Kidney Research Institute and Harborview Medical Center, University of Washington, Seattle, Washington, USA.
Kidney Int. 2013 Nov;84(5):989-97. doi: 10.1038/ki.2013.145. Epub 2013 Apr 24.
Whether higher serum phosphorus levels are associated with a higher risk for death and/or progression of chronic kidney disease (CKD) is not well established, and whether the association is confounded by access and barriers to care is unknown. To answer these questions, data of 10,672 individuals identified to have CKD (estimated glomerular filtration rate <60 ml/min per 1.73 m(2)) from those participating in a community-based screening program were analyzed. Over a median follow-up of 2.3 years, there was no association between quartiles of serum phosphorus and all-cause mortality (adjusted hazards ratio for serum phosphorus over 3.3 to 3.7, over 3.7 to 4.1, and over 4.1 mg/dl, respectively: 1.22 (0.95-1.56), 1.00 (0.76-1.32), and 1.00 (0.75-1.33); reference, serum phosphorus of 3.3 mg/dl and below). Individuals in the highest quartile for serum phosphorus had a significantly higher risk for progression to end-stage renal disease (ESRD) (unadjusted hazards ratio, 6.72 (4.16-10.85)); however, the risk became nonsignificant on adjustment for potential confounders. There was no appreciable change in hazards ratio with inclusion of variables related to access and barriers to care. Additional analyses in subgroups based on 12 different variables yielded similar negative associations. Thus, in the largest cohort of individuals with early-stage CKD to date, we could not validate an independent association of serum phosphorus with risk for death or progression to ESRD.
血清磷水平升高是否与慢性肾脏病(CKD)患者的死亡风险和(或)疾病进展风险升高相关尚未明确,而且这种相关性是否受到获得医疗服务的机会和障碍的影响也尚不清楚。为了回答这些问题,我们对参加社区筛查项目的 10672 名 CKD 患者(估算肾小球滤过率<60 ml/min/1.73 m2)的数据进行了分析。在中位随访 2.3 年期间,血清磷四分位与全因死亡率之间没有相关性(血清磷超过 3.3-3.7、3.7-4.1 和超过 4.1 mg/dl 时的校正后危害比分别为:1.22(0.95-1.56)、1.00(0.76-1.32)和 1.00(0.75-1.33);参考值为血清磷<3.3 mg/dl)。血清磷最高四分位组患者进展为终末期肾病(ESRD)的风险显著升高(未校正危害比为 6.72(4.16-10.85));然而,在调整潜在混杂因素后,这种风险不再具有统计学意义。纳入与获得医疗服务的机会和障碍相关的变量后,危害比没有明显变化。基于 12 个不同变量的亚组分析得出了类似的阴性关联。因此,在迄今最大的早期 CKD 患者队列中,我们无法证实血清磷与死亡风险或进展为 ESRD 的风险之间存在独立关联。