Vitamin D affects the risk of disease activity in multiple sclerosis.

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY
Antonino Giordano, Ferdinando Clarelli, Béatrice Pignolet, Elisabetta Mascia, Melissa Sorosina, Kaalindi Misra, Laura Ferrè, Florence Bucciarelli, Ali Manouchehrinia, Lucia Moiola, Vittorio Martinelli, Maria A Rocca, Roland Liblau, Massimo Filippi, Federica Esposito
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Abstract

Background: Vitamin D (VitD) affects the risk of multiple sclerosis (MS), but the impact on disease activity is controversial. We assessed whether VitD is associated with the No-Evidence of Disease Activity-3 (NEDA-3) status at 2 years from disease-modifying treatment (DMT) start, and whether this association is causal or the result of confounding factors. Furthermore, we explored if a genetic predisposition to higher VitD levels affects the risk of disease activity.

Methods: 230 untreated relapsing-remitting MS patients underwent serum 25-OH-vitamin-D measurement, and the association between seasonally adjusted VitD and disease activity was tested. Modelling a Polygenic Risk Score from a Genome-Wide Association Study on ~400 000 individuals, we studied the impact of genetic predisposition to higher VitD on the NEDA-3 status in 1408 independent MS patients. Two-sample Mendelian randomisation (MR) was used to assess causality.

Results: Lower baseline VitD was associated with decreased probability of NEDA-3 at 2 years (p=0.019). Particularly, VitD levels <20 ng/mL conferred an over twofold risk of disease activity (OR 2.36, 95% CI 1.30 to 3.88, p=0.0037). Genetic predisposition to higher VitD levels was associated with delayed age at MS onset (p=0.018) and with a higher probability of NEDA-3 status (p=0.034). MR confirmed causality between VitD and the risk of disease activity (p=0.041).

Conclusions: VitD levels before DMT start affect the risk of disease activity in MS. Genetic predisposition to higher VitD levels confers a lower risk of disease activity and is associated with delayed MS onset. Our work prompts future prospective studies regarding VitD supplementation and lifestyle interventions to hamper disease activity in MS.

维生素 D 会影响多发性硬化症的疾病活动风险。
背景:维生素 D(VitD)会影响多发性硬化症(MS)的发病风险,但其对疾病活动性的影响还存在争议。我们评估了维生素 D 是否与疾病缓解治疗(DMT)开始两年后的无疾病活动证据-3(NEDA-3)状态有关,以及这种关联是因果关系还是混杂因素的结果。此外,我们还探讨了较高维生素D水平的遗传易感性是否会影响疾病活动的风险。方法:230名未经治疗的复发性缓解型多发性硬化症患者接受了血清25-OH-维生素D测定,并检测了经季节性调整的维生素D与疾病活动之间的关联。通过对约 40 万人进行的全基因组关联研究中的多基因风险评分建模,我们研究了高 VitD 遗传易感性对 1408 名独立多发性硬化症患者 NEDA-3 状态的影响。结果显示,基线VitD较低的多发性硬化症患者的NEDA-3状态较好,而基线VitD较高的多发性硬化症患者的NEDA-3状态较差:结果:基线 VitD 较低与 2 年后 NEDA-3 的概率降低有关(p=0.019)。结论:DMT开始前的VitD水平与NEDA-3的概率相关:DMT开始前的VitD水平会影响多发性硬化症的疾病活动风险。VitD水平较高的遗传易感性会降低疾病活动的风险,并与多发性硬化症的延迟发病有关。我们的研究提示今后应开展有关补充维生素 D 和生活方式干预的前瞻性研究,以阻碍多发性硬化症的疾病活动。
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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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