Giordano Antonino, Clarelli Ferdinando, Pignolet Béatrice, Mascia Elisabetta, Sorosina Melissa, Misra Kaalindi, Ferrè Laura, Bucciarelli Florence, Manouchehrinia Ali, Moiola Lucia, Martinelli Vittorio, Rocca Maria A, Liblau Roland, Filippi Massimo, Esposito Federica
Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Università Vita Salute San Raffaele, Milano, Italy.
J Neurol Neurosurg Psychiatry. 2025 Jan 16;96(2):170-176. doi: 10.1136/jnnp-2024-334062.
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.
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.
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).
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(VitD)会影响多发性硬化症(MS)的发病风险,但对疾病活动的影响存在争议。我们评估了VitD是否与疾病修饰治疗(DMT)开始2年后的无疾病活动证据-3(NEDA-3)状态相关,以及这种关联是因果关系还是混杂因素导致的结果。此外,我们还探讨了较高VitD水平的遗传易感性是否会影响疾病活动风险。
对230例未经治疗的复发缓解型MS患者进行血清25-羟基维生素D测量,并测试经季节调整的VitD与疾病活动之间的关联。通过对约400,000人的全基因组关联研究构建多基因风险评分,我们研究了较高VitD水平的遗传易感性对1408例独立MS患者NEDA-3状态的影响。采用两样本孟德尔随机化(MR)评估因果关系。
较低的基线VitD与2年后NEDA-3概率降低相关(p = 0.019)。特别是,VitD水平<20 ng/mL使疾病活动风险增加两倍以上(OR 2.36,95%CI 1.30至3.88,p = 0.0037)。较高VitD水平的遗传易感性与MS发病年龄延迟相关(p = 0.018),且与NEDA-3状态的概率较高相关(p = 0.034)。MR证实了VitD与疾病活动风险之间的因果关系(p = 0.041)。
DMT开始前的VitD水平会影响MS的疾病活动风险。较高VitD水平的遗传易感性使疾病活动风险降低,并与MS发病延迟相关。我们的工作促使未来开展关于补充VitD和生活方式干预以抑制MS疾病活动的前瞻性研究。