Human Nutrition Research Unit, Department of Agricultural, Food and Nutritional Science, Division of Human Nutrition, University of Alberta, Edmonton, Alberta, T6G 2E1, Canada.
Department of Applied Nutrition, Nutrition Institute, Rio de Janeiro State University, Rio de Janeiro, 20550-900, Brazil.
Clin Nutr. 2022 Jun;41(6):1218-1227. doi: 10.1016/j.clnu.2022.04.017. Epub 2022 Apr 19.
Chronic kidney disease (CKD) is associated with a reduction in bone mineral density (BMD), but less is understood regarding the relation between BMD and muscle mass, especially in non-dialysis dependent-CKD (NDD-CKD). The aim of this study was to explore the prevalence and association of low BMD (osteopenia and osteoporosis) with markers of muscle mass and function in patients with NDD-CKD.
This cross-sectional observational study included patients with NDD-CKD. Routine biochemical parameters including those related to mineral and bone metabolism were evaluated. Body composition was assessed by dual energy x-ray absorptiometry (DXA) for BMD (g/cm), total and trunk body fat (%), total lean soft tissue (LST; kg), and appendicular skeletal muscle mass (ASM; kg) as the sum of the LST from the limbs. The latter two variables were used as markers of muscle mass, together with its height indexed values: ASM/height as ASM index (ASMI; kg/m), and LST/height as LST index (LSTI, kg/m). Muscle quality index (MQI) was calculated as handgrip strength (HGS)/mean ASM (kg/kg). Osteosarcopenia was defined according to referenced cut-points for patients presenting with low ASMI, HGS and BMD.
Patients (n = 257, 57.6% males) had a mean age = 64.8 ± 12.9 years, estimated glomerular filtration rate (eGFR) = 30.1 ± 12.9 ml/min and body mass index (BMI) = 26.8 ± 4.8 kg/m. Patients with low BMD (39.4%) presented with lower BMI, LST, LSTI, ASM and ASMI for both sexes. BMD was positively and significantly correlated with LST, LSTI, ASM, ASMI and HGS. Low ASM was associated with low BMD (odds-ratio-OR; 95% confidence interval-CI: males OR = 4.54, 2.02-10.21; females OR = 4.45, 1.66-11.93). Linear multiple regression analysis (adjusted for sex and eGFR) showed significant associations between T-score with HGS (R = 0.288, R adjusted = 0.272, standardized coefficient β = 0.536, p < 0.0001) and also with MQI (R = 0.095, R adjusted = 0.075, standardized coefficient β = 0.309, p = 0.024). Osteosarcopenia was present in about 7% of participants and similarly distributed between sexes.
Low BMD was prevalent, and associated with low markers of muscle mass and quality, in NDD-CKD patients of both sexes. In view of the known significance of these conditions, targeted interventions are needed to optimize body composition and functional status of these patients.
慢性肾脏病(CKD)与骨密度(BMD)降低有关,但对于 BMD 与肌肉质量之间的关系,特别是在非透析依赖性 CKD(NDD-CKD)患者中,了解较少。本研究的目的是探讨 NDD-CKD 患者低 BMD(骨质疏松症和骨质疏松症)与肌肉质量和功能标志物的患病率和相关性。
本横断面观察性研究纳入了 NDD-CKD 患者。评估了常规生化参数,包括与矿物质和骨代谢相关的参数。通过双能 X 射线吸收法(DXA)评估身体成分,用于 BMD(g/cm)、全身和躯干脂肪(%)、全身瘦软组织(LST;kg)和四肢 LST 之和的四肢附属骨骼肌质量(ASM;kg)。后两个变量被用作肌肉质量的标志物,与其身高指数值一起使用:ASM/身高作为 ASMI(kg/m)和 LST/身高作为 LSTI(kg/m)。肌肉质量指数(MQI)计算为握力强度(HGS)/平均 ASM(kg/kg)。根据低 ASMI、HGS 和 BMD 患者的参考切点定义了骨肌减少症。
患者(n=257,57.6%为男性)的平均年龄为 64.8±12.9 岁,估计肾小球滤过率(eGFR)为 30.1±12.9ml/min,体重指数(BMI)为 26.8±4.8kg/m。低 BMD(39.4%)的患者无论男女 BMI、LST、LSTI、ASM 和 ASMI 均较低。BMD 与 LST、LSTI、ASM、ASMI 和 HGS 呈正相关且具有显著意义。低 ASM 与低 BMD 相关(男性比值比[OR];95%置信区间[CI]:OR=4.54,2.02-10.21;女性 OR=4.45,1.66-11.93)。线性多元回归分析(按性别和 eGFR 调整)显示 T 评分与 HGS(R=0.288,R 调整=0.272,标准化系数β=0.536,p<0.0001)和 MQI(R=0.095,R 调整=0.075,标准化系数β=0.309,p=0.024)之间存在显著相关性。骨肌减少症约占参与者的 7%,且在男女之间分布相似。
NDD-CKD 患者无论男女,低 BMD 均较为普遍,且与肌肉质量和质量标志物降低有关。鉴于这些情况的已知重要性,需要采取有针对性的干预措施,以优化这些患者的身体成分和功能状态。