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血管危险因素与继发进展型多发性硬化症中的灰质萎缩相关。

Vascular risk factors are associated with grey matter atrophy in secondary progressive multiple sclerosis.

作者信息

John Nevin A, Li Yingtong, De Angelis Floriana, Stutters Jonathan, Prados Ferran, Doshi Anisha, Calvi Alberto, Williams Thomas, Plantone Domenico, Phan Thanh, Gandini Wheeler-Kingshott Claudia A M, Barkhof Frederik, Chataway Jeremy

机构信息

Department of Medicine, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia.

Department of Neurology, Monash Health, Melbourne, Victoria, Australia.

出版信息

Eur J Neurol. 2025 Jan;32(1):e16586. doi: 10.1111/ene.16586.

Abstract

BACKGROUND

Comorbidities including vascular risk factors can be associated with whole and regional brain atrophy in multiple sclerosis (MS). This has been examined in mixed MS cohorts in prospective or observational studies; however, the association between vascular comorbidities (VCM) in secondary progressive MS (SPMS) and brain atrophy has been less well studied. The aim was to investigate the cross-sectional and longitudinal association between VCM, comorbidity burden and brain atrophy in SPMS.

METHODS

Post hoc analysis of 445 participants from the MS-Secondary Progressive multi-arm trial (MS-SMART)-a multi-arm multicentre phase-2b randomised placebo-controlled trial of three agents in SPMS (NCT01910259). VCM (hypertension, hyperlipidaemia) but also asthma, hypothyroidism and osteoporosis were recorded. Regional and whole brain volume (WBV), and percentage brain volume change were calculated using SIENAX and SIENA, respectively. Multiple linear regression was used to investigate the cross-sectional and longitudinal relationships between VCM, overall comorbidity count and whole brain, grey matter (GM) and white matter (WM) atrophy.

RESULTS

The cohort was predominantly female (67%), mean age 55 with median EDSS 6.0. In total, 13% and 9% had hypertension and hyperlipidaemia, respectively. In cross-sectional regression models, VCM was associated with decreased cortical GM volume [(hypertension β = -0.30, 95%CI -0.54 to -0.06, p = 0.01) (hyperlipidaemia β = -0.37, 95%CI -0.64 to -0.09, p = 0.008)]; but not WBV. Having ≥2 comorbidities was also associated with decreased cortical GM volume (β = -0.36, 95%CI -0.61 to -0.10, p = 0.007). No relationship was observed between VCM/comorbidity count and whole brain or GM atrophy rate over 96 weeks.

CONCLUSIONS

People with SPMS with VCM or increased overall comorbidity burden showed reduced whole brain and especially cortical grey matter volumes, but no significant impact on subsequent 2-year atrophy rate was detected.

摘要

背景

包括血管危险因素在内的合并症可能与多发性硬化症(MS)的全脑和局部脑萎缩有关。这一点已在前瞻性或观察性研究中的混合MS队列中得到检验;然而,继发进展型MS(SPMS)中的血管合并症(VCM)与脑萎缩之间的关联研究较少。目的是研究SPMS中VCM、合并症负担与脑萎缩之间的横断面和纵向关联。

方法

对来自MS-继发进展多臂试验(MS-SMART)的445名参与者进行事后分析,该试验是一项多臂多中心2b期随机安慰剂对照试验,研究三种药物对SPMS的疗效(NCT01910259)。记录了VCM(高血压、高脂血症)以及哮喘、甲状腺功能减退和骨质疏松症。分别使用SIENAX和SIENA计算局部和全脑体积(WBV)以及脑体积变化百分比。采用多元线性回归研究VCM、总体合并症计数与全脑、灰质(GM)和白质(WM)萎缩之间的横断面和纵向关系。

结果

该队列主要为女性(67%),平均年龄55岁,EDSS中位数为6.0。总体上,分别有13%和9%的人患有高血压和高脂血症。在横断面回归模型中,VCM与皮质GM体积减少有关[(高血压β=-0.30,95%CI -0.54至-0.06,p=0.01)(高脂血症β=-0.37,95%CI -0.64至-0.09,p=0.008)];但与WBV无关。合并症≥2种也与皮质GM体积减少有关(β=-0.36,95%CI -0.61至-0.10,p=0.007)。在96周内,未观察到VCM/合并症计数与全脑或GM萎缩率之间的关系。

结论

患有VCM或合并症负担增加的SPMS患者全脑尤其是皮质灰质体积减少,但未检测到对随后2年萎缩率有显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fef0/11653023/24151cca69e9/ENE-32-e16586-g002.jpg

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