Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis

Michele Zorzetto, Ilaria Ferrarotti, Rocco Trisolini, Luigi Lazzari Agli, Roberta Scabini, Monique Novo, Annalisa De Silvestri, Marco Patelli, Miryam Martinetti, MariaClara Cuccia, Venerino Poletti, Ernesto Pozzi, Maurizio Luisetti

Research output: Contribution to journalArticle

Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic, fibrotic disorder underlain by aberrant wound healing of repeated lung injury. Environmental triggers and genetic background are likely to act as modifiers of the fibrotic response. Erythrocyte complement receptor 1 is a membrane protein mediating the transport of immune complexes to phagocytes. Three gene polymorphisms are related to the erythrocyte surface density of complement receptor 1 molecules, which in turn are related to the rate of immune complexes' clearance. There is evidence of association between sarcoidosis and the complement receptor 1 gene. We wondered whether IPF is associated with the complement receptor 1 gene alleles coding for a reduced molecule/erythrocyte ratio. We studied 74 patients and 166 control subjects. Three polymorphic sites of the gene, A3650G exon 22, HindIII RFLP intron 27, and C5507G exon 33, were analyzed and found to be in linkage disequilibrium. The GG genotype for the C5507G exon 33 polymorphism was significantly more common in patients with IPF than in control subjects (odds ratio = 6.232, 95% confidence interval = 2.198-18.419, p = 0.00023). The significant difference was found in both sexes. These findings agree with speculations on the role of the complement receptor 1 gene in idiopathic pulmonary fibrosis.

Original languageEnglish
Pages (from-to)330-334
Number of pages5
JournalAmerican Journal of Respiratory and Critical Care Medicine
Volume168
Issue number3
DOIs
Publication statusPublished - Aug 1 2003

Fingerprint

Complement C1
Complement Receptors
Idiopathic Pulmonary Fibrosis
Exons
Erythrocytes
Genes
Antigen-Antibody Complex
Membrane Transport Proteins
Linkage Disequilibrium
Lung Injury
Sarcoidosis
Phagocytes
Restriction Fragment Length Polymorphisms
Wound Healing
Introns
Alleles
Odds Ratio
Genotype
Confidence Intervals

Keywords

  • Association study
  • Candidate gene
  • Gene sequencing
  • Immune complexes
  • Polymerase chain reaction

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine

Cite this

Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis. / Zorzetto, Michele; Ferrarotti, Ilaria; Trisolini, Rocco; Agli, Luigi Lazzari; Scabini, Roberta; Novo, Monique; De Silvestri, Annalisa; Patelli, Marco; Martinetti, Miryam; Cuccia, MariaClara; Poletti, Venerino; Pozzi, Ernesto; Luisetti, Maurizio.

In: American Journal of Respiratory and Critical Care Medicine, Vol. 168, No. 3, 01.08.2003, p. 330-334.

Research output: Contribution to journalArticle

Zorzetto, M, Ferrarotti, I, Trisolini, R, Agli, LL, Scabini, R, Novo, M, De Silvestri, A, Patelli, M, Martinetti, M, Cuccia, M, Poletti, V, Pozzi, E & Luisetti, M 2003, 'Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis', American Journal of Respiratory and Critical Care Medicine, vol. 168, no. 3, pp. 330-334. https://doi.org/10.1164/rccm.200302-221OC
Zorzetto, Michele ; Ferrarotti, Ilaria ; Trisolini, Rocco ; Agli, Luigi Lazzari ; Scabini, Roberta ; Novo, Monique ; De Silvestri, Annalisa ; Patelli, Marco ; Martinetti, Miryam ; Cuccia, MariaClara ; Poletti, Venerino ; Pozzi, Ernesto ; Luisetti, Maurizio. / Complement receptor 1 gene polymorphisms are associated with idiopathic pulmonary fibrosis. In: American Journal of Respiratory and Critical Care Medicine. 2003 ; Vol. 168, No. 3. pp. 330-334.
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