Lp. Svetkey et al., Angiotensinogen genotype and blood pressure response in the Dietary Approaches to Stop Hypertension (DASH) study, J HYPERTENS, 19(11), 2001, pp. 1949-1956
Citations number
50
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Objective To determine the relationship between angiotensinogen (ANG) genot
ype and blood pressure response to the dietary patterns of the Dietary Appr
oaches to Stop Hypertension (DASH) trial. The angiotensin converting enzyme
(ACE) gene was also tested.
Design The DASH trial was a randomized outpatient feeding study comparing t
he effects on blood pressure (BP) of three dietary patterns: a control diet
, similar to typical American intake; a 'fruits and vegetables' diet (F/V)
that is rich in fruits and vegetables but otherwise resembles the control d
iet; and the DASH diet that is reduced in fats and that emphasizes fruits,
vegetables and low-fat dairy products. Participants' genotype was also dete
rmined.
Setting Four clinical sites.
Participants Adults with above-optimal BP or stage I hypertension.
Intervention Participants ate one of the three dietary patterns for 8 weeks
. Sodium intake and weight were held constant. In 356 of 459 DASH participa
nts, DNA was extracted from leukocytes and genotyped for the G-6A ANG polym
orphism and the D/I ACE polymorphism, by the polymerase chain reaction.
Main outcomes Genotype at ANG and ACE loci; BP after 8 weeks of interventio
n diet.
Results There was no association between ACE genotype and BP response. Asso
ciations with ANG polymorphism were significant: net systolic and diastolic
BP response to the DASH diet was greatest in individuals with the AA genot
ype (-6.93/-3.68 mmHg) and least in those with the GG genotype (-2.80/0.20
mmHg). A similar relationship existed for the F/V diet.
Conclusions ANG genotype is associated with BP response to the DASH diet Th
e AA genotype confers excess risk of hypertension and is associated with in
creased responsiveness to diet. (C) 2001 Lippincott Williams & Wilkins.