Progress and Future Aspects in Genetics of Human Hypertension

Author:

Zhao Qi,Kelly Tanika N.,Li Changwei,He Jiang

Publisher

Springer Science and Business Media LLC

Subject

Internal Medicine

Reference98 articles.

1. Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H, et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012;380:2224–60.

2. Danaei G, Finucane MM, Lin JK, Singh GM, Paciorek CJ, Cowan MJ, et al. National, regional, and global trends in systolic blood pressure since 1980: systematic analysis of health examination surveys and epidemiological studies with 786 country-years and 5.4 million participants. Lancet. 2011;377:568–77.

3. Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet. 2006;367:1747–57.

4. Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J. Global burden of hypertension: analysis of worldwide data. Lancet. 2005;365:217–23.

5. •• Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011;478:103–9. To date, this is the largest meta-analysis of genome-wide association studies (GWAS) of the phenotypes of blood pressure by the International Consortium of Blood Pressure (ICBP). It included a discovery GWAS among 69,395 individuals and a combined sample of about 200,000 Europeans. It identified 16 novel loci associated with blood pressure. A genetic risk score calculated by GWAS significant variants was associated with hypertension, left ventricular wall thickness, stroke, and coronary artery disease.

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