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Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study.
Aikens, Rachael C; Zhao, Wei; Saleheen, Danish; Reilly, Muredach P; Epstein, Stephen E; Tikkanen, Emmi; Salomaa, Veikko; Voight, Benjamin F.
Afiliación
  • Aikens RC; Department of Biology, Swarthmore College, Swarthmore, PA.
  • Zhao W; Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Saleheen D; Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Reilly MP; Center for Non-Communicable Diseases, Karachi, Pakistan.
  • Epstein SE; Department of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Tikkanen E; Cardiology Division, Department of Medicine, and the Irving Institute for Clinical and Translational Research, Columbia University, New York, NY.
  • Salomaa V; MedStar Heart & Vascular Institute, MedStar Washington Hospital Center, Washington, DC.
  • Voight BF; Department of Public Health, University of Helsinki, Helsinki, Finland.
Diabetes ; 66(2): 543-550, 2017 02.
Article en En | MEDLINE | ID: mdl-27702834
ABSTRACT
Observational studies have shown that elevated systolic blood pressure (SBP) is associated with future onset of type 2 diabetes, but whether this association is causal is not known. We applied the Mendelian randomization framework to evaluate the causal hypothesis that elevated SBP increases risk for type 2 diabetes. We used 28 genetic variants associated with SBP and evaluated their impact on type 2 diabetes using a European-centric meta-analysis comprising 37,293 case and 125,686 control subjects. We found that elevation of SBP levels by 1 mmHg due to our genetic score was associated with a 2% increase in risk of type 2 diabetes (odds ratio 1.02, 95% CI 1.01-1.03, P = 9.05 × 10-5). To limit confounding, we constructed a second score based on 13 variants exclusively associated with SBP and found a similar increase in type 2 diabetes risk per 1 mmHg of genetic elevation in SBP (odds ratio 1.02, 95% CI 1.01-1.03, P = 1.48 × 10-3). Sensitivity analyses using multiple, alternative causal inference measures and simulation studies demonstrated consistent association, suggesting robustness of our primary observation. In line with previous reports from observational studies, we found that genetically elevated SBP was associated with increased risk for type 2 diabetes. Further work will be required to elucidate the biological mechanism and translational implications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Sanguínea / Diabetes Mellitus Tipo 2 Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Diabetes Año: 2017 Tipo del documento: Article País de afiliación: Panamá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Sanguínea / Diabetes Mellitus Tipo 2 Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Diabetes Año: 2017 Tipo del documento: Article País de afiliación: Panamá
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