Serum Angiotensin-Converting Enzyme Activity,... : Chest (original) (raw)
Clinical Investigation: Interstitial Lung Disease
Serum Angiotensin-Converting Enzyme Activity, Concentration, and Specific Activity in Granulomatous Interstitial Lung Disease, Tuberculosis, and COPD*
- Edmund A. W. Brice
- Wulfie Friedlander
- Eric D. Bateman
- Ralph E. Kirsch
Chest
107
(
3
)
:p
706
-
710
,
March 1995
.
Angiotensin-converting enzyme (ACE) activity in serum is used as an aid to the diagnosis and follow-up of patients with sarcoidosis. A theoretical limitation of measurements of activity is that these may be affected by the presence of pharmacologic or endogenous inhibitors of ACE. Immunoassays of ACE concentration avoid this problem and, when combined with tests of ACE activity, permit calculation of specific activity of ACE. In this study, we set out to develop a sensitive radioimmunoassay for ACE to compare results obtained with this method with results of ACE activity and calculated ACE specific activity in patients suffering from a variety of lung diseases. In a group of control subjects (n equals 32), the ACE concentration was 453.7 plus minus 159.8 (SD) ng/mL; 95% confidence interval (CI), 398.34 to 509.06, but levels were significantly elevated in sarcoidosis (979.3 plus minus 558.6 ng/mL; 95% CI, 827.5 to 1,131.1; n equals 51; p less than 0.001 vs control subjects), silicosis (646.5 plus minus 239.1 ng/mL; 95% CI, 544.2 to 748.8; n equals 21; p less than 0.01), and miliary tuberculosis (647.0 plus minus 217.1 ng/mL; 95% CI, 551.9 to 742.1; n equals 29; p less than 0.01). The levels were normal in COPD, interstitial pulmonary fibrosis, and active cavitary pulmonary tuberculosis. The overall correlation between ACE activity and concentration measurements was strong (r equals 0.93). No evidence of endogenous ACE inhibition was observed in any of the disease categories studied except in COPD where an elevation of ACE specific activity was observed, raising the possibility that in this condition different isozymes of ACE with higher specific activity might be released.
(Chest 1995; 107:706-10)