TY - JOUR
T1 - Anti-inflammatory effects of dietary Vitamin D 3 in patients with multiple sclerosis
AU - Hashemi, Reza
AU - Morshedi, Mohammad
AU - Jafarabadi, Mohammad Asghari
AU - Altafi, Davar
AU - Hosseini-Asl, Seyed Saeed
AU - Rafie-Arefhosseini, Seyed
N1 - Funding Information:
This study was financially supported by the Nutrition Research Center, Tabriz University of Medical Sciences, Tabriz, Iran, and Ardabil University of Medical Sciences, Ardabil, Iran. The results of this article were extracted from the MSc. Thesis of Reza Hashemi (Grant no.: 5/D/960060) was registered at Tabriz University of Medical Sciences, Tabriz, Iran.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Objective To assess the effects of dietary vitamin D 3 on proinflammatory (interleukin-17A [IL-17A] and IL-6) and anti-inflammatory (IL-10) cytokines. Methods Our study was conducted on 75 participants who were divided into 3 groups: multiple sclerosis participants (MSPs, n = 25), first-degree relative participants (FDRPs, n = 25), and healthy participants (HPs, n = 25). All groups received 50,000 IU vitamin D 3 /wk for 8 weeks. Serum 25-(OH) vitamin D 3 levels and messenger RNA (mRNA) expression levels of ILs were determined using electrochemiluminescence assay and real-time PCR, respectively. Results Vitamin D 3 affected the levels of IL-17A, IL-10, and IL-6 among the 3 groups (p < 0.001 for all). Levels of IL-17A (MSPs: fold change [FC] = 5.9, p = 0.014; FDRPs: FC = 5.2, p = 0.006; HPs: FC = 4.2, p = 0.012) and IL-6 (MSPs: FC = 5.6, p = 0.003; FDRPs: FC = 5.5, p = 0.002; HPs: FC = 5.1, p < 0.001) were downregulated after vitamin D 3 treatment. In addition, levels of IL-10 (MSPs: FC = 6.2, p = 0.005; FDRPs: FC = 4.6, p < 0.001; HPs: FC = 5.2, p < 0.001) were upregulated after 8 weeks. Conclusions Although supplementation with vitamin D 3 reduced the mRNA expression levels of IL-17A and IL-6, it increased the mRNA expression level of IL-10 in all groups. However, these effects were more considerable in the MSP group than in the other groups. Of interest, in a deficiency state of serum vitamin D3, IL-17A expression had a positive feedback effect on the expression of IL-6. Conversely, in the sufficient state, IL-10 expression had a negative feedback effect on the expression of IL-17A and IL-6.
AB - Objective To assess the effects of dietary vitamin D 3 on proinflammatory (interleukin-17A [IL-17A] and IL-6) and anti-inflammatory (IL-10) cytokines. Methods Our study was conducted on 75 participants who were divided into 3 groups: multiple sclerosis participants (MSPs, n = 25), first-degree relative participants (FDRPs, n = 25), and healthy participants (HPs, n = 25). All groups received 50,000 IU vitamin D 3 /wk for 8 weeks. Serum 25-(OH) vitamin D 3 levels and messenger RNA (mRNA) expression levels of ILs were determined using electrochemiluminescence assay and real-time PCR, respectively. Results Vitamin D 3 affected the levels of IL-17A, IL-10, and IL-6 among the 3 groups (p < 0.001 for all). Levels of IL-17A (MSPs: fold change [FC] = 5.9, p = 0.014; FDRPs: FC = 5.2, p = 0.006; HPs: FC = 4.2, p = 0.012) and IL-6 (MSPs: FC = 5.6, p = 0.003; FDRPs: FC = 5.5, p = 0.002; HPs: FC = 5.1, p < 0.001) were downregulated after vitamin D 3 treatment. In addition, levels of IL-10 (MSPs: FC = 6.2, p = 0.005; FDRPs: FC = 4.6, p < 0.001; HPs: FC = 5.2, p < 0.001) were upregulated after 8 weeks. Conclusions Although supplementation with vitamin D 3 reduced the mRNA expression levels of IL-17A and IL-6, it increased the mRNA expression level of IL-10 in all groups. However, these effects were more considerable in the MSP group than in the other groups. Of interest, in a deficiency state of serum vitamin D3, IL-17A expression had a positive feedback effect on the expression of IL-6. Conversely, in the sufficient state, IL-10 expression had a negative feedback effect on the expression of IL-17A and IL-6.
UR - http://www.scopus.com/inward/record.url?scp=85060878962&partnerID=8YFLogxK
U2 - 10.1212/NXG.0000000000000278
DO - 10.1212/NXG.0000000000000278
M3 - Article
C2 - 30533524
AN - SCOPUS:85060878962
SN - 2376-7839
VL - 4
JO - Neurology: Genetics
JF - Neurology: Genetics
IS - 6
M1 - e278
ER -