Source:http://linkedlifedata.com/resource/pubmed/id/15135805
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2004-5-11
|
pubmed:abstractText |
Cytokines and chemokines have been implicated in the pathogenesis of Type 1 diabetes mellitus (T1DM) and its microvascular complications. Recently, genetic variants of monocyte chemotactic protein-1 (MCP-1), CC-chemokine receptor 2 (CCR2), CC-chemokine receptor 5 (CCR5) genes have been identified. The aim was to investigate whether genetic variants of the MCP-1 G(-2518)A, CCR2B 64I, CCR5 G(59029)A, and CCR5 Delta32 are associated with T1DM and its microvascular complications. Two hundred and sixty patients with T1DM with and without diabetic microvascular complications, and 104 normal controls were recruited for this study. Genotypes of the MCP-1 G(-2518)A, CCR2B 64I, CCR5 G(59029)A, and CCR5 delta32 were performed by polymerase chain reaction followed by digestion with appropriate restriction endonucleases. Frequencies of the MCP-1 A(-2518) allele (74.6% vs. 63.5%, p < 0.003) and A/A genotype (54.5% vs. 34.6%, p < 0.001, Pc = 0.002) were significantly higher in patients with T1DM compared with normal controls. CCR5 G(59029) was slightly increased in the patients with microvascular complications compared with the uncomplicated (21.4% vs. 10%, p < 0.03, Pc = ns). The frequency of haplotype G/G/W was slightly increased in the patients with diabetic complications compared to the uncomplicated (39.6% vs. 28.8%, p < 0.02, Pc = ns). These results suggest that polymorphisms of the MCP-1, CCR2 and CCR5 genes may be associated with T1DM and its complications.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCL2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/CCR2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR5,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
1043-4666
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 2004 Elsevier Ltd.
|
pubmed:issnType |
Print
|
pubmed:day |
7
|
pubmed:volume |
26
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
114-21
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15135805-Adolescent,
pubmed-meshheading:15135805-Adult,
pubmed-meshheading:15135805-Chemokine CCL2,
pubmed-meshheading:15135805-Chemokines,
pubmed-meshheading:15135805-Child,
pubmed-meshheading:15135805-Child, Preschool,
pubmed-meshheading:15135805-Diabetes Mellitus, Type 1,
pubmed-meshheading:15135805-Female,
pubmed-meshheading:15135805-Humans,
pubmed-meshheading:15135805-Infant,
pubmed-meshheading:15135805-Male,
pubmed-meshheading:15135805-Middle Aged,
pubmed-meshheading:15135805-Polymorphism, Genetic,
pubmed-meshheading:15135805-Receptors, CCR2,
pubmed-meshheading:15135805-Receptors, CCR5,
pubmed-meshheading:15135805-Receptors, Chemokine
|
pubmed:year |
2004
|
pubmed:articleTitle |
Polymorphisms of chemokine and chemokine receptor genes in Type 1 diabetes mellitus and its complications.
|
pubmed:affiliation |
Molecular Medicine Research Group, Peninsula Medical School, Universities of Exeter and Plymouth, Plymouth PL6 8BX, UK.
|
pubmed:publicationType |
Journal Article
|