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Articles |
1
Servicio Cardiología, Hospital de Cabueñes, 33280 Gijón, Spain.
2
Laboratorio Genética Molecular-Instituto
Investigación Nefrológica and
3
Servicio
Cardiología, Hospital Central de Asturias, 33006 Oviedo, Spain.
4
Servicio Medicina Interna, Hospital Monte Naranco,
E-33006 Oviedo, Spain.
a Author for correspondence. Fax 34-985-273657; e-mail
ecoto{at}hcas.Insalud.es
Background: Several studies based on different populations worldwide have described an association between cardiovascular diseases and genetic variations in the apolipoprotein E (APOE), angiotensinogen (AGT), angiotensin receptor type 1 (AT1R), and angiotensin-converting enzyme (ACE) genes. In addition, there is growing evidence of an interaction between hypercholesterolemia and the renin-angiotensin system in the risk for hypertension and atherosclerosis.
Methods: To determine whether the DNA polymorphisms in
APOE (
2,
3, and
4 alleles), AGT
(M235T), AT1R (1166 A/C),
and ACE (I/D) are
associated with early onset of myocardial infarction (MI), we genotyped
220 patients and 200 controls <55 years of age. Patients and controls
were males from the same homogeneous Caucasian population. Data
concerning hypertension, diabetes, and tobacco consumption were
recorded. The lipid profiles of patients and controls were also
determined.
Results: APOE, ACE,
AGT, and AT1R allele and genotype
frequencies did not differ between patients and controls. None of these
polymorphisms was related to the biochemical values in patients
or controls. The frequency of individuals who were both
APOE
4 allele carriers
and AGT-TT homozygotes was significantly higher in
patients than in controls (11% vs 3.5%; P =
0.0037). In patients, the frequency of
4 carriers was significantly higher
(P <0.00001) in those who were AGT-TT
(46%) than those who were AGT-MT/MM
(14%). Mean cholesterol was significantly higher in
AGT-TT + APOE
34/44 patients than in the
TM/MM +
34/44 or
TT +
23/33 genotypes
(P = 0.029).
Conclusions: Our data suggest a synergistic effect between the
APOE and AGT polymorphisms and early MI.
The increased risk could be mediated in part through higher cholesterol
concentrations among individuals who are AGT-TT +
APOE
4 allele
carriers.
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