Serum lysozyme is used as a marker of sarcoidosis disease activity. In this
study we examined the association between lysozyme levels and the clinical
features of sarcoidosis and thus the clinical usability of this parameter
in a large population. One hundred ten sarcoidosis patients from central Ja
pan were examined for clinical features and serum lysozyme level at the fir
st visit to our hospital and on a regular basis thereafter. The sensitivity
of lysozyme for predicting sarcoidosis was 79.1%, whereas that of serum an
giotensin-converting enzyme (ACE) was 59.0%. Even in the cases without an e
levated serum ACE level, a value of 72.1% was obtained. The serum lysozyme
level demonstrated a significant tendency to increase with the number of or
gans involved (p < 0.01). There were significant differences among the four
radiographic stages (p < 0.05). The maximum serum lysozyme levels of patie
nts without a disappearance of abnormal shadows on chest radiography within
5 years were significantly greater than those of individuals with a disapp
earance (p < 0.05). A positive correlation between serum lysozyme and serum
ACE levels was observed. Because serum lysozyme is much less specific for
sarcoidosis than serum ACE, its diagnostic value may be limited. However, t
he sensitivity was high even when serum ACE levels were within normal limit
s and correlated well with clinical features in sarcoidosis. Therefore, thi
s parameter seems suitable for disease monitoring in proven cases.