Deakin University, IMPACT - the Institute for Mental and Physical Health and Clinical Translation, School of Medicine, Health Education and Research Building, Level 3 (Barwon Health), PO Box 281, Geelong, VIC, 3220, Australia.
Barwon Health, Geelong, Australia.
Calcif Tissue Int. 2022 Oct;111(4):396-408. doi: 10.1007/s00223-022-01004-9. Epub 2022 Jul 14.
Medications used to treat hypertension may affect fracture risk. This study investigated fracture risk for users of angiotensin converting enzyme inhibitors (ACEI) or angiotensin II receptor blockers (ARB). Participants (899 men, median age 70.3 yr (59.9-79.1), range 50.0-96.6 yr; 574 women, median age 65.5 yr (58.1-75.4), range 50.1-94.6 yr) were from the Geelong Osteoporosis Study. Medication use was self-reported and incident fractures were ascertained using radiological reports. Bone mineral density (BMD) was measured at the femoral neck. Participants were divided into four groups: (1) non-users without hypertension, (2) non-users with hypertension, (3) ACEI users and (4) ARB users. Dosage was calculated using the defined daily dose (DDD) criteria. Participants were followed from date of visit to first fracture, death or 31 December 2016, whichever occurred first. Cox proportional hazards models were used for analyses. At least one incident fracture was sustained by 156 men and 135 women over a median(IQR) of 11.5(6.2-13.2) and 10.9(6.3-11.6) years of follow-up, respectively. In unadjusted analyses, compared to non-users without hypertension, men in all three other groups had a higher risk of fracture (Hazard Ratio (HR, 95%CI) 1.54, 1.00-2.37; 1.90, 1.18-3.05; 2.15, 1.26-3.66), for non-users with hypertension, ACEI and ARB users, respectively). Following adjustment for age, prior fracture and BMD, these associations became non-significant. A dose effect for ARB use was observed; men using lower doses had a higher risk of fracture than non-users without hypertension, in both unadjusted (2.66, 1.34-5.29) and adjusted (2.03, 1.01-4.08) analyses, but this association was not observed at higher doses. For women, unadjusted analyses showed a higher risk for ACEI users compared to non-users without hypertension (1.74, 1.07-2.83). This was explained after adjustment for age, alcohol consumption, prior fracture and BMD (1.28, 0.74-2.22). No other differences were observed. In men, lower dose (0 < DDD ≤ 1) ARB use was associated with an increased risk of fracture. ACEI or ARB use was not associated with increased risk of incident fracture in women. These findings may be important for antihypertensive treatment decisions in individuals with a high risk of fracture.
用于治疗高血压的药物可能会影响骨折风险。本研究调查了血管紧张素转换酶抑制剂(ACEI)或血管紧张素 II 受体阻滞剂(ARB)使用者的骨折风险。参与者(899 名男性,中位年龄 70.3 岁(59.9-79.1),范围 50.0-96.6 岁;574 名女性,中位年龄 65.5 岁(58.1-75.4),范围 50.1-94.6 岁)来自吉朗骨质疏松症研究。用药情况为自我报告,使用放射学报告确定骨折事件。采用股骨颈骨密度(BMD)测量法。参与者被分为四组:(1)无高血压的非使用者,(2)有高血压的非使用者,(3)ACEI 使用者和(4)ARB 使用者。根据规定日剂量(DDD)标准计算剂量。从就诊日期开始随访至首次骨折、死亡或 2016 年 12 月 31 日,以先发生者为准。采用 Cox 比例风险模型进行分析。至少有 156 名男性和 135 名女性在中位(IQR)11.5(6.2-13.2)和 10.9(6.3-11.6)年的随访中发生了一次以上的骨折事件。在未调整分析中,与无高血压的非使用者相比,所有其他三组男性的骨折风险更高(风险比(HR,95%CI)1.54,1.00-2.37;1.90,1.18-3.05;2.15,1.26-3.66),非使用者高血压、ACEI 和 ARB 使用者)。在调整年龄、既往骨折和 BMD 后,这些关联不再具有统计学意义。ARB 使用率呈剂量效应;与无高血压的非使用者相比,使用低剂量的男性骨折风险更高,未调整(2.66,1.34-5.29)和调整(2.03,1.01-4.08)后,风险均升高,但在高剂量下并未观察到这种关联。对于女性,未调整分析显示 ACEI 使用者与无高血压的非使用者相比,骨折风险更高(1.74,1.07-2.83)。在调整年龄、饮酒、既往骨折和 BMD 后,这一关联得到了解释(1.28,0.74-2.22)。未观察到其他差异。对于男性,低剂量(0<DDD<=1)ARB 使用率与骨折风险增加相关。ACEI 或 ARB 的使用与女性的骨折风险增加无关。这些发现可能对高骨折风险个体的降压治疗决策具有重要意义。