Schelleman Hedi, Klungel Olaf H, van Duijn Cornelia M, Witteman Jacqueline C M, Hofman Albert, de Boer Anthonius, Stricker Bruno H Ch
Department of Epidemiology & Biostatistics, Erasmus MC, Rotterdam, Netherlands.
Ann Pharmacother. 2006 Feb;40(2):212-8. doi: 10.1345/aph.1G316. Epub 2006 Jan 31.
Despite the availability of a variety of effective drugs, inadequate control of blood pressure is common. There are some indications that the angiotensin-converting enzyme (ACE) gene modifies the response to antihypertensive drugs, but the results have been inconclusive.
To investigate whether the insertion/deletion polymorphism of the ACE gene modifies blood pressure differences among subjects using diuretics, beta-blockers, calcium-channel antagonists, or ACE inhibitors.
Data were used from the Rotterdam Study, a population-based, prospective, cohort study in the Netherlands, which started in 1990 and included 7983 subjects aged 55 years or older. Data from 3 subsequent cross-sectional investigations were used, as well. Subjects were included if they had high blood pressure during one or more examinations and/or used monotherapy with a diuretic, beta-blocker, calcium-channel antagonist, or ACE inhibitor. A marginal, generalized, linear model was used to assess the association between the mean difference in systolic/diastolic blood pressure and antihypertensive classes stratified by the 3 genotypes.
In total, 3025 hypertensive individuals were included, and 6500 measurements of blood pressure were taken. The percentages of DD, ID, and II genotypes were 28.3%, 51.4%, and 20.3%, respectively. The mean differences in systolic blood pressure between the II and DD genotypes were 0.23 mm Hg (95% CI -5.48 to 5.94) for diuretics, -2.41 mm Hg (95% CI -6.72 to 1.90) for beta-blockers, 2.12 mm Hg (95% CI -4.64 to 8.89) for calcium-channel antagonists, and -2.01 mm Hg (95% CI -9.82 to 5.79) for ACE inhibitors.
The adjusted mean difference in diastolic and systolic blood pressure among diuretic, beta-blocker, calcium-channel antagonist, or ACE inhibitor users was not modified by the ACE insertion/deletion polymorphism.
尽管有多种有效药物可供使用,但血压控制不佳的情况很常见。有迹象表明,血管紧张素转换酶(ACE)基因会改变对抗高血压药物的反应,但结果尚无定论。
研究ACE基因的插入/缺失多态性是否会改变使用利尿剂、β受体阻滞剂、钙通道拮抗剂或ACE抑制剂的受试者之间的血压差异。
使用来自鹿特丹研究的数据,这是一项于1990年在荷兰开展的基于人群的前瞻性队列研究,纳入了7983名55岁及以上的受试者。还使用了随后3次横断面调查的数据。如果受试者在一次或多次检查中患有高血压和/或使用利尿剂、β受体阻滞剂、钙通道拮抗剂或ACE抑制剂进行单药治疗,则将其纳入研究。使用边际广义线性模型评估按3种基因型分层的收缩压/舒张压平均差异与抗高血压药物类别之间的关联。
总共纳入了3025名高血压个体,并进行了6500次血压测量。DD、ID和II基因型的百分比分别为28.3%、51.4%和20.3%。对于利尿剂,II型和DD型基因型之间的收缩压平均差异为0.23 mmHg(95%CI -5.48至5.94);对于β受体阻滞剂,为-2.41 mmHg(95%CI -6.72至1.90);对于钙通道拮抗剂,为2.12 mmHg(95%CI -4.64至8.89);对于ACE抑制剂,为-2.01 mmHg(95%CI -9.82至5.79)。
ACE插入/缺失多态性并未改变利尿剂、β受体阻滞剂、钙通道拮抗剂或ACE抑制剂使用者舒张压和收缩压的校正平均差异。