TY - JOUR
T1 - Angiotensin converting enzyme (ACE) gene expression in the human left ventricle
T2 - Effect of ACE gene insertion/deletion polymorphism and left ventricular function
AU - Davis, Gershan K.
AU - Millner, Russell W.J.
AU - Roberts, David H.
PY - 2001/9/3
Y1 - 2001/9/3
N2 - Aims: We investigated the effect of the angiotensin converting enzyme (ACE) I/D polymorphism and left ventricular (LV) function on ACE gene expression in tru-cut LV myocardial biopsies from 50 consecutive patients (II: 18, ID: 18, DD: 14; 40 males) with ischaemic heart disease undergoing coronary artery bypass grafting (CABG). Methods: The polymerase chain reaction was used for ACE genotyping. LV function [normal (n = 22) or impaired] was determined by left ventriculography at cardiac catheterisation prior to bypass surgery. ACE expression was determined (n = 46) by a competitive quantitative reverse transcription PCR assay using 5 x 105, 12.5 x 105 and 20 x 105 copies of a mutant DNA internal standard (IS). PCR products were analysed by negative film photography and laser densitometry to determine the number of ACE transcripts present. Results: Mean age was similar (II: 59.1 ± 10.4, ID: 57.0 ± 10.6, DD: 61.4 ± 6.2; P = NS) with no differences between groups in sex (P = 0.25); hypertension, P = 0.31; previous myocardial infarction, P = 0.44; LV function, P = 0.23; and ACE inhibitor therapy, P = 0.06. ACE expression per 100 ng of total RNA varied with genotype [< 5 x 105 copies in II: 6, 5-12.5 x 105 copies in II: 6, ID: 16, DD: 4; and > 12.5 x 105 (II: 4, ID: 2, DD: 8), Kendall's tau-b coefficient (τ(b)) = 0.43, P = 0.003]. Impaired LV function also correlated with higher levels of ACE expression, Kendall's τ(b) = 0.40, P = 0.001. Conclusion: ACE gene expression in the left ventricle varied with ACE genotype and LV function in IHD patients undergoing CABG. (C) 2000 European Society of Cardiology.
AB - Aims: We investigated the effect of the angiotensin converting enzyme (ACE) I/D polymorphism and left ventricular (LV) function on ACE gene expression in tru-cut LV myocardial biopsies from 50 consecutive patients (II: 18, ID: 18, DD: 14; 40 males) with ischaemic heart disease undergoing coronary artery bypass grafting (CABG). Methods: The polymerase chain reaction was used for ACE genotyping. LV function [normal (n = 22) or impaired] was determined by left ventriculography at cardiac catheterisation prior to bypass surgery. ACE expression was determined (n = 46) by a competitive quantitative reverse transcription PCR assay using 5 x 105, 12.5 x 105 and 20 x 105 copies of a mutant DNA internal standard (IS). PCR products were analysed by negative film photography and laser densitometry to determine the number of ACE transcripts present. Results: Mean age was similar (II: 59.1 ± 10.4, ID: 57.0 ± 10.6, DD: 61.4 ± 6.2; P = NS) with no differences between groups in sex (P = 0.25); hypertension, P = 0.31; previous myocardial infarction, P = 0.44; LV function, P = 0.23; and ACE inhibitor therapy, P = 0.06. ACE expression per 100 ng of total RNA varied with genotype [< 5 x 105 copies in II: 6, 5-12.5 x 105 copies in II: 6, ID: 16, DD: 4; and > 12.5 x 105 (II: 4, ID: 2, DD: 8), Kendall's tau-b coefficient (τ(b)) = 0.43, P = 0.003]. Impaired LV function also correlated with higher levels of ACE expression, Kendall's τ(b) = 0.40, P = 0.001. Conclusion: ACE gene expression in the left ventricle varied with ACE genotype and LV function in IHD patients undergoing CABG. (C) 2000 European Society of Cardiology.
KW - Angiotensin converting enzyme
KW - Gene polymorphism
KW - Myocardium
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U2 - 10.1016/S1388-9842(00)00070-2
DO - 10.1016/S1388-9842(00)00070-2
M3 - Article (journal)
C2 - 10938484
AN - SCOPUS:0033857041
SN - 1388-9842
VL - 2
SP - 253
EP - 256
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 3
ER -