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. 2010 Jul 26;2(7):187–197. doi: 10.4330/wjc.v2.i7.187

Table 4.

Effect of renin-angiotensin-aldosterone system gene polymorphisms on survival of patients with heart failure

Ref. Sample, design1 Endpoints Follow-up (mo) Mortality rate (%) SNP Main findings
Angiotensinogen
[75] 822 AD, HZ 12 24 M235T No association with endpoints
[78] 2273 AD, HT 48 18 M235T No association with endpoints
[83] 4513 AD 48 49.7 M235T, T174M Increased mortality in 174M patients
Angiotensin-converting enzyme
[75] 822 AD, HZ 12 24 I/D No association with endpoints
[73] 1943 AD, HT 60 42 I/D Increased risk of death in DD patients
[78] 2273 AD, HT 48 18 I/D No association with endpoints
[84] 3283 AD, HT 3-38 23 I/D Decreased survival in D allele patients untreated with beta-blockers. No differences in treated patients
[85] 4793 AD, HT 3-62 28.6 I/D Decreased survival in D allele patients untreated with β-blockers. No differences in treated patients and decreased impact with high dose ACE inhibitors
[86] 3233 AD, HZ 10 (median) 9.6 I/D Associated with severity of disease (NYHA class)
Angiotensin-II receptor type 1
[73] 1943 AD, HT 60 42 A1166C Not associated with end-points. Increased risk of mortality as haplotype (ACE DD)
[75] 822 AD, HZ 12 24 A1166C No correlation with mortality rate
[78] 2273 AD, HT 48 18 A1166C No association with endpoints
Aldosterone
[87] 3542 AD, HZ 12 3.4 -344 T/C Decreased survival in C allele patients. Isosorbide dinitrate and hydralazine improved composite score in TT genotype but had no impact on C allele
1

Study design;

2

Placebo controlled randomized trial;

3

Non-randomized, single group assignment. SNP: Single nucleotide polymorphism; AD: All cause mortality; CD: Cardiac mortality; HT: Heart transplantation; HZ: Hospitalizations; ACE: Angiotensin-converting enzyme.