CORRELATIONS BETWEEN CLINICAL ACTIVITY, ENDOSCOPIC SEVERITY, AND BIOLOGICAL PARAMETERS IN COLONIC OR ILEOCOLONIC CROHNS-DISEASE - A PROSPECTIVE MULTICENTER STUDY OF 121 CASES
C. Cellier et al., CORRELATIONS BETWEEN CLINICAL ACTIVITY, ENDOSCOPIC SEVERITY, AND BIOLOGICAL PARAMETERS IN COLONIC OR ILEOCOLONIC CROHNS-DISEASE - A PROSPECTIVE MULTICENTER STUDY OF 121 CASES, Gut, 35(2), 1994, pp. 231-235
The relationships between clinical activity, endoscopic severity, and
biological parameters in Crohn's disease have not been thoroughly inve
stigated and a link was therefore sought between these three elements.
The following parameters were determined simultaneously in 121 consec
utive patients with colonic or ileocolonic Crohn's disease: Crohn's di
sease activity index, Crohn's disease endoscopic index of severity, an
d serum albumin, alpha(2)-globulin, alpha(1)-antitrypsin, orosomucoid,
C reactive protein, erythrocyte sedimentation rate, platelets, lympho
cyte and polymorphonuclear cell counts, haematocrit, and faecal alpha(
1)-antitrypsin concentration. The distribution of these parameters was
studied and transformation was used so that data matched the normal d
istribution closely. A weak but significant correlation (r=0.32; p<0.0
01) was found between clinical and endoscopic indices in the whole gro
up of patients and this correlation seemed to be homogenous in various
patient subgroups (clinically quiescent or active disease, pure colon
ic disease, untreated patients). Endoscopic or clinical indices were a
lso found to be weakly linked with biological parameters (r<0.50). Ste
pwise linear regression identified C reactive protein as predictive of
the clinical index, and, successively, alpha(2)-globulin, erythrocyte
sedimentation rate, faecal alpha(1)-antitrypsin, serum orosomucoid, a
nd alpha(1)-antitrypsin as predictive of the endoscopic index. Both pr
edictions were poor - the biological variables accounting for only 22
and 44% respectively of the clinical and endoscopic index variations.
In conclusion, Crohn's disease clinical activity seems to be virtually
independent of the severity of the mucosal lesions and biological act
ivity.