de Vries Frank, Pouwels Sander, Bracke Madelon, Lammers Jan-Willem, Leufkens Hubert, Klungel Olaf, van Staa Tjeerd
Utrecht Institute for Pharmaceutical Sciences, Division of Pharmacoepidemiology and Pharmacotherapy, Universiteit Utrecht, Utrecht, The Netherlands.
J Hypertens. 2008 Jan;26(1):124-9. doi: 10.1097/HJH.0b013e3282f0ab4a.
Use of inhaled corticosteroids may reduce the risk of acute myocardial infarction (MI) through reductions in systemic inflammation and C-reactive protein.
To examine the association between the use of inhaled corticosteroids and the risk of non-fatal acute MI.
In the Dutch PHARMO record linkage system database, we conducted a case-control study (2476 MI cases), nested in a cohort of antihypertensive drug users. The use of inhaled corticosteroids 100 days before the index date was compared with never use. We adjusted the analyses for the severity of the underlying respiratory disease and general drug and disease history.
We found that the use of inhaled corticosteroids was not associated with a decreased risk of non-fatal MI in antihypertensive drug users after adjustment for the underlying respiratory disease severity, adjusted odds ratio (OR) 1.24, 95% confidence interval (CI) 0.97-1.57. A higher daily dose (adjusted OR 1.82, 95% CI 0.80-4.13) and longer duration of use (adjusted OR 1.28, 95% CI 0.90-1.81) were not associated with a decreased risk of non-fatal MI. An inhaled corticosteroid dispensing in the 30 days before the index date was not protective but resulted in a 1.7-fold increased risk of non-fatal MI.
Our results do not support the hypothesis that inhaled corticosteroids protect against the risk of non-fatal MI by a reduction of systemic inflammation.
吸入性糖皮质激素的使用可能通过减轻全身炎症反应和降低C反应蛋白水平来降低急性心肌梗死(MI)的风险。
研究吸入性糖皮质激素的使用与非致命性急性心肌梗死风险之间的关联。
在荷兰PHARMO记录链接系统数据库中,我们开展了一项病例对照研究(2476例心肌梗死病例),该研究嵌套于一组抗高血压药物使用者队列中。将索引日期前100天吸入性糖皮质激素的使用情况与从未使用过的情况进行比较。我们对分析结果进行了调整,以考虑潜在呼吸系统疾病的严重程度以及一般用药和疾病史。
我们发现,在对潜在呼吸系统疾病严重程度进行调整后,吸入性糖皮质激素的使用与抗高血压药物使用者中非致命性心肌梗死风险的降低无关,调整后的比值比(OR)为1.24,95%置信区间(CI)为0.97 - 1.57。更高的每日剂量(调整后的OR为1.82,95%CI为0.80 - 4.13)和更长的使用持续时间(调整后的OR为1.28,95%CI为0.90 - 1.81)与非致命性心肌梗死风险的降低无关。索引日期前30天的吸入性糖皮质激素配药并无保护作用,反而导致非致命性心肌梗死风险增加了1.7倍。
我们的研究结果不支持吸入性糖皮质激素通过减轻全身炎症反应来预防非致命性心肌梗死风险这一假说。