rdf:type |
|
lifeskim:mentions |
umls-concept:C0011854,
umls-concept:C0011860,
umls-concept:C0017337,
umls-concept:C0022638,
umls-concept:C0027567,
umls-concept:C0033422,
umls-concept:C0034987,
umls-concept:C0038323,
umls-concept:C1167622,
umls-concept:C1521761,
umls-concept:C1882417
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pubmed:issue |
1
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pubmed:dateCreated |
2009-2-24
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pubmed:abstractText |
Ketosis prone type 2 diabetes (KPD) is an atypical form of diabetes described mainly in people of sub-Saharan African origin. Its pathogenesis is unknown, although we have previously described a high prevalence of glucose-6-phosphate-dehydrogenase (G6PD) deficiency in patients with KPD. However, 50% of these deficient patients lacked the G6PD gene mutation. The isoforms of the transcription factor sterol regulatory element binding protein 1 (SREBP-1) are known to stimulate G6PD gene expression, and some polymorphisms in the SREBP-1 gene (SREBF-1) have been described only in Africans. We investigated one of these, the Arg585Gln polymorphism, in a candidate gene approach for KPD.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
Feb
|
pubmed:issn |
1262-3636
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pubmed:author |
pubmed-author:BoudouPP,
pubmed-author:ChoukemS-PSP,
pubmed-author:EberleDD,
pubmed-author:FoufelleFF,
pubmed-author:GautierJ-FJF,
pubmed-author:HadjadjSS,
pubmed-author:IbrahimFF,
pubmed-author:MoulinPP,
pubmed-author:SobngwiEE,
pubmed-author:VexiauPP,
pubmed-author:VilletteJ-MJM
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pubmed:issnType |
Print
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pubmed:volume |
35
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
20-4
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pubmed:meshHeading |
pubmed-meshheading:19062325-Adult,
pubmed-meshheading:19062325-African Continental Ancestry Group,
pubmed-meshheading:19062325-Amino Acid Substitution,
pubmed-meshheading:19062325-Arginine,
pubmed-meshheading:19062325-C-Peptide,
pubmed-meshheading:19062325-Cross-Sectional Studies,
pubmed-meshheading:19062325-Diabetes Mellitus, Type 1,
pubmed-meshheading:19062325-Diabetes Mellitus, Type 2,
pubmed-meshheading:19062325-Female,
pubmed-meshheading:19062325-Glutamine,
pubmed-meshheading:19062325-Humans,
pubmed-meshheading:19062325-Lipids,
pubmed-meshheading:19062325-Male,
pubmed-meshheading:19062325-Middle Aged,
pubmed-meshheading:19062325-Polymorphism, Genetic,
pubmed-meshheading:19062325-Sterol Regulatory Element Binding Protein 1
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pubmed:year |
2009
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pubmed:articleTitle |
The polymorphism Arg585Gln in the gene of the sterol regulatory element binding protein-1 (SREBP-1) is not a determinant of ketosis prone type 2 diabetes (KPD) in Africans.
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pubmed:affiliation |
Service de diabétologie et d'endocrinologie, hôpital Saint-Louis, 1, avenue Claude-Vellefaux, 75475 Paris cedex 10, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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