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PMID: 20943049 Published · ppublish English Journal Article

A study of Adenosine-Deaminase genetic polymorphism in rheumatoid arthritis.

International journal of immunopathology and pharmacology ·Vol. 23 ·No. 3 ·2010-00-00 ·Pages 791-5

Sebastiani GD, Bottini N, Greco E, Saccucci P, Canu G, Lucarelli P, Gloria-Bottini F, Fontana L

Abstract

Recent investigations suggest that Adenosine Deaminase (ADA) could play a role in susceptibility to rheumatoid arthritis (RA). The purpose of our study is to investigate the possible role of genetic variability of ADA in the susceptibility to RA. We studied three intragenic ADA polymorphisms, ADA1, ADA2 and ADA6, in a sample of 91 subjects with RA and in 246 healthy subjects from the same Caucasian population and compared genotype and pairwise haplotype distributions between cases and controls. No statistically significant differences between RA and controls are observed for ADA genotypes. A border line difference for ADA1-ADA2 haplotype distribution is observed due to a decreased proportion of ADA1 *2/ADA2 *2 haplotype in RA compared to controls. Our data indicate a border line effect of ADA gene polymorphism on susceptibility to RA that need to be confirmed in other clinical settings.

MeSH Terms
Adenosine Deaminase/genetics Alleles Amino Acid Substitution Arthritis, Rheumatoid/epidemiology,genetics Codon/genetics DNA/genetics DNA Primers Exons/genetics Female Genotype Haplotypes Humans Male Middle Aged Polymorphism, Genetic/genetics Reverse Transcriptase Polymerase Chain Reaction Rome/epidemiology
Chemicals
Codon DNA Primers DNA Adenosine Deaminase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Sebastiani G D
St. Camillo Hospital, Rheumatology Unit, Rome, Italy.
Bottini N
Greco E
Saccucci P
Canu G
Lucarelli P
Gloria-Bottini F
Fontana L
Article Info
Journal
International journal of immunopathology and pharmacology
Abbr.
Int J Immunopathol Pharmacol
ISSN
0394-6320
Published
2010-00-00
Pages
791-5
Language
English
Region
England
NLM ID
8911335
Subset
IM
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