Sustained Improvement of Arterial Stiffness and Blood Pressure after Long-Term Rosuvastatin Treatment in Patients with Inflammatory Joint Diseases: Results from the RORA-AS Study

PLoS One. 2016 Apr 19;11(4):e0153440. doi: 10.1371/journal.pone.0153440. eCollection 2016.

Abstract

Objective: Patients with inflammatory joint diseases (IJD) have a high prevalence of hypertension and increased arterial stiffness. The aim of the present study was to evaluate the effect of long-term rosuvastatin treatment on arterial stiffness, measured by augmentation index (AIx) and aortic pulse wave velocity (aPWV), and blood pressure (BP) in IJD patients with established atherosclerosis.

Methods: Eighty-nine statin naïve IJD patients with carotid atherosclerotic plaque(s) (rheumatoid arthritis n = 55, ankylosing spondylitis n = 23, psoriatic arthritis n = 11) received rosuvastatin for 18 months to achieve low-density lipoprotein cholesterol goal ≤1.8 mmol/L. Change in AIx (ΔAIx), aPWV (ΔaPWV), systolic BP (ΔsBP) and diastolic BP (ΔdBP) from baseline to study end was assessed by paired samples t-tests. Linear regression was applied to evaluate associations between cardiovascular disease (CVD) risk factors, rheumatic disease specific variables and medication, and ΔAIx, ΔaPWV, ΔsBP and ΔdBP.

Results: AIx, aPWV, sBP and dBP were significantly reduced from baseline to study end. The mean (95%CI) changes were: ΔAIx: -0.34 (-0.03, -0.65)% (p = 0.03), ΔaPWV: -1.69 (-0.21, -3.17) m/s2 (p = 0.03), ΔsBP: -5.27 (-1.61, -8.93) mmHg (p = 0.004) and ΔdBP -2.93 (-0.86, -5.00) mmHg (p = 0.01). In linear regression models, ∆aPWV was significantly correlated with ΔsBP and ΔdBP (for all: p<0.001).

Conclusions: There is an unmet need of studies evaluating CVD prevention in IJD patients. We have shown for the first time that long-term intensive lipid lowering with rosuvastatin improved arterial stiffness and induced a clinically significant BP reduction in patients with IJD. These improvements were linearly correlated and may represent novel insight into the pleiotropic effects by statins.

Trial registration: ClinicalTrials.gov NCT01389388.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aorta / drug effects
  • Aorta / metabolism
  • Arthritis, Psoriatic / drug therapy
  • Arthritis, Psoriatic / metabolism
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / metabolism
  • Atherosclerosis / metabolism
  • Blood Pressure / drug effects*
  • Blood Pressure Determination / methods
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / metabolism
  • Cholesterol, LDL / metabolism
  • Female
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Inflammation / drug therapy*
  • Joint Diseases / drug therapy*
  • Male
  • Middle Aged
  • Pulse Wave Analysis / methods
  • Risk Factors
  • Rosuvastatin Calcium / therapeutic use*
  • Spondylitis, Ankylosing / drug therapy
  • Spondylitis, Ankylosing / metabolism
  • Vascular Stiffness / drug effects*

Substances

  • Cholesterol, LDL
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Rosuvastatin Calcium

Associated data

  • ClinicalTrials.gov/NCT01389388

Grants and funding

AGS and SR received grants from The South-Eastern Norway Regional Health Authority to conduct the RORA-AS study (http://www.helse-sorost.no/omoss_/english_/), Grant numbers: 2013064 and 2013010. The study medication (rosuvastatin) in the RORA-AS study was provided by AstraZeneca (http://www.astrazeneca.com/). AstraZeneca had no further involvement in the study concerning data collection, analyses, interpretation or publication.