Department of Nephrology, Monash Medical Centre, Melbourne, Australia.
Am J Kidney Dis. 2013 Jul;62(1):58-66. doi: 10.1053/j.ajkd.2013.03.010. Epub 2013 Apr 23.
Low serum 25-hydroxyvitamin D (25[OH]D) levels have been associated with chronic kidney disease in cross-sectional studies. However, this association has not been studied prospectively in a large general population-based cohort.
Prospective cohort study.
SETTING & PARTICIPANTS: 6,180 adults 25 years or older participating in the baseline and 5-year follow-up phases of the Australian Diabetes, Obesity and Lifestyle (AusDiab) Study.
Serum 25(OH)D levels <15 ng/mL were considered deficient.
OUTCOMES & MEASUREMENTS: Incident chronic kidney disease was defined as being negative at baseline but positive after 5 years for (1) reduced estimated glomerular filtration rate (eGFR; <60 mL/min/1.72 m²) or (2) albuminuria (spot urine albumin-creatinine ratio ≥2.5 mg/mmol [≥22.1 mg/g] for men and ≥3.5 mg/mmol [≥30.9 mg/g] for women).
623 (10.9%) participants were vitamin D deficient, 161 developed incident reduced eGFR, and 222 developed incident albuminuria. In participants with and without vitamin D deficiency, annual age-standardized incidences were 0.92% (95% CI, 0.56%-1.30%) and 0.59% (95% CI, 0.51%-0.68%), respectively, for eGFR <60 mL/min/1.72 m² and 1.50% (95% CI, 1.06%-1.95%) and 0.66% (95% CI, 0.56%-0.76%), respectively, for albuminuria. In multivariate regression models, vitamin D deficiency was associated significantly with the 5-year incidence of albuminuria (OR, 1.71; 95% CI, 1.12-2.61; P = 0.01), but not reduced eGFR (OR, 0.93; 95% CI, 0.53-1.66; P = 0.8).
The observational nature of the study does not account for unmeasured confounders. Only baseline 25(OH)D level was measured and therefore may not accurately reflect lifetime levels. Differences in baseline characteristics of participants who were included compared with those excluded due to missing data or follow-up may limit the applicability of results to the original AusDiab cohort.
Our prospective cohort study shows that vitamin D deficiency is associated with a higher annual incidence of albuminuria and reduced eGFR and independently predicts the 5-year incidence of albuminuria. These associations warrant further exploration in long-term prospective clinical trials.
在横断面研究中,低血清 25-羟维生素 D(25[OH]D)水平与慢性肾脏病有关。然而,在大型一般人群队列中,尚未前瞻性研究这种相关性。
前瞻性队列研究。
参加澳大利亚糖尿病、肥胖和生活方式(AusDiab)研究基线和 5 年随访阶段的 6180 名 25 岁或以上的成年人。
血清 25(OH)D 水平<15ng/mL 被认为是不足的。
新发生的慢性肾脏病定义为基线时为阴性,但 5 年后为(1)肾小球滤过率(eGFR)降低(<60mL/min/1.72m²)或(2)白蛋白尿(尿液白蛋白-肌酐比值≥2.5mg/mmol[≥22.1mg/g]男性和≥3.5mg/mmol[≥30.9mg/g]女性)。
623 名(10.9%)参与者存在维生素 D 缺乏,161 名参与者出现新发生的 eGFR 降低,222 名参与者出现新发生的白蛋白尿。在有和没有维生素 D 缺乏的参与者中,eGFR<60mL/min/1.72m²的年标化发生率分别为 0.92%(95%CI,0.56%-1.30%)和 0.59%(95%CI,0.51%-0.68%),白蛋白尿的年标化发生率分别为 1.50%(95%CI,1.06%-1.95%)和 0.66%(95%CI,0.56%-0.76%)。在多变量回归模型中,维生素 D 缺乏与白蛋白尿的 5 年发生率显著相关(OR,1.71;95%CI,1.12-2.61;P=0.01),但与 eGFR 降低无关(OR,0.93;95%CI,0.53-1.66;P=0.8)。
该研究的观察性质不能说明未测量的混杂因素。仅测量了基线 25(OH)D 水平,因此可能无法准确反映终生水平。由于数据缺失或随访而被纳入和排除的参与者在基线特征上存在差异,这可能限制了研究结果在原始 AusDiab 队列中的适用性。
我们的前瞻性队列研究表明,维生素 D 缺乏与白蛋白尿的更高年度发生率和 eGFR 降低有关,并且独立预测白蛋白尿的 5 年发生率。这些关联需要在长期前瞻性临床试验中进一步探讨。