Department of Nephrology, University of Queensland at Princess Alexandra Hospital, Brisbane, Australia.
BMC Nephrol. 2009 Dec 10;10:41. doi: 10.1186/1471-2369-10-41.
Approximately 50% of patients with stage 3 Chronic Kidney Disease are 25-hydroxyvitamin D insufficient, and this prevalence increases with falling glomerular filtration rate. Vitamin D is now recognised as having pleiotropic roles beyond bone and mineral homeostasis, with the vitamin D receptor and metabolising machinery identified in multiple tissues. Worryingly, recent observational data has highlighted an association between hypovitaminosis D and increased cardiovascular mortality, possibly mediated via vitamin D effects on insulin resistance and inflammation. The main hypothesis of this study is that oral Vitamin D supplementation will ameliorate insulin resistance in patients with Chronic Kidney Disease stage 3 when compared to placebo. Secondary hypotheses will test whether this is associated with decreased inflammation and bone/adipocyte-endocrine dysregulation.
METHODS/DESIGN: This study is a single-centre, double-blinded, randomised, placebo-controlled trial. Inclusion criteria include; estimated glomerular filtration rate 30-59 ml/min/1.73 m(2); aged >or=18 on entry to study; and serum 25-hydroxyvitamin D levels <75 nmol/L. Patients will be randomised 1:1 to receive either oral cholecalciferol 2000IU/day or placebo for 6 months. The primary outcome will be an improvement in insulin sensitivity, measured by hyperinsulinaemic euglycaemic clamp. Secondary outcome measures will include serum parathyroid hormone, cytokines (Interleukin-1beta, Interleukin-6, Tumour Necrosis Factor alpha), adiponectin (total and High Molecular Weight), osteocalcin (carboxylated and under-carboxylated), peripheral blood mononuclear cell Nuclear Factor Kappa-B p65 binding activity, brachial artery reactivity, aortic pulse wave velocity and waveform analysis, and indirect calorimetry. All outcome measures will be performed at baseline and end of study.
To date, no randomised controlled trial has been performed in pre-dialysis CKD patients to study the correlation between vitamin D status with supplementation, insulin resistance and markers of adverse cardiovascular risk. We remain hopeful that cholecalciferol may be a safe intervention, with health benefits beyond those related to bone-mineral homeostasis.
Australian and New Zealand Clinical Trials Registry ACTRN12609000246280.
约 50%的 3 期慢性肾脏病患者存在 25-羟维生素 D 不足,且随着肾小球滤过率下降,这种患病率会增加。目前,维生素 D 被认为具有除骨和矿物质稳态以外的多种作用,维生素 D 受体和代谢机制已在多种组织中被发现。令人担忧的是,最近的观察性数据表明,维生素 D 缺乏症与心血管死亡率增加之间存在关联,这可能是通过维生素 D 对胰岛素抵抗和炎症的影响介导的。本研究的主要假设是,与安慰剂相比,口服维生素 D 补充剂可改善 3 期慢性肾脏病患者的胰岛素抵抗。次要假设将检验这是否与炎症减少和骨/脂肪细胞内分泌失调有关。
方法/设计:这是一项单中心、双盲、随机、安慰剂对照试验。纳入标准包括:估计肾小球滤过率 30-59ml/min/1.73m²;入组时年龄≥18 岁;血清 25-羟维生素 D 水平<75nmol/L。患者将以 1:1 的比例随机接受口服胆钙化醇 2000IU/天或安慰剂治疗 6 个月。主要结局将是通过高胰岛素正葡萄糖钳夹测量胰岛素敏感性的改善。次要结局测量包括甲状旁腺激素、细胞因子(白细胞介素-1β、白细胞介素-6、肿瘤坏死因子-α)、脂联素(总和高分子量)、骨钙素(羧化和未羧化)、外周血单个核细胞核因子 Kappa-B p65 结合活性、肱动脉反应性、主动脉脉搏波速度和波形分析以及间接热量测定。所有结局测量将在基线和研究结束时进行。
迄今为止,尚未在透析前 CKD 患者中进行随机对照试验,以研究维生素 D 状态与补充、胰岛素抵抗和不良心血管风险标志物之间的相关性。我们仍然希望胆钙化醇可能是一种安全的干预措施,其健康益处不仅与骨矿物质稳态有关。
澳大利亚和新西兰临床试验注册 ACTRN12609000246280。