Affiliations 

  • 1 Department of Pharmacology, School of Pharmaceutical Sciences, Shoolini University, Solan, Himachal Pradesh, India
  • 2 Pranveer Singh Institute of Technology, Pharmacy, Kanpur, Uttar Pradesh, India
  • 3 Raja Balwant Singh Engineering Technical Campus, Bichpuri, Agra, India
  • 4 Department of Anesthesia, Mediclinic Aljowhara Hospital, Al Ain, United Arab Emirates
  • 5 School of Pharmacy, Babu Banarasi Das University, Lucknow, Uttar Pradesh, India
  • 6 Department of Pharmacology, Bromatology and Toxicology, Faculty of Pharmacy and Biochemistry, Universidad Nacional Mayor de San Marcos, Lima 15001, Peru
  • 7 Amity Institute of Pharmacy, Amity University, Noida, Uttar Pradesh, India
  • 8 Jeffrey Cheah School of Medicine and Health Sciences, Monash University, Jalan Lagoon Selatan, Bandar Sunway, 47500 Selangor Darul Ehsan, Malaysia
  • 9 School of Health Sciences and Technology, University of Petroleum and Energy Studies, Bidholi, Dehradun, Uttarakhand, India
  • 10 Amity School of Pharmaceutical Sciences, Amity University, Mohali, Punjab, India
  • 11 Department of Pharmacology, Delhi Pharmaceutical Sciences and Research University, Pushp Vihar, Delhi, India
Can J Physiol Pharmacol, 2024 May 01;102(5):305-317.
PMID: 38334084 DOI: 10.1139/cjpp-2023-0259

Abstract

Mostly, cardiovascular diseases are blamed for casualties in rheumatoid arthritis (RA) patients. Customarily, dyslipidemia is probably the most prevalent underlying cause of untimely demise in people suffering from RA as it hastens the expansion of atherosclerosis. The engagement of inflammatory cytokines like tumor necrosis factor-α (TNF-α), interleukin-1 (IL-1), interleukin-6 (IL-6), etc., is crucial in the progression and proliferation of both RA and abnormal lipid parameters. Thus, lipid abnormalities should be monitored frequently in patients with both primary and advanced RA stages. An advanced lipid profile examination, i.e., direct role of apolipoproteins associated with various lipid molecules is a more dependable approach for better understanding of the disease and selecting suitable therapeutic targets. Therefore, studying their apolipoproteins is more relevant than assessing RA patients' altered lipid profile levels. Among the various apolipoprotein classes, Apo A1 and Apo B are primarily being focused. In addition, it also addresses how calculating Apo B:Apo A1 ratio can aid in analyzing the disease's risk. The marketed therapies available to control lipid abnormalities are associated with many other risk factors. Hence, directly targeting Apo A1 and Apo B would provide a better and safer option.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.