Vitamin D and neurology

Vitamin D
Drug class

Molecular structure of Vitamin D3 with the common reasons for use and the biological target.

Class identifiers
Use Rickets, osteoporosis, vitamin D deficiency
ATC code A11CC
Biological target vitamin D receptor
Clinical data
Drugs.com MedFacts Natural Products
External links
MeSH D014807
In Wikidata

Vitamin D is a steroid hormone that plays a vital role in calcium and phosphate absorption. In recent studies, several associations between low levels of vitamin D, or hypovitaminosis D, and neuropsychiatric disorders have begun to surface.[1] These disorders include, but are not limited to: Alzheimer's disease, Parkinson's disease, multiple sclerosis, epilepsy, and schizophrenia.[1]

Physiology

Vitamin D is mainly found in the body in two forms: vitamin D3 and vitamin D2. Vitamin D3, or cholecalciferol, is formed in the skin after exposure to sunlight or ultra violet radiation. Vitamin D2, or ergocalciferol, is obtained from various food sources including milk and fish.[2] These two forms of vitamin D are metabolized in the liver and stored as 25-hydroxyvitamin D.[3] Before biological use, the storage form must be converted into an active form. One common active form is 1,25 dihydroxyvitamin D.[3] The term vitamin D in this article, refers to group of molecules including cholecalciferol,ergocalciferol, 25-hydroxyvitamin D, and the active forms. The role of vitamin D is best characterized as enabling calcium absorption and regulating calcium homeostasis. Vitamin D also play a role in phosphate absorption.[4]

Hypovitaminosis D

Hypovitaminosis D is described as any deficiency of vitamin D. A vitamin D blood concentration standard for diagnosing hypovitaminosis D does not exist. In the past, hypovitaminosis D has been defined by blood concentrations lower than 20 ng/ mL.[5] However, in more recent literature many researchers have considered 30 ng/ mL to be an insufficient concentration of vitamin D.[5] Subnormal levels of vitamin D are usually caused by poor nutrition or a lack of sun exposure.[4] Risk factors for hypovitaminosis D include premature birth, darker skin pigmentation, obesity, malabsorption, and older age.

Vitamin D and the central nervous system

Location in the central nervous system

The brain requires the use of many neurosteroids to develop and function properly. These molecules are often identified as one of many common substances including thyroid hormones, glucocorticoids, and androgens. However in recent studies, throughout the brain and spinal fluid, vitamin D has begun to surface as one of these neurosteroids.

Location of brain regions related to vitamin D.

Function in the central nervous system

The presence of vitamin D, its activating enzyme, and VDR in the brain leads researchers to question what role vitamin D plays in the brain. Research suggests that vitamin D may function as a modulator in brain development and as a neuroprotectant.[1] In recent studies, vitamin D has exhibited an association with the regulation of nerve growth factor (NGF) synthesis. NGF is responsible for the growth and survival of neurons.[7] This relationship has also been studied in embryonic and neonatal rats. Developmental vitamin D deficient (DVD) rats have decreased levels of neurotrophic factors, increased mitosis, and decreased apoptosis. These findings suggest that vitamin D potentially affects the development of neurons as well as their maintenance and survival. Current research is underway investigating whether vitamin D is a factor contributing to normal brain functioning.

Vitamin D and neurological disorders

Hypovitaminosis D is associated with several neuropsychiatric disorders including dementia, Parkinson's disease, multiple sclerosis, epilepsy, and schizophrenia. There are several proposed mechanisms by which hypovitaminosis D may impact these disorders. One of these mechanisms is through neuronal apoptosis. Neuronal apoptosis is the programmed death of the neurons. Hypovitaminosis D causes this specific apoptosis by decreasing the expression of cytochrome C and decreasing the cell cycle of neurons. Cytochrome C is a protein that promotes the activation of pro-apoptotic factors.[8] A second mechanism is through the association of neurotrophic factors like nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF). These neurotrophic factors are proteins that are involved in the growth and survival of developing neurons and they are involved in the maintenance of mature neurons.[9]

Dementia: Alzheimer's disease

Notice the shrunken and enlarged portions of the brain
The image compares the brain of a normal adult to that of a patient with Alzheimer's disease

"Dementia" is a term referring to neurodegenerative disorders characterized by a loss of memory and such brain functions executive functioning. Included under this umbrella term is Alzheimer's disease. Alzheimer's disease is characterized by the loss of cortical functions like language and motor skills.[6] Patients with Alzheimer's disease exhibit an extreme shrinkage of the cerebral cortex and hippocampus with an enlargement of the ventricles. In several recent studies, higher vitamin D levels have been associated with lower risks of developing Alzheimer's disease.[10] Alzheimer's disease is associated with a decrease in vitamin D receptors in the Cornu Ammonius areas (CA 1& 2) of the hippocampus.[6] The hippocampus is a portion of the limbic system responsible for memory and spatial navigation. Additionally, certain VDR haplotypes were detected with increased frequency in patients with Alzheimer's disease while other VDR haplotypes were detected with decreased frequency, suggesting that specific haplotypes may increase or decrease risk of developing Alzheimer's.[11][12] It is hypothesized that this lack of VDRs in the hippocampus prevents the proper functioning (ie. memory) of this structure.

Parkinson's disease

This image depicts the circuits of the basal ganglia in patients with Parkinson's disease. Pay close attention to the role of the substantia nigra and the dopaminergic neurons

Parkinson's disease is characterized by progressive deterioration of movement and coordination. Patients with Parkinson's disease lose dopaminergic (DA) neurons in the substantia nigra.,[13] a part of the brain that plays a central role in such brain functions as reward, addiction, and coordination of movement. Studies suggest that low vitamin D levels could play a role in PD, and in one case report, vitamin D supplements lessened parkinsonian symptoms. In a study of vitamin D receptor knockout mice, mice without VDR exhibited motor impairments similar to impairments seen in patients with Parkinson's disease.[6] One proposed mechanism linking vitamin D to Parkinson's disease involves the Nurr 1 gene. Vitamin D deficiency is associated with decreased expression of the Nurr1 gene, a gene responsible for development of DA neurons. It is therefore plausible that a lack of Nurr1 expression leads to impaired DA neuronal development. Failure to form DA neurons would lead to lower dopamine concentrations in the basal ganglia. Additionally, rats lacking Nurr1 exhibited hypoactivity followed by death shortly after birth.[13]

Multiple sclerosis

Multiple sclerosis (MS) is an autoimmune disease causing demyelination within the central nervous system.[14] In the central nervous system, there are many cells encased in a fatty coating called the myelin sheath. This sheath allows for informational signals to be transmitted at greater speeds down through the cell. In multiple sclerosis, this sheath deterioration causes a slower transmission of nerve signals. This ultimately results in severe motor deficits.

The prevalence of MS is associated with latitude. In this image, red indicates a high prevalence of MS while yellow indicates a lower prevalence

There is a well-established global correlation between multiple sclerosis and latitude; there is a higher multiple sclerosis prevalence in northeastern regions than in the south and western regions. At the same time, on average higher vitamin D levels are found in the south and western regions than in the northeast.[14] Based on this correlation and other studies, the higher intake of vitamin D is associated with a lower risk for MS.[14] The mechanism for this association is not fully established, however, a proposed mechanism involves inflammatory cytokines. Hypovitaminosis D is associated with an increase in proinflammatory cytokines and decrease in anti-inflammatory cytokines. The increase in these specific cytokines is associated with the degradation of the myelin sheath.[15]

Epilepsy and seizures

Seizures are disturbances in brain activities where neurons fire abnormally. Epilepsy is a condition in which a person experiences repeated seizures. In one pilot small pilot study (Christiansen, 1974,BMJ),vitamin D supplementation, but not placebo treatment was associated with decreased seizures. Vitamin D regulates proconvulsant and anticonvulsant factors. More specifically, Vitamin D is involved in the down regulation of cytokine IL-6, which is a proconvulsant.[6] Additionally, vitamin D is associated with the up regulation of neurotrophic factors: GDNF and TN3. These neurotrophic factors are anticonvulsant. In the absence or depletion of vitamin D, research suggests that the proconvulsant factors will not be down regulated and the anticonvulsant factors will not be up regulated. It is hypothesized that this disturbance in homeostasis may lower the threshold for convulsive activity. Lastly, vitamin D has also been shown to promote the expression of calcium binding proteins that are known to possess anti-epileptic properties.[6]

Schizophrenia

The effects of Schizophrenia on the brain

Schizophrenia is a neuropsychiatric disorder characterized by the inability to perceive reality and think clearly. This condition has genetic and developmental causes.[16] In this disorder, vitamin D is believed to be involved in the development of the brain during the gestational period. Gestational vitamin D deficiency in rats is associated with reduced levels of neurotrophic factors NGF and GDNF.[6] NGF is the nerve growth factor, which is involved in neurotransmission. GDNF is the glial cell lined derived neurotrophic factor, which is involved in the survival and differentiation of dopaminergic neurons.

Other hypovitaminosis D associations

Hypovitaminosis D has also been associated with many other conditions, including both neurological and non neurological conditions. These include but are not limited to autism, diabetes, and osteoporosis.[1]

Future research: cause or effect

Hypovitaminosis D has been associated with many neurological conditions. However, an actual mechanism of attack for each of the conditions has yet to be solidified. Many researchers have questioned whether the depletion of vitamin D actually causes these disorders or if vitamin D is a symptom of these disorders. Future research is needed to fully answer these questions.

See also

References

  1. 1 2 3 4 5 6 7 Harms, L. R., Burne, T. H. J., Eyles, D. W., & McGrath, J. J. (2011). Vitamin D and the brain. Best practice & research. Clinical endocrinology & metabolism, 25(4), 657-69. Elsevier Ltd. doi:10.1016/j.beem.2011.05.009
  2. ↑ Lips, P. (2006). Vitamin D physiology. Progress in biophysics and molecular biology, 92(1), 4-8. doi:10.1016/j.pbiomolbio.2006.02.016
  3. 1 2 Christakos, S., Ajibade, D.V., Dhawan, P., Fechner, A. J., Mady, L.J. (2011). NIH Public Access. Endocrinology And Metabolism, 39(2), 243-253. doi:10.1016/j.ecl.2010.02.002.Vitamin
  4. 1 2 Harvey, M. (2012, October 17). Interview by TN Smith [Audio Tape Recording]. Vitamin d and neuropsychiatric disorders
  5. 1 2 Llewellyn, D. J., Lang, I. a, Langa, K. M., Muniz-Terrera, G., Phillips, C. L., Cherubini, A., Ferrucci, L., et al. (2010). Vitamin D and risk of cognitive decline in elderly persons. Archives of internal medicine, 170(13), 1135-41. doi:10.1001/archinternmed.2010.173
  6. 1 2 3 4 5 6 7 Evatt, M. L. (2012, October 25). Interview by T.N. Smith [Personal Interview]. Vitamin d deficiency and associated neurological conditions., Atlanta, Ga.
  7. ↑ Garcion, E., Wion-barbot, N., Montero-menei, C. N., Berger, F., & Wion, D. (2002). New clues about vitamin D functions in the nervous system. Trends Endocrinol Metab. 2002 13(3):100-105.
  8. ↑ Goodsell, D.S. (2004). The molecular perspective: cytochrome c and apoptosis. The Oncologist Fundamentals of Cancer Medicine. 2004(9),226-227
  9. ↑ Deister, C. and C.E. Schmidt, Optimizing neurotrophic factor combinations for neurite outgrowth. Journal of Neural Engineering, 2006. 3: p. 172-179.
  10. ↑ Annweiler, C., Rolland, Y., Schott, A. M., Blain, H., Vellas, B., Herrmann, F. R., & Beauchet, O. (2012). Higher vitamin D dietary intake is associated with lower risk of alzheimer's disease: a 7-year follow-up . Journals of Gerontology
  11. ↑ Gezen-ak, D., Dursun, E., Bilgiç, B., Hanağasi, H., Ertan, T., Gürvit, H., Emre, M., et al. (2012). Vitamin D Receptor Gene Haplotype Is Associated with Late-Onset Alzheimer ’ s Disease. October, 189-196. doi:10.1620/tjem.228.189.Correspondence
  12. ↑ Valdivielso, J. M., & Fernandez, E. (2006). Vitamin D receptor polymorphisms and diseases. Clinica chimica acta; international journal of clinical chemistry, 371(1-2), 1-12. doi:10.1016/j.cca.2006.02.016
  13. 1 2 Vinh Quôc Luong, K., & Thi Hoàng Nguyên, L. (2012). Vitamin D and Parkinson’s disease. Journal of neuroscience research, 90(12), 2227-36. doi:10.1002/jnr.23115
  14. 1 2 3 Pierrot-Deseilligny, C., & Souberbielle, J.-C. (2010). Is hypovitaminosis D one of the environmental risk factors for multiple sclerosis? Brain : a journal of neurology, 133(Pt 7), 1869-88. doi:10.1093/brain/awq147
  15. ↑ Manuscript, A. (2009). NIH Public Access. Neuroscience, 1119-1147. doi:10.1100/tsw.2008.140.Cytokines
  16. ↑ Picchioni, M. M., & Murray, R. M. (2007). Schizophrenia. Current, 335(July), 91-95. doi:10.1136/bmj.39227.616447.BE
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