Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1997-7-18
|
pubmed:abstractText |
In insulin-dependent (Type 1) diabetes mellitus (IDDM) the development of nephropathy is partly due to genetic susceptibility. Previously one study has demonstrated a relationship between a HindIII restriction polymorphism of the collagen IV alpha 1-chain gene and diabetic nephropathy. The aim of the present study was to evaluate such as association in a case-control study including 207 Danish IDDM patients: 116 with nephropathy (urinary albumin excretion rate (AER) > 300 mg 24 h-1) and 91 without nephropathy (AER < 30 mg 24 h-1). Using genomic DNA, HindIII restriction fragment length analysis revealed a bi allele polymorphism visualized by southern hybridization with a cDNA probe recognizing the collagen IV alpha 1-chain gene. No differences in genotype frequencies or allele frequencies were demonstrated comparing patients with and without nephropathy: p = 0.39 and p = 0.96, respectively. Neither were there any difference in genotype frequencies or allele frequencies when the patients were stratified according to the presence of proliferative retinopathy: p = 0.44 and p = 0.84, respectively. Pooling the diabetic groups revealed genotype frequencies and allele frequencies comparable to those found in 57 healthy unrelated Danish individuals. We conclude that in a Danish IDDM population a HindIII restriction polymorphism of the collagen IV alpha 1-chain gene is not associated with diabetic nephropathy, diabetic retinopathy or with diabetes per se.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0742-3071
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
143-7
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:9047092-Adult,
pubmed-meshheading:9047092-Albuminuria,
pubmed-meshheading:9047092-Alleles,
pubmed-meshheading:9047092-Collagen,
pubmed-meshheading:9047092-Denmark,
pubmed-meshheading:9047092-Diabetes Mellitus, Type 1,
pubmed-meshheading:9047092-Diabetic Nephropathies,
pubmed-meshheading:9047092-Diabetic Retinopathy,
pubmed-meshheading:9047092-Female,
pubmed-meshheading:9047092-Follow-Up Studies,
pubmed-meshheading:9047092-Genotype,
pubmed-meshheading:9047092-Hemoglobins,
pubmed-meshheading:9047092-Humans,
pubmed-meshheading:9047092-Male,
pubmed-meshheading:9047092-Polymorphism, Genetic,
pubmed-meshheading:9047092-Restriction Mapping,
pubmed-meshheading:9047092-Time Factors
|
pubmed:year |
1997
|
pubmed:articleTitle |
Genetic variation of a collagen IV alpha 1-chain gene polymorphism in Danish insulin-dependent diabetes mellitus (IDDM) patients: lack of association to nephropathy and proliferative retinopathy.
|
pubmed:affiliation |
Steno Diabetes Center, Gentofte, Denmark.
|
pubmed:publicationType |
Journal Article
|