Division of Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
J Nephrol. 2013 May-Jun;26(3):485-94. doi: 10.5301/jn.5000185. Epub 2012 Sep 13.
Reduced bone mineral density (BMD) is common in end-stage renal disease (ESRD) patients and predicts outcomes. The chronic kidney disease-mineral bone disorder contributes to low BMD in ESRD; however, the impact of classical risk factors for osteoporosis in the general population, such as body weight and fat mass, remains less well defined in ESRD subjects.
BMD, body composition (dual-energy X-ray absorptiometry), nutritional status (subjective global assessment), hand grip strength and multiple biomarkers were investigated in 361 patients (218 males; 60.4%) starting on dialysis. The relations between BMD, body composition and biomarkers were analyzed at baseline, and the impact of BMD on mortality was analyzed prospectively.
In univariate analysis, T-score correlated with fat mass (r = 0.308, p<0.001), lean body mass (r = 0.278, p<0.001), leptin (r = 0.124, p = 0.028) as well as the anabolic marker insulin-like growth factor-1 (IGF-1; r = 0.301, p<0.001), and its binding proteins IGFBP-1 (r = -0.342, p<0.001) and IGFBP-3 (0.231, p<0.001). BMD T-score was independently associated with age, total fat mass, intact parathyroid hormone and presence of wasting. During 5 years of follow-up, 87 deaths were recorded. Each unit of increase of T-score was associated with decreased all-cause mortality, which persisted after multivariate adjustment (hazard ratio = 0.824, 95% confidence interval, 0.681-0.996).
BMD is associated with body composition, especially total fat mass, nutritional status and mortality risk in ESRD patients.
在终末期肾病(ESRD)患者中,骨矿物质密度(BMD)降低很常见,并且可以预测预后。慢性肾脏病-矿物质和骨异常导致 ESRD 患者的低 BMD;然而,在 ESRD 患者中,人群中骨质疏松症的经典危险因素(如体重和脂肪量)的影响仍不太明确。
对 361 名开始透析的患者(218 名男性;60.4%)进行了 BMD、身体成分(双能 X 射线吸收法)、营养状况(主观整体评估)、握力和多种生物标志物的研究。在基线时分析了 BMD、身体成分和生物标志物之间的关系,并前瞻性分析了 BMD 对死亡率的影响。
在单变量分析中,T 评分与脂肪量(r = 0.308,p<0.001)、瘦体重(r = 0.278,p<0.001)、瘦素(r = 0.124,p = 0.028)以及合成代谢标志物胰岛素样生长因子-1(IGF-1;r = 0.301,p<0.001)和其结合蛋白 IGFBP-1(r = -0.342,p<0.001)和 IGFBP-3(0.231,p<0.001)相关。BMD T 评分与年龄、总脂肪量、完整甲状旁腺激素和消瘦的存在独立相关。在 5 年的随访期间,记录到 87 例死亡。T 评分每增加一个单位,全因死亡率就会降低,这种关联在多变量调整后仍然存在(风险比=0.824,95%置信区间,0.681-0.996)。
BMD 与身体成分,特别是总脂肪量、营养状况和 ESRD 患者的死亡风险相关。