Key result
Adenosine-Deaminase genetic polymorphisms showed no statistically significant differences in genotype distribution between rheumatoid arthritis patients and healthy controls.
Why the study?
Does genetic variability of Adenosine Deaminase (ADA) play a role in susceptibility to rheumatoid arthritis?
Case-Control (n=337)
Does genetic variability of Adenosine Deaminase (ADA) play a role in susceptibility to rheumatoid arthritis?
There is a borderline effect of ADA gene polymorphism on susceptibility to rheumatoid arthritis that requires further confirmation.
ADA polymorphisms show no RA association in this case-control study; leaves open a possible borderline effect needing larger confirmation.
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.
No takes yet. Share an insight, caveat, or question.
Sebastiani et al. (2010) conducted a case-control in Rheumatoid arthritis (n=337). Adenosine-Deaminase (ADA) genetic polymorphisms vs. Healthy controls was evaluated on Genotype and pairwise haplotype distributions. Adenosine-Deaminase genetic polymorphisms showed no statistically significant differences in genotype distribution between rheumatoid arthritis patients and healthy controls.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: