P. Fogar et al., Transforming growth factor beta, fibrogenesis and hyperglycemia in patients with chronic pancreatitis, J MED, 29(5-6), 1998, pp. 277-287
It has been suggested that transforming growth factor beta (TGFb) mediates
liver fibrosis, which can be monitored by the serum determination of the N-
terminal peptide of type III procollagen (PIIIP) and laminin. Fibrosis is a
lso an important phenomenon in patients with chronic pancreatitis (CP). In
23 patients with CP, 38 with liver cirrhosis (LC) and 20 healthy controls w
e compared the serum patterns of PIIIP, laminin and TGFb and assessed wheth
er in CP these markers are correlated with exocrine and endocrine function.
In patients with LC, PIIIP and laminin levels were significantly higher, w
hereas TGFb levels were significantly lower than those of controls. In CP p
atients, no significant variations were found for PIIIP and laminin, althou
gh levels were high in 7/23 and in 5/23 patients, respectively. TGFb levels
in CP patients were higher than those in LC patients, levels being raised
in 6/23 patients. In LC patients an inverse correlation was found between P
IIIP and TGFb, whereas in CP patients, a direct correlation was found betwe
en TGFb and PIIIP. Moreover, in CP patients, there was also a positive corr
elation between TGFb and fasting serum glucose levels, while laminin was co
rrelated with PABA test results. In conclusion: serum biochemical markers o
f liver fibrosis can be considered of limited value in assessing pancreatic
fibrosis; in liver cirrhosis there may be a negative feed-back regulation
between TGFb production and the fibrogenetic process; and in chronic pancre
atitis TGFb appears to favor fibrosis on the one hand and the development o
f hyperglycemia on the other.