New England Research Institutes, Inc., Watertown, Massachusetts.
Evans Department of Medicine and Whitaker Cardiovascular Institute, Boston University, Boston, Massachusetts.
J Urol. 2015 Feb;193(2):612-7. doi: 10.1016/j.juro.2014.08.108. Epub 2014 Sep 6.
Increasing evidence of a link between erectile dysfunction and cardiovascular disease suggests a shared vascular etiology with endothelial dysfunction as a plausible underlying biological mechanism. To our knowledge whether this association is different for large arterial endothelium compared to microvascular endothelium has not yet been established. We investigated the association of erectile dysfunction with macrovascular and microvascular endothelial function.
A sample of 390 men with a mean age of 55.5 years was recruited from the BACH survey, a population based survey of urological symptoms. Erectile dysfunction was assessed using IIEF-5. The percent of brachial artery flow mediated dilatation, a measure of macrovascular function, and hyperemic flow velocity in cm per second, a measure of microvascular function, were assessed by ultrasound. Linear regression was used to assess the association of erectile dysfunction and endothelial function, and adjust for potential confounders.
Reactive hyperemia was lower in men with vs without erectile dysfunction (mean ± SE 97.1 ± 2.5 vs 106.0 ± 1.6 cm per second, p = 0.003). However, the difference in flow mediated dilatation between men with vs without erectile dysfunction was statistically nonsignificant (mean 6.6% ± 0.33% vs 7.2% ± 0.24%, p = 0.147). The association of erectile dysfunction with reactive hyperemia was attenuated but it remained statistically significant in men with moderate to severe erectile dysfunction (IIEF-5 less than 12) after adjusting for traditional cardiovascular risk factors (p = 0.038).
These results provide evidence of greater microvascular than macrovascular endothelial dysfunction as a potential contributor to erectile dysfunction and an underlying mechanism linking erectile dysfunction and cardiovascular disease.
越来越多的证据表明勃起功能障碍与心血管疾病之间存在关联,提示内皮功能障碍是一种共同的血管发病机制,可能是潜在的生物学机制。据我们所知,这种关联在大动脉内皮与微血管内皮之间是否不同尚未确定。我们研究了勃起功能障碍与大血管和微血管内皮功能的关系。
从基于人群的泌尿系统症状 BACH 调查中招募了 390 名平均年龄为 55.5 岁的男性。使用 IIEF-5 评估勃起功能障碍。通过超声评估肱动脉血流介导的扩张率(反映大血管功能的指标)和每秒厘米的高流量速度(反映微血管功能的指标)。使用线性回归评估勃起功能障碍与内皮功能之间的关联,并调整潜在的混杂因素。
与无勃起功能障碍的男性相比,勃起功能障碍男性的反应性充血较低(平均±SE 97.1±2.5 与 106.0±1.6cm/s,p=0.003)。然而,勃起功能障碍男性与无勃起功能障碍男性之间的血流介导扩张差异无统计学意义(平均 6.6%±0.33%与 7.2%±0.24%,p=0.147)。在调整传统心血管危险因素后,勃起功能障碍与反应性充血之间的关联减弱,但在中重度勃起功能障碍(IIEF-5 小于 12)男性中仍具有统计学意义(p=0.038)。
这些结果提供了证据表明,微血管内皮功能障碍比大血管内皮功能障碍更为严重,可能是勃起功能障碍的一个潜在原因,也是勃起功能障碍与心血管疾病之间的潜在机制。