The Effect of Smoking on Long-term Gray Matter Atrophy and Clinical Disability in Patients with Relapsing-Remitting Multiple Sclerosis.

IF 7.5
Ingrid Anne Lie, Kristin Wesnes, Silje S Kvistad, Iman Brouwer, Stig Wergeland, Trygve Holmøy, Rune Midgard, Alla Bru, Astrid Edland, Randi Eikeland, Sonia Gosal, Hanne F Harbo, Grethe Kleveland, Yvonne S Sørenes, Nina Øksendal, Frederik Barkhof, Hugo Vrenken, Kjell-Morten Myhr, Lars Bø, Øivind Torkildsen
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引用次数: 4

Abstract

Background and objectives: The relationship between smoking, long-term brain atrophy, and clinical disability in patients with multiple sclerosis (MS) is unclear. Here, we assessed long-term effects of smoking by evaluating MRI and clinical outcome measures after 10 years in smoking and nonsmoking patients with relapsing-remitting MS (RRMS).

Methods: We included 85 treatment-naive patients with RRMS with recent inflammatory disease activity who participated in a 10-year follow-up visit after a multicenter clinical trial of 24 months. Smoking status was decided for each patient by 2 separate definitions: by serum cotinine levels measured regularly for the first 2 years of the follow-up (during the clinical trial) and by retrospective patient self-reporting. At the 10-year follow-up visit, clinical tests were repeated, and brain atrophy measures were obtained from MRI using FreeSurfer. Differences in clinical and MRI measurements at the 10-year follow-up between smokers and nonsmokers were investigated by 2-sample t tests or Mann-Whitney tests and linear mixed-effect regression models. All analyses were conducted separately for each definition of smoking status.

Results: After 10 years, smoking (defined by serum cotinine levels) was associated with lower total white matter volume (β = -21.74, p = 0.039) and higher logT2 lesion volume (β = 0.22, p = 0.011). When defining smoking status by patient self-reporting, the repeated analyses found an additional association with lower deep gray matter volume (β = -2.35, p = 0.049), and smoking was also associated with a higher score (higher walking impairment) on the log timed 25-foot walk test (β = 0.050, p = 0.039) after 10 years and a larger decrease in paced auditory serial addition test (attention) scores (β = -3.58, p = 0.029).

Discussion: Smoking was associated with brain atrophy and disability progression 10 years later in patients with RRMS. The findings imply that patients should be advised and offered aid in smoking cessation shortly after diagnosis, to prevent long-term disability progression.

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吸烟对复发-缓解型多发性硬化症患者长期灰质萎缩和临床残疾的影响。
背景与目的:吸烟、长期脑萎缩和多发性硬化症(MS)患者临床残疾之间的关系尚不清楚。在这里,我们通过评估吸烟和不吸烟的复发-缓解型MS (RRMS)患者10年后的MRI和临床结果来评估吸烟的长期影响。方法:我们纳入了85例未接受治疗且近期有炎症性疾病活动的RRMS患者,这些患者在进行了24个月的多中心临床试验后进行了10年的随访。每位患者的吸烟状况由两种不同的定义来确定:在随访的前2年(临床试验期间)通过定期测量血清可替宁水平和通过回顾性患者自我报告。在10年的随访中,重复临床试验,并使用FreeSurfer通过MRI获得脑萎缩测量。通过两样本t检验或Mann-Whitney检验和线性混合效应回归模型,研究吸烟者和非吸烟者在10年随访期间的临床和MRI测量的差异。所有的分析都是针对每个吸烟状态的定义分别进行的。结果:10年后,吸烟(以血清可替宁水平定义)与总白质体积降低(β = -21.74, p = 0.039)和logT2病变体积增加(β = 0.22, p = 0.011)相关。当通过患者自我报告来定义吸烟状态时,重复分析发现,吸烟与深部灰质体积降低有额外的关联(β = -2.35, p = 0.049),吸烟还与10年后对数计时25英尺步行测试(β = 0.050, p = 0.039)的更高分数(更高的步行障碍)有关(β = -3.58, p = 0.029),并与节律性听觉系列附加测试(注意力)分数的更大下降有关(β = -3.58, p = 0.029)。讨论:吸烟与RRMS患者10年后脑萎缩和残疾进展有关。研究结果表明,在诊断后不久,应该建议并帮助患者戒烟,以防止长期残疾进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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