Type 1 diabetes: evidence of interaction between ACP1 and ADA1 gene polymorphisms.

Abstract:

BACKGROUND:ACP1 (acid phosphatase locus 1, a cytosolic low-molecular-weight phosphotyrosin phosphatase) and ADA1 (adenosine deaminase locus 1) are two polymorphic systems involved in immune reactions. Observed interactions at the biochemical and clinical levels between the two systems prompted this investigation of a possible interaction concerning susceptibility to type 1 diabetes. MATERIAL/METHODS:Two hundred eighty-seven children admitted consecutively to the hospital for type 1 diabetes and 727 healthy newborn infants were studied. All were from the Caucasian Italian population living in the central area of Italy. ACP1 and ADA1 genotypes were determined by DNA analysis. RESULTS:In the type 1 diabetics the distribution of ACP1 genotypes was dependent on the ADA1 genotypes, showing an excess of the low-activity *A/*A and *A/*B genotypes in the ADA1*2 carriers compared with the ADA1*1/*1 subjects (OR: 2.200, 95%CI: 1.133-4.298). Such an association was not present in the healthy newborn infants. CONCLUSIONS:This investigation based on the biological effects of ACP1 and ADA1 on the immune system and on the known biochemical interaction between the two systems showed a significant interaction between the two system concerning susceptibility to type 1 diabetes. The low-activity ACP1 genotypes *A/*A and *A/*B carrying the low-activity ADA1*2 allele were more common in type 1 diabetic than in healthy newborns (OR: 1.699 95%CI: 1.066-2.702).

journal_name

Med Sci Monit

authors

Saccucci P,Manca Bitti ML,Bottini N,Rapini N,Piccinini S,D'Annibale F,Chiarelli F,Verrotti A,Bottini E,Gloria-Bottini F

subject

Has Abstract

pub_date

2009-10-01 00:00:00

pages

CR511-517

issue

10

eissn

1234-1010

issn

1643-3750

pii

878212

journal_volume

15

pub_type

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