Turner S T, Schwartz G L, Chapman A B, Boerwinkle E
Division of Hypertension, Department of Internal Medicine, Mayo Clinic and Foundation, 200 First Street S.W., Rochester, MN 55905, USA.
Curr Hypertens Rep. 2001 Oct;3(5):410-5. doi: 10.1007/s11906-001-0059-x.
Sequencing of the human genome has elevated the potential for genetic information to aid in the prevention, diagnosis, and treatment of common chronic diseases. One beneficial application of genetic information is the identification of variants that influence response to pharmaceutical agents used to lower blood pressure and prevent target organ complications of hypertension. Knowledge of genetic variants that influence blood pressure response to antihypertensive drugs may allow more individualized tailoring of antihypertensive drug therapy, and provide greater insight into the molecular mechanisms regulating blood pressure levels and causing hypertension.
人类基因组测序提高了利用遗传信息预防、诊断和治疗常见慢性病的可能性。遗传信息的一个有益应用是识别那些影响用于降低血压和预防高血压靶器官并发症的药物反应的变异。了解影响血压对抗高血压药物反应的遗传变异,可能会使抗高血压药物治疗更加个体化,并能更深入地洞察调节血压水平和导致高血压的分子机制。