ADENOSINE-DEAMINASE (ADA) ISOENZYME ANALYSIS IN PLEURAL EFFUSIONS - DIAGNOSTIC ROLE, AND RELEVANCE TO THE ORIGIN OF INCREASED ADA IN TUBERCULOUS PLEURISY
L. Valdes et al., ADENOSINE-DEAMINASE (ADA) ISOENZYME ANALYSIS IN PLEURAL EFFUSIONS - DIAGNOSTIC ROLE, AND RELEVANCE TO THE ORIGIN OF INCREASED ADA IN TUBERCULOUS PLEURISY, The European respiratory journal, 9(4), 1996, pp. 747-751
The rise in adenosine deaminase (ADA) activity in the pleural fluid of
tuberculous pleurisy patients, though used for diagnosis, is of unkno
wn origin. In this work, we determined ADA activity and the activities
of 2'-deoxyadenosine deaminase and ADA-2 in 350 patients. We also con
sidered whether the results throw light on the origin of high pleural
fluid ADA in tuberculous pleurisy and estimated the diagnostic efficie
ncy of 2'-deoxyadenosine deaminase, ADA-2 and total ADA activities wit
h and without the inclusion of the 2'-deoxyadenosine deaminase/ADA act
ivity ratio in a combined criterion. The 350 pleural effusions were cl
assified by previously established criteria as transudates (60 males/1
8 females) or as tuberculous (49 males/27 females), neoplastic (50 mal
es/39 females), parapneumonic (36 males/19 females), empyematous (11 m
ales/3 females), or miscellaneous (25 males/13 females) exudates. Tota
l ADA, ADA-2 and 2'-deoxyadenosine deaminase activities were, respecti
vely, 127.5+/-2.9, 103+/-29.5 and 42.8+/-14 U . L(-1) in tuberculous e
xudates. With diagnostic thresholds of 47, 40 and 22 U . L(-1) respect
ively, the sensitivities of ADA, ADA-2 and 2'-deoxyadenosine deaminase
for tuberculosis were 100, 100 and 95%; their specificities 91, 96 an
d 92%; and their efficiencies 93, 97 and 93%, respectively. One hundre
d and one effusions (all 76 tuberculous, 12 neoplastic, 4 parapneumoni
c and 9 empyematous exudates) had total ADA levels >47 U . L(-1); of t
hese, 8 neoplastic, 1 parapneumonic and all the tuberculous exudates h
ad a 2'-deoxyadenosine deaminase/ADA activity ratio <0.49. The criteri
on of simultaneously having ADA >47 U . L(-1), ADA-2 >40 U . L(-1) and
a 2'-deoxyadenosine deaminase/ADA activity ratio <0.49 was satisfied
by all the tuberculous effusions but only eight others (all neoplastic
) (sensitivity 100%, specificity 97%, efficiency 98%). We conclude tha
t: 1) high total ADA activity in tuberculous pleural effusions is due
mainly to an increase in ADA-2, and, therefore, originated from the on
ly known source monocytes and macrophages; 2) ADA-2 was a more efficie
nt diagnostic marker of tuberculous pleurisy than total ADA activity,
although the difference was not statistically significant; and 3) amon
g effusions with high total ADA the 2'-deoxyadenosine deaminase/ADA ac
tivity ratio differentiates tuberculous effusions from empyemas and pa
rapneumonic effusions, but fails to discriminate well between tubercul
ous and neoplastic effusions.