Source:http://linkedlifedata.com/resource/pubmed/id/11571669
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2001-9-25
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pubmed:abstractText |
The recently described mutations within the human adipocyte-specific apM-1 gene might play a role in the pathogenesis of obesity, type 2 diabetes and related metabolic disorders. DESIGN: Frequency of apM-1 gene polymorphisms and their association with metabolic parameters was evaluated in a population-based sample of 556 type 2 (316 males / 240 females) diabetic patients. PCR-based RFLP analysis was performed in blood samples. The T --> G transition at nucleotide +45 within exon-2 [Gly15Gly] was detected with an allelic frequency of 0.91 for the wildtype allele and 0.09 for the mutated allele. The missense point mutation (TAC --> CAC) at nucleotide +331 within exon 3 [Tyr111His] was detected with an allelic frequency of 0.97 and 0.03, respectively. These frequencies did not differ from a non-diabetic cohort examined earlier. Concerning the Gly15Gly polymorphism, the TT-genotype was found in 457 (82.2%) and the TG-genotype in 99 (17.8%), concerning the Tyr111His polymorphism, TT-genotype was found in 525 (94.4) and TC-genotype in 31 (5.6%) of type 2 diabetic patients. In TG-genotype as compared to TT-genotype significantly more patients had LDL-serum levels in high LDL-classes (<150 mg/dl: 24.4% (TG) vs. 41.4% (TT), 150mg/dl to 190mg/dl: 40.0% (TG) vs. 33.9% (TT), >190 mg/l: 35.6% (TG) vs. 25.0% (TT); p = 0.010). No differences in serum levels of lipids were found in genotype-subgroups of the Tyr111His polymorphism. Thus, Gly15Gly polymorphism of apM-1 gene might play a role in dyslipidaemia in type 2 diabetic patients.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adiponectin,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol,
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins
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pubmed:status |
MEDLINE
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pubmed:issn |
0947-7349
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
109
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
320-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11571669-Adipocytes,
pubmed-meshheading:11571669-Adiponectin,
pubmed-meshheading:11571669-Aged,
pubmed-meshheading:11571669-Amino Acid Sequence,
pubmed-meshheading:11571669-Amino Acid Substitution,
pubmed-meshheading:11571669-Cholesterol,
pubmed-meshheading:11571669-Cholesterol, LDL,
pubmed-meshheading:11571669-Cohort Studies,
pubmed-meshheading:11571669-Diabetes Mellitus, Type 2,
pubmed-meshheading:11571669-European Continental Ancestry Group,
pubmed-meshheading:11571669-Female,
pubmed-meshheading:11571669-Humans,
pubmed-meshheading:11571669-Intercellular Signaling Peptides and Proteins,
pubmed-meshheading:11571669-Male,
pubmed-meshheading:11571669-Middle Aged,
pubmed-meshheading:11571669-Polymorphism, Genetic,
pubmed-meshheading:11571669-Proteins
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pubmed:year |
2001
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pubmed:articleTitle |
Gly15Gly polymorphism within the human adipocyte-specific apM-1gene but not Tyr111His polymorphism is associated with higher levels of cholesterol and LDL-cholesterol in caucasian patients with type 2 diabetes.
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pubmed:affiliation |
Department of Internal Medicine I, University of Regensburg, D-93042 Regensburg, Germany. Bettina.Zietz@klinik.uni-regensburg.de
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pubmed:publicationType |
Journal Article
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