DIABETIC COMPLICATIONS AND THE GENETICS OF SIGNAL-TRANSDUCTION - A STUDY OF RETINOPATHY IN NIDDM

Citation
N. Lucarini et al., DIABETIC COMPLICATIONS AND THE GENETICS OF SIGNAL-TRANSDUCTION - A STUDY OF RETINOPATHY IN NIDDM, Disease markers, 13(3), 1997, pp. 169-176
Citations number
32
Categorie Soggetti
Genetics & Heredity",Pathology
Journal title
ISSN journal
02780240
Volume
13
Issue
3
Year of publication
1997
Pages
169 - 176
Database
ISI
SICI code
0278-0240(1997)13:3<169:DCATGO>2.0.ZU;2-I
Abstract
Cytosolic low molecular weight acid phosphatase (ACP1) is a high polym orphic phosphotyrosine-protein-phosphatase involved in signal transduc tion. In NIDDM subjects we have found that ACP1 genotype is a highly s ignificant predictor of retinopathy, suggesting that genetic variabili ty of signal transduction may have an important role in the susceptibi lity to this complication. Adenosine deaminase, ABO blood groups and s everal clinical variables have been also considered. The results point out the importance of interactions between generic systems. Among non -genetic variables dislipidemia and treatment with insulin are signifi cantly associated with retinopathy.