Department of Cardiothoracic Surgery, The First People's Hospital of Yunnan Province, Kunming, Yunnan, China.
Health Research Institute, University of Canberra, Kirinari St, Bruce, ACT, 2617, Australia.
Cardiovasc Diabetol. 2019 Jan 30;18(1):14. doi: 10.1186/s12933-019-0817-1.
Carotid artery intima-media thickness (cIMT) progression is a surrogate marker of atherosclerosis with a high predictive value for future CVD risk. This study evaluates the comparative efficacies of lipid lowering, hypoglycemic, antihypertensive and antiplatelet medications on cIMT progression.
We conducted a network meta-analysis (NMA) to evaluate the relative efficacies of several drug classes in modifying cIMT progression. After a literature search in several electronic databases, studies were selected by following predetermined eligibility criteria. An inverse variance-heterogeneity model was used for NMA. Sensitivity analyses were performed to check the reliability of the overall NMA, and transitivity analyses were performed to examine the effects of modifiers on the NMA outcomes.
Data were taken from 47 studies (15,721 patients; age: 60.2 years [95% confidence interval (CI) 58.8, 61.6]; BMI: 27.2 kg/m [95% CI 26.4, 28.0]; and gender: 58.3% males [95% CI 48.3, 68.3]). Treatment duration was 25.8 months [95% CI 22.9, 28.7]. Of the 13 drug classes in the network, treatment with phosphodiesterase III inhibitors was the most effective in retarding annual mean cIMT against network placebo (weighted mean difference (WMD) - 0.059 mm [95% CI - 0.099, - 0.020) followed by the calcium channel blockers (WMD - 0.055 mm [95% CI - 0.099, 0.001]) and platelet adenosine diphosphate inhibitors (WMD - 0.033 mm [95% CI - 0.058, 0.008]). These 3 drug classes also attained the same positions when the NMA was conducted by using first-year changes in mean cIMT. In transitivity analyses, longer treatment duration, higher body mass index (BMI), and a higher baseline cIMT were found to be independently associated with a lesser reduction in annual mean cIMT. However, in a multivariate analysis with these 3 modifiers, none of these factors was significantly associated with annual change in mean cIMT. In the placebo group, age was inversely associated with annual change in mean cIMT independently.
Phosphodiesterase III inhibitors and calcium channel blockers are found more effective than other drug classes in retarding cIMT progression. Age, BMI, and baseline cIMT may have some impact on these outcomes.
颈动脉内膜中层厚度(cIMT)进展是动脉粥样硬化的替代标志物,对未来心血管疾病风险具有较高的预测价值。本研究评估了降脂、降糖、降压和抗血小板药物对 cIMT 进展的相对疗效。
我们进行了一项网络荟萃分析(NMA),以评估几种药物类别的相对疗效,以改变 cIMT 的进展。在几个电子数据库中进行文献检索后,根据预先确定的纳入标准选择研究。采用逆方差-异质性模型进行 NMA。进行敏感性分析以检查整体 NMA 的可靠性,并进行转换分析以检查修饰符对 NMA 结果的影响。
数据来自 47 项研究(15721 名患者;年龄:60.2 岁[95%置信区间(CI)58.8,61.6];BMI:27.2kg/m[95%CI 26.4,28.0];性别:58.3%男性[95%CI 48.3,68.3])。治疗持续时间为 25.8 个月[95%CI 22.9,28.7]。在网络中的 13 种药物类别中,磷酸二酯酶 III 抑制剂在阻止年度平均 cIMT 相对于网络安慰剂方面最为有效(加权平均差异(WMD)-0.059mm[95%CI-0.099,-0.020]),其次是钙通道阻滞剂(WMD-0.055mm[95%CI-0.099,0.001])和血小板二磷酸腺苷抑制剂(WMD-0.033mm[95%CI-0.058,0.008])。当使用第一年平均 cIMT 的变化进行 NMA 时,这 3 种药物类别也处于相同位置。在转换分析中,发现治疗持续时间较长、体重指数(BMI)较高和基线 cIMT 较高与每年平均 cIMT 的减少较少独立相关。然而,在使用这 3 个修饰符进行的多变量分析中,这些因素均与平均 cIMT 的年度变化无显著相关性。在安慰剂组中,年龄与平均 cIMT 的年度变化呈负相关。
与其他药物类别相比,磷酸二酯酶 III 抑制剂和钙通道阻滞剂在减缓 cIMT 进展方面更为有效。年龄、BMI 和基线 cIMT 可能对这些结果有一定影响。