Effectiveness of Vitamin D on Neurological and Mental Disorders
Abstract
:1. Introduction
2. Materials and Methods
2.1. Inclusion and Exclusion Criteria
- Vitamin D supplementation: The review specifically sought to examine research that investigated the effects of vitamin D supplementation on various health outcomes.
- Specific mental health disorders: The included studies covered a range of mental health conditions, such as those outlined in the search terms—depression, epilepsy, bipolar disorder, schizophrenia, and neuroinflammation.
- Studies that focused on mental or neurological disorders other than the key conditions of interest, namely depression, bipolar disorder, schizophrenia, and neuroinflammation.
- Studies that examined the effects of vitamins other than vitamin D.
- Studies that utilized multiple nutrients or supplements rather than focusing solely on vitamin D.
- Studies that covered a range of mental health disorders rather than concentrating on the specific conditions outlined.
- Comparative studies that did not include a vitamin D supplementation intervention.
2.2. Search Strategy
2.3. Data Extraction
3. Results
4. Discussion
5. Conclusions
Limitations
Funding
Conflicts of Interest
References
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Parameter | Inclusion Criteria | Exclusion Criteria |
---|---|---|
Population | Adults and children with specific mental health disorders (depression, bipolar and schizophrenia), and neurological disorders including (epilepsy and neuroinflammation) | Studies include other disorders, such as eating disorders and intellectual disabilities |
Intervention | Vitamin D supplementation | Nutrients apart from vitamin D and other combined nutrients |
Comparison | Influence of vitamin D on specified disorder assessed | No specificity in the comparison |
Outcomes | Specific mental disorders including (depression, bipolar and schizophrenia), and neurological disorders including (epilepsy, and neuroinflammation) | Generalised mental or neurological health and comparison of different disorders in a single study. |
Study design | Peer-reviewed studies published in English, including those that utilized; randomised controlled trials, retrogressive studies, randomised crossover trials, cohort studies, case-control studies, cross-sectional studies, systematic reviews, meta-analyses, and exception of experimental studies. | Articles not published in English, including websites, letters to the editor, expert opinions, case studies, case reports, and reports. |
Author, Year | Study Design | Country (Location) | Study Group | Time |
---|---|---|---|---|
Depression | ||||
Mousa et al., 2018 [28] | Cross-sectional study and randomised placebo-controlled trial. | Melbourne, Australia | Obese adults with BMI >25 kg/m2 from the age of 18 to 60 serum 25(OH)D concentrations <50 without clinical depression | Undefined |
Jorde et al., 2008 [29] | Cross-sectional study and randomized double blind controlled trial | Norway | 441 subjects (body mass index 28–47 kg m−2, 159 men and 282 women, aged 21–70 years) | Undefined |
Sharifi et al., 2019 [30] | Double-Blind Randomised Placebo-Controlled Trial. | Shariati Hospital in Tehran | Patients above 35 years and with a BMI equal to and lower or higher than 25 Kg/m2 | December 2014 and January 2015 |
de Koning et al., 2015 [31] | Randomised placebo-controlled clinical trial | Amsterdam, Netherlands | Older adults between 60 and 80 years. | June 2013 and April 2015 |
Gowda et al., 2015 [32] | Meta-analysis of Undefined. randomised controlled. trials | Undefined | Individuals aged ≥18 y who were diagnosed with depressive disorder | Up to 2014 |
Bipolar | ||||
Marsh et al., 2017 [33] | Double-blind placebo-controlled trial. | Massachusetts, USA | 18–70 years old with DSM IV bipolar Depression and Vitamin D deficiency (<30 ng/mL) Bipolar patients. | June 2013 and April 2015 |
Pirotta et al., 2015 [34] | Double-blinded, placebo-controlled randomized trial | Melbourne, Australia | Men and women (age > 60 with serum 25(OH) D concentrations | Undefined |
Petrov et al., 2018 [35] | Longitudinal study | USA | A total of 36 participants (Youth aged 6–12) who were divided into three categories: non-mood controls (n = 13), bipolar disorder (BD) (n = 12) and major Depressive Disorder (MDD) (n = 11) | Undefined |
Schizophrenia | ||||
Krivoy et al., 2017 [36] | Randomized, Double-Blind, Placebo-controlled Clinical trial | Geha Mental Health Center, Israel | Schizophrenia patients who had been maintained on clozapine treatment for at least 18 weeks and had low levels of vitamin D (<75 nmol/L) | 1 May 2014 to 30 September 2016. |
Valipour et al., 2014 [37] | Systematic Review and Meta-Analysis of Observational Studies | Undefined | Patients with schizophrenia | Up to October 2013 |
Sheikhmoonesi et al., 2016 [38] | Randomized controlled trial | Iran | Patients aged 18 to 65 years who met the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria for a diagnosis of schizophrenia. All participants had baseline serum vitamin D concentrations less than 30 ng/mL, indicating either vitamin D deficiency (less than 20 ng/mL) or vitamin D insufficiency (21 to 29 ng/mL). | March 2013–September 2013 |
Epilepsy | ||||
Alhaidari et al., 2022 [39] | Retrospective analytical medical record review | Outpatient epilepsy research clinic in Saudi Arabia | Epileptic patients older than 14 years. | November 2016 and April 2020 |
Hollo et al., 2012 [40] | Pilot study | Budapest, Hungary | Patients between 19 years and 60 years. | Undefined |
Mishra et al., 2023 [41] | Randomised Controlled Trial | Undefined | Children aged 2 to 12 years old with epilepsy. | Undefined |
Al Khalifah et al., 2018 [42] | Randomised pragmatic trial protocol | Paediatric neurology clinic at King Saud University Medical City, Saudi Arabia. | Children aged 2 to 16 years with epilepsy. | December 2017 and December 2019 |
Neuroinflammation | ||||
Jiang et al., 2022 [43] | Experimental study (behavioural tests in traumatic brain injury rats) | Beijing, China | Sprague-Dawley (SD) rats (age, 12–16 weeks, weighing 280–320 g). | Undefined |
Author, Year | Outcome | Conclusion from Studies | Quality Based on NOS |
---|---|---|---|
Depression | |||
Mousa et al., 2018 [28] | No significant reduction in Beck Depression inventory score in patients included in the study. | Non-supporting | 6 |
Jorde et al., 2008 [29] | Overweight and obese subjects with serum 25(OH)D levels <40 nmol L−1 have higher (more depressive) scores on the BDI. A significant improvement BDI scores. | Supporting | 6 |
Sharifi et al., 2019 [30] | Patients with sufficient baseline vitamin D may benefit from supplementation more than vitamin D-deficient patients, which indicates that higher serum vitamin D levels may be needed for its antidepressant effect. | Supporting | 8 |
de Koning et al., 2015 [31] | Supplementation with 1200 IU/d vitamin D for 12 months did not affect depressive symptoms and physical functioning in older persons with relatively low vitamin D status. | Supporting | 6 |
Gowda et al., 2015 [32] | The study did not support the evidence for the efficacy of vitamin D in improving depression among adults. | Inconclusive | 6 |
Bipolar | |||
Marsh et al., 2017 [33] | Despite a more significant rise in Vitamin D levels in the Vitamin D supplementation group, there was no significant difference in reducing depressive symptoms. Additionally, Vitamin D3 supplementation vs. placebo did not improve reduction in mood elevation or anxiety symptoms. | Non-supporting | 7 |
Pirotta et al., 2015 [34] | Daily supplementation with 2000 IU of vitamin D3 for ten weeks had no significant effect on neuroplasticity compared to placebo, but the finding that vitamin D treatment alone was associated with a decrease in corticospinal excitability and intracortical inhibition. | Inconclusive | 6 |
Petrov et al., 2018 [35] | Increased levels of Vitamin D Binding Protein (DBP) in participants with bipolar disorder (BD) compared to the non-mood control group. | Supportive | 6 |
Schizophrenia | |||
Krivoy et al., 2017 [36] | Providing vitamin D supplements did not demonstrate a clear superior benefit compared to the placebo treatment when evaluating the primary outcomes related to psychotic, depressive, and metabolic outcomes. A mild positive effect of vitamin D supplementation seen on cognitive performance in the participants. | Inconclusive | 7 |
Valipour et al., 2014 [37] | A strong association between vitamin D deficiency and schizophrenia. | Supportive | 6 |
Sheikhmoonesi et al., 2016 [38] | No relationship between serum vitamin D level changes and the improvement of negative and positive symptoms in schizophrenic patients | Not supporting | 6 |
Epilepsy | |||
Alhaidari et al., 2022 [39] | Patients with high vitamin D levels had reasonable seizure control compared with those with low levels. | Inconclusive (Recommended RCT) | 6 |
Hollo et al., 2012 [40] | Supplementation of vitamin D had a significant impact on decreasing seizures. | Supporting. | 7 |
Mishra et al., 2023 [41] | Supplementation of vitamin D had a significant impact on decreasing seizures. | Supporting. | 7 |
Al Khalifah et al., 2018 [42] | The results proved the efficacy of maintaining higher vitamin D levels and its impacts on seizure control and bone health for children with epilepsy. | Supporting. | 6 |
Neuroinflammation | |||
Jiang et al., 2022 [43] | Vitamin D effectively alleviated neurocognitive deficits, brain oedema, and blood brain barrier disruption, and promoted hippocampal neuronal survival in vivo and in vitro. | Supporting | - |
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AlGhamdi, S.A. Effectiveness of Vitamin D on Neurological and Mental Disorders. Diseases 2024, 12, 131. https://doi.org/10.3390/diseases12060131
AlGhamdi SA. Effectiveness of Vitamin D on Neurological and Mental Disorders. Diseases. 2024; 12(6):131. https://doi.org/10.3390/diseases12060131
Chicago/Turabian StyleAlGhamdi, Shareefa Abdullah. 2024. "Effectiveness of Vitamin D on Neurological and Mental Disorders" Diseases 12, no. 6: 131. https://doi.org/10.3390/diseases12060131
APA StyleAlGhamdi, S. A. (2024). Effectiveness of Vitamin D on Neurological and Mental Disorders. Diseases, 12(6), 131. https://doi.org/10.3390/diseases12060131