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July 8, 2014Hypertension110 citations

Dose-Dependent Arterial Destiffening and Inward Remodeling After Olmesartan in Hypertensives With Metabolic Syndrome

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SLStéphane LaurentPBPierre Boutouyrie

Key Result

Olmesartan at 40 and 80 mg significantly reduced pulse wave velocity compared with 20 mg (-0.61 m/s blood pressure-independent reduction; P=0.0066) at 52 weeks.

Key Points

  • This study investigates whether different doses of olmesartan can remodel the arterial wall in hypertensive patients with metabolic syndrome over a long-term period.
  • Phase III, multicenter, randomized, double-blind study
  • Participants (N=133) received olmesartan at 20 mg, 40 mg, or 80 mg for 1 year
  • Measurements included blood pressure and aortic stiffness at baseline, 24 weeks, and 52 weeks.
  • Pulse wave velocity significantly decreased in each group (P<0.001) over time with no significant time-dose interaction
  • Combining 40 and 80 mg olmesartan resulted in a significant reduction in pulse wave velocity (-0.61 m/s, P=0.0066) compared to 20 mg
  • Patients on 40 and 80 mg showed significant inward carotid remodeling, indicating improved arterial elasticity.

Study Design

Type

RCT (n=133)

Blinding

double-blind

Randomization

randomized

Multicenter

Yes

Structured PICO

Does high-dose olmesartan (40-80 mg) improve arterial destiffening and remodeling compared to low-dose (20 mg) in patients with hypertension and metabolic syndrome?

P
Population
133 subjects with hypertension and metabolic syndrome followed for 1 year.
I
Intervention
Olmesartan 40 mg (n=42) or 80 mg (n=47) oral once a day for 1 year
C
Comparator
Olmesartan 20 mg (n=44) oral once a day for 1 year
O
Outcome
Aortic stiffness (carotid-femoral pulse wave velocity) and carotid parameters at 52 weekssurrogate

Higher doses of olmesartan (40 and 80 mg) significantly remodel and destiffen the arterial wall during long-term treatment, partly independent of blood pressure reduction, compared to the 20 mg dose.

Main Result

Mean Difference: -0.61

p-value: p=0.0066

Abstract

Whether angiotensin receptor blockers can dose-dependently remodel the arterial wall during long-term treatment has been largely debated. In this phase III, multicenter, randomized, double-blind, parallel-group study, 133 subjects with hypertension and metabolic syndrome were assigned to olmesartan, either 20 mg (n=44), 40 mg (n=42), or 80 mg (n=47) once a day, according to a force titration design during a 1-year period. Office blood pressure, 24-hour blood pressure, aortic stiffness (carotid-femoral pulse wave velocity), and carotid parameters were measured at baseline, 24 weeks, and 52 weeks. Pulse wave velocity significantly decreased (P<0.001) with time in each group, with no significant time-dose interaction, despite a tendency (P=0.0685) for a smaller effect of 20 mg, compared with 40 and 80 mg at week 52. When the 40 and 80 mg doses were combined (40/80 mg versus 20 mg), a significant blood pressure-independent reduction in pulse wave velocity (-0.61 m/s) was observed at week 52 (P=0.0066), whereas the nonadjusted reduction was -1.31 m/s (P<0.0001). By contrast, after 20 mg, the blood pressure-independent reduction in pulse wave velocity was not significant. Patients receiving the highest dose of olmesartan (40 and 80 mg) had an inward carotid remodeling and were shifted toward a lower elastic modulus at a given circumferential wall stress, indicating an improvement in the intrinsic elastic properties of the carotid artery wall material. These data suggest that 40 and 80 mg olmesartan were able to significantly remodel and destiffen the arterial wall material during long-term treatment, partly independently of blood pressure, compared with 20 mg.

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Cite This Study

Laurent et al. (2014) conducted an RCT in hypertension and metabolic syndrome (n=133). Olmesartan vs. 20 mg once a day was evaluated on pulse wave velocity at week 52 (MD -0.61 m/s, p=0.0066). Olmesartan at 40 and 80 mg significantly reduced pulse wave velocity compared with 20 mg (-0.61 m/s blood pressure-independent reduction; P=0.0066) at 52 weeks.

synapsesocial.com/papers/6a22243c20559d46645817b7https://doi.org/10.1161/hypertensionaha.114.03282
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