Takemoto Y, Sakatani M, Takami S, Tachibana T, Higaki J, Ogihara T, Miki T, Katsuya T, Tsuchiyama T, Yoshida A, Yu H, Tanio Y, Ueda E
Department of Medicine, National Kinki Central Hospital, Osaka, Japan.
Thorax. 1998 Jun;53(6):459-62. doi: 10.1136/thx.53.6.459.
Serum angiotensin converting enzyme (SACE) is considered to reflect disease activity in sarcoidosis. SACE activity is increased in many patients with active sarcoid lesions. The mechanism for the increased SACE activity in this disease has not been clarified. ACE insertion/deletion (I/D) gene polymorphism has been reported to have an association with SACE levels in sarcoidosis, but no evidence of an association between angiotensin II receptor gene polymorphism and SACE in this disease has been found. A study of the association of angiotensin II receptor gene polymorphisms with sarcoidosis was therefore undertaken.
ACE (I/D), angiotensin II type 1 receptor (AGTR1), and angiotensin II type 2 receptor (AGTR2) gene polymorphisms were investigated by polymerase chain reaction (PCR) and SACE levels were measured in three groups of patients: those with sarcoidosis or tuberculosis and normal controls.
There was no difference in allele frequency of AGTR1 and AGTR2 polymorphism among the three groups. Neither AGTR1 nor AGTR2 polymorphisms were associated with sarcoidosis. SACE activity was higher in patients with sarcoidosis with the AGTR1 A/C genotype than in others. However, this tendency was not detected in patients with tuberculosis.
The AGTR1 allele C is associated with high activity of SACE in patients with sarcoidosis. It is another predisposing factor for high levels of SACE in patients with sarcoidosis and is considered to be an independent factor from the ACE D allele for high levels of SACE in sarcoidosis. This fact could be one of the explanations for the increased SACE activity in sarcoidosis.
血清血管紧张素转换酶(SACE)被认为可反映结节病的疾病活动情况。许多有活动性结节病病变的患者SACE活性升高。该疾病中SACE活性升高的机制尚未阐明。据报道,ACE插入/缺失(I/D)基因多态性与结节病中的SACE水平有关,但尚未发现血管紧张素II受体基因多态性与该疾病中SACE之间存在关联的证据。因此,开展了一项关于血管紧张素II受体基因多态性与结节病关联的研究。
采用聚合酶链反应(PCR)研究ACE(I/D)、血管紧张素II 1型受体(AGTR1)和血管紧张素II 2型受体(AGTR2)基因多态性,并对三组患者(结节病患者、结核病患者和正常对照)的SACE水平进行测量。
三组之间AGTR1和AGTR2多态性的等位基因频率没有差异。AGTR1和AGTR2多态性均与结节病无关。AGTR1 A/C基因型的结节病患者的SACE活性高于其他患者。然而,在结核病患者中未发现这种趋势。
AGTR1等位基因C与结节病患者SACE的高活性相关。它是结节病患者SACE高水平的另一个易感因素,并且被认为是结节病中SACE高水平的与ACE D等位基因无关的独立因素。这一事实可能是结节病中SACE活性升高的解释之一。