Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-10-19
pubmed:abstractText
The aim of this study was to investigate whether an association exists between the angiotensin converting enzyme (ACE) insertion/deletion (I/D) polymorphism and microvascular complications of type 2 diabetes mellitus in Turkish patients. A total of 239 type 2 diabetic patients and 138 sex and age matched control subjects were included into the study. The I/D polymorphism was determined by polymerase chain reaction (PCR). Nephropathy status was determined according to urinary albumin/creatinine ratio (microg/mg) (<30 normoalbuminuria, 30-300 microalbuminuria, >300 macroalbuminuria) and retinopathy was evaluated by fundoscopic examination and by flourescein fundus angiography. The distribution of ACE I/D polymorphism and allele frequencies in diabetic patients were not significantly different from controls, DD genotype 32.2 versus 37.2%; ID genotype 50.6 versus 47.1%; and II 17.2 versus 15.2%; D allele 57.5 versus 61.2%; I allele 42.5 versus 38.8%. Genotype distribution between normo-, micro- and macroalbuminuric patients did not differ significantly (DD:ID:II (%), normoalbuminuria, 35:46:19; microalbuminuria, 28:55:17; macroalbuminuria, 31:55:14). There was also no difference in genotype distribution between patients with and without retinopathy (DD:ID:II (%), retinopathy positive, 32:51:17; retinopathy negative, 33:49:18). In conclusion, the ACE I/D polymorphism does not seem to be associated with diabetic nephropathy and retinopathy in Turkish type 2 diabetic patients.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0168-8227
pubmed:author
pubmed:issnType
Print
pubmed:volume
54
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
95-104
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11640993-Adult, pubmed-meshheading:11640993-Aged, pubmed-meshheading:11640993-Albuminuria, pubmed-meshheading:11640993-Blood Pressure, pubmed-meshheading:11640993-Cholesterol, pubmed-meshheading:11640993-Cholesterol, HDL, pubmed-meshheading:11640993-Cholesterol, LDL, pubmed-meshheading:11640993-DNA Primers, pubmed-meshheading:11640993-Diabetes Mellitus, Type 2, pubmed-meshheading:11640993-Diabetic Angiopathies, pubmed-meshheading:11640993-Diabetic Nephropathies, pubmed-meshheading:11640993-Female, pubmed-meshheading:11640993-Hemoglobin A, Glycosylated, pubmed-meshheading:11640993-Humans, pubmed-meshheading:11640993-Male, pubmed-meshheading:11640993-Middle Aged, pubmed-meshheading:11640993-Peptidyl-Dipeptidase A, pubmed-meshheading:11640993-Polymorphism, Genetic, pubmed-meshheading:11640993-Triglycerides, pubmed-meshheading:11640993-Turkey
pubmed:year
2001
pubmed:articleTitle
Angiotensin-converting enzyme gene polymorphism and microvascular complications in Turkish type 2 diabetic patients.
pubmed:affiliation
Department of Internal Medicine, Medical Faculty, Gaziantep University, TR-27070, Gaziantep, Turkey. araz@gantep.edu.tr
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't