机构地区:[1]安徽医科大学附属省立医院风湿免疫科,合肥230001
出 处:《中华内科杂志》2017年第3期179-183,共5页Chinese Journal of Internal Medicine
基 金:国家自然科学基金(81373186)
摘 要:目的研究长期服用小剂量泼尼松对缓解期系统性红斑狼疮(SLE)患者骨密度的影响。方法选长期服用小剂量泼尼松的女性缓解期SLE患者118例,同时选年龄、性别、BMI相匹配的健康对照者29例。采用双能X线吸收法测所有受试者骨密度,分析骨密度与病程及泼尼松剂量的相关性。结果118例女性缓解期SLE患者中骨量减少50例(42.4%),骨质疏松17例(14.4%)。股骨颈、股骨、桡骨远端、桡骨、腰椎(L2~4)的骨密度口服泼尼松≤7.5 mg/d SLE患者[(0.897±0.116) g/cm2,(0.931±0.115) g/cm^2,(0.366±0.058) g/cm^2,(0.523±0.054) g/cm^2,(1.052±0.143) g/cm^2]、泼尼松7.5~10 mg/d者[(0.871±0.138) g/cm^2, (0.935±0.143) g/cm^2, (0.358±0.055) g/cm^2, (0.515±0.056) g/cm^2, (1.056±0.140)g/cm^2]均低于健康对照者[(1.020±0.107) g/cm^2, (1.081±0.129) g/cm^2, (0.393±0.524) g/cm^2, (0.556±0.050) g/cm^2, (1.239±0.114)g/cm^2,P〈0.05]。SLE病程≤3年者、SLE病程4~5年者、SLE病程6~10年者、SLE病程〉10年者上述检测部位的骨密度均低于健康对照者(P〈0.05),SLE病程〉10年者上述检测部位的骨密度均低于SLE病程≤3年者、SLE病程4~5年者、SLE病程6~10年者(P〈0.05)。多因素logistic回归分析显示,累积泼尼松剂量与骨量减少相关(OR=1.069,95% CI 1.008~1.133,P=0.025),补充钙剂(OR=0.343,95% CI 0.135~0.868,P=0.024)、阿法骨化醇(OR=0.320,95% CI 0.112~0.913,P=0.033)是骨密度的保护性因素。结论缓解期SLE患者长期服用小剂量泼尼松导致不同程度的骨密度减低,以腰椎和股骨颈的发生率最高。长期应用泼尼松≤7.5 mg/d也导致骨密度明显减低。补充钙剂、阿法骨化醇是骨密度的保护性因素。Objective To investigate the effect of long-term low dose prednisone administration on bone mineral density (BMD) in patients with inactive systemic lupus erythematosus (SLE). Methods A total of 118 inactive female SLE patients with long-term administration of low dose prednisone were recruited from the Department of Rheumatology and Immunology at An hui Provincial Hospital. All patients were given low dose prednisone for long-term ( ≤ 10 mg/d, more than half a year). According to prednisone doses, subjects were divided into two groups, namely group A ( ≤7.5 mg/d) and group B (7.5 - 10 mg/d). In addition, patients were also divided into four groups based on the duration of administration, including group Ⅰ ≤3 years, Ⅱ from 4 - 5 years, Ⅲ 6 - 10 years and Ⅳ 〉 10 years. Twenty-nine healthy people were recruitedas normal controls. The BMD was measured by dual energy X-ray absorptiometry. The association of BMD with prednisone dose and duration was compared between different groups. Results The incidence of osteopenia in all patients with SLE was 42. 4% (50/118), and the incidence of osteoporosis was 14. 4% (17/118). BMD of all bone sites in both group A and B were significantly lower than that in normal control group (P 〈 0. 05 ). Similarly, the BMD of all bone sites in group Ⅰ , Ⅱ ,Ⅲ and Ⅳ were significantly decreased (P 〈 0. 05 ). What needed to be stressed was the BMD in group Ⅳ was lower than those in other three groups ( P 〈 0. 05 ). Multiple logistic regression analysis showed that the cumulative prednisone dose was the risk factor for osteopenia, while taking calcium and alfacalcidol were protective factors. Conclusion Long-term use of low dose prednisone result in the decrease of BMD in patients with inactive SLE. The lumbar spine and femoral neck had more severe osteopenia. Long-term administration of prednisone, even less than 7.5 rag/d, can also cause osteopenia. Calcium and alfacalcidol were protective factors of BMD.
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