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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.
Abstract:
An open, pilot study tested the safety and efficacy of an acid stable form of the angiogenic protein basic fibroblast growth factor (bFGF) for healing of non-steroidal anti-inflammatory drug (NSAID) associated gastric ulcers in five patients with nine gastric ulcers that were resistant to conventional treatment (4) or had relapsed (5). Oral bFGF treatment for four weeks was safe and well tolerated. There was no evidence of systemic absorption. After four weeks, four ulcers had healed and there was a 89 (3)% mean (SEM) reduction in the area of the others. A controlled, comparative trial of this novel growth factor treatment is warranted.
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.
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