ASSOCIATION BETWEEN ANGIOTENSIN-II RECEPTOR GENE POLYMORPHISM AND SERUM ANGIOTENSIN-CONVERTING ENZYME (SACE) ACTIVITY IN PATIENTS WITH SARCOIDOSIS
Citation
Y. Takemoto et al., ASSOCIATION BETWEEN ANGIOTENSIN-II RECEPTOR GENE POLYMORPHISM AND SERUM ANGIOTENSIN-CONVERTING ENZYME (SACE) ACTIVITY IN PATIENTS WITH SARCOIDOSIS, Thorax, 53(6), 1998, pp. 459-462
Categorie Soggetti
Respiratory System
SICI code
0040-6376(1998)53:6<459:ABARGP>2.0.ZU;2-8
Abstract
Background-Serum angiotensin converting enzyme (SACE) is considered to
reflect disease activity in sarcoidosis. SAGE activity is increased i
n many patients with active sarcoid lesions. The mechanism for the inc
reased SAGE activity in this disease has not been clarified. ACE inser
tion/deletion (I/D) gene polymorphism has been reported to have an ass
ociation with SAGE levels in sarcoidosis, but no evidence of an associ
ation between angiotensin II receptor gene polymorphism and SAGE in th
is disease has been found. A study of the association of angiotensin I
I receptor gene polymorphisms with sarcoidosis was therefore undertake
n. Methods-ACE (I/D), angiotensin II type 1 receptor (AGTR1), and angi
otensin II type 2 receptor (AGTR2) gene polymorphisms were investigate
d by polymerase chain reaction (PCR) and SAGE levels were measured in
three groups of patients: those with sarcoidosis or tuberculosis and n
ormal controls. Results-There was no difference in allele frequency of
AGTR1 and AGTR2 polymorphism among the three groups. Neither AGTR1 no
r AGTR2 polymorphisms were associated with sarcoidosis. SAGE activity
was higher in patients with sarcoidosis with the AGTR1 AIC genotype th
an in others. However, this tendency was not detected in patients with
tuberculosis. Conclusions-The AGTR1 allele C is associated with high
activity of SAGE in patients with sarcoidosis. It is another predispos
ing factor for high levels of SAGE in patients with sarcoidosis and is
considered to be an independent factor from the ACE D allele for high
levels of SAGE in sarcoidosis. This fact could be one of the explanat
ions for the increased SAGE activity in sarcoidosis.