Basic fibroblast growth factor treatment for non-steroidal anti-inflammatory drug associated gastric ulceration

M A Hull1, D J Cullen, N Hudson

  • 1Division of Gastroenterology, University Hospital, Queen's Medical Centre, Nottingham.

Gut
|November 1, 1995
PubMed

Insights

This pilot study shows oral basic fibroblast growth factor (bFGF) is a safe treatment for non-steroidal anti-inflammatory drug (NSAID)-associated gastric ulcers. The treatment led to significant ulcer healing and area reduction in patients resistant to conventional therapies.

Area of Science:

  • Gastroenterology
  • Regenerative Medicine
  • Pharmacology

Background:

  • Non-steroidal anti-inflammatory drug (NSAID)-associated gastric ulcers are a common clinical challenge.
  • Ulcers resistant to conventional treatment or those that relapse pose significant therapeutic difficulties.
  • Angiogenic proteins like basic fibroblast growth factor (bFGF) show potential for tissue repair.

Purpose of the Study:

  • To evaluate the safety and efficacy of an acid-stable form of bFGF in treating NSAID-associated gastric ulcers.
  • To assess the healing of gastric ulcers resistant to or relapsed after conventional treatments.

Main Methods:

  • An open, pilot study involving five patients with nine gastric ulcers.
  • Treatment with oral, acid-stable bFGF for a duration of four weeks.
  • Monitoring for safety, tolerability, and systemic absorption.

Main Results:

  • Oral bFGF treatment was found to be safe and well tolerated.
  • No evidence of systemic absorption of bFGF was detected.
  • After four weeks, four out of nine ulcers healed completely.
  • The remaining ulcers showed an 89% mean reduction in area.

Conclusions:

  • Acid-stable oral bFGF is a potentially safe and effective therapeutic option for NSAID-associated gastric ulcers.
  • The promising results warrant further investigation in a controlled, comparative trial.
  • Novel growth factor-based therapies represent a promising avenue for refractory ulcer treatment.

Related Concept Videos

Peptic Ulcer Disease IV: Management01:26

Peptic Ulcer Disease IV: Management

Medical treatment strategies for peptic ulcers encompass various methods. The primary goal of treatment is to diminish gastric acidity and strengthen mucosal defense mechanisms.
The therapeutic approach involves ensuring adequate rest, implementing drug therapy, promoting smoking cessation, making dietary modifications, and emphasizing long-term follow-up care.
Pharmacological management
The prevailing therapy for peptic ulcers involves a combination of managing the patient's current...
576
Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents01:20

Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents

The gastric mucosa produces prostaglandins E2 (PGE2) and prostacyclin (PGI2), crucial in maintaining gastric health. They exert cytoprotective effects, including increasing bicarbonate secretion, releasing protective mucin, reducing gastric acid output, and preventing harmful vasoconstriction. These effects are mediated through various receptors, such as EP1, EP2, EP3, and EP4.
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
1.3K
Drugs for Peptic Ulcer Disease: Sucralfate as Mucosal Protective Agents01:24

Drugs for Peptic Ulcer Disease: Sucralfate as Mucosal Protective Agents

In the intricate landscape of the gastric lumen, excessive acid secretion disrupts the natural defense mechanisms, weakening the mucus-bicarbonate barrier. This vulnerability allows pepsin to infiltrate epithelial cells, digesting mucosal proteins and triggering erosion, leading to ulcer formation.
In this scenario, mucosal protective agents like sucralfate play an essential role. Sucralfate, a complex of sulfated sucrose and aluminum hydroxide, demonstrates its usefulness in acidic conditions,...
1.8K
Drugs for Treatment of Ulcerative Colitis in IBD01:29

Drugs for Treatment of Ulcerative Colitis in IBD

Ulcerative colitis is a chronic inflammatory condition primarily affecting the colon and rectum. The primary drugs used in the treatment of ulcerative colitis are aminosalicylates. They exhibit anti-inflammatory and immunosuppressive properties. They modulate inflammatory mediators and inhibit the activity of nuclear factor κB (NF-κB). Aminosalicylates also reduce inflammation by inhibiting prostaglandin and leukotriene production and decreasing neutrophil chemotaxis and superoxide...
577
Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors01:13

Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors

Peptic ulcers, often induced by H. pylori infections or NSAID usage, arise from disruptions in the delicate balance of gastric acid production. Peptic ulcers stem from heightened gastric acid levels due to H. pylori infections or NSAID use. The protective mucus layer diminishes in the presence of these factors, allowing gastric acid to erode the stomach lining and form ulcers.
Gastric acid, a potent cocktail of hydrogen and chloride ions, is produced in specialized parietal cells within the...
1.0K
Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors01:24

Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors

Peptic ulcer disease, commonly called PUD, represents a multifaceted condition characterized by disruptions in the lining of the gastrointestinal (GI)  tract. Central to the protection of the gastrointestinal lining is the mucosal-bicarbonate barrier. This physiological defense mechanism is a formidable shield against the corrosive effects of gastric acid and pepsin secretion in the stomach. Its role is pivotal in maintaining the structural integrity of the stomach's inner lining.
1.3K