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作 者:石明亮 谢栋 杨立利 SHI Mingliang;XIE Dong;YANG Lili(Spine Center,Department of Orthopedics,Shanghai Changzheng Hospital,the Second Affiliated Hospital of Naval Medical University,Shanghai 200003,China;Department of Orthopedics,No.905 Hospital of PLA Navy,Shanghai 200052,China)
机构地区:[1]海军军医大学第二附属医院(上海长征医院)脊柱外科,上海200003 [2]中国人民解放军海军第九零五医院骨科,上海200052
出 处:《中国骨质疏松杂志》2024年第5期673-678,共6页Chinese Journal of Osteoporosis
基 金:国家自然科学基金面上项目(82372431);上海市卫健委“卫生健康领军人才”计划(2022LJ007);上海市科委“科技创新行动计划”自然科学基金(22ZR1476700);上海市科委“科技创新行动计划”科技支撑项目(201409003200)。
摘 要:目的采用双向和多变量孟德尔随机化方法探讨不同部位骨密度与椎间盘退变的因果关联。方法椎间盘退变的遗传工具变量来自FinnGen数据库;骨质疏松症、腰椎骨密度、股骨颈骨密度、全身骨密度和足跟骨密度5个独立遗传工具变量来自GEFOS联盟和英国生物银行。逆方差加权法作为主要分析方法,并采用了严格的框架,包括双向、多变量孟德尔随机化和多种敏感性分析,以避免潜在的混杂偏倚。结果遗传预测骨质疏松症是椎间盘退变发生的负向影响因素(OR=0.017,P=1.718E-02)。此外,正向孟德尔随机化分析表明,腰椎骨密度(OR=1.131,95%CI:1.053~1.214,P=6.915E-04)、全身骨密度(OR=1.148,95%CI:1.093~1.206,P=4.221E-08)和足跟骨密度(OR=1.061,95%CI:1.016~1.109,P=7.871E-03)与椎间盘退变发生显著正相关。而在多变量模型中,仅发现腰椎骨密度与椎间盘退变具有正向因果效应(OR=1.120,95%CI:1.003~1.250,P=4.493E-02)。反向分析结果表明,椎间盘退变可影响腰椎骨密度(Beta=0.142,95%CI:0.052~0.233,P=2.078E-03),而未发现对其他部位骨密度具有类似影响。异质性、多效性和统计效能分析结果肯定了上述发现的稳健性。结论遗传预测骨质疏松症是椎间盘退变发生的负向影响因素。此外,本研究还强调腰椎骨密度与椎间盘退变具有双向因果关联。Objective Bidirectional and multivariable Mendelian randomization(MR)method were employed to investigate the causal association between bone mineral density(BMD)and intervertebral disc degeneration(IVDD)at different sites.Methods Genetic instrumental variables for IVDD were sourced from the FinnGen database.Five independent genetic instrumental variables for osteoporosis,lumbar spine BMD,femoral neck BMD,total body BMD,and heel BMD,were acquired from the GEFOS consortium and the UK Biobank.Our primary analytical approach was based on inverse-variance weighted,and we adhered to a robust framework that encompassed bidirectional,multivariable,and multiple sensitivity analyses to mitigate the risk of potential confounding biases.Results The occurrence of IVDD was negatively influenced by genetically predicted osteoporosis(OR=0.017,P=1.718E-02).Univariable MR analyses revealed significant positive associations between lumbar spine BMD(OR=1.131,95%CI:1.053-1.214,P=6.915E-04),total body BMD(OR=1.148,95%CI:1.093-1.206,P=4.221E-08),heel BMD(OR=1.061,95%CI:1.016-1.109,P=7.871E-03),and the occurrence of IVDD.However,in the multivariable model,only genetically predicted lumbar spine BMD demonstrated a positive causal effect on the risk of IVDD(OR=1.120,95%CI:1.003-1.250,P=4.493E-02).Results from the reverse causality study suggested a potential reverse causal association between lumbar spine BMD and IVDD(Beta=0.142,95%CI:0.052-0.233,P=2.078E-03),with no similar associations found for BMD at other sites.Sensitivity analysis affirmed the robustness of our findings.Conclusion Genetically predicted osteoporosis is a negative influence on the occurrence of IVDD.In addition,this study emphasizes a bidirectional causal association between lumbar spine BMD and IVDD.
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