rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2007-5-9
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pubmed:abstractText |
The insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme gene (ACE) is associated with altered serum ACE activity. Raised ACE levels and the ACE DD genotype are associated with a 3.2 to 6.8-fold increased risk of severe hypoglycemia in type 1 diabetes. This relationship has not been assessed in type 2 diabetes. We aimed to test for association of the ACE I/D polymorphism with severe hypoglycemia in type 2 diabetes. Patients with type 2 diabetes (n = 308), treated with insulin (n = 124) or sulphonylureas (n = 184), were classified according to whether or not they had previously experienced severe hypoglycemia. Samples of DNA were genotyped for the ACE I/D polymorphism using two alternative polymerase chain reactions to prevent mistyping due to preferential amplification of the D allele. Overall, 12% of patients had previously experienced one or more episodes of severe hypoglycemia. This proportion did not differ between genotype groups (odds ratio (95% confidence limits) for carriers of D allele relative to II homozygotes: 0.79 (0.35-1.78)). This study found no evidence for association of the ACE I/D polymorphism with severe hypoglycemia frequency in patients with type 2 diabetes. However, we cannot rule out a smaller effect (odds ratio </= 1.78). Our results suggest that any effect of ACE genotype on severe hypoglycemia risk in type 2 patients is likely to be smaller than that seen in type 1 diabetes. We recommend future larger-scale studies.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-10319862,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-10376450,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-10391391,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-10841123,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11331618,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11380755,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11418149,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11431175,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11522714,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11723093,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-11756350,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-12136392,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-12547848,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-12637987,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-15589062,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-15642485,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-1976655,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-7555560,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-7587846,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-7589820,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-7773733,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8268786,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8366922,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8485954,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8485955,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8521557,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8596493,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8720609,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-8941475,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-9049480,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-9264004,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-9321743,
http://linkedlifedata.com/resource/pubmed/commentcorrection/17487330-9454524
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:status |
PubMed-not-MEDLINE
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pubmed:issn |
1614-0575
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pubmed:author |
|
pubmed:issnType |
Electronic
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
76-81
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pubmed:dateRevised |
2009-11-18
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pubmed:year |
2006
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pubmed:articleTitle |
The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetes.
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pubmed:affiliation |
Institute of Biomedical and Clinical Science, Peninsula Medical School, Exeter, United Kingdom.
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pubmed:publicationType |
Journal Article
|