Key takeaways:
~For some people, supplementing with low-dose lithium orotate helps with anxiety, mood, and anger issues.
~For others, lithium orotate supplements seem to have little or no noticeable effect on mood.
~Research shows that small amounts of lithium (natural mineral) influence mood, aggression, neuroinflammation, and more.
~Vitamin B12 comes into play here as well, and lithium orotate along with B12 may help with mood and cognition.
In this article, we will explore the potential lithium orotate benefits, backed by research studies, and discuss its impact on mood, anxiety, and cognition. Members will see their genotype report below, plus additional solutions in the Lifehacks section. Join today.
What is low-dose lithium orotate?
Lithium is a naturally occurring mineral found in foods at concentrations dependent upon the mineral content of the soil. It is also an essential element that people need – in small amounts. High amounts of lithium are toxic.[ref]
We get roughly 3 -4 mg of lithium per day naturally in our food and water, although this varies depending on where you live and where your food was grown.
Lithium orotate is a type of natural mineral supplement, and it comes in doses ranging from 5 to 10 mg of elemental lithium. (Just to be clear — I’m not talking about the high dose prescription lithium carbonate that is used for bipolar disorder. Lithium orotate is a different formulation and a whole lot lower dose.)
The science behind lithium orotate’s positive effects:
Studies show that low amounts of lithium, such as what is found in lithium orotate supplements, can help with mood, neuroinflammation, circadian rhythm, ADHD, and more.
Let’s dive into the research on lithium for mood, explore the cellular changes, and understand the mechanisms of action in the brain.
Naturally occurring levels of lithium impact depression and aggression:
Lithium is found in drinking water in varying amounts, depending on the naturally occurring lithium levels in the soil.
Researchers have looked at areas that have higher levels of lithium in the water and compared them to areas with low lithium levels.
Several studies show that areas with higher lithium levels in their drinking water have lower levels of depression and decreased aggression.
- A meta-analysis of studies on lithium in water showed that suicide rates were >50% lower in areas with higher lithium in the drinking water.[ref]
- Another study found that homicide rates were lower in areas with higher levels of lithium in the water supply.[ref]
In addition to epidemiological studies showing that lithium in drinking water reduces suicide rates, research on prescription lithium chloride also indicates that it reduces suicide attempts, independent of its effect on mood in bipolar disorder.[ref][ref]
Lithium orotate benefits: Impact on circadian rhythm and sleep
One way that lithium interacts with mood is by inhibiting GSK3B (glycogen synthase kinase 3beta). GSK3B acts on many different pathways in the body, including circadian rhythm and neuronal plasticity.[ref]
Dysregulation of GSK3B is linked to bipolar disorder, depression, and Alzheimer’s disease.[ref]
Lithium competes with magnesium in binding with GSK3B and inhibiting GSK3B. Through its impact on GSK3B, researchers think lithium can modulate the activity of many different pathways including circadian rhythm. Additionally, lithium may take the place of magnesium in other proteins that need magnesium.[ref]
GSK3B interacts with circadian rhythm and sleep issues, which can be at the heart of depression and mood disorders. Thus, lithium may impact mood and sleep through modifying GSK3B.
What is the connection between lithium orotate, mood, and B vitamins?
Clinicians for more than a decade have recognized that lithium orotate and vitamin B12 act synergistically.
For example, Amy Yasko, PhD, states that “Lithium not only plays a role in mood, glutamate control and limiting aggression but also has been shown to be involved in B12 transport.”[ref] In addition to Dr. Yasko’s clinical work associating B12 and lithium, several studies are showing this as well.[ref]
Research studies on lithium and B vitamins:
- People who take prescription levels of lithium long-term for bipolar disorder tend to have lower serum levels of B12 (thus possibly more B12 in cells) than people using other medications.[ref]
- A study that analyzed lithium in hair samples in various locations and populations “suggests a role of lithium in the transport and distribution of vitamin B12.”[ref]
- A recent study (Feb. 2020) finds that for animal models of bipolar disorder, lithium works better in conjunction with folate (vitamin B9).[ref]
Why is vitamin B12 important to your mood?
Vitamin B12 and folate (B9) are required to produce tetrahydrobiopterin (BH4), which is involved in the production of the neurotransmitters serotonin, melatonin, dopamine, norepinephrine, and epinephrine.[ref]
A deficiency of vitamin B12 has been shown to cause symptoms that “may include agitation, irritability, negativism, confusion, disorientation, amnesia, impaired concentration and attention, and insomnia..” Additionally vitamin B12 deficiency increases the relative risk of depression, bipolar disorder, panic disorder, psychosis, phobias, and dementia.[ref]
Lithium reduces neuroinflammation:
Several studies have found that lithium reduces arachidonic acid production in the brain. Arachidonic acid is an inflammatory lipid. Some researchers theorize that this reduction in neuroinflammation is one of the ways prescription-strength lithium chloride works for people with bipolar disorder.[ref][ref]
The reduction in arachidonic acid isn’t an immediate change, though. Animal studies using higher lithium levels, similar to levels found in prescription lithium, show that lipid levels in the brain change within a month. Specifically, choline and phosphatidylcholine levels increased while sphingomyelin levels decreased.[ref]
Phosphatidylcholine and choline are well-studied for brain benefits and are frequently used as supplements to improve cognitive performance.
Related article: Types of Supplemental Choline
ADHD:
Some clinicians recommend low-dose lithium orotate for ADHD.[ref] In adults with ADHD, a study using high-dose lithium found that it was as effective as methylphenidate in reducing irritability, aggressive outbursts, and more.[ref] In animals, lithium increases working memory.[ref]
Related article: ADHD Genes
Lithium orotate supplements and doses:
Low-dose lithium orotate supplements are available in many health and supplement stores. They are also readily available online. Supplemental doses of lithium range from 5 mg to 20mg of elemental lithium.
Note: If you have medical questions about lithium orotate as a supplement, talk to your doctor or pharmacist. This is especially important if you are on medications for a mood disorder.
Safety studies specific to lithium orotate:
While lithium has been used for more than a century for bipolar disorder, there are possible side effects with the high dose prescription levels of lithium.
But what about low-dose lithium orotate?
A 2021 animal study investigated the safety of using lithium orotate. The results showed no genotoxic effects, meaning that it wouldn’t damage DNA. There were no adverse side effects or organ damage in the animal trial. The highest dose tested in animals was 400 mg/kg/day with no observable adverse effects.[ref]
How long does lithium orotate take to work?
Anecdotally, a 5 or 10mg lithium orotate supplement helps some people feel less irritable, angry, or anxious. It may take a week to notice the effect on mood. However, not everyone notices a difference in mood.
It is likely that genetics, diet, stress level, and daily exposure to lithium through drinking water/foods all come together to determine whether supplemental lithium affects an individual’s mood. The genetics part is explained in more detail below.
In addition to improving anxiety and irritability symptoms, there may be other benefits to low-dose lithium, such as Alzheimer’s prevention.
What is ‘microdosing’ lithium?
Several recent peer-reviewed studies reference microdosing of lithium for Alzheimer’s disease prevention or treatment. Essentially, the term microdosing just means a low dose compared to prescription lithium.
For example, clinical trials using a 300 mcg dose of lithium refer to it as microdosing. However, trials using up to 5 mg of elemental lithium also refer to it as microdosing.[ref][ref][ref]
I am bringing up microdosing because the right dose of lithium for Alzheimer’s prevention may be different than for someone who is using lithium orotate for mood regulation..
Lithium Orotate Genotype Report:
Not a member? Join here. Membership lets you see your data right in each article and also gives you access to the members-only information in the Lifehacks sections.
The MTR and MTRR genes are important in vitamin B12 usage in the methylation cycle. Dr. Yasko explains her research on the effects of lithium. She makes the case that lithium, through the inhibition of thioredoxin, can increase COMT, an enzyme that regulates and degrades dopamine, epinephrine, and norepinephrine.
I want to be really clear here… This information is based on online recommendations from clinicians – not peer-reviewed research studies. There are no research studies connecting lithium orotate to specific B12 variants.
MTR Polymorphisms (SNPs):
Check your genetic data for rs1805087 (23andMe v4, v5; AncestryDNA):
- A/A: typical
- A/G: increased enzyme activity, possibly more responsive to lithium orotate supplements for irritability, anxiety
- G/G: increased enzyme activity[ref], possibly more responsive to lithium orotate supplements for irritability, anxiety
Members: Your genotype for rs1805087 is —.
The rs1805087 variant is also known as A2756G. The G allele causes an increase in activity, thus possibly causing a decrease in methyl groups available for other pathways to use and also using up methylB12 more quickly than normal.[ref]
MTRR Polymorphisms (SNPs):
Methionine synthase reductase (MTRR) has several fairly common variants that affect the production of the MTRR enzyme, which regenerates vitamin B12 (methylcobalamin) for use by MTR and other enzymes. The variant rs1801394 is also known as A66G, and it decreases this enzyme’s efficiency. It is a fairly common variant carried by about half the population.
Check your genetic data for rs1801394 (23andMe v4, v5; AncestryDNA):
Members: Your genotype for rs1801394 is —.
COMT genetic variant: rs4680
One well-studied variant of the COMT gene is rs4680, often referred to as Val158Met. In looking at research studies, the G is “Val” and the A allele is usually noted as “Met”.
- The G allele (Val) has higher COMT enzymatic activity, causing a more rapid breakdown of the neurotransmitters and, thus, lower dopamine levels. In most populations, the G allele is the most common.[ref]
- The A allele (Met) has lower COMT enzyme activity and, thus, higher dopamine levels. This variant of the COMT enzyme seems to have lower activity because it breaks down faster at normal body temperature.[ref]
Check your genetic data for rs4680 (23andMe v4, v5; AncestryDNA):
- G/G: higher COMT activity, lower dopamine & norepinephrine, higher pain tolerance (Val)
- A/G: intermediate COMT activity (most common genotype)
- A/A: 40% lower COMT activity, higher dopamine & norepinephrine, lower pain tolerance (Met), reduced stress resiliency
Members: Your genotype for rs4680 is —.
Genetic variants that impact lithium carbonate (prescription lithium):
Keep in mind that the amount of lithium in the prescription medication is orders of magnitude higher than supplemental lithium orotate. What I find interesting is that genome-wide genetic studies (GWAS) link lithium as an ion to channels that directly affect neurons.
ACCN1 gene: codes for a cation channel in neurons that is responsive to sodium, potassium, and lithium
Check your genetic data for rs11869731 (23andMe v5):
- C/C: may be more likely to respond to lithium for bipolar disorder[ref][ref]
- C/G: typical response
- G/G: typical response
Members: Your genotype for rs11869731 is —.
CACNG2 gene: calcium channel gamma-2 subunit
Check your genetic data for rs2284018 (23andMe v4, v5):
- C/C: may be more likely to respond to lithium for bipolar disorder[ref][ref]
- C/T: may be more likely to respond to lithium for bipolar disorder
- T/T: typical response rate
Members: Your genotype for rs2284018 is —.
BDNF gene: codes for brain-derived neurotrophic factor, which is important in the way neurotransmitters work and in neuroplasticity.
Check your genetic data for rs6265 Val66Met (23andMe v4, v5; AncestryDNA):
- T/T: decreased BDNF[ref] referred to in studies as Met/Met; introversion, resilient to adverse events, a quicker decline in Alzheimer’s[ref][ref][ref] may have a better response to lithium carbonate for bipolar disorder[ref]
- C/T: somewhat decreased BDNF, referred to as Val/Met;
- C/C: typical BDNF, referred to as Val/Val
Members: Your genotype for rs6265 is —.
GADL1 gene: encodes glutamate decarboxylase-like protein 1
Check your genetic data for rs17026688 (23andMe v4; AncestryDNA):
- C/C: Typical
- C/T: more likely to respond to lithium carbonate for bipolar disorder
- T/T: more likely to respond to lithium carbonate for bipolar disorder[ref]
Members: Your genotype for rs17026688 is —.
Lifehacks:
The rest of this article explains the research on using lithium orotate as a supplement. It is for Genetic Lifehacks members only. Consider joining today to see the rest of this article.
Member Content:
An active subscription is required to access this content.
Join Here for full access to this article, genotype reports, and much more!
Already a member? Log in below.
Related Articles and Topics:
Is inflammation causing your depression and anxiety?
Research over the past two decades clearly shows a causal link between increased inflammatory markers and depression. Genetic variants in the inflammatory-related genes can increase the risk of depression and anxiety.
Lithium Orotate: Mood, Alzheimer’s Prevention, and Telomeres
Lithium is a naturally occurring mineral that we consume in small amounts each day. Research now shows that low doses of lithium may impact mood, Alzheimer’s disease, and telomere length.
Depression, Genetics, and Circadian Rhythm
For some people, circadian disruption can be chronic – and at the heart of depression or mood disorders. Genetic variants play a role in this susceptibility. Fortunately, some solutions may help.
Anxiety and Genetics
This article covers genetic variants related to anxiety disorders. Genetic variants combine with environmental factors (nutrition, sleep, relationships, etc), when it comes to anxiety. There is not a single “anxiety gene”. Instead, many genes can be involved – and many genetic pathways to target for solutions.
Cortisol and HPA Axis Dysfunction
Cortisol is a hormone produced by the adrenal glands in times of stress, and it also plays many roles in your normal bodily functions. It is a multi-purpose hormone that needs to be in the right amount (not too high, not too low) and at the right time. Your genes play a big role in how likely you are to have problems with cortisol.
References:
Basselin, Mireille, et al. “Lithium Modifies Brain Arachidonic and Docosahexaenoic Metabolism in Rat Lipopolysaccharide Model of Neuroinflammation.” Journal of Lipid Research, vol. 51, no. 5, May 2010, pp. 1049–56. PubMed Central, https://doi.org/10.1194/jlr.M002469.
Cervantes, P., et al. “Vitamin B12 and Folate Levels and Lithium Administration in Patients with Affective Disorders.” Biological Psychiatry, vol. 45, no. 2, Jan. 1999, pp. 214–21. PubMed, https://doi.org/10.1016/s0006-3223(97)00544-1.
Chen, Jingshan, et al. “Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on MRNA, Protein, and Enzyme Activity in Postmortem Human Brain.” American Journal of Human Genetics, vol. 75, no. 5, Nov. 2004, pp. 807–21. PubMed, https://doi.org/10.1086/425589.
Coppen, Alec, and Christina Bolander-Gouaille. “Treatment of Depression: Time to Consider Folic Acid and Vitamin B12.” Journal of Psychopharmacology (Oxford, England), vol. 19, no. 1, Jan. 2005, pp. 59–65. PubMed, https://doi.org/10.1177/0269881105048899.
Del Matto, L., et al. “Lithium and Suicide Prevention in Mood Disorders and in the General Population: A Systematic Review.” Neuroscience & Biobehavioral Reviews, vol. 116, Sept. 2020, pp. 142–53. ScienceDirect, https://doi.org/10.1016/j.neubiorev.2020.06.017.
Fortinguerra, Stefano, et al. “Pharmacogenomic Characterization in Bipolar Spectrum Disorders.” Pharmaceutics, vol. 12, no. 1, Dec. 2019, p. 13. PubMed Central, https://doi.org/10.3390/pharmaceutics12010013.
Geoffroy, Pierre A., et al. “Lithium Response in Bipolar Disorders and Core Clock Genes Expression.” The World Journal of Biological Psychiatry: The Official Journal of the World Federation of Societies of Biological Psychiatry, vol. 19, no. 8, Dec. 2018, pp. 619–32. PubMed, https://doi.org/10.1080/15622975.2017.1282174.
Giotakos, Orestis, George Tsouvelas, et al. “A Negative Association between Lithium in Drinking Water and the Incidences of Homicides, in Greece.” Biological Trace Element Research, vol. 164, no. 2, Apr. 2015, pp. 165–68. PubMed, https://doi.org/10.1007/s12011-014-0210-6.
Giotakos, Orestis, Paul Nisianakis, et al. “Lithium in the Public Water Supply and Suicide Mortality in Greece.” Biological Trace Element Research, vol. 156, no. 1–3, Dec. 2013, pp. 376–79. PubMed, https://doi.org/10.1007/s12011-013-9815-4.
Health, Holistic. Lithium Connection – Yasko Protocol Conference. 2011. Vimeo, https://vimeo.com/26165981.
Hidvégi, Anna, et al. “[Results of investigations on the association between lithium levels in drinking water and suicidal behaviour in the population: a narrative review].” Psychiatria Hungarica: A Magyar Pszichiatriai Tarsasag Tudomanyos Folyoirata, vol. 31, no. 3, 2016, pp. 221–30.
“Home.” Dr. Amy Yasko, https://dramyyasko.com/. Accessed 14 May 2022.
Jakobsson, Eric, et al. “Towards a Unified Understanding of Lithium Action in Basic Biology and Its Significance for Applied Biology.” The Journal of Membrane Biology, vol. 250, no. 6, 2017, pp. 587–604. PubMed Central, https://doi.org/10.1007/s00232-017-9998-2.
Kennedy, David O. “B Vitamins and the Brain: Mechanisms, Dose and Efficacy—A Review.” Nutrients, vol. 8, no. 2, Jan. 2016, p. 68. PubMed Central, https://doi.org/10.3390/nu8020068.
Li, Dankang, et al. “Associations of MTRR A66G Polymorphism and Promoter Methylation with Ischemic Stroke in Patients with Hyperhomocysteinemia.” The Journal of Gene Medicine, vol. 22, no. 5, May 2020, p. e3170. PubMed, https://doi.org/10.1002/jgm.3170.
Li, Xiaohua, and Richard S. Jope. “Is Glycogen Synthase Kinase-3 a Central Modulator in Mood Regulation?” Neuropsychopharmacology, vol. 35, no. 11, Oct. 2010, pp. 2143–54. PubMed Central, https://doi.org/10.1038/npp.2010.105.
Lin, Zhong, et al. “Interactions between Genetic Variants Involved in the Folate Metabolic Pathway and Serum Lipid, Homocysteine Levels on the Risk of Recurrent Spontaneous Abortion.” Lipids in Health and Disease, vol. 18, June 2019, p. 143. PubMed Central, https://doi.org/10.1186/s12944-019-1083-7.
Ma, Xian-Yong, et al. “Association between BDNF Rs6265 and Obesity in the Boston Puerto Rican Health Study.” Journal of Obesity, vol. 2012, Dec. 2012, p. e102942. www.hindawi.com, https://doi.org/10.1155/2012/102942.
Mandelman, Samuel D., and Elena L. Grigorenko. “BDNF Val66Met and Cognition: All, None, or Some? A Meta-Analysis of the Genetic Association.” Genes, Brain, and Behavior, vol. 11, no. 2, Mar. 2012, pp. 127–36. PubMed Central, https://doi.org/10.1111/j.1601-183X.2011.00738.x.
Menegas, Samira, et al. “Efficacy of Folic Acid as an Adjunct to Lithium Therapy on Manic-like Behaviors, Oxidative Stress and Inflammatory Parameters in an Animal Model of Mania.” Metabolic Brain Disease, vol. 35, no. 2, Feb. 2020, pp. 413–25. PubMed, https://doi.org/10.1007/s11011-019-00503-3.
Murbach, Timothy S., et al. “A Toxicological Evaluation of Lithium Orotate.” Regulatory Toxicology and Pharmacology, vol. 124, Aug. 2021, p. 104973. ScienceDirect, https://doi.org/10.1016/j.yrtph.2021.104973.
Nunes, Marielza Andrade, Natalia Mendes Schöwe, et al. “Chronic Microdose Lithium Treatment Prevented Memory Loss and Neurohistopathological Changes in a Transgenic Mouse Model of Alzheimer’s Disease.” PloS One, vol. 10, no. 11, 2015, p. e0142267. PubMed, https://doi.org/10.1371/journal.pone.0142267.
Nunes, Marielza Andrade, Tania Araujo Viel, et al. “Microdose Lithium Treatment Stabilized Cognitive Impairment in Patients with Alzheimer’s Disease.” Current Alzheimer Research, vol. 10, no. 1, Jan. 2013, pp. 104–07. PubMed, https://doi.org/10.2174/1567205011310010014.
Ozan, Erol, et al. “The Effect of Depression, BDNF Gene Val66met Polymorphism and Gender on Serum BDNF Levels.” Brain Research Bulletin, vol. 81, no. 1, Jan. 2010, pp. 61–65. ScienceDirect, https://doi.org/10.1016/j.brainresbull.2009.06.022.
Priebe, Garrick A., and Mark M. Kanzawa. “Reducing the Progression of Alzheimer’s Disease in Down Syndrome Patients with Micro-Dose Lithium.” Medical Hypotheses, vol. 137, Apr. 2020, p. 109573. PubMed, https://doi.org/10.1016/j.mehy.2020.109573.
Rapoport, Stanley I. “Lithium and the Other Mood Stabilizers Effective in
Bipolar Disorder Target the Rat Brain Arachidonic Acid Cascade.” ACS Chemical Neuroscience, vol. 5, no. 6, May 2014, pp. 459–67. PubMed Central, https://doi.org/10.1021/cn500058v.
Rybakowski, J. K., et al. “Prophylactic Lithium Response and Polymorphism of the Brain-Derived Neurotrophic Factor Gene.” Pharmacopsychiatry, vol. 38, no. 4, July 2005, pp. 166–70. PubMed, https://doi.org/10.1055/s-2005-871239.
Schrauzer, G. N., et al. “Lithium in Scalp Hair of Adults, Students, and Violent Criminals. Effects of Supplementation and Evidence for Interactions of Lithium with Vitamin B12 and with Other Trace Elements.” Biological Trace Element Research, vol. 34, no. 2, Aug. 1992, pp. 161–76. PubMed, https://doi.org/10.1007/BF02785244.
Schrauzer, G. N., and K. P. Shrestha. “Lithium in Drinking Water and the Incidences of Crimes, Suicides, and Arrests Related to Drug Addictions.” Biological Trace Element Research, vol. 25, no. 2, May 1990, pp. 105–13. PubMed, https://doi.org/10.1007/BF02990271.
Silberberg, Gilad, et al. “Stargazin Involvement with Bipolar Disorder and Response to Lithium Treatment.” Pharmacogenetics and Genomics, vol. 18, no. 5, May 2008, pp. 403–12. PubMed, https://doi.org/10.1097/FPC.0b013e3282f974ca.
Stern, Shani, et al. “Prediction of Response to Drug Therapy in Psychiatric Disorders.” Open Biology, vol. 8, no. 5, May 2018, p. 180031. PubMed Central, https://doi.org/10.1098/rsob.180031.
Tufan, Ali Evren, et al. “Mood Disorder with Mixed, Psychotic Features Due to Vitamin B12 Deficiency in an Adolescent: Case Report.” Child and Adolescent Psychiatry and Mental Health, vol. 6, June 2012, p. 25. PubMed Central, https://doi.org/10.1186/1753-2000-6-25.
Voineskos, Aristotle N., et al. “The Brain-Derived Neurotrophic Factor Val66Met Polymorphism and Prediction of Neural Risk for Alzheimer Disease.” Archives of General Psychiatry, vol. 68, no. 2, Feb. 2011, pp. 198–206. PubMed, https://doi.org/10.1001/archgenpsychiatry.2010.194.
Wang, Liang-Jen, et al. “A Potential Interaction between COMT and MTHFR Genetic Variants in Han Chinese Patients with Bipolar II Disorder.” Scientific Reports, vol. 5, Mar. 2015, p. 8813. PubMed Central, https://doi.org/10.1038/srep08813.
Weiner, Alexandra S., et al. “Methylenetetrahydrofolate Reductase C677T and Methionine Synthase A2756G Polymorphisms Influence on Leukocyte Genomic DNA Methylation Level.” Gene, vol. 533, no. 1, Jan. 2014, pp. 168–72. PubMed, https://doi.org/10.1016/j.gene.2013.09.098.
Zanni, Giulia, et al. “Lithium Accumulates in Neurogenic Brain Regions as Revealed by High Resolution Ion Imaging.” Scientific Reports, vol. 7, Jan. 2017, p. 40726. PubMed Central, https://doi.org/10.1038/srep40726.