (34.6%)</td><td align="center" valign="middle" >6 (14%)</td><td align="center" valign="middle" >524 (25.4%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  rowspan="4"  >Combined medication</td><td align="center" valign="middle" >Nil</td><td align="center" valign="middle" >1143 (97.4%)</td><td align="center" valign="middle" >197 (91.6%)</td><td align="center" valign="middle" >218 (85.8%)</td><td align="center" valign="middle" >187 (96.4%)</td><td align="center" valign="middle" >177 (97.3%)</td><td align="center" valign="middle" >42 (97.7%)</td><td align="center" valign="middle" >1964 (25.4%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Aspirin</td><td align="center" valign="middle" >19 (1.6%)</td><td align="center" valign="middle" >18 (8.4%)</td><td align="center" valign="middle" >19 (7.5%)</td><td align="center" valign="middle" >3 (1.5%)</td><td align="center" valign="middle" >4 (2.2%)</td><td align="center" valign="middle" >1 (2.3%)</td><td align="center" valign="middle" >64 (3.1%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >NSAIDs</td><td align="center" valign="middle" >9 (0.8%)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >15(5.9%)</td><td align="center" valign="middle" >4 (2.1%)</td><td align="center" valign="middle" >1 (0.5%)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >29 (1.4%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >Coumadin</td><td align="center" valign="middle" >3 (0.3%)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2 (0.8%)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >5 (2%)</td><td align="center" valign="middle" >0.384b</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >Risk factors</td><td align="center" valign="middle" >Nil</td><td align="center" valign="middle" >1105 (94.1%)</td><td align="center" valign="middle" >193 (89.8%)</td><td align="center" valign="middle" >218 (85.8%)</td><td align="center" valign="middle" >163 (84%)</td><td align="center" valign="middle" >173 (95.2%)</td><td align="center" valign="middle" >17 (39.5%)</td><td align="center" valign="middle" >1869 (90.6%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >GI bleeds</td><td align="center" valign="middle" >23 (2%)</td><td align="center" valign="middle" >10 (4.6%)</td><td align="center" valign="middle" >21 (8.3%)</td><td align="center" valign="middle" >22 (11.3%)</td><td align="center" valign="middle" >3 (1.6%)</td><td align="center" valign="middle" >9 (20.9%)</td><td align="center" valign="middle" >88 (4.3%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >BWL</td><td align="center" valign="middle" >25 (2.1%)</td><td align="center" valign="middle" >6 (2.8%)</td><td align="center" valign="middle" >9 (3.5%)</td><td align="center" valign="middle" >4 (2.1%)</td><td align="center" valign="middle" >3 (1.6%)</td><td align="center" valign="middle" >11 (25.6%)</td><td align="center" valign="middle" >58 (2.8%)</td><td align="center" valign="middle" >0.001b</td></tr><tr><td align="center" valign="middle" >Poor drug response</td><td align="center" valign="middle" >20 (1.7%)</td><td align="center" valign="middle" >6 (2.8%)</td><td align="center" valign="middle" >6 (2.4%)</td><td align="center" valign="middle" >5 (2.6%)</td><td align="center" valign="middle" >3 (1.6%)</td><td align="center" valign="middle" >1 (2.3%)</td><td align="center" valign="middle" >41 (2%)</td><td align="center" valign="middle" >0.630b</td></tr><tr><td align="center" valign="middle" >Dysphagia</td><td align="center" valign="middle" >1 (0.1%)</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >5 (11.6%)</td><td align="center" valign="middle" >6 (3%)</td><td align="center" valign="middle" >0.001b</td></tr></tbody></table></table-wrap><p><sup>a</sup>Kruskal-Wallis 1-Way Anova test; <sup>b</sup>Pearson’s Chi-square test <sup>**</sup>: P &lt; 0.05; Abbreviations: BWL, body weight loss; DU, duodenal ulcers; GI, gastrointestinal; GU, gastric ulcers; H.P., Helicobacter pylori; NSAIDs: nonsteroidal anti-inflammatory drugs.</p><p>esophageal or gastric malignancy (50 - 59 years), as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>. We also found that more male patients had peptic ulcers, reflux esophagitis and malignancy, more female patients had normal endoscopic findings, and the numbers of male and female patients with gastritis were similar.</p><p>The ratio of H. pylori infection, shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>, was highest in the patients with duodenal ulcers (60.3%), followed by those with gastritis (40.5%), gastric ulcers (40%), malignancy (18.9%), normal endoscopic findings (18.2%) and reflux esophagitis (6.7%).</p><p>Tracing the past medication history of the patients in our study, a significantly higher ratio of patients with gastritis (8.4%) and gastric ulcers (7.5%) had taken aspirin recently, and similarly, a higher proportion of patients with gastric ulcers (5.9%) had a history of NSAIDs usage compared to the other groups. There was no significant difference of coumadin usage among patients in these five groups. As shown in <xref ref-type="table" rid="table1">Table 1</xref>, the patients with esophageal or gastric malignancy had the highest ratio of risk factors, including body weight loss, signs of gastrointestinal bleeding and dysphagia. There was no significant difference in poor response to medication.</p></sec><sec id="s4"><title>4. Discussion</title><p>The definition of dyspepsia that is generally accepted by most clinicians is the presence of upper abdominal pain or discomfort with or without other upper gastrointestinal symptoms, such as nausea, belching and vomiting [<xref ref-type="bibr" rid="scirp.46968-ref1">1</xref>] . The precise pathophysiology of this condition remains unclear, but it is thought to result from a combination of visceral hypersensitivity, gastric motor dysfunction and psychological factors [<xref ref-type="bibr" rid="scirp.46968-ref7">7</xref>] . Cases of dyspepsia in pre-</p><p>vious reports were mostly caused by the functional subtype (50% - 70%); others were mainly caused by three major structural subtypes: peptic ulcer disease (10%), gastro-esophageal refIux (20%), and malignancy (2%) [<xref ref-type="bibr" rid="scirp.46968-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.46968-ref8">8</xref>] . Our research reported a similar finding, although it was not a population-based survey.</p><fig-group id="fig1"><caption><title>Figure 1</title><p> The distribution of age among the dyspeptic patients with different etiology</p></caption><fig id ="fig1_1"><label>Age (years)</label><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\1-1900214x\b7f798c5-c2e2-417a-bcbb-dcc8913de5a1.png"/></fig></fig-group><fig id="fig2"><label>Figure 2</label><caption><p> The ratio of H. pylori infection among the dyspeptic patients with different etiology</p></caption><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\1-1900214x\05ce3841-d477-4973-a5de-d5a649670d8b.png"/></fig><p>The peak prevalence of organic dyspepsia was in patients between the ages of 45 and 54 years in a Canadian survey, [<xref ref-type="bibr" rid="scirp.46968-ref9">9</xref>] whilst functional dyspepsia appeared to peak in Chinese subjects aged 41 - 50 years, [<xref ref-type="bibr" rid="scirp.46968-ref10">10</xref>] and in Japanese adults aged 50 - 59 years [<xref ref-type="bibr" rid="scirp.46968-ref11">11</xref>] . The average age for peak prevalence in our patients with dyspepsia was 51.0 &#177; 16.4 years. Among these patients, cases of the organic and functional type peaked at 55.8 &#177; 16.4 and 47.4 &#177; 15.4 years, respectively. Patients with organic dyspepsia were significantly older than those with functional dyspepsia, implying that the diagnostic yield of upper endoscopy in patients in the former group increases with advancing age [<xref ref-type="bibr" rid="scirp.46968-ref5">5</xref>] . <sup></sup></p><p>Most population-based studies have obtained relatively similar male-female ratios, and the majority of them have shown no differences in dyspepsia prevalence between genders [<xref ref-type="bibr" rid="scirp.46968-ref1">1</xref>] . However, some studies have noted a consistent female preponderance with functional dyspepsia [<xref ref-type="bibr" rid="scirp.46968-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.46968-ref13">13</xref>] . In a previous study of 2018 health check attendees, female gender was found to be the only independent risk factor for functional dyspepsia [<xref ref-type="bibr" rid="scirp.46968-ref14">14</xref>] . Similarly, our patients showed a parallel pattern, in which female predominance existed in patients with functional dyspepsia (male/female: 40.3%/59.7%) and male predominance was noted in patients with organic dyspepsia (male/female: 56.8%/43.2%). The male-female ratio of the overall patients with dyspepsia was similar (male/female: 47.4%/52.6%).</p><p>The effect of aspirin and NSAIDs on dyspeptic symptoms has been examined specifically in some population-based studies, which concluded the regular usage of NSAIDs and aspirin is strongly associated with organic dyspepsia and is thought to be solely responsible for 4% of dyspepsia cases in the community [<xref ref-type="bibr" rid="scirp.46968-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.46968-ref16">16</xref>] . The results of our study provide solid evidence of the relationship between aspirin or NSAIDs usage and peptic ulcer disease, especially in patients with gastric ulcers. However, we did not find any evidence that coumadin caused symptoms of dyspepsia.</p><p>A previous population-based study investigated the association of H. pylori infection with dyspepsia, and it revealed H. pylori status to be predictive of organic dyspepsia. Furthermore, the authors concluded that H. pylori infection had a 5% population-attributable risk for dyspepsia assuming a causal association [<xref ref-type="bibr" rid="scirp.46968-ref16">16</xref>] . Chronic gastric and duodenal ulcers are usually caused by H. pylori (up to 70% and 95% of patients are infected, respectively, but this varies geographically). According to a previous study, between 30% and 65% of patients diagnosed with functional dyspepsia had H. pylori-induced gastritis [<xref ref-type="bibr" rid="scirp.46968-ref16">16</xref>] .<sup> </sup>However, the association between H. pylori and functional dyspepsia remains unclear. Our patients, with either organic or functional dyspepsia, had a lower ratio of H. pylori infection, and this may be because of the relatively high sanitation level in our country.</p><p>There were some limitations in our study. Firstly, our study, a form of referral-based endoscopy, as opposed to a population-based study, may be less representative of the general population due to selection bias. Secondly, there are other causes of dyspepsia which we did not take into account, such as gallstones, chronic pancreatitis, medications, metabolic disturbances and intestinal angina. Including these causes would result in overestimation of the proportion of patients with functional dyspepsia. Thirdly and fourthly, the retrospective study design and the lack of randomization, respectively, were major limitations of this study. Although the duration of this study was designed to be as long as one year, it is possible that there were unmeasured differences among these subgroups.</p></sec><sec id="s5"><title>5. Conclusion</title><p>“Dyspepsia” refers to a collection of upper gastrointestinal symptoms. In this study, the prevalence of etiologies among the Chinese population in Taiwan was similar to that in previous reports. Patients with organic dyspepsia, compared to patients with functional dyspepsia, are older, male, and have a higher H. pylori infection ratio, a positive relationship with aspirin or NSAIDs usage, and more risk factors. 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