School of Cardiovascular Medicine & Sciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.
J Clin Endocrinol Metab. 2018 May 1;103(5):2026-2032. doi: 10.1210/jc.2018-00004.
Soluble Klotho (sKlotho) is a circulating hormone with cardiovascular-renal protective effects. Whether sKlotho predicts estimated glomerular filtration rate (eGFR) decline in patients with type 2 diabetes mellitus (T2DM) with relatively preserved renal function is unknown.
DESIGN, SETTING, PARTICIPANTS, AND MEASUREMENTS: Single-center observational follow-up study of 101 patients with T2DM and eGFR >45 mL/min [91% on renin angiotensin system (RAS) blockade] followed for a median of 9 years (range, 2 to 13 years).
Primary outcome was a >50% decline in eGFR. sKlotho, serum phosphorus, serum calcium, and fibroblast growth factor-23 levels were measured from stored samples collected at baseline. Patients were followed up with standardized clinical and biochemical measurements.
Patients with residual microalbuminuria (MA) despite RAS blockade (n = 53) had significantly lower levels of sKlotho [median, 184.7 pg/mL; interquartile range (IQR), 130.5 to 271.8 pg/mL) compared with patients without MA (n = 39; median, 235.2 pg/mL; IQR, 172.0 to 289.4 pg/mL; P = 0.03). Of the cohort, 21% reached the primary outcome. In a competing risk analysis, a 10% higher sKlotho level reduced the incidence of the primary outcome by 12% (hazard ratio, 0.27; 95% confidence interval, 0.15 to 0.52; P < 0.001] independent of traditional risk factors. Patients with sKlotho below the median of 204.4 pg/mL had nearly a fourfold higher cumulative incidence of the primary outcome compared with those above the median (24% vs 6.2%; P = 0.01).
In patients with T2DM with relatively preserved eGFR, reduced levels of sKlotho predict renal function decline independent of traditional risk markers. sKlotho is a biomarker of renal dysfunction and a potential treatment target for renoprotection in T2DM.
可溶性 Klotho(sKlotho)是一种具有心血管-肾脏保护作用的循环激素。在肾功能相对保留的 2 型糖尿病(T2DM)患者中,sKlotho 是否可预测估算肾小球滤过率(eGFR)下降尚不清楚。
设计、地点、参与者和测量方法:这是一项单中心观察性随访研究,共纳入 101 例 eGFR>45mL/min(91%接受肾素-血管紧张素系统(RAS)阻滞剂治疗)的 T2DM 患者,中位随访时间为 9 年(范围为 2 至 13 年)。
主要结局为 eGFR 下降>50%。从基线时采集的储存样本中测量 sKlotho、血清磷、血清钙和成纤维细胞生长因子-23 水平。通过标准化的临床和生化测量对患者进行随访。
尽管接受 RAS 阻滞剂治疗,但仍存在微量白蛋白尿(MA)的患者(n=53)的 sKlotho 水平显著较低[中位数为 184.7pg/mL;四分位距(IQR)为 130.5 至 271.8pg/mL],而无 MA 的患者(n=39)的 sKlotho 水平较高[中位数为 235.2pg/mL;IQR 为 172.0 至 289.4pg/mL;P=0.03]。在该队列中,21%的患者达到了主要结局。在竞争风险分析中,sKlotho 水平每升高 10%,主要结局的发生率降低 12%(风险比,0.27;95%置信区间,0.15 至 0.52;P<0.001),独立于传统危险因素。sKlotho 水平低于中位数 204.4pg/mL 的患者的主要结局累积发生率几乎是中位数以上患者的四倍(24%比 6.2%;P=0.01)。
在 eGFR 相对保留的 T2DM 患者中,sKlotho 水平降低可预测肾功能下降,独立于传统风险标志物。sKlotho 是肾功能障碍的生物标志物,也是 T2DM 患者肾脏保护的潜在治疗靶点。