Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 May 15;11(3):349-357.
doi: 10.5009/gnl16055.

Functional Dyspepsia: Advances in Diagnosis and Therapy

Affiliations
Review

Functional Dyspepsia: Advances in Diagnosis and Therapy

Nicholas J Talley. Gut Liver. .

Abstract

Functional dyspepsia (FD) is a common but under-recognized syndrome comprising bothersome recurrent postprandial fullness, early satiety, or epigastric pain/burning. Epidemiologically, there are two clinically distinct FD syndromes (although these often overlap clinically): postprandial distress syndrome (PDS; comprising early satiety or meal-related fullness) and epigastric pain syndrome. Symptoms of gastroesophageal reflux disease overlap with FD more than expected by chance; a subset has pathological acid reflux. The pretest probability of FD in a patient who presents with classical FD symptoms and no alarm features is high, approximately 0.7. Coexistent heartburn should not lead to the exclusion of FD as a diagnosis. One of the most exciting observations in FD has been the consistent finding of increased duodenal eosinophilia, notably in PDS. Small bowel homing T cells, signaling intestinal inflammation, and increased cytokines have been detected in the circulation, and elevated tumor necrosis factor-α levels have been significantly correlated with increased anxiety. Postinfectious gastroenteritis is a risk factor for FD. Therapeutic options remain limited and provide only symptomatic benefit in most cases. Only one therapy is known to change the natural history of FD-Helicobacter pylori eradication. Treatment of duodenal eosinophilia is under investigation.

Keywords: Epidemiology; Functional dyspepsia.

PubMed Disclaimer

Conflict of interest statement

CONFLICTS OF INTEREST

Dr Talley is funded by the National Health and Medical Reearch Council of Australia. He has received grant support from Commonwealth Diagnostic Laboratories, Prometheus, GI Therapies, Janssen, Abbott, Pfizer and Salix, and consulted for Allergan, Yuhan, Adelphi Values and GI Therapies.

Figures

Fig. 1
Fig. 1
Increased duodenal eosinophils in a patient with functional dyspepsia (H&E, ×40) (with permission from Walker MM and Talley NJ, 2016).

References

    1. Talley NJ, Ford AC. Functional dyspepsia. N Engl J Med. 2015;373:1853–1863. doi: 10.1056/NEJMra1501505. - DOI - PubMed
    1. Tack J, Talley NJ, Camilleri M, et al. Functional gastroduodenal disorders. Gastroenterology. 2006;130:1466–1479. doi: 10.1053/j.gastro.2005.11.059. - DOI - PubMed
    1. Camilleri M, Dubois D, Coulie B, et al. Prevalence and socioeconomic impact of upper gastrointestinal disorders in the United States: results of the US Upper Gastrointestinal Study. Clin Gastroenterol Hepatol. 2005;3:543–552. doi: 10.1016/S1542-3565(05)00153-9. - DOI - PubMed
    1. Ford AC, Marwaha A, Sood R, Moayyedi P. Global prevalence of, and risk factors for, uninvestigated dyspepsia: a meta-analysis. Gut. 2015;64:1049–1057. doi: 10.1136/gutjnl-2014-307843. - DOI - PubMed
    1. Ford AC, Marwaha A, Lim A, Moayyedi P. What is the prevalence of clinically significant endoscopic findings in subjects with dyspepsia? Systematic review and meta-analysis. Clin Gastroenterol Hepatol. 2010;8:830–837.e2. doi: 10.1016/j.cgh.2010.05.031. - DOI - PubMed