Survey of Turkish systemic lupus erythematosus patients for a particular mutation of C1Q deficiency

Clin Exp Rheumatol. 2000 Jan-Feb;18(1):75-7.

Abstract

Objective: Hereditary C1q deficiency is a rare disease and up to now only 41 cases have been reported. Since all but 3 cases developed SLE or SLE-like disease, C1q deficiency represents the most powerful disease susceptibility gene identified for the development of SLE in humans. A molecular defect in homozygous C1q deficiency has been identified in 13 families. Four of these families are Turkish in origin and they all share the same mutation which is a CAG to TAG change at codon 186 in the A chain. This led us to investigate whether this mutation might be found in Turkish SLE patients and whether it could cause increased disease susceptibility when expressed in the heterozygous form.

Methods: We screened 65 Turkish lupus patients and 49 healthy Turkish individuals by carrying out an amplification of exon 2 of the A chain and restriction enzyme analysis for the C1qA mutation.

Results: We found no other example of this mutation in either the homozygous or heterozygous forms.

Conclusion: C1q deficiency is one of the very strong disease susceptibility genes in lupus and may cause SLE via a critical role in the physiological clearance of apoptotic cells. However, C1q deficiency caused by a particular mutation in the A chain in a heterozygous form is not found in the Turkish SLE population.

MeSH terms

  • Adolescent
  • Adult
  • Alleles
  • Base Sequence / genetics
  • Child
  • Complement C1q / deficiency*
  • Complement C1q / genetics*
  • Female
  • Health Surveys*
  • Heterozygote
  • Homozygote
  • Humans
  • Lupus Erythematosus, Systemic / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Turkey

Substances

  • Complement C1q