E. Bhatia et al., EXOCRINE PANCREATIC AND BETA-CELL FUNCTION IN MALNUTRITION-RELATED DIABETES AMONG NORTH INDIANS, Diabetes care, 18(8), 1995, pp. 1174-1178
Citations number
29
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
OBJECTIVE - To compare the pancreatic exocrine and beta-cell function
in the two variants of malnutrition-related diabetes mellitus (MRDM):
fibrocalculous pancreatic diabetes (FCPD) and protein-deficient pancre
atic diabetes (PDPD). RESEARCH DESIGN AND METHODS - Fecal chymotrypsin
(FCT) and fasting C-peptide levels were measured in 20 consecutive pa
tients with FCPD and 19 with PDPD. FCPD was diagnosed by pancreatic ca
lcification on ultrasonography, while the diagnosis of PDPD was made o
n the basis of low body mass index, severe diabetes requiring insulin
therapy, and ketosis resistance on interruption of insulin. Twenty pat
ients with type I diabetes and 32 healthy subjects served as control s
ubjects. RESULTS - Both FCPD and PDPD patients had diminished levels o
f FCT when compared with those of control subjects and patients with t
ype I diabetes. However, FCT levels were significantly lower in subjec
ts with FCPD (median 0.4 U/g, range 0-8.9 U/g), in comparison with tho
se with PDPD (4.7 U/g, 0.6-40.5 U/g; P < 0.001). Of the FCPD patients,
13 of 20 (65%) had severe exocrine pancreatic deficiency (FCT <1 U/g)
vs. 3 of 19 (15.8%) PDPD subjects (P < 0.01). In comparison with cont
rol subjects, fasting serum C-peptide levels were significantly dimini
shed in both MRDM groups. However, C-peptide levels in subjects with F
CPD (mean +/- SE, 0.22 +/- 0.04 nmol/l) and PDPD (0.26 +/- 0.04 nmol/l
) were comparable. CONCLUSIONS - Among the two variants of MRDM, subje
cts with FCPD have severe pancreatic exocrine deficiency in comparison
with those with PDPD, even though their C-peptide levels are comparab
ly diminished. This suggests that the pathogenesis of these two entiti
es may differ or that the genetic and/or environmental factors leading
to exocrine damage are different.