Marshfield Clinic Research Institute, Marshfield, WI; University of Wisconsin School of Medicine and Public Health, Madison, WI.
Marshfield Clinic Research Institute, Marshfield, WI.
Am J Med. 2020 Aug;133(8):994-998. doi: 10.1016/j.amjmed.2020.01.023. Epub 2020 Feb 24.
Inflammation is intimately involved in the pathogenesis of atherosclerosis and is accurately measured by high-sensitivity C-reactive protein (hs-CRP), a sensitive marker for future risk of cardiovascular disease. The Correlation between Oral Health and Systemic Inflammation (COHESION) trial was designed to test the hypothesis that PlaqueHD, a plaque-identifying toothpaste, reduces hs-CRP.
The trial was designed initially to include 132 subjects with hs-CRP between 2.0 and 10.0 mg/L but instead randomized 112 between 0.5 and 10.0, of which 103 had baseline and follow-up data and comprised the intention-to-treat sample. Of these, a prespecified subgroup analysis included 40 with baseline hs-CRP >2.0 and all hs-CRP <10. Because the distribution of hs-CRP was skewed toward higher values, to achieve normality assumptions, the significance of changes in hs-CRP between groups over time was tested on log-transformed data using a mixed effects analysis of variance.
The intention-to-treat analysis showed no significant differences between the PlaqueHD and placebo group (P = .615). The prespecified subgroup analysis showed a significant difference between the PlaqueHD and placebo group (P = .047). Results of the analysis showed a reduction in hs-CRP at follow-up of 0.58 in the PlaqueHD and an increase of 0.55 in the placebo group.
These findings are compatible with those of a prior pilot trial that also suggested benefits only in subjects with baseline elevations. Future trials targeting reductions of hs-CRP levels should randomize subjects with baseline hs-CRP between 2.0 and 10.0 mg/L.
炎症与动脉粥样硬化的发病机制密切相关,可通过高敏 C 反应蛋白(hs-CRP)准确测量,hs-CRP 是心血管疾病未来风险的敏感标志物。口腔健康与全身炎症相关性研究(COHESION)旨在验证 PlaqueHD(一种菌斑识别牙膏)可降低 hs-CRP 的假设。
该试验最初设计纳入 132 例 hs-CRP 为 2.0 至 10.0 mg/L 的受试者,但实际纳入 112 例 hs-CRP 为 0.5 至 10.0 的受试者,其中 103 例有基线和随访数据,构成意向治疗样本。其中,一个预先指定的亚组分析包括 40 例基线 hs-CRP>2.0 且所有 hs-CRP<10 的受试者。由于 hs-CRP 的分布偏向较高值,为了满足正态性假设,使用混合效应方差分析对时间点两组间 hs-CRP 的变化进行对数转换后进行组间差异的显著性检验。
意向治疗分析显示 PlaqueHD 组与安慰剂组之间无显著差异(P=0.615)。预先指定的亚组分析显示 PlaqueHD 组与安慰剂组之间存在显著差异(P=0.047)。分析结果显示 PlaqueHD 组随访时 hs-CRP 降低 0.58,安慰剂组升高 0.55。
这些发现与之前一项初步试验结果一致,该试验也提示仅在基线升高的受试者中获益。未来针对 hs-CRP 水平降低的试验应将基线 hs-CRP 为 2.0 至 10.0 mg/L 的受试者随机分组。