Associations between APOE genotypes and disease susceptibility, joint damage and lipid levels in patients with rheumatoid arthritis

PLoS One. 2013 Apr 17;8(4):e60970. doi: 10.1371/journal.pone.0060970. Print 2013.

Abstract

Objective: Apolipoprotein E (APOE) genotypes are associated with cardiovascular disease (CVD) and lipid levels. In rheumatoid arthritis (RA), an association has been found with disease activity. We examined the associations between APOE genotypes and disease susceptibility and markers of disease severity in RA, including radiographic joint damage, inflammatory markers, lipid levels and cardiovascular markers.

Method: A Norwegian cohort of 945 RA patients and 988 controls were genotyped for two APOE polymorphisms. We examined longitudinal associations between APOE genotypes and C-reactive protein (CRP), erythrocyte sedimentation rate (ESR) as well as hand radiographs (van der Heijde Sharp Score(SHS)) in 207 patients with 10 year longitudinal data. Lipid levels, cardiovascular markers and history of CVD were compared across genotypes in a cross sectional study of 136 patients. Longitudinal radiological data of cohorts from Lund and Leiden were available for replication. (N = 935, with 4799 radiographs).

Results: In the Norwegian cohort, associations between APOE genotypes and total cholesterol (TC) and low-density lipoproteins (LDL) were observed (ε2 < ε3/ε3 < ε4, p = 0.03 and p = 0.02, respectively). No association was present for acute phase reactant or CVD markers, but a longitudinal linear association between APOE genotypes and radiographic joint damage was observed (p = 0.007). No association between APOE genotypes and the severity of joint destruction was observed in the Lund and Leiden cohorts, and a meta- analysis combining all data was negative.

Conclusion: APOE genotypes are associated with lipid levels in patients with RA, and may contribute to dyslipidemia in some patients. APOE genotypes are not consistently associated with markers of inflammation or joint destruction in RA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute-Phase Reaction / blood
  • Acute-Phase Reaction / complications
  • Acute-Phase Reaction / genetics
  • Apolipoproteins E / genetics*
  • Arthritis, Rheumatoid / blood*
  • Arthritis, Rheumatoid / complications
  • Arthritis, Rheumatoid / diagnostic imaging
  • Arthritis, Rheumatoid / genetics*
  • Arthrography
  • Blood Sedimentation
  • C-Reactive Protein / metabolism
  • Cardiovascular Diseases / blood
  • Cardiovascular Diseases / complications
  • Cardiovascular Diseases / genetics
  • Case-Control Studies
  • Demography
  • Disease Progression
  • Female
  • Genetic Association Studies*
  • Genetic Predisposition to Disease*
  • Humans
  • Joints / pathology*
  • Lipids / blood*
  • Longitudinal Studies
  • Male
  • Meta-Analysis as Topic
  • Middle Aged
  • Norway

Substances

  • Apolipoproteins E
  • Lipids
  • C-Reactive Protein

Grants and funding

This work has been funded through grants from the Southern and Eastern Health Region of Norway (Helse Sør Øst). The work of AK and DPCdR is supported by grants of the Dutch Arthritis Foundation (Reumafonds). The work of AHMvdHvM is supported by the Dutch organization of Health research and development (Zon-MW). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.