Dhingra Ravi, Sullivan Lisa M, Fox Caroline S, Wang Thomas J, D'Agostino Ralph B, Gaziano J Michael, Vasan Ramachandran S
National Heart, Lung, and Blood Institute's Framingham Heart Study, Framingham, MA 01702-5803, USA.
Arch Intern Med. 2007 May 14;167(9):879-85. doi: 10.1001/archinte.167.9.879.
Higher levels of serum phosphorus and the calcium-phosphorus product are associated with increased mortality from cardiovascular disease (CVD) in patients with chronic kidney disease (CKD) or prior CVD. However, it is unknown if serum phosphorus levels influence vascular risk in individuals without CKD or CVD.
We prospectively evaluated 3368 Framingham Offspring study participants (mean age, 44 years; 51% were women) free of CVD and CKD. We used multivariable Cox models to relate serum phosphorus and calcium levels to CVD incidence.
On follow-up (mean duration, 16.1 years), there were 524 incident CVD events (159 in women). In multivariable analyses and adjusting for established risk factors and additionally for glomerular filtration rate and for hemoglobin, serum albumin, proteinuria, and C-reactive protein levels, a higher level of serum phosphorus was associated with an increased CVD risk in a continuous fashion (adjusted hazard ratio per increment of milligrams per deciliter, 1.31; 95% confidence interval, 1.05-1.63; P=.02; P value for trend across quartiles = .004). Individuals in the highest serum phosphorus quartile experienced a multivariable-adjusted 1.55-fold CVD risk (95% confidence interval, 1.16%-2.07%; P=.004) compared with those in the lowest quartile. These findings remained robust in time-dependent models that updated CVD risk factors every 4 years and in analyses restricted to individuals without proteinuria and an estimated glomerular filtration rate greater than 90 mL/min per 1.73 m(2). Serum calcium was not related to CVD risk.
Higher serum phosphorus levels are associated with an increased CVD risk in individuals free of CKD and CVD in the community. These observations emphasize the need for additional research to elucidate the potential link between phosphorus homeostasis and vascular risk.
在慢性肾脏病(CKD)患者或既往有心血管疾病(CVD)的患者中,血清磷水平升高及钙磷乘积升高与心血管疾病死亡率增加相关。然而,血清磷水平是否会影响无CKD或CVD的个体的血管风险尚不清楚。
我们对3368名无CVD和CKD的弗雷明汉心脏研究后代队列参与者(平均年龄44岁;51%为女性)进行了前瞻性评估。我们使用多变量Cox模型来关联血清磷和钙水平与CVD发病率。
在随访期间(平均时长16.1年),共发生524例CVD事件(女性159例)。在多变量分析中,在调整了既定风险因素以及肾小球滤过率、血红蛋白、血清白蛋白、蛋白尿和C反应蛋白水平后,血清磷水平升高与CVD风险呈持续增加的关联(每增加毫克/分升的校正风险比为1.31;95%置信区间为1.05 - 1.63;P = 0.02;四分位数间趋势的P值 = 0.004)。血清磷最高四分位数的个体与最低四分位数的个体相比,多变量调整后的CVD风险高1.55倍(95%置信区间为1.16% - 2.07%;P = 0.004)。这些发现在每4年更新CVD风险因素的时间依赖性模型以及仅限于无蛋白尿且估计肾小球滤过率大于90 mL/min/1.73 m²个体的分析中仍然稳健。血清钙与CVD风险无关。
在社区中无CKD和CVD的个体中,较高的血清磷水平与CVD风险增加相关。这些观察结果强调需要进一步研究以阐明磷稳态与血管风险之间的潜在联系。