A. Augarten et al., Serum lipase levels pre and post Lundh meal: evaluation of exocrine pancreatic status in cystic fibrosis, INT J CL L, 28(4), 1998, pp. 226-229
Citations number
18
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH
Determination of pancreatic function is essential in cystic fibrosis. The m
ost-reliable method is by measuring pancreatic enzymes in the duodenum foll
owing intravenous or oral stimulation. However, this is invasive, time cons
uming, and expensive. Indirect tests are non-invasive but lack accuracy. Th
is study examines a simple test which combines pancreatic stimulation by Lu
ndh meal and sequential serum lipase measurements. The test was performed o
n three groups: group A, 36 cystic fibrosis patients carrying two mutations
associated with severe disease and pancreatic insufficiency (Delta F508, W
1282X, G542X, N1303K, S549R); group B, 8 compound heterozygote cystic fibro
sis patients carrying one mutation causing mild disease with pancreatic suf
ficiency (3849 + 10 kb C --> T); group C, 17 healthy individuals. Basal lip
ase levels were 2-16.5, 16.4-73, and 8.5-27.8 U/l in groups A, B, and C, re
spectively, with some overlapping between groups. There were three patterns
of lipase activity(1) consistently low levels (group A) suggested a severe
ly affected insufficient pancreas; (2) normal basal levels followed by a li
near rise peaking 30 min after the meal (found in 16 of 17 healthy individu
als and 3 patients of group B) reflecting an unaffected sufficient pancreas
; (3) elevated lipase levels not influenced by the meal (5 patients of grou
p B). This reflects an ongoing destructive process in the pancreas which wi
ll eventually result in conversion from pancreatic sufficiency to pancreati
c insufficiency. Hence serum lipase activity prior to and 30 min after Lund
h meal is a good indicator of pancreatic status allowing categorization of
cystic fibrosis patients as pancreatic insufficient, pancreatic sufficient,
or pancreatic sufficient with late conversion to insufficiency.