Lack of linkage and association of adrenomedullin and its receptor genes in French Caucasian rheumatoid arthritis trio families

Clin Exp Rheumatol. 2008 Nov-Dec;26(6):1083-6.

Abstract

Objective: Rheumatoid arthritis (RA) is characterized by hyperplasia of fibro-blast-like synoviocytes (FLSs), in part due to apoptosis resistance. Adrenomedullin, an anti-apoptotic peptide, is secreted more by RA than osteoarthritis FLSs. Adrenomedullin binds to a heterodimeric functional receptor, of calcitonin receptor-like receptor (CRLR) coupled with a receptor activity-modifying protein-2 (RAMP-2), which is also overexpressed by rheumatoid synoviocytes. Since adrenomedullin decreases RA FLS apoptosis, possibly contributing to the development of pannus, study of adrenomedullin and its receptor genes might reveal a linkage and association in French Caucasian RA trio families.

Methods: Within each of 100 families, one RA-affected patient and both parents underwent genotyping for polymorphisms of adrenomedullin, CRLR and RAMP-2, by PCR-restricted fragment-length polymorphism (RFLP) or Taqman 5' allelic discrimination assay. Statistical analysis relied on the transmission disequilibrium test, the affected family-based controls and the genotype relative risk. Haplotypes of CRLR were inferred, and linkage and association studies were performed.

Results: No significant transmission disequilibrium or association between the three genes and RA was observed. CRLR haplotypes revealed two major haplotypes, but no significant linkage with RA.

Conclusion: Our findings provided no significant linkage or association of adrenomedullin and CRLR-RAMP-2 genes with RA in the studied trio families. The two CRLR polymorphisms rs3771076 and rs3771084 should be investigated in larger samples.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenomedullin / genetics*
  • Adult
  • Arthritis, Rheumatoid / ethnology*
  • Arthritis, Rheumatoid / genetics*
  • Calcitonin Receptor-Like Protein
  • Family Health
  • Female
  • France / epidemiology
  • Genetic Predisposition to Disease / ethnology
  • Haplotypes
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Linkage Disequilibrium
  • Male
  • Membrane Proteins / genetics*
  • Polymorphism, Restriction Fragment Length
  • Receptor Activity-Modifying Proteins
  • Receptors, Calcitonin / genetics*
  • Risk Factors
  • White People / statistics & numerical data
  • Young Adult

Substances

  • ADM protein, human
  • CALCRL protein, human
  • Calcitonin Receptor-Like Protein
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Receptor Activity-Modifying Proteins
  • Receptors, Calcitonin
  • Adrenomedullin