ACE gene insertion/deletion polymorphism has a mild influence on the acute development of left ventricular dysfunction in patients with ST elevation myocardial infarction treated with primary PCI
- Jiri Parenica†1Email author,
- Monika Pavkova Goldbergova†2,
- Petr Kala1,
- Jiri Jarkovsky3,
- Martin Poloczek1,
- Jan Manousek1,
- Krystyna Prymusova1,
- Lenka Kubkova1,
- Daniela Tomcikova3,
- Ondrej Toman1,
- Martin Tesak1,
- Josef Tomandl4,
- Anna Vasku2 and
- Jindrich Spinar1
© Parenica et al; licensee BioMed Central Ltd. 2010
Received: 16 April 2010
Accepted: 17 December 2010
Published: 17 December 2010
We evaluated the associations among angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism, ACE activity and post-myocardial infarction (MI) left ventricular dysfunction and acute heart failure (AHF) early after presentation with MI with ST-segment elevation (STEMI).
A total of 556 patients with STEMI treated by primary PCI (421 patients without AHF and 135 patients with AHF) were the study population. The activity of BNP, NT-ProBNP and ACE were measured at hospital admission and 24 h after MI onset. Left ventricular angiography was done before PCI; echocardiography was undertaken between the third and fifth day after MI.
In comparison with the II genotypes group, the DD/ID group had a higher level of ACE activity upon hospital admission (p < 0.001). We found a significantly higher level of ACE activity in patients with moderate LV dysfunction (EF 40-54%) in comparison both with patients with preserved LV function (EF ≥55%) and with patients with severe LV dysfunction (p = 0.028). A non-significant trend towards a higher incidence of mild AHF (22.1% vs. 16.02%, p = 0,093), a significantly higher value of end-systolic volume (ESV/BSA) (30.0 ± 12.3 vs. 28.5 ± 13.0; p < 0.05) and lower EF (50.2 ± 11.1 vs. 52.7 ± 11.7; p < 0.05) in the DD/ID genotypes group was noted. Even after multiple adjustments according to multivariate models, the EF for the DD/ID group remained significantly lower (p = 0,033). The DD/ID genotypes were associated with a significantly higher risk of EF <45% (OR 2.04 [95% CI 1.28; 3.25]).
These results suggest that the I/D polymorphism of ACE is associated with the development of LV dysfunction in the acute phase after STEMI. We demonstrated for the first time an association of the low ACE activity with the severe LV dysfunction, although patients with moderate LV dysfunction had higher level ACE activity than patients with preserved LV function.
The angiotensin-converting enzyme (ACE) is a membrane-bound, zinc metalloendopeptidase involved in the metabolism of many small peptides, particularly in activating angiotensin I to angiotensin II and inactivating bradykinin via the kallikrein-kininogen system. The enzyme is expressed on the surface of cells in many tissues, and its richest source is the lung. ACE also circulates in a soluble form produced by proteolytic cleavage of the extracellular portion from endothelial cells. Angiotensin II increases contraction of vascular smooth muscle cells. It also affects proliferation of smooth muscle cells; adhesion and diapedesis of monocytes through stimulation of expression of several adhesion molecules and chemoattractants; and the adhesion and aggregation of platelets. Angiotensin II stimulates inflammatory/fibrogenic responses during MI, thus promoting scar formation. On the other hand Angiotensin II-induced reactive oxygen species production may further damage myocardium in the border zones and enlarge infarct size . The ACE gene is located on chromosome 17q23. In the intron 16 of the ACE gene is an I/D polymorphism which contains an insertion (I) and deletion (D)--the presence or absence of 287 bp Alu repeat [2, 3]. Homozygotes for the deletion allele (DD) have serum ACE levels higher (on average) as those homozygous for the insertion allele (II), whereas heterozygotes (ID) have intermediate levels [2–4]. The genetic effect accounts for 28%-47% of the total variance of serum ACE [2, 3]. Also cardiac ACE activity is higher in subjects with the DD genotype . Early treatment by ACE inhibitors after myocardial infarction (MI) decreases adverse remodeling of the left ventricle, the incidence of heart failure, and mortality [5–11]. Several smaller studies found an increased risk of left ventricular enlargement or remodeling among individuals with the DD/ID genotype after MI [12–16], others were negative, but in the presence of ACEI therapy .
However recently published results detected new single-nucleotid polymorphisms associated with low mRNA expression and with adverse cardiovascular outcomes .
Based on these results, we hypothesized a higher activity of ACE in the acute stage of ST segment elevation myocardial infarction (STEMI) in patients with DD/ID genotypes compared with individuals homozygous for the insertion allele (II). We investigated if the ACE I/D polymorphism and levels of ACE activity in the acute period after STEMI treated with primary PCI were associated with post-MI left ventricular dysfunction and evidence of acute heart failure.
Written informed consent was obtained from all subjects before participation in the study. The study protocol complied with the Declaration of Helsinki, and was approved by the local Ethics Committee of Faculty Hospital Brno and by the Ethics Committee of the Masaryk University in Brno (Brno, Czech Republic).
From November 2005 to October 2008, 913 patients with STEMI were referred for primary percutaneous coronary intervention (PCI). They were admitted to the Coronary Care Unit (CCU) of Internal Cardiological Department of Faculty Hospital Brno. The diagnosis of STEMI was based on symptoms consistent with MI in conjuction with appropriate changes on electrocardiography (ECG) (ST-segment elevation or new left bundle branch block (LBBB)) and elevation in the levels of markers of myocardial necrosis (troponin I). Time from the onset of chest pain until primary PCI was <12 h. Standard therapy, including ACE inhibitors, beta-blockers and statins, was given as soon as possible after primary PCI. Exclusion criteria were: age >80 years (n = 112); known or newly diagnosed malignancy; inflammatory diesease or connective-tissue diesease; known previous LV dysfunction; estimated life expectancy <12 months (n = 48); refusal to sign the consent inform or non-compliance (n = 74); geographic reasons (distance from the place of residence to the hospital of >100 km without the possibility of follow-up; n = 35). In total, 51 patients were not included because of technical and organizational problems. Genotypes were not obtained for 37 patients. In total, 556 consecutive patients with STEMI were included in the present study. A control population of 200 healthy subjects (age, 48-80 years; median, 65 years; 76.5% male) without a history of CAD or heart failure were evaluated by specialized cardiologists in the Brno region. The diagnosis of acute heart failure was assessed according to clinical signs upon hospital admission and/or during hospitalization (Killip class I-IV). Mild acute heart failure was defined as pulmonary congestion with wet rales in the lower half of the lung fields or S3 gallop. The study population was divided into two groups according to ACE I/D polymorphism (DD/ID group and II group).
Samples of venous blood for analyses of the activity of B-type natriuretic peptide (BNP), N-terminal pro B-type natriuretic peptide (NT-ProBNP) and ACE were drawn immediately upon hospital admission before primary PCI (sample 1). Blood samples were drawn again at 24 h after the onset of chest pain (sample 2). Samples were centrifuged within 20 min in a refrigerated centrifuge, and the plasma and serum stored at -80°C. Standard biochemical and hematological blood tests were done immediately at hospital admission before primary PCI and 24 h after the onset of chest pain (including Troponin-I ADSV, Abbott Laboratories, Abbott Park, USA). BNP was analyzed using the AxSYM BNP-Microparticle Enzyme Immunoassay (Abbott Laboratories, Abbott Park, USA). NT-ProBNP was analyzed using the Cobas E411 NT-proBNP Imunoassay Kit (Roche Diagnostics, Indianapolis). The activity of ACE was analysed using ACE kinetic assay (Bühlmann laboratories AG, Switzerland).
Echocardiography was carried out during the index admission (between the third and fifth day after MI onset). Left ventricular end-systolic volume (LVESV), left ventricular end-diastolic volume (LVEDV), and left ventricular ejection fraction (LVEF) were estimated using the bi-planar Simpson's rule from apical two- and four-chamber views (93.8% and 94.6% of all measurements in DD/ID genotype group, resp. in II genotype group) or by the Teicholz formula. Echocardiography was assessed by two operators using Vivid 7 or Vivid i (GE Vingmed Ultrasound).
Ejection fraction (EF) was determined by LV angiography (5-F pigtail catheter) before primary PCI. A diseased coronary vessel was defined as having ≥50% reduction of the intraluminal diameter of any of the coronary arteries (left main, left anterior descending, left circumflex, right coronary) or the main branches with a diameter ≥2.0 mm. Significant left main artery stenosis was classified as "two-vessel disease".
DNA was extracted from peripheral leukocytes using the standard proteinase K technique. Genotyping of the insertion/deletion polymorphism in angiotensin I-converting enzyme (I/D ACE) was done using polymerase chain reaction (PCR) methods according to the method of Rigat and Shanmugam . DNA amplification was undertaken in a volume of 25 μL containing 50 ng genomic DNA with 1 unit Taq polymerase (MBI Ferments, USA). Using gel electrophoresis, PCR products were distinguished at 1.5% Serva with ethidium bromide in UV light as a 190 bp fragment in the absence of an Alu repeat insertion and a 490 bp fragment in the presence of the insertion (genotypes described as II-490 bp, ID-490+190 bp, and DD-190 bp). Blind samples were used to control the reliability of genotyping.
Summary statistics for categorical variables are shown as frequencies. Normally distributed continuous variables are shown as mean and SD or median and 5-95th percentile range for variables with non-normal distribution. Within all groups, the distributions of genotypes and consistency of genotype frequencies with the Hardy-Weinberg equilibrium were tested using the χ2 test on a contingency table of observed versus predicted genotype frequencies. The allelic frequences were compared by Fisher's exact test. The point estimates of the risk, the odds ratio (OR) and 95% confidence interval (CI) based on logistic regression were estimated and supplemented by their significance (Ward's test). Changes within groups were analyzed by Wilcoxon signed-ranks test, and differences between two groups were analyzed by the Mann-Whitney U test. Correlations were analyzed by Spearman's rank order correlation coefficient. A probability value of α < 0.05 was considered to indicate significance. Multivariate linear regression was applied for adjustment of markers of LV dysfunction on the influence of other variables. Preselection of variables based on univariate linear regression and a backward stepwise algorithm were used for the definition of these models. The power of tests and sample size were evaluated by EpiInfo6. Statistical analyses were undertaken using Stat View version 8.0 (SAS Institute Incorporated, 2008), SPSS 18.0.3 (IBM, Corporation 2010) and STATISTICA 8.0 (StatSoft, Inc. 2008).
Baseline characteristics of patients, treatment, and neurohumoral measurements in the ACE genotype group
N = 556
N = 393
N = 163
DD/ID vs. II
62.7 ± 10.5
62.7 ± 10.3
62.6 ± 10.8
83.9 ± 14.0
84.2 ± 14.1
83.1 ± 13.9
28.1 ± 3.9
28.1 ± 4.0
27.9 ± 3.7
BP systolic (mmHg)
135.6 ± 27.0
135.3 ± 27.2
136.1 ± 26.5
BP diastolic (mmHg)
74.7 ± 14.4
74.5 ± 14.2
75.1 ± 15.0
Heart rate (per min)
73.0 (52.0; 107.6)
72.0 (50.4; 109.4)
Time delay (min)
245.0 (122.1; 667.0)
228.0 (121.6; 590.2)
Mild AHF (%)
ACE inhibitors (%)
AT II (%)
8.2 (5.7; 17.4)
7.7 (5.3; 16.7)
Troponin I (ng/mL)
48.9 (3.2; 186.5)
52.2 (2.4; 181.3)
BNP at hospital admission (pg/mL)
66.2 (15.0; 504.1)
68.0 (15.0; 491.0)
BNP after 24 h (pg/ml)
286.7 (68.1; 892.9)
269.3 (70.0; 1145.5)
NT-ProBNP at hospital admission (pg/mL)
223.0 (33.0-4 233.0)
230.0 (33.0; 4512.0)
183.0 (28.1; 5350.2)
NT-ProBNP after 24 h (pg/mL)
ACE activity (IU/L)
33.6 (4.1; 70.6)
24.1 (4.4; 63.8)
Significant differences were not observed in the distributions of ACE genotypes and/or allele frequences between patients with acute MI (DD 29.5%, ID 41.2%, II 29.3%; I 46.5%, D 53.5%) and healthy controls (DD 28.1%, ID 50.7%, II 21.2%; D 50.1%, I 49.9%) (p = NS).
In comparison with the II genotype group, the DD genotype group had a higher level of ACE activity upon admission, while ID genotype group had an intermediate level of ACE activity (medians of ACE activities of DD vs ID vs II genotype groups were 36.7 U/L vs 31.4 U/L vs 24.1 U/L, p < 0.001). We found a significantly higher level of ACE activity for patients with moderate LV dysfunction (EF 40-54%; n = 301; described by median and 5-95th percentile (30.9 U/L (10.2-65.5)) in comparison both with patients with preserved LV function (EF ≥55%; n = 185; 28.5 U/L (8.2-60.4)) and in patients with severe LV dysfunction (EF ≤40%; n = 70; level of ACE activity 27.8 U/L (5.4-62.6)) (p = 0.028). Using multivariate linear regression, only age, previous treatment with ACE inhibitors or AT1-antagonists and I/D polymorphism were detected as variables with a statistically significant influence on ACE activity (25% of variability of ACE activity was explained by a given model; 4.9% of the total variability of ACE activity could be explained by ACE gene I/D polymorphism in this model).
Invasive and echocardiographic measurements
N = 556
N = 393
N = 163
DD/ID vs. II
1.89 ± 0.80
1.92 ± 0.80
1.83 ± 0.80
IRA - LM
IRA - LAD (%)
IRA - RCx (%)
IRA - RCA (%)
TIMI after PCI
49.4 ± 12.2
49.3 ± 21.4
49.7 ± 12.0
62.4 ± 17.0
62.1 ± 16.9
63.2 ± 17.5
29.6 ± 12.5
30.0 ± 12.3
28.5 ± 13.0
EF (echo) (%)
50.9 ± 11.3
50.2 ± 11.1
52.7 ± 11.7
Multivariate models for adjusting of parameters of left ventricle dysfunction
Ejection fraction (echo)
Ejection fraction (angiography)
IRA - RIA
Time delay (min)
ACE gene polymorphism and prognosis after MI
Samani  concluded that I/D polymorphism did not significantly influence the risk of mortality after MI in a group of 684 patients with MI. Yoshida  revealed that the endpoints of the study (cardiac death, reccurent MI or unstable angina) were significantly associated with the ACE ID polymorphism (RR = 4.49), and that the DD/ID genotype was associated with a higher occurrence of the endpoints. Similar results were revealed by Palmer . In a study of 978 patients after MI, the DD/ID genotypes were associated with a higher risk of mortality with an OR of 8.03 (95% CI, 2.16-29.88; p < 0.05). In the present study, an association of in-hospital mortality and I/D ACE polymorphism was not observed. This was probably because of the very short duration of follow-up (this work explored only the time of hospitalization) and fewer subjects.
ACE gene polymorphism, the level of ACE activity and left ventricle function
Circulating ACE probably originates from vascular endothelial cells. Higher levels of plasma ACE were found for the DD/ID genotypes of healthy subjects  as well as of patients with CAD [22, 23]. At the same time Danser  explored ACE activity in the cardiac tissue of subjects who died of non-cardiac disorders, and the highest levels were in subjects with the DD genotype. An elevated activity of ACE during the acute phase of STEMI in association with I/D polymorphism ACE has not been documented. We demonstrated for the first time a clear association of a higher activity of ACE in DD genotype group in comparison with II group in acute phase of STEMI, while the ID genotype group had an intermediate level of ACE activity. There is a lack of data concerning the ACE activity and its interaction with AHF and LV dysfunction. Cambien  indicated that a higher level of ACE in plasma could be a risk factor for MI independent of the I/D polymorphism. Nakai  concluded that the deletion polymorphism of the ACE gene was associated with a higher activity of ACE in serum and carried an increased risk of CAD in Japanese subjects. Other results were presented by Gardemann , who concluded that increased ACE activity was not a risk factor for CAD or MI. A completely new look Johnson  brought at 2009, he detected three promotor single-nucleotide polymorphisms (SNPs) of the ACE gene connected with reduced ACE mRNA expression in cardiac tissue. These identified SNPs (rs7213516 and rs4290) were tested in a large cohort of 1032 hypertonics and they were associated with adverse cardiovascular outcomes, largely attributable to nonfatal MI in African Americans. The high allele frequency was found in African Americans (16%), but low in Hispanics (4%) and very low in Caucasians (< 1%). We do not suppose these SNPs play a relevant role in our study population according to low allele frequency in Caucasians only 1 or 2 subjects could be expected. But very important is an idea that very low level of ACE activity could be harmfull. So far the higher levels of ACE activity associated with DD/ID genotypes of ACE were connected with worse prognosis , but existing results were not consistent [23, 24]. For the first time our results suggest a non-linear type of a dependence of ACE activity and adverse cardiac outcomes. As we showed, higher levels of ACE activity were associated with moderate LV dysfunction (EF 40-54%), but lower levels of ACE activity were found in patients with preserved LV function (EF ≥ 55%) as well as in patients with severe LV dysfunction (EF < 40%). The results of Johnson study  and the Valsartan Heart Failure (Val-HeFT) trial  raise the possibility, that excessive neurohormonal inhibition may contribute to adverse outcomes in heart failure treatment.
ACE gene polymorphism and LV systolic dysfunction after MI
Infarct size is one of the most important determinants of the progression of the LVEDV . Pinto et al.  reported that enlargement of the left ventricle 12 months after an anterior MI was more pronounced in patients with the DD genotype than in patients with the ID or II genotypes. They did not find any differences in the volumes of the left ventricle in the acute stage of MI . Ohmichi  associated the DD and ID genotypes of the ACE gene with the progression of the left ventricular end-diastolic volume index (LVEDVI) and end-systolic volume index (LVESVI) 4 months after MI. Multiple regression analysis revealed that the LVESVI at echocardiography 7 ± 4 days after MI and ACE I/D polymorphism are predictors of the increases in the LVEDVI a LVESVI on the second echocardiogram. In a group of 43 patients with old anteroseptal MI-treated PCI (they were not treated by ACE inhibitors), Nagashi  found a significantly higher LV end-systolic and end-diastolic dimension in the deletion group. Ulgen  proved the relationship of ACE gene polymorphism and LV remodeling in the early period in 142 patients with anterior MI. Echocardiographic examinations were undertaken within 24 h of MI and on the fifth day. LV systolic diameters, diastolic diameters and EF between the first and second echocardiographic results were significantly different in the DD group. Palmer  demonstrated a significantly greater LVEDV and the increased LVESV bordered on significance when 223 DD individuals were compared with grouped ID ad II patients (n = 572). This was not confirmed in a study by Zee , which provided no evidence of an association of the ACE I/D polymorphism with the risk of LV remodeling post-MI in the presence of ACE-I therapy. During the fifth day after MI, we demonstrated a significantly greater LVESVI and worse EF for the DD/ID genotypes in a homogenous group of patients with STEMI despite treatment by primary PCI and full pharmacological treatment (including ACE inhibitors given as soon as possible). We consider the difference of EF between the both genotype groups on the border of clinical significance, the absolute value of the EF difference was only 1.5% after adjustments for other variables. This borderline influence of ACE polymorphism may explain inconsistent results of previous smaller studies on the development of left ventricular dysfunction, especially when ACE inhibitors were administered.
ACE gene polymorphism and AHF
We did not find data in the literature concerning the clinical signs of AHF during the acute stages of MI and polymorphism of the ACE gene. An accurate assignation of diagnosis of acute heart failure could be influenced in border line by individual assessment of the subject status. We found a non-significant trend for an association of I/D ACE polymorphism and signs of mild AHF.
ACE gene polymorphism and BNP and NT-proBNP
BNP is a cardiac hormone that is secreted mainly from the ventricles in response to excessive stretching of cardiomyocytes. NT-proBNP is an inactive molecule resulting from the cleavage of the prohormone Pro-BNP. Palmer  showed that patients with the DD genotype had a significantly higher plasma level of BNP, N-terminal BNP, and endothelin levels within 96 h after MI than those observed in the II/ID group. These data was in correlation with a greater LVEDV in the DD group. In our study a significant association between DD/ID polymorphism of the ACE gene and BNP or NT-proBNP was not found even after the multiple adjustments for variables significantly influencing the level of BNP or NT-proBNP. Probably the later assesment of BNP/NT-proBNP after MI (96 hours in Palmer study vs 24 hours after MI onset in our study) is likely more relevant to determine subsequent development of left ventricular dysfunction in which the ACE polymorphism may participate.
Comparison with previous studies
Previous studies have not defined exactly the type of MI (NSTEMI or STEMI) and the manner of revascularization. Just the type and time of revascularization are crucial factors for the dysfunction and remodeling of the left ventricle and congestive heart failure. Primary PCI is associated with a significant reduction in mortality and reinfarction in patients with STEMI, above all in patients with AHF [27, 28]. Several trials and studies proved a positive influence of treatment by ACE inhibitors for the progression of LV remodeling and heart failure. Although patients had full treatment of acute coronary syndrome with STEMI--revascularization by primary PCI (PCI was succesful in 97.5% of patients), ACE inhibitors, beta-blockers and statins were usually administered immediately after PCI, we found a border interaction between I/D ACE polymorphism and signs of LV systolic dysfunction up to 5 days after MI. For the first time we confirmed definitely that the level of ACE activity is influenced by I/D polymorphism in acute stage of myocardial infarction, although only small part of ACE activity variability may be explained by this polymorphism. We demonstrated that the higher level of ACE activity is associated with the development of the moderate left ventricular dysfunction in comparison with ACE activity in patients with preserved left ventricular function. However the severe left ventricular dysfunction (EF < 40%) was associated also with low ACE activity. These new results may help explain ambiquous findings of previous studies.
Limitation of the study
Although our study population belongs to larger cohorts, on which interraction between left ventricular dysfunction and I/D polymorphism was investigated so far, a much larger group would be better to set up. The results brought new information about interraction among I/D gene polymorphism, ACE activity and the development of left ventricular dysfunction. However we do not believe the stratification of patients according to I/D polymorphism and ACE activity is useful in the daily clinical practice.
The present study clearly demonstrated an association between I/D gene polymorphism and the development of LV dysfunction in the acute stage of STEMI despite revascularization by primary PCI and early treatment using ACE inhibitors and beta-blockers. For the first time we confirmed definitely that the level of ACE activity is influenced by I/D polymorphism also in acute stage of myocardial infarction. We demonstrated that higher level of ACE activity was associated with the development of the moderate left ventricular dysfunction in comparison with ACE activity of patients with preserved left ventricular function, however the severe left ventricular dysfunction (EF < 40%) was associated with low ACE activity as well.
This study was supported by a research grant of IGA 1A 9880-3.
- Yao S: Myocardial repair/remodeling following infarction: roles of local factors. Cardiovasc Res. 2009, 81: 482-490.Google Scholar
- Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F: An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. Journal of Clinical Investigation. 1990, 86: 1343-1346. 10.1172/JCI114844.View ArticlePubMedPubMed CentralGoogle Scholar
- Tiret L, Rigat B, Visvikis S, Breda C, Corvol P, Cambien F, et al: Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels. American Journal of Human Genetics. 1992, 51: 197-205.PubMedPubMed CentralGoogle Scholar
- Danser AHJ, Schalekamp MADH, Bax WA, Van den Brink AM, Saxena PR, Riegger GAJ, et al: Angiotensin-converting enzyme in the human heart: Effect of the deletion/insertion polymorphism. Circulation. 1995, 92: 1387-1388.View ArticlePubMedGoogle Scholar
- ISIS-4: A randomised factorial trial assessing early oral captopril, oral mononitrate, and intravenous magnesium sulphate in 58 050 patients with suspected acute myocardial infarction. The Lancet. 1995, 345: 669-682. 10.1016/S0140-6736(95)90865-X.
- Gruppo Italiano per lo Studio della Soprawivenza nell'Infarto Miocardico: GISSI-3: effects of lisiriopril and transdermal glyceryl trinitrate singly and together on 6-week mortality and ventricular function after acute myocardial infarction. The Lancet. 1994, 343: 1115-1122.Google Scholar
- The Acute Infarction Ramipril Efficacy (AIRE) Study Investigators: Effect of ramipril on mortality and morbidity of survivors of acute myocardial infarction with clinical evidence of heart failure. The Lancet. 1993, 342: 821-828.Google Scholar
- Borghi C, Cicero AFG, Ambrosioni E: Effects of early treatment with zofenopril in patients with myocardial infarction and metabolic syndrome: The SMILE Study. Vascular Health and Risk Management. 2008, 4: 665-671.PubMedPubMed CentralGoogle Scholar
- Pfeffer MA, Braunwald E, Moye LA, Basta L, Brown J, Cuddy TE, et al: Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction - Results of the survival and ventricular enlargement trial. New England Journal of Medicine. 1992, 327: 669-677. 10.1056/NEJM199209033271001.View ArticlePubMedGoogle Scholar
- Køber L, Torp-Pedersen C, Carlsen JE, Bagger H, Eliasen P, Lyngborg K, et al: A clinical trial of the angiotensin-converting-enzyme inhibitor trandolapril in patients with left ventricular dysfunction after myocardial infarction. New England Journal of Medicine. 1995, 333: 1670-1676.View ArticlePubMedGoogle Scholar
- Ertl G, Kloner RA, Alexander RW, Braunwald E: Limitation of experimental infarct size by an angiotensin-converting enzyme inhibitor. Circulation. 1982, 65: 40-48.View ArticlePubMedGoogle Scholar
- Palmer BR, Pilbrow AP, Yandle TG, Frampton CM, Richards AM, Nicholls MG, et al: Angiotensin-converting enzyme gene polymorphism interacts with left ventricular ejection fraction and brain natriuretic peptide levels to predict mortality after myocardial infarction. Journal of the American College of Cardiology. 2003, 41: 729-736. 10.1016/S0735-1097(02)02927-3.View ArticlePubMedGoogle Scholar
- Ulgen MS, Ozturk O, Alan S, Kayrak M, Turan Y, Tekes S, et al: The relationship between angiotensin-converting enzyme (insertion/deletion) gene polymorphism and left ventricular remodeling in acute myocardial infarction. Coronary Artery Disease. 2007, 18: 10.1097/MCA.0b013e328010a4c4.Google Scholar
- Nagashima J, Musha H, So T, Kunishima T, Nobuoka S, Murayama M: Effect of angiotensin-converting enzyme gene polymorphism on left ventricular remodeling after anteroseptal infarction. Clinical Cardiology. 1999, 22: 587-590. 10.1002/clc.4960220909.View ArticlePubMedGoogle Scholar
- Ohmichi N, Iwai N, Maeda K, Shimoike H, Nakamura Y, Izumi M, et al: Genetic basis of left ventricular remodeling after myocardial infarction. International Journal of Cardiology. 1996, 53: 265-272. 10.1016/0167-5273(96)02562-4.View ArticlePubMedGoogle Scholar
- Pinto YM, Van Gilst WH, Herre Kingma J, Schunkert H: Deletion-type allele of the angiotensin-converting enzyme gene is associated with progressive ventricular dilation after anterior myocardial infarction. Journal of the American College of Cardiology. 1995, 25: 1622-1626. 10.1016/0735-1097(95)00090-Q.View ArticlePubMedGoogle Scholar
- Zee RYL, Solomon SD, Ajani UA, Pfeffer MA, Lindpaintner K: A prospective evaluation of the angiotensin-converting enzyme D/I polymorphism and left ventricular remodeling in the 'Healing and Early Afterload Reducing Therapy' Study. Clinical Genetics. 2002, 61: 21-25. 10.1034/j.1399-0004.2002.610104.x.View ArticlePubMedGoogle Scholar
- Johnson A, Gong Y, Wang D, Langaee T, Shin J, Cooper-DeHof R, et al: Promoter polymorphism in ACE (Angiotensin I-converting enzyme) associated with clinical outcomes in hypertension. Clin Pharmacol Ther. 2009, 85: 36-44. 10.1038/clpt.2008.194.View ArticlePubMedGoogle Scholar
- Rigat B, Hubert C, Corvol P, Soubrier F: PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1). Nucleic Acids Research. 1992, 20: 1433-10.1093/nar/20.6.1433-a.View ArticlePubMedPubMed CentralGoogle Scholar
- Samani NJ, Thompson JR, O'Toole L, Channer K, Woods KL: A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction. Circulation. 1996, 94: 708-712.View ArticlePubMedGoogle Scholar
- Yoshida M, Iwai N, Ohmichi N, Izumi M, Nakamura Y, Kinoshita M: D allele of the angiotensin-converting enzyme gene is a risk factor for secondary cardiac events after myocardial infarction. International Journal of Cardiology. 1999, 70: 119-125. 10.1016/S0167-5273(99)00064-9.View ArticlePubMedGoogle Scholar
- Cambien F, Costerousse O, Tiret L, Poirier O, Lecerf L, Gonzales MF, et al: Plasma level and gene polymorphism of angiotensin-converting enzyme in relation to myocardial infarction. Circulation. 1994, 90: 669-676.View ArticlePubMedGoogle Scholar
- Gardemann A, Weiss T, Schwartz O, Eberbach A, Katz N, Hehrlein FW, et al: Gene polymorphism but not catalytic activity of angiotensin I-converting enzyme is associated with coronary artery disease and myocardial infarction in low-risk patients. Circulation. 1995, 92: 2796-2799.View ArticlePubMedGoogle Scholar
- Nakai K, Itoh C, Miura Y, Hotta K, Musha T, Itoh T, et al: Deletion polymorphism of the angiotensin I-converting enzyme gene is associated with serum ACE concentration and increased risk for CAD in the Japanese. Circulation. 1994, 90: 2199-2202.View ArticlePubMedGoogle Scholar
- Cohn J, Tognoni G, Valsartan Heart Failure Trial Investigators: A randomized trial of the angiotensin-receptor blocker valsartan in chronic heart failure. New England Journal of Medicine. 2001, 345: 1667-1675. 10.1056/NEJMoa010713.View ArticlePubMedGoogle Scholar
- Pfeffer MA, Braunwald E: Ventricular remodeling after myocardial infarction: Experimental observations and clinical implications. Circulation. 1990, 81: 1161-1172.View ArticlePubMedGoogle Scholar
- Rott D, Behar S, Leor J, Hod H, Boyko V, Mandelzweig L, et al: Effect on survival of acute myocardial infarction in Killip classes II or III patients undergoing invasive coronary procedures. American Journal of Cardiology. 2001, 88: 618-623. 10.1016/S0002-9149(01)01802-1.View ArticlePubMedGoogle Scholar
- Flaherty JD, Bax JJ, De Luca L, Rossi JS, Davidson CJ, Filippatos G, et al: Acute Heart Failure Syndromes in Patients With Coronary Artery Disease. Early Assessment and Treatment. Journal of the American College of Cardiology. 2009, 53: 254-263. 10.1016/j.jacc.2008.08.072.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2261/10/60/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.