多发性硬化症患者的跌倒、骨折和虚弱风险:一项旨在确定共同遗传基因的孟德尔随机研究。

IF 2.4 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Journal of Bone and Mineral Metabolism Pub Date : 2024-05-01 Epub Date: 2024-05-27 DOI:10.1007/s00774-024-01504-8
Sohyun Jeong, Ming-Ju Tsai, Changbing Shen, Yi-Hsiang Hsu
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引用次数: 0

摘要

导言:多发性硬化症(MS)患者通常会出现以骨矿物质密度(BMD)降低和肌肉无力为特征的肌肉骨骼疾病。然而,其根本病因仍不清楚。我们的目的是确定共同的多向遗传效应,并估计多发性硬化症与肌肉骨骼疾病之间的因果关系:我们使用近期大规模全基因组关联研究(GWAS)的汇总统计数据进行了关联不平衡评分回归(LDSR)、共定位和孟德尔随机化(MR)分析,这些研究涵盖了多发性硬化症、跌倒、骨折和虚弱。其他 MR 分析还探讨了与肌肉骨骼风险因素(如 BMD、瘦体重、握力和维生素 D)之间的因果关系:在 LDSR 分析中,我们观察到多发性硬化症与跌倒之间存在中度遗传相关性(RG = 0.10,P 值 = 0.01),但多发性硬化症与骨折或虚弱之间不存在遗传相关性。MR显示多发性硬化症与骨折和虚弱没有因果关系,但与跌倒有中度关联(OR:1.004,FDR q值=0.018)。我们进一步使用 9 个 SNPs 进行了共定位分析,这些 SNPs 在 MR 中与 MS 和跌倒均有显著关联。两个 SNP(ANKRD55 基因上的 rs7731626 和 OS9 基因上的 rs701006)显示出较高的共定位后验概率(PP.H4 = 0.927),表明 MS 和跌倒之间存在潜在的多向效应。这九个基因与中枢神经系统发育和炎症信号通路有关:我们发现了多发性硬化症与跌倒之间潜在的多向遗传效应。然而,我们的分析并未发现多发性硬化症与跌倒、骨折或虚弱风险增加之间存在因果关系。这表明,临床研究中经常报告的多发性硬化症患者的肌肉骨骼疾病更可能是由于疾病进展和治疗相关的继发性因素造成的,而不是由多发性硬化症本身直接引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Falls, fracture and frailty risk in multiple sclerosis: a Mendelian Randomization study to identify shared genetics.

Falls, fracture and frailty risk in multiple sclerosis: a Mendelian Randomization study to identify shared genetics.

Introduction: Patients with multiple sclerosis (MS) commonly present musculoskeletal disorders characterized by lower bone mineral density (BMD) and muscle weakness. However, the underlying etiology remains unclear. Our objective is to identify shared pleiotropic genetic effects and estimate the causal relationship between MS and musculoskeletal disorders.

Materials and methods: We conducted linkage disequilibrium score regression (LDSR), colocalization, and Mendelian randomization (MR) analyses using summary statistics from recent large-scale genome-wide association studies (GWAS), encompassing MS, falls, fractures, and frailty. Additional MR analyses explored the causal relationship with musculoskeletal risk factors, such as BMD, lean mass, grip strength, and vitamin D.

Results: We observed a moderate genetic correlation between MS and falls (RG = 0.10, P-value = 0.01) but not between MS with fracture or frailty in the LDSR analyses. MR revealed MS had no causal association with fracture and frailty but a moderate association with falls (OR: 1.004, FDR q-value = 0.018). We further performed colocalization analyses using nine SNPs that exhibited significant associations with both MS and falls in MR. Two SNPs (rs7731626 on ANKRD55 and rs701006 on OS9 gene) showed higher posterior probability of colocalization (PP.H4 = 0.927), suggesting potential pleiotropic effects between MS and falls. The nine genes are associated with central nervous system development and inflammation signaling pathways.

Conclusion: We found potential pleiotropic genetic effects between MS and falls. However, our analysis did not reveal a causal relationship between MS and increased risks of falls, fractures, or frailty. This suggests that the musculoskeletal disorders frequently reported in MS patients in clinical studies are more likely attributed to secondary factors associated with disease progression and treatment, rather than being directly caused by MS itself.

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来源期刊
Journal of Bone and Mineral Metabolism
Journal of Bone and Mineral Metabolism 医学-内分泌学与代谢
CiteScore
6.30
自引率
3.00%
发文量
89
审稿时长
6-12 weeks
期刊介绍: The Journal of Bone and Mineral Metabolism (JBMM) provides an international forum for researchers and clinicians to present and discuss topics relevant to bone, teeth, and mineral metabolism, as well as joint and musculoskeletal disorders. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. Acceptance is based on the originality, significance, and validity of the material presented. The journal is aimed at researchers and clinicians dedicated to improvements in research, development, and patient-care in the fields of bone and mineral metabolism.
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