Evaluation of lipid profile, macular toxicity and clinical manifestations according to APO E genotype in systemic lupus erythematosus and rheumatoid arthritis patients treated with chloroquine

Scand J Rheumatol. 2002;31(1):32-7. doi: 10.1080/030097402317255345.

Abstract

Objective: To investigate the effect of APO E gene polymorphism over lipid profile, macular toxicity and clinical manifestations in RA and SLE patients treated with chloroquine.

Materials and methods: We studied 45 RA and 29 SLE patients treated with chloroquine who were classified based on the therapeutic regime of chloroquine into three groups: A) Cumulative dose of 100-300 g, B) >300 g and C) Never received chloroquine. Clinical evaluation, fasting lipid profile, visual field testing and stereoscopic photos of the retina were performed. APO E genotype was determined by PCR-RFLP.

Results: Reduced apo B levels in RA and SLE according to the cumulative dose of chloroquine 2/3 APO E genotype in a subset of SLE patients were observed. Macular toxicity was independent of both APO E genotype and cumulative chloroquine dose.

Conclusions: Reduced apo B levels were observed associated to chloroquine treatment and 2/3 APO E genotype.

Publication types

  • Clinical Trial

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antirheumatic Agents / adverse effects*
  • Apolipoproteins E / genetics*
  • Arthritis, Rheumatoid / blood
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / genetics*
  • Chloroquine / adverse effects*
  • DNA / analysis
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Lipids / blood*
  • Lupus Erythematosus, Systemic / blood
  • Lupus Erythematosus, Systemic / drug therapy
  • Lupus Erythematosus, Systemic / genetics*
  • Macula Lutea / drug effects*
  • Male
  • Middle Aged
  • Ophthalmoscopy
  • Polymerase Chain Reaction
  • Polymorphism, Genetic
  • Polymorphism, Restriction Fragment Length
  • Retinal Diseases / chemically induced*
  • Retrospective Studies

Substances

  • Antirheumatic Agents
  • Apolipoproteins E
  • Lipids
  • Chloroquine
  • DNA