Wang X, Yan S, Liu C, Xu Y, Wan L, Wang Y, Gao W, Meng S, Liu Y, Liu R, Xu D
Department of Rheumatology and Immunology, The Affiliated Hospital of Weifang Medical University, Weifang, 261000, Shandong Province, China.
Department of Anorectal Surgery, The Affiliated Hospital of Weifang Medical University, Weifang, 261000, China.
Osteoporos Int. 2016 Apr;27(4):1413-1423. doi: 10.1007/s00198-015-3449-7. Epub 2016 Jan 11.
Previous studies suggested possible bone loss and fracture risk in patients with systemic lupus erythematosus (SLE). The aim of this systematic review and meta-analysis was to assess the strength of the relationship of SLE with fracture risk and the mean difference of bone mineral density (BMD) levels between SLE patients and controls. Literature search was undertaken in multiple indexing databases on September 26, 2015. Studies on the relationship of SLE with fracture risk and the mean difference of BMD levels between SLE patients and controls were included. Data were combined using standard methods of meta-analysis. Twenty-one studies were finally included into the meta-analysis, including 15 studies on the mean difference of BMD levels between SLE patients and controls, and 6 studies were on fracture risk associated with SLE. The meta-analysis showed that SLE patients had significantly lower BMD levels than controls in the whole body (weighted mean difference [WMD] = -0.04; 95 % CI -0.06 to -0.02; P < 0.001), femoral neck (WMD = -0.06; 95 % CI -0.07 to -0.04; P < 0.001), lumbar spine (WMD = -0.06; 95 % CI -0.09 to -0.03; P < 0.001), and total hip (WMD = -0.05; 95 % CI -0.06 to -0.03; P < 0.001). In addition, the meta-analysis also showed that SLE was significantly associated with increased fracture risk of all sites (relative risk [RR] = 1.97, 95 % CI 1.20-3.25; P = 0.008). Subgroup analysis by adjustment showed that SLE was significantly associated with increased fracture risk of all sites before and after adjusting for confounding factors (unadjusted RR = 2.07, 95 % CI 1.46-2.94, P < 0.001; adjusted RR = 1.22, 95 % CI 1.05-1.42, P = 0.01). Subgroup analysis by types of fracture showed that SLE was significantly associated with increased risks of hip fracture (RR = 1.99, 95 % CI 1.55-2.57; P < 0.001), osteoporotic fracture (RR = 1.36, 95 % CI 1.21-1.53; P < 0.001), and vertebral fracture (RR = 2.97, 95 % CI 1.71-5.16; P < 0.001). This systematic review and meta-analysis provides strong evidence for the relationship of SLE with bone loss and fracture risk.
既往研究提示系统性红斑狼疮(SLE)患者可能存在骨质流失及骨折风险。本系统评价和荟萃分析的目的是评估SLE与骨折风险之间关系的强度,以及SLE患者与对照组之间骨密度(BMD)水平的平均差异。2015年9月26日在多个索引数据库进行了文献检索。纳入了关于SLE与骨折风险之间关系以及SLE患者与对照组之间BMD水平平均差异的研究。采用标准的荟萃分析方法合并数据。最终有21项研究纳入荟萃分析,其中15项研究涉及SLE患者与对照组之间BMD水平的平均差异,6项研究涉及与SLE相关的骨折风险。荟萃分析显示,SLE患者全身BMD水平显著低于对照组(加权平均差异[WMD] = -0.04;95%可信区间[-0.06,-0.02];P < 0.001),股骨颈(WMD = -0.06;95%可信区间[-0.07,-0.04];P < 0.001),腰椎(WMD = -0.06;95%可信区间[-0.09,-0.03];P < 0.001)和全髋关节(WMD = -0.05;95%可信区间[-0.06,-0.03];P < 0.001)。此外,荟萃分析还显示,SLE与所有部位骨折风险增加显著相关(相对风险[RR] = 1.97,95%可信区间[1.20,3.25];P = 0.008)。校正后的亚组分析显示,在调整混杂因素前后,SLE与所有部位骨折风险增加均显著相关(未校正RR = 2.07,95%可信区间[1.46,2.94],P < 0.001;校正RR = 1.22,95%可信区间[1.05,1.42],P = 0.01)。按骨折类型进行的亚组分析显示,SLE与髋部骨折风险增加显著相关(RR = 1,99,95%可信区间[1.55,2.57];P < 0.001)、骨质疏松性骨折(RR = 1.36,95%可信区间[1.21,1.53];P < 0.001)和椎体骨折(RR = 2.97,95%可信区间[1.71,5.16];P < 0.001)。本系统评价和荟萃分析为SLE与骨质流失及骨折风险之间的关系提供了有力证据。