| Literature DB >> 33297350 |
Yi-Ming Chen1,2,3, Po-Ku Chen4,5,6, Ching-Kun Chang4,5, Chi-Chen Lin2,5, Hsin-Hua Chen1,2,3, Joung-Liang Lan4,6,7,8, Shih-Hsin Chang4,6, Der-Yuan Chen4,5,6,8.
Abstract
Apolipoprotein E (ApoE) polymorphism and adipokines are linked to atherosclerosis. We aimed to investigate the associations of apoE genotypes with adipokines, inflammatory parameters, and cardiovascular disease (CVD) risks in rheumatoid arthritis (RA) patients. We enrolled 152 RA patients and 49 healthy control (HC) subjects. The apoE genotyping was determined by a polymerase chain reaction, while plasma levels of adipokines and inflammatory cytokines were measured with ELISA. Although apoE genotypes distributions were indistinguishable between RA patients and HC, we found significantly higher levels of apoE and adipokines in RA patients compared with HC. RA patients with ε2ε3 genotype had lower levels of TNF-α, IL-6, resistin, and visfatin, but higher leptin levels compared with ε3ε3 genotype patients. Patients with ε3ε4 genotype had significantly higher low-density lipoprotein-cholesterol (LDL-C) levels and atherogenic index scores compared with ε2ε3 genotype carriers. Moreover, patients with ε2ε3 genotype had significantly lower 10-year CVD risk than ε3ε3 or ε3ε4 genotype patients. ε3ε4 genotype and adiponectin levels were independent predictors of a high 10-year CVD risk. RA patients with ε2ε3 genotype are associated with lower levels of TNF-α, IL-6, resistin, visfatin, and CVD risk, while RA patients with ε3ε4 genotype exhibited higher levels of LDL-C, insulin resistance, and higher CVD risks.Entities:
Keywords: adipokines; apoE genotypes; cardiovascular disease (CVD); lipid profile; rheumatoid arthritis (RA)
Year: 2020 PMID: 33297350 PMCID: PMC7762228 DOI: 10.3390/life10120330
Source DB: PubMed Journal: Life (Basel) ISSN: 2075-1729