Prospective controlled trial of a standardized meal stimulation test in the detection of pancreaticoduodenal endocrine tumours in patients with multiple endocrine neoplasia type 1

Citation
P. Langer et al., Prospective controlled trial of a standardized meal stimulation test in the detection of pancreaticoduodenal endocrine tumours in patients with multiple endocrine neoplasia type 1, BR J SURG, 88(10), 2001, pp. 1403-1407
Citations number
19
Categorie Soggetti
Surgery,"Medical Research Diagnosis & Treatment
Journal title
BRITISH JOURNAL OF SURGERY
ISSN journal
00071323 → ACNP
Volume
88
Issue
10
Year of publication
2001
Pages
1403 - 1407
Database
ISI
SICI code
0007-1323(200110)88:10<1403:PCTOAS>2.0.ZU;2-I
Abstract
Background: Use of a standardized meal stimulation test has been recommende d for the early diagnosis of pancreaticoduodenal endocrine tumours (PETs) i n patients with multiple endocrine neoplasia type 1 (MEN 1). The diagnostic value of this test was re-evaluated. Methods: In a prospective, controlled trial 58 standardized meal stimulatio n tests (563 kcal) were performed in 12 patients with MEN 1 and histologica lly, biochemically and/or radiologically confirmed PETs (group 1), 11 carri ers of an MEN 1 mutation with no evidence of PETs (group 2) and in 27 healt hy controls (group 3). Serum pancreatic polypeptide (PP) and gastrin concen trations were measured before and during the test meal. Results: Patients in group 1 had significantly higher mean basal serum PP a nd gastrin concentrations than patients in group 2 and controls (P < 0.05). In all three groups an increase in serum PP was observed after meal stimul ation, but there was no significant difference between the groups. No incre ase in gastrin level was found in any of the groups after meal stimulation. Conclusion: The standardized meal stimulation test does not reliably indica te the presence of PETs in patients with MEN 1, whereas raised basal serum PP and gastrin levels do. The expensive and time-consuming meal test can be excluded from MEN 1 screening programmes.