Rtl. Couper et al., LONGITUDINAL EVALUATION OF SERUM TRYPSINOGEN MEASUREMENT IN PANCREATIC-INSUFFICIENT AND PANCREATIC-SUFFICIENT PATIENTS WITH CYSTIC-FIBROSIS, The Journal of pediatrics, 127(3), 1995, pp. 408-413
We studied serial measurements of serum cationic trypsinogen in patien
ts with cystic fibrosis to assess the predictability of changes in ind
ividuals and the value of longitudinal measurement in defining pancrea
tic status, Three hundred twenty-nine patients with cystic fibrosis, a
ged 3 days to 40 years, had serum levels of trypsinogen measured on 2
to 12 occasions for periods ranging from 1 week to 7 years, Patients w
ere classified into three groups on the basis of 72-hour fecal fat stu
dies performed at the time of diagnosis, Two hundred thirty-three pati
ents had pancreatic insufficiency (Pi), 78 had pancreatic sufficiency
(PS), and 18 had PS at diagnosis but acquired PI during follow-up (PS
--> PI). Infants with PI had greatly elevated serum trypsinogen levels
that fell sharply in the first years of life, so that by age 7 years
more than 95% had subnormal values; individual patient values followed
a predictable course similar to previously reported cross-sectional a
ge-related values, In patients with PS, serum trypsinogen levels gener
ally remained within or above the normal range and, after age 10 years
, were well above the upper limit for Pi patients. Within-patient vari
ance was significantly greater (p < 0.0001) in patients with PS than i
n those with PI who were older than 7 years of age, Changes in patient
s within PS --> PI generally followed the pattern seen in patients wit
h PI, but values in older patients tended to be in the higher range, W
e conclude that serial measurement of serum trypsinogen is a valuable
tool for monitoring the pancreatic status of patients with cystic fibr
osis and PS.