Effect of Pravastatin on Erythrocyte Membrane Fatty Acid Contents in Patients With Chronic Kidney Disease

Sponsor
Dong-A University (Other)
Overall Status
Completed
CT.gov ID
NCT02992548
Collaborator
(none)
62
2
1
40
31
0.8

Study Details

Study Description

Brief Summary

Treatment using statin has been decreased the risk of cardiovascular events in pre-dialysis CKD population. Supplementation with omega-3 fatty acid (FA) lowers the risk of cardiovascular death in patients with myocardial infarction. This cardioprotective effect of omega-3 FA can be explained by anti-inflammatory, anti-oxidative, or anti-thrombotic effects. Statin such as pravastatin is also known to have anti-inflammatory and antioxidant properties, suggesting that statin may replace the cardioprotective effect of omega-3 fatty acids. Erythrocyte membrane oleic acid is significantly higher in patients with acute coronary syndrome than control subjects. The cardioprotective effect of omega-3 FA may also be related to decreased oleic acid content of erythrocyte membrane. There is no report about the effect of statin on FA including erythrocyte membrane oleic acid. As omega-3 FAs are recognized as therapeutic agents for reducing triglycerides, statin may affect on the erythrocyte membrane FA. Therefore, pravastatin supplementation can modify erythrocyte membrane FA contents including oleic acid in CKD patients.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Patients with chronic kidney disease (CKD) have higher risk of death and cardiovascular disease than general population. Treatment using statin has been decreased the risk of cardiovascular events in pre-dialysis CKD population. Supplementation with omega-3 fatty acid (FA) lowers the risk of cardiovascular death in patients with myocardial infarction. This cardioprotective effect of omega-3 FA can be explained by anti-inflammatory, anti-oxidative, or anti-thrombotic effects. Statin such as pravastatin is also known to have anti-inflammatory and antioxidant properties, suggesting that statin may replace the cardioprotective effect of omega-3 fatty acids.

Omega-3 FA such as EPA (eicosapentaenoic acid), DHA (docosahexaenoic acid), and EPA/arachidonic acid ratio are well known as key indicators of cardiovascular disease. In addition, erythrocyte membrane oleic acid is significantly higher in patients with acute coronary syndrome than control subjects. The cardioprotective effect of omega-3 FA may also be related to decreased oleic acid content of erythrocyte membrane. There is no report about the effect of statin on FA including erythrocyte membrane oleic acid. As omega-3 FAs are recognized as therapeutic agents for reducing triglycerides, statin may affect on the erythrocyte membrane FA. Therefore, pravastatin supplementation can modify erythrocyte membrane FA contents including oleic acid in CKD patients.

Study Design

Study Type:
Interventional
Actual Enrollment :
62 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Pravastatin on Erythrocyte Membrane Fatty Acid Contents in Patients With Chronic Kidney Disease
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Dec 31, 2018
Actual Study Completion Date :
Dec 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: pravastatin group

Use of pravastatin 20mg to 40mg

Drug: Pravastatin

Outcome Measures

Primary Outcome Measures

  1. mean change of erythrocyte membrane fatty acid including oleic acid [24 weeks after intervention]

Secondary Outcome Measures

  1. mean change of total cholesterol [24 weeks after intervention]

  2. mean change of triglyceride [24 weeks after intervention]

  3. mean change of LDL-cholesterol [24 weeks after intervention]

  4. mean change of HDL-cholesterol [24 weeks after intervention]

  5. mean change of adiponectin [24 weeks after intervention]

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • CKD patients who agreed with written informed consent

  • CKD patients who do not take statin

  • Who have LDL cholesterol over 100mg/dL and coronary vascular disease(CVD) or equivalent risk; Who have LDL cholesterol over 130mg/dL and two or more coronary vascular risk; Whose LDL cholesterol over 160mg/dL in patient with CKD stage 1 to 5 without dialysis.

Exclusion Criteria:
  • Patients with acute illness, a history of active infection, CVD, acute kidney injury during the past 3 months, or a history of malignancy or liver disease

  • Patients using statin, omega-3 fatty acid or sevelamer hydrochloride within 3 months

  • Patients who experienced side effects by statin treatment

  • Pregnant or pregnancy expected CKD patients

  • Patient with dyslipidemia due to nephrotic syndrome

  • Patient taken imaging study using contrast media during the past 14 days

  • Patient with albumin level < 3.0 g/dL

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dong-A University Busan Korea, Republic of 602715
2 Inje University, Pusan Paik Hospital Busan Korea, Republic of

Sponsors and Collaborators

  • Dong-A University

Investigators

  • Principal Investigator: Won Suk An, MD, Dong-A University
  • Study Director: Yeong Hoon Kim, MD, Inje University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
WON SUK AN, Professor, Dong-A University
ClinicalTrials.gov Identifier:
NCT02992548
Other Study ID Numbers:
  • prava_2016
First Posted:
Dec 14, 2016
Last Update Posted:
Mar 11, 2019
Last Verified:
Mar 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by WON SUK AN, Professor, Dong-A University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2019