The Effect of Atorvastatin on Lipid Profile and Inflammatory Marker in patient with Diabetes Dyslipidemia

Rezlie Bellatasie, Suharjono Suharjono, Wiwid Samsulhadi, Nur Palestin Ayumuyas

Research output: Contribution to journalArticlepeer-review

Abstract

Inflammation is the underlying cause of several comorbid diseases, including macrovascular complications that cause the highest mortality in diabetes patients. One of the pro-inflammatory cytokines used to assess inflammatory conditions in diabetes and its complications is IL-6. This study intends to analyze the effect of atorvastatin administration on lipid profile and inflammatory markers after 30 days and the correlation between lipid profile and IL-6. An observational prospective cohort study was conducted from November 2017 to January 2018 and approved by the ethical committee of General Hajj Hospital, Surabaya. Nineteen patients who met the inclusion criteria and signed the informed consent enrolled in this study. The measurement of lipid profile and IL-6 level were done twice, before and after 30 days of atorvastatin therapy. After atorvastatin administration, there was a 40.55% decrease in LDL level, a 15.34% decrease in TG level, a 30.70% decrease in total cholesterol level, which was statistically significant (p<0.05), and a 6.06% increase in HDL level. There was a 5.76% decrease in the IL-6 level (p>0.05). In conclusion, atorvastatin administration can improve lipid profile in diabetes patients with dyslipidemia. There was a decrease in IL-6 but not statistically different. From statistical analysis, there is no correlation found between lipid profile and IL-6.

Original languageEnglish
Pages (from-to)4105-4110
Number of pages6
JournalResearch Journal of Pharmacy and Technology
Volume15
Issue number9
DOIs
Publication statusPublished - Sept 2022

Keywords

  • Atorvastatin
  • IL-6
  • diabetes
  • dyslipidemia
  • lipid profile

Fingerprint

Dive into the research topics of 'The Effect of Atorvastatin on Lipid Profile and Inflammatory Marker in patient with Diabetes Dyslipidemia'. Together they form a unique fingerprint.

Cite this