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[title] => [A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose.]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Paterson+AD">Paterson AD , Waggott D , Boright AP , Hosseini SM , Shen E , Sylvestre MP , Wong I , Bharaj B , Cleary PA , Lachin JM , MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium) , Below JE , Nicolae D , Cox NJ , Canty AJ , Sun L , Bull SB ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Diabetes, Volume 59, p.539-49 (2010)</div>
<h3>URL:</h3><a href="http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614">http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614</a>
<h3>Abstract:</h3> <p>{OBJECTIVE: Glycemia is a major risk factor for the development of long-term complications in type 1 diabetes; however, no specific genetic loci have been identified for glycemic control in individuals with type 1 diabetes. To identify such loci in type 1 diabetes, we analyzed longitudinal repeated measures of A1C from the Diabetes Control and Complications Trial. RESEARCH DESIGN AND METHODS: We performed a genome-wide association study using the mean of quarterly A1C values measured over 6.5 years, separately in the conventional (n = 667) and intensive (n = 637) treatment groups of the DCCT. At loci of interest, linear mixed models were used to take advantage of all the repeated measures. We then assessed the association of these loci with capillary glucose and repeated measures of multiple complications of diabetes. RESULTS: We identified a major locus for A1C levels in the conventional treatment group near SORCS1 (10q25.1</p>
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[biblio_secondary_title] => [Diabetes]
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[biblio_authors] => [Paterson AD , Waggott D , Boright AP , Hosseini SM , Shen E , Sylvestre MP , Wong I , Bharaj B , Cleary PA , Lachin JM , MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium) , Below JE , Nicolae D , Cox NJ , Canty AJ , Sun L , Bull SB , ]
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[biblio_year] => [2010]
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[biblio_pages] => [539-49]
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[biblio_abst_e] => [{OBJECTIVE: Glycemia is a major risk factor for the development of long-term complications in type 1 diabetes; however, no specific genetic loci have been identified for glycemic control in individuals with type 1 diabetes. To identify such loci in type 1 diabetes, we analyzed longitudinal repeated measures of A1C from the Diabetes Control and Complications Trial. RESEARCH DESIGN AND METHODS: We performed a genome-wide association study using the mean of quarterly A1C values measured over 6.5 years, separately in the conventional (n = 667) and intensive (n = 637) treatment groups of the DCCT. At loci of interest, linear mixed models were used to take advantage of all the repeated measures. We then assessed the association of these loci with capillary glucose and repeated measures of multiple complications of diabetes. RESULTS: We identified a major locus for A1C levels in the conventional treatment group near SORCS1 (10q25.1]
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Paterson+AD">Paterson AD , Waggott D , Boright AP , Hosseini SM , Shen E , Sylvestre MP , Wong I , Bharaj B , Cleary PA , Lachin JM , MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium) , Below JE , Nicolae D , Cox NJ , Canty AJ , Sun L , Bull SB ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Diabetes, Volume 59, p.539-49 (2010)</div>
<h3>URL:</h3><a href="http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614">http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614</a>
<h3>Abstract:</h3> <p>{OBJECTIVE: Glycemia is a major risk factor for the development of long-term complications in type 1 diabetes; however, no specific genetic loci have been identified for glycemic control in individuals with type 1 diabetes. To identify such loci in type 1 diabetes, we analyzed longitudinal repeated measures of A1C from the Diabetes Control and Complications Trial. RESEARCH DESIGN AND METHODS: We performed a genome-wide association study using the mean of quarterly A1C values measured over 6.5 years, separately in the conventional (n = 667) and intensive (n = 637) treatment groups of the DCCT. At loci of interest, linear mixed models were used to take advantage of all the repeated measures. We then assessed the association of these loci with capillary glucose and repeated measures of multiple complications of diabetes. RESULTS: We identified a major locus for A1C levels in the conventional treatment group near SORCS1 (10q25.1</p>
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<div class="biblio_authors"><h3>Authors:</h3> <a href="/biblio/author/Paterson+AD">Paterson AD , Waggott D , Boright AP , Hosseini SM , Shen E , Sylvestre MP , Wong I , Bharaj B , Cleary PA , Lachin JM , MAGIC (Meta-Analyses of Glucose and Insulin-related traits Consortium) , Below JE , Nicolae D , Cox NJ , Canty AJ , Sun L , Bull SB ,</a></div>
<div class="biblio_source"><h3>Source: </h3> Diabetes, Volume 59, p.539-49 (2010)</div>
<h3>URL:</h3><a href="http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614">http://diabetes.diabetesjournals.org/cgi/pmidlookup?view=long&pmid=19875614</a>
<h3>Abstract:</h3> <p>{OBJECTIVE: Glycemia is a major risk factor for the development of long-term complications in type 1 diabetes; however, no specific genetic loci have been identified for glycemic control in individuals with type 1 diabetes. To identify such loci in type 1 diabetes, we analyzed longitudinal repeated measures of A1C from the Diabetes Control and Complications Trial. RESEARCH DESIGN AND METHODS: We performed a genome-wide association study using the mean of quarterly A1C values measured over 6.5 years, separately in the conventional (n = 667) and intensive (n = 637) treatment groups of the DCCT. At loci of interest, linear mixed models were used to take advantage of all the repeated measures. We then assessed the association of these loci with capillary glucose and repeated measures of multiple complications of diabetes. RESULTS: We identified a major locus for A1C levels in the conventional treatment group near SORCS1 (10q25.1</p>
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