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Prognostic value of serum pepsinogen I in children with peptic ulcer
G Oderda1, F Altare, D Dell'Olio
1Sezione di Gastroenterologia, Università di Torino, Italia.
Insights
Serum pepsinogen I levels in children with peptic ulcer disease (PUD) can predict relapse. Higher pretreatment PG I levels indicate a higher risk of ulcer recurrence after ranitidine treatment.
Area of Science:
- Pediatric Gastroenterology
- Biomarker Research
- Peptic Ulcer Disease
Background:
- Peptic ulcer disease (PUD) affects children, with recurrence being a concern after treatment.
- Serum pepsinogen I (PG I) is a potential biomarker for gastric conditions.
- Understanding predictors of PUD relapse in children is crucial for effective management.
Purpose of the Study:
- To investigate the role of serum PG I levels as a predictor of PUD relapse in children.
- To evaluate the efficacy of ranitidine in treating PUD in a pediatric population.
- To correlate PG I levels with gastric acid secretion.
Main Methods:
- Radioimmunoassay was used to measure serum PG I levels in children with PUD and controls.
- Upper gastrointestinal endoscopy was performed to diagnose and monitor PUD.
- Gastric acid secretion (maximal acid output) was assessed after pentagastrin stimulation.
Main Results:
- Ranitidine healed PUD in 93.5% of pediatric patients, but a 41.9% relapse rate was observed long-term.
- Children with PUD often exhibited higher maximal acid output compared to controls.
- Significantly higher pretreatment serum PG I levels were found in patients who relapsed compared to non-relapsers and controls.
Conclusions:
- Pretreatment serum PG I levels may accurately predict which children with PUD will not relapse after ranitidine treatment.
- Elevated serum PG I levels above 56.7 ng/ml in pediatric patients with PUD are associated with a higher risk of relapse.
- Serum PG I shows promise as a predictive biomarker for PUD recurrence in children.
Abstract:
Serum pepsinogen I (PG I) levels were determined by radioimmunoassay in 23 children with peptic ulcer disease (PUD) before and after treatment with ranitidine and in 44 children who were being investigated for recurrent abdominal pain. Upper gastrointestinal endoscopy was performed in all. No lesions were detected in controls, while 18 patients showed a duodenal ulcer, 4 had an antral ulcer, and 1 had both. An 8-week course of ranitidine healed PUD in 93.5% of them, while long-term (1-5 years) endoscopic follow-up showed a 41.9% ulcer relapse rate after stopping treatment. Gastric acid secretion after pentagastrin stimulation [maximal acid output (MAO)] was tested in all controls and in 22 PUD patients: While controls had normal MAO values for their age, 65% of patients had a secretion above the normal range. No significant correlation was detected between serum PG I and MAO either in controls or in patients. Mean serum PG I concentrations were not significantly higher in the whole patient group than in controls, but PUD patients who relapsed after discontinuing ranitidine treatment had shown on admission significantly higher PG I levels when compared both with those who did not relapse and with controls. All patients who relapsed, but only 42.8% of those who did not, had a serum PG I concentration above the normal upper limit for a pediatric population (56.7 ng/ml). None of the PUD patients who had serum PG I levels under this limit relapsed. Our results suggest that pretreatment serum PG I levels in children with PUD may predict fairly accurately which will not relapse after attaining ulcer healing by a short-term ranitidine course.
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