Open AccessDeletion Polymorphism of the Angiotensin I‐Converting Enzyme Gene Associates with Increased Risk for Late Potentials in Patients with Myocardial Infarction
Author(s) -
Nakai Kenji,
Chiba Naoki,
Shobuzawa Minoru,
Musha Takehiko,
Shiroto Takahiro,
Hosokawa Shunichi,
Kamata Junya,
Suzuki Tomomi,
Aoki Hidehiko,
Saiki Seiichi,
Hiramori Katsuhiko
Publication year - 1996
Publication title -
annals of noninvasive electrocardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.494
H-Index - 48
eISSN - 1542-474X
pISSN - 1082-720X
DOI - 10.1111/j.1542-474x.1996.tb00297.x
Subject(s) - medicine , ejection fraction , myocardial infarction , cardiology , qrs complex , genotype , angiotensin converting enzyme , infarction , pathogenesis , endocrinology , diastole , gene polymorphism , polymorphism (computer science) , gene , heart failure , blood pressure , biology , genetics
Background: The pathogenesis of the occurrence of late potentials (LP) has not been fully elucidated. Deletion polymorphism in the Angiotensin I‐converting enzyme (ACE) gene may relate the myocarclial remodeling after the myocardial infarction (Ml). The purpose of this study was to evaluate the significance of ACE gene polymorphism for the occurrence of LPs after Ml. Methods: A 287 base pair (bp) insertion/deletion polymorphism in intron 16 of the ACE gene was determined by polymerase chain reaction and LPs were also examined by signal‐averaged EGC in 136 patients with Ml. Polymorphism of the ACE gene was characterized by three genotypes: II, ID, and DD. Signal‐averaged ECG were recorded using X, Y, Z leads and LP were defined by time‐domain analysis as low amplitude potentials exceeding 20 ms after the QRS‐end and filtered QRS >115 ms. Results: Positive LPs were noted in 40 of 136 patients with Ml. No differences could be detected between patients with LP‐positive and LP‐negative for the location of Ml, the success rate of reperfusion therapy, and left ventricular end‐diastolic volume (126 ± 40 vs 113 ± 43 mL/m 2 ). In patients with LP‐positive compared with those in LP‐negative, filtered QRS was significantly higher (135 ± 8 vs 107 ± 8 ms), left ventricular ejection fraction was lower (47 ± 12 vs 54%± 11 %), and peak was higher (3602 ± 2928 vs 2614 ± 2360 IU/L). The frequency of ACE/DD genotype was associated with patients with LP‐positive (18 of DD, 18 of ID, and 4 of II for patients with LP‐positive, while 25 of DD, 42 of ID, and 29 of II for patients with LP‐negative). In the study population, the ACE / DD genotype was associated with patients with LP‐positive when compared with the ACE ID & II genotype (x 2 = 4.7, P = 0.03). Conclusion: ACE/DD genotype of the ACE gene may be associated with the occurrence of LP after Ml.