Blood pressure is linked to salt intake and modulated by the angiotensinogen gene in normotensive and hypertensive elderly subjects

Citation
Ag. Johnson et al., Blood pressure is linked to salt intake and modulated by the angiotensinogen gene in normotensive and hypertensive elderly subjects, J HYPERTENS, 19(6), 2001, pp. 1053-1060
Citations number
20
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
JOURNAL OF HYPERTENSION
ISSN journal
02636352 → ACNP
Volume
19
Issue
6
Year of publication
2001
Pages
1053 - 1060
Database
ISI
SICI code
0263-6352(200106)19:6<1053:BPILTS>2.0.ZU;2-O
Abstract
Objectives To evaluate salt sensitivity in elderly subjects with different forms of hypertension and controls and to investigate any modulation by gen otype Design Randomized, double-blinded, placebo-controlled latin-square Setting Tertiary referral hospital Participants Community subjects (n = 46) aged greater than or equal to 60 y ears classified as isolated systolic hypertension [ISH; systolic blood pres sure (SBP)greater than or equal to 160, diastolic blood pressure (DBP)< 90 mmHg, n =191, diastolic a systolic hypertension (SDH; DBP greater than or e qual to 90 mmHg, n =10)and normotension (SBP < 160, DBP < 90 mmHg, n = 17). Intervention: Four 14 day treatments, 50, 100, 200 and 300 mmol/day of sodi um chloride supplementation interspersed with 14 day washout periods on a s alt-restricted diet. Main outcome measures The 24 h blood pressure, heart rate, weight, urinary sodium and creatinine clearance measured during baseline, treatment and was hout periods and angiotensinogen (AGT) and angiotensin converting enzyme(AC E)genotypes. Results For the entire cohort, the mean a standard error (SE) of change fro m baseline in SEP for 50, 100, 200 and 300 mmol/day salt was 7.7 +/- 2.4, 1 2.1 +/- 2.4, 16.6 +/- 3.0, 18.5 +/- 2.6 mmHg, respectively. For DBP, the re spective changes were: -0.1 +/- 1.5, 2.4 +/- 1.6, 3.0 +/- 1.5, 5.8 +/- 1.7 mmHg. The increase in SEP among ISH subjects was significantly higher than among subjects in the SDH and normotensive groups (P < 0.05). AGT genotype influenced the effect of salt dose on the change in DBP (P= 0.006) but not SEP (P= 0.7). Conclusions In healthy, older subjects, a linear increase in BP occurred wi th increasing salt dose, it appeared most pronounced in ISH subjects and co uld be modulated by AGT genotype.