Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11482
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dc.contributor.authorPatel, Sheila Ken
dc.contributor.authorWai, Bryanen
dc.contributor.authorMacIsaac, Richard Jen
dc.contributor.authorGrant, Sharon Len
dc.contributor.authorVelkoska, Elenaen
dc.contributor.authorOrd, Michelleen
dc.contributor.authorPanagiotopoulos, Siannaen
dc.contributor.authorJerums, Georgeen
dc.contributor.authorSrivastava, Piyush Men
dc.contributor.authorBurrell, Louise Men
dc.date.accessioned2015-05-16T01:05:40Z-
dc.date.available2015-05-16T01:05:40Z-
dc.date.issued2012-04-26en
dc.identifier.citationCardiovascular Diabetology 2012; 11(): 42en
dc.identifier.govdoc22533709en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11482en
dc.description.abstractConnective tissue growth factor (CTGF) has been implicated in the cardiac and kidney complications of type 2 diabetes, and the CTGF -945 G/C polymorphism is associated with susceptibility to systemic sclerosis, a disease characterised by tissue fibrosis. This study investigated the association of the CTGF -945 G/C promoter variant with cardiac complications (left ventricular (LV) hypertrophy (LVH), diastolic and systolic dysfunction) and chronic kidney disease (CKD) in type 2 diabetes.The CTGF -945 G/C polymorphism (rs6918698) was examined in 495 Caucasian subjects with type 2 diabetes. Cardiac structure and function were assessed by transthoracic echocardiography. Kidney function was assessed using estimated glomerular filtration rate (eGFR) and albuminuria, and CKD defined as the presence of kidney damage (decreased kidney function (eGFR <60 ml/min/1.73 m2) or albuminuria).The mean age ± SD of the cohort was 62 ± 14 years, with a body mass index (BMI) of 31 ± 6 kg/m2 and median diabetes duration of 11 years [25th, 75th interquartile range; 5, 18]. An abnormal echocardiogram was present in 73% of subjects; of these, 8% had LVH alone, 74% had diastolic dysfunction and 18% had systolic ± diastolic dysfunction. CKD was present in 42% of subjects. There were no significant associations between the CTGF -945 G/C polymorphism and echocardiographic parameters of LV mass or cardiac function, or kidney function both before and after adjustment for covariates of age, gender, BMI, blood pressure and hypertension. CTGF -945 genotypes were not associated with the cardiac complications of LVH, diastolic or systolic dysfunction, nor with CKD.In Caucasians with type 2 diabetes, genetic variation in the CTGF -945 G/C polymorphism is not associated with cardiac or kidney complications.en
dc.language.isoenen
dc.subject.otherAgeden
dc.subject.otherAlbuminuria.geneticsen
dc.subject.otherChi-Square Distributionen
dc.subject.otherConnective Tissue Growth Factor.geneticsen
dc.subject.otherDiabetes Mellitus, Type 2.complications.ethnology.geneticsen
dc.subject.otherDiabetic Nephropathies.diagnosis.ethnology.genetics.physiopathologyen
dc.subject.otherDiastole.geneticsen
dc.subject.otherEuropean Continental Ancestry Group.geneticsen
dc.subject.otherFemaleen
dc.subject.otherGene Frequencyen
dc.subject.otherGenetic Predisposition to Diseaseen
dc.subject.otherGlomerular Filtration Rate.geneticsen
dc.subject.otherHumansen
dc.subject.otherHypertrophy, Left Ventricular.ethnology.genetics.physiopathology.ultrasonographyen
dc.subject.otherKidney.physiopathologyen
dc.subject.otherLinear Modelsen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherMultivariate Analysisen
dc.subject.otherPhenotypeen
dc.subject.otherPolymorphism, Geneticen
dc.subject.otherPromoter Regions, Geneticen
dc.subject.otherRenal Insufficiency, Chronic.diagnosis.ethnology.genetics.physiopathologyen
dc.subject.otherRisk Assessmenten
dc.subject.otherRisk Factorsen
dc.subject.otherSystole.geneticsen
dc.subject.otherVentricular Dysfunction, Left.ethnology.genetics.physiopathology.ultrasonographyen
dc.subject.otherVentricular Function, Left.geneticsen
dc.subject.otherVictoria.epidemiologyen
dc.titleThe CTGF gene -945 G/C polymorphism is not associated with cardiac or kidney complications in subjects with type 2 diabetes.en
dc.typeJournal Articleen
dc.identifier.journaltitleCardiovascular diabetologyen
dc.identifier.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1186/1475-2840-11-42en
dc.description.pages42en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/22533709en
dc.identifier.orcid0000-0002-0845-0001-
dc.identifier.orcid0000-0003-1863-7539-
dc.type.austinJournal Articleen
local.name.researcherBurrell, Louise M
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptOffice for Research-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
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