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Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis
- Source :
- Cardiovascular Diabetology, Cardiovascular Diabetology; Vol 12
- Publication Year :
- 2013
- Publisher :
- Springer Science and Business Media LLC, 2013.
-
Abstract
- Background Left ventricular hypertrophy has multiple aetiologies including diabetes and genetic factors. We aimed to identify genetic variants predicting left ventricular hypertrophy in diabetic individuals. Methods Demographic, echocardiographic, prescribing, morbidity, mortality and genotyping databases connected with the Genetics of Diabetes Audit and Research in Tayside, Scotland project were accurately linked using a patient-specific identifier. Left ventricular hypertrophy cases were identified using echocardiographic data. Genotyping data from 973 cases and 1443 non-left ventricular hypertrophy controls were analysed, investigating whether single nucleotide polymorphisms associated with left ventricular hypertrophy in previous Genome Wide Association Studies predicted left ventricular hypertrophy in our population of individuals with type 2 diabetes. Meta-analysis assessed overall significance of these single nucleotide polymorphisms, which were also used to create gene scores. Logistic regression assessed whether these scores predicted left ventricular hypertrophy. Results Two single nucleotide polymorphisms previously associated with left ventricular hypertrophy were significant: rs17132261: OR 2.03, 95% CI 1.10-3.73, p-value 0.02 and rs2292462: OR 0.82, 95% CI 0.73-0.93 and p-value 2.26x10-3. Meta-analysis confirmed rs17132261 and rs2292462 were associated with left ventricular hypertrophy (p=1.03x10-8 and p=5.86x10-10 respectively) and one single nucleotide polymorphisms in IGF1R (rs4966014) became genome wide significant upon meta-analysis although was not significant in our study. Gene scoring based on published single nucleotide polymorphisms also predicted left ventricular hypertrophy in our study. Rs17132261, within SLC25A46, encodes a mitochondrial phosphate transporter, implying abnormal myocardial energetics contribute to left ventricular hypertrophy development. Rs2292462 lies within the obesity-implicated neuromedin B gene. Rs4966014 lies within the IGF1R1 gene. IGF1 signalling is an established factor in cardiac hypertrophy. Conclusions We created a resource to study genetics of left ventricular hypertrophy in diabetes and validated our left ventricular hypertrophy phenotype in replicating single nucleotide polymorphisms identified by previous genome wide association studies investigating left ventricular hypertrophy.
- Subjects :
- Male
medicine.medical_specialty
Neurokinin B
Endocrinology, Diabetes and Metabolism
Population
Genome-wide association study
Single-nucleotide polymorphism
Type 2 diabetes
030204 cardiovascular system & hematology
Left ventricular hypertrophy
Polymorphism, Single Nucleotide
Receptor, IGF Type 1
Mitochondrial Proteins
03 medical and health sciences
0302 clinical medicine
Ventricular hypertrophy
Diabetes mellitus
Internal medicine
Type 2 diabetes mellitus
Genetics
medicine
Humans
Phosphate Transport Proteins
Genetic Predisposition to Disease
education
Aged
Ultrasonography
Original Investigation
030304 developmental biology
0303 health sciences
education.field_of_study
business.industry
Case-control study
Middle Aged
medicine.disease
3. Good health
Diabetes Mellitus, Type 2
Case-Control Studies
Cardiology
Female
Hypertrophy, Left Ventricular
Cardiology and Cardiovascular Medicine
business
Genome-Wide Association Study
Subjects
Details
- ISSN :
- 14752840
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Cardiovascular Diabetology
- Accession number :
- edsair.doi.dedup.....c6f7220470570c340ac02e39f7b6bc3a
- Full Text :
- https://doi.org/10.1186/1475-2840-12-109