Higher 25-hydroxyvitamin D Is Associated with Lower Relapse Risk in Multiple Sclerosis

被引:367
作者
Simpson, Steve, Jr. [1 ]
Taylor, Bruce [1 ]
Blizzard, Leigh [1 ]
Ponsonby, Anne-Louise [2 ]
Pittas, Fotini [1 ]
Tremlett, Helen [3 ]
Dwyer, Terence [2 ]
Gies, Peter [4 ]
van der Mei, Ingrid [1 ]
机构
[1] Menzies Res Inst, Hobart, Tas 7001, Australia
[2] Univ Melbourne, Murdoch Childrens Res Inst, Melbourne, Vic, Australia
[3] Univ British Columbia, Div Neurol, Fac Med, Vancouver, BC V5Z 1M9, Canada
[4] Australian Radiat Protect & Nucl Safety Agcy, Ultraviolet Radiat Sect, Yallambie, Vic, Australia
基金
英国医学研究理事会;
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; VITAMIN-D STATUS; 1,25-DIHYDROXYVITAMIN D-3; SERUM; 25-HYDROXYCHOLECALCIFEROL; ULTRAVIOLET-RADIATION; HUMAN PLASMA; METABOLITE; AUSTRALIA; HORMONE; PEOPLE;
D O I
10.1002/ana.22043
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: A protective association between higher vitamin D levels and the onset of multiple sclerosis (MS) has been demonstrated; however, its role in modulating MS clinical course has been little studied. We investigated whether higher levels of serum 25-hydroxyvitamin D (25-OH-D) were associated with a lower risk of relapses in people with MS. Methods: We conducted a prospective cohort study of 145 participants with relapsing-remitting MS from 2002 to 2005. Serum 25-OH-D levels were measured biannually, and the hazard of relapse was assessed using survival analysis. Results: There was an inverse linear relationship between 25-OH-D levels and the hazard of relapse over the subsequent 6 months, with hazard ratio (HR) 0.91 (95% confidence interval [CI]: 0.85-0.97) per 10nmol/l increase in 25-OH-D level (p = 0.006). When variation due to timing of blood collection was removed by estimating 25-OH-D at the start of each season, this association persisted, with HR 0.90 (95% Cl, 0.83-0.98) per 10nmol/l increase (p = 0.016). Taking into account the biological half-life of 25-OH-D, we estimated 25-OH-D at monthly intervals, resulting in a slightly enhanced association, with HR 0.88 (95% Cl, 0.82-0.95) per 10nmol/l increase (p = 0.001). Adjusting for potential confounders did not alter these findings. Interpretation: In this prospective population-based cohort study, in a cohort largely on immunomodulatory therapy, higher 25-OH-D levels were associated with a reduced hazard of relapse. This occurred in a dose-dependent linear fashion, with each 10nmol/l increase in 25-OH-D resulting in up to a 12% reduction in risk of relapse. Clinically, raising 25-OH-D levels by 50nmol/l could halve the hazard of a relapse. ANN NEUROL 2010;68:193-203
引用
收藏
页码:193 / 203
页数:11
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