BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.
Authors: R Takayanagi; K Ohnaka; Y Sakai; R Nakao; T Yanase; M Haji; T Inagami; H Furuta; D F Gou; M Nakamuta Journal: Biochem Biophys Res Commun Date: 1992-03-16 Impact factor: 3.575
Authors: L Tiret; A Bonnardeaux; O Poirier; S Ricard; P Marques-Vidal; A Evans; D Arveiler; G Luc; F Kee; P Ducimetière Journal: Lancet Date: 1994-10-01 Impact factor: 79.321
Authors: A Bonnardeaux; E Davies; X Jeunemaitre; I Féry; A Charru; E Clauser; L Tiret; F Cambien; P Corvol; F Soubrier Journal: Hypertension Date: 1994-07 Impact factor: 10.190
Authors: Alexandra Dadarlat-Pop; Dana Pop; Lucia Procopciuc; Adela Sitar-Taut; Dumitru Zdrenghea; Gyorgy Bodizs; Raluca Tomoaia; Diana Gurzau; Florina Fringu; Silvana Susca-Hojda; Anca D Buzoianu Journal: Int J Gen Med Date: 2021-05-06
Authors: Thomas W Lindner; Charles D Deakin; Hildegunn Aarsetøy; Sten Rubertsson; Jon-Kenneth Heltne; Eldar Søreide Journal: Open Heart Date: 2014-08-14