Vitamin B7, more commonly known as biotin, is a B vitamin. Like all B-type vitamins, biotin aids the body in breaking down carbohydrates, fats, and proteins for energy production. It also has roles in maintaining healthy skin, hair, and nervous system function.<\/p>\n
Read this post to learn more about the potential health benefits of biotin.<\/p>\n
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Biotin, also known as vitamin B7, is a water-soluble B-complex vitamin essential for the growth and development of all organisms [R<\/a>].<\/p>\n As a coenzyme of carboxylase enzymes, vitamin B7 is involved in the metabolism of fatty acids, amino acids, and carbohydrates [R<\/a>].<\/p>\n Biotin has been shown to be important for many health factors including supporting neurological functions, steadying blood sugar levels, DNA stability, and hair, skin and nail health [R<\/a>, R<\/a>].<\/p>\n The body cannot synthesize vitamin B7, so it needs to be obtained regularly from the diet and intestinal bacteria [R<\/a>].<\/p>\n Biotin can be found in a wide variety of foods including animal liver, egg yolks, cow milk, and some fruits and vegetables [R<\/a>].<\/p>\n Although vitamin B7 deficiency is rare, it can be dangerous if left untreated. Suboptimal levels or marginal deficiencies, which are a lot more common, have been linked to a variety of negative health effects including growth retardation, neurological dysfunction, hair loss, skin rash, muscle pain<\/a>, and anemia [R<\/a>].<\/p>\n Groups at risk for biotin deficiency include smokers, alcoholics, pregnant women, and people with inflammatory bowel disease (IBD)<\/a> [R<\/a>, R<\/a>, R<\/a>, R<\/a>].<\/p>\n Oral vitamin B7 supplements are completely absorbed even at high pharmacological doses (81.9 micromoles taken orally or 18.4 micromoles taken intravenously) [R<\/a>].<\/p>\n Biotin is absorbed via a sodium-dependent multivitamin transporter (SMVT) in the small and large intestines [R<\/a>].<\/p>\n After transport from the intestines into the systemic circulation, biotin is taken up by the liver and eventually crosses the blood-brain barrier into the central nervous system [R<\/a>].<\/p>\n Soon after oral ingestion by humans, single high doses of biotin (600 micrograms and 900 micrograms) are eliminated from the circulation leading to a significant increase of urinary excretion. Therefore, for prolonged maintenance of blood biotin levels, lower doses (300 micrograms) each day for a week are recommended [R<\/a>].<\/p>\n Roughly half of the absorbed vitamin B7 undergoes metabolism to bisnorbiotin and biotin sulfoxide prior to excretion. Vitamin B7, bisnorbiotin, and biotin sulfoxide are present in molar ratios of approximately 3:2:1 in human urine and blood [R<\/a>].<\/p>\n The elimination half-life time of biotin is approximately 1 hour, 50 minutes [R<\/a>].<\/p>\n Biotin is a coenzyme for carboxylases, the enzymes that assist in the metabolism of fats, proteins, and carbohydrates for energy production [R<\/a>].<\/p>\n These enzymes are essential for the following processes:<\/p>\n Inadequate vitamin B7 levels in the body can slow down metabolism, which may lead to fatigue, digestive problems, and weight gain [R<\/a>].<\/p>\n Biotin is required for myelin<\/a> sheath formation, a fatty substance that surrounds nerves and facilitates nerve impulse conduction. As such, biotin deficiency can delay myelination [R<\/a>].<\/p>\n Biotin deficiency can also lead to a number of other neurological symptoms, including seizures, lack of muscle coordination, learning disabilities, hallucinations, depression<\/a>, and lethargy. Most of these conditions can be resolved with biotin supplementation [R<\/a>, R<\/a>, R<\/a>].<\/p>\n High-dose biotin supplementation (5-10 mg\/kg\/day) was also effective in treating biotin-responsive basal ganglia<\/a> disease, a rare brain metabolic condition characterized by seizures, confusion, and abnormal coordination, in a review of 18 cases [R<\/a>].<\/p>\n Multiple sclerosis<\/a> is an autoimmune disorder characterized by myelin damage and loss. Given its role in fatty acid synthesis and energy production (both are needed for myelin repair and axonal survival), it has been proposed that biotin may be effective in limiting or reversing multiple sclerosis-related impairments [R<\/a>].<\/p>\n In fact, 2 clinical trials on 177 people found that high-dose vitamin B7 treatment was able to reverse disease progression and improve symptoms in patients with progressive multiple sclerosis. However, the treatment had little or no effectiveness at improving visual acuity in another trial on 93 people with multiple sclerosis [R<\/a>, R<\/a>, R<\/a>].<\/p>\n Vitamin B7 is needed for white blood cell development and its deficiency is linked to impaired immune function and an increased risk of infection [R<\/a>, R<\/a>].<\/p>\n It increases the production of Th1<\/a> cytokines like IL-1\u03b2<\/a> and IFN-\u03b3<\/a>, which are essential for eliciting an immune response to fight bacterial and viral infections [R<\/a>].<\/p>\n Inadequate levels of vitamin B7 are associated with decreased antibody synthesis, T cell decay, and lower amounts of spleen cells and T cells in both animals and humans [R<\/a>, R<\/a>, R<\/a>].<\/p>\n Decreased rates of cellular proliferation during biotin deficiency may account for some of these adverse effects on immune function [R<\/a>].<\/p>\n A deficiency of biotinidase, an enzyme that helps recycle biotin, is associated with chronic vaginal candidiasis and is treatable with biotin supplementation. Since 1 in every 123 people is believed to be biotinidase-deficient, women with chronic vaginal candidiasis may be responsive to biotin treatment [R<\/a>].<\/p>\n Biotin may help lower blood sugar levels by increasing insulin production, enhancing glucose uptake in muscle cells, and stimulating glucokinase<\/a>, an enzyme in the liver that promotes glycogen synthesis [R<\/a>, R<\/a>, R<\/a>].<\/p>\n Daily supplementation of vitamin B7 decreased fasting<\/a> blood sugar concentrations by an average of approximately 45% in a clinical trial on 43 people with type 2 diabetes [R<\/a>].<\/p>\n This vitamin increased the activity of 3 enzymes involved in glucose breakdown (pyruvate carboxylase, acetyl-CoA carboxylase, and propionyl-CoA carboxylase) in a clinical trial on 30 people [R<\/a>].<\/p>\n Its combination with chromium<\/a> picolinate improved blood sugar management in 2 clinical trials on almost 500 uncontrolled diabetics [R<\/a>, R<\/a>].<\/p>\n Furthermore, high doses improved the symptoms of a nerve damage condition commonly exhibited in diabetic patients (diabetic neuropathy) [R<\/a>].<\/p>\n All in all, the evidence suggests that supplementation with biotin, especially in combination with chromium picolinate, may help control blood sugar levels and reduce the risk of diabetic neuropathy. You may use biotin as a complementary approach to managing your blood sugar levels if your doctor determines that it may be helpful in your case. Never take biotin in place of the antidiabetic medication prescribed by your doctor.<\/p>\n Biotin is required for normal fat metabolism, which is critical for maintaining heart and blood vessel health [R<\/a>, R<\/a>, R<\/a>].<\/p>\n In combination with chromium<\/a> picolinate, vitamin B7 helped reduce heart disease risk factors by increasing high-density lipoprotein (HDL<\/a>) levels and decreasing low-density lipoprotein (LDL<\/a>) levels, especially in 2 clinical trials on almost 400 diabetic patients with heart disease [R<\/a>, R<\/a>].<\/p>\n Pharmacological doses of biotin (15,000 mcg\/day) were also effective in lowering blood triglyceride concentrations in 33 patients with elevated triglyceride levels [R<\/a>].<\/p>\n Although limited, the evidence suggests that biotin may help reduce the risk of heart disease. You may discuss with your doctor if it may be recommendable in your case.<\/p>\n Biotin deficiency is linked to a number of skin conditions, including seborrheic dermatitis (cradle cap) and eczema [R<\/a>, R<\/a>].<\/p>\n This may be related to biotin\u2019s roles in fatty acid synthesis and metabolism, which is critical for skin health [R<\/a>].<\/p>\n Skin cells are particularly dependent on fat production since they require extra protection against damage and water loss from constant outdoor exposure [R<\/a>].<\/p>\n Inadequate levels of vitamin B7 can also lead to hair loss, which is reversible with supplementation. Although some studies have found that vitamin B7 promotes hair growth in women with thinning hair, there is minimal evidence to support that it promotes hair growth in otherwise healthy individuals [R<\/a>, R<\/a>, R<\/a>, R<\/a>].<\/p>\n Biotin may enhance the quality of brittle nails, with affected patients exhibiting firmer, harder, and thicker nails after treatment [R<\/a>, R<\/a>, R<\/a>].<\/p>\n Again, the evidence is limited but suggests that biotin may improve hair, skin, and nail health. Discuss with your doctor if you can obtain any of these benefits by supplementing with biotin.<\/p>\n Marginal biotin deficiency is common during pregnancy due to the increased biotin demands from the growing fetus [R<\/a>].<\/p>\n In animals, even a subclinical level of biotin deficiency can result in cleft palate and limb abnormalities [R<\/a>].<\/p>\n It is hypothesized that a low biotin status during pregnancy may increase the risk of birth defects in humans by altering fat metabolism and increasing genomic instability, both of which can lead to the development of chromosomal abnormalities and fetal malformations [R<\/a>, R<\/a>].<\/p>\n In human embryonic palatal (roof of the mouth) stem cells, vitamin B7 depletion was found to suppress carboxylase production and cellular proliferation, indicating that lower levels of vitamin B7 may delay or halt the growth of the embryonic palate, resulting in cleft palate development [R<\/a>].<\/p>\n However, definitive evidence establishing the connection between biotin deficiency in humans and the development of birth defects is currently lacking and thus, more research is required [R<\/a>].<\/p>\n Biotin covalently binds to histones, DNA binding proteins that help fold and package DNA into chromatin. The addition of biotin to histones plays a significant role in cellular proliferation, gene silencing, and DNA repair and stability [R<\/a>, R<\/a>, R<\/a>].<\/p>\n Low levels of biotin can lead to inadequate histone biotinylation, which may result in genomic instability and abnormal gene expression (cellular production) and thus increases the risks of cancer. These effects have been shown to increase cancer risk in fruit flies and cell-based studies [R<\/a>, R<\/a>, R<\/a>].<\/p>\n However, higher levels of biotin (up to 600 micrograms) were actually found to increase <\/em>genomic instability and damage in 1 study in humans. This suggests that biotin\u2019s DNA stabilizing effects may be dose-dependent [R<\/a>].<\/p>\n In any case, the causal link between histone biotinylation and DNA damage risk in humans remains to be investigated [R<\/a>].<\/p>\n Research from mouse models and human white blood cells<\/a> indicates that biotin deficiency may increase the production of proinflammatory cytokines and aggravate inflammatory conditions [R<\/a>, R<\/a>].<\/p>\n In biotin-deficient mice with nickel allergies, biotin supplementation decreased the production of pro-inflammatory cytokines and improved allergic inflammation, suggesting a potential therapeutic effect of biotin against inflammatory and allergic diseases in humans [R<\/a>].<\/p>\n This may be a result of decreased NF-\u03baB<\/a> activity, which is activated during vitamin B7 deficiency [R<\/a>, R<\/a>].<\/p>\n The BTD gene<\/a> encodes biotinidase, an enzyme that recycles biotin. Biotinidase transports free biotin through the bloodstream and attaches biotin to other proteins [R<\/a>].<\/p>\n Single nucleotide polymorphisms (SNPs) in the BTD genome include the following:<\/p>\n The SLC5A6 gene<\/a> encodes the sodium-dependent multivitamin transporter that helps transport biotin into cells [R<\/a>].<\/p>\n This gene encodes holocarboxylase synthetase (HLCS), an enzyme that attaches biotin molecules to histones and carboxylase enzymes. Mutations in this gene can reduce biotin binding to molecules and suppress carboxylase activity, resulting in impaired protein, fat, and carbohydrate metabolism. They can also affect the production of genes that are important for normal development [R<\/a>, R<\/a>].<\/p>\n Biotin covalently binds to histones using the enzyme HLCS and is involved in gene silencing, DNA repair, chromatin structure, and transposon repression [R<\/a>].<\/p>\n Contact your doctor or pharmacist if you notice any side effects after supplementing with biotin. <\/em><\/p>\n Call your doctor for medical advice about side effects. In the US, you may report side effects to the FDA at 1-800-FDA-1088 or at <\/em>www.fda.gov\/medwatch<\/em><\/a>. In Canada, you may report side effects to Health Canada at 1-866-234-2345.<\/em><\/p>\n Biotin is generally considered safe and no toxicity has been reported for doses up to 300 mg\/day orally and 20 mg intravenously [R<\/a>, R<\/a>].<\/p>\n Since it is a water-soluble vitamin, vitamin B7 overdose is unlikely as excess amounts are excreted in the urine [R<\/a>].<\/p>\n High-dose vitamin B7 supplementation may skew thyroid test results and mimic the laboratory pattern of Grave\u2019s disease [R<\/a>].<\/p>\n Supplement\/Herb\/Nutrient-drug interactions can be dangerous and, in rare cases, even life-threatening. Always consult your doctor before supplementing and let them know about all drugs and supplements you are using or considering.<\/em><\/p>\n Lipoic acid<\/a> competes with vitamin B7 for binding to the sodium-dependent multivitamin transporter (SMVT) in the intestine, so long-term use of lipoic acid could result in depleted vitamin B7 levels [R<\/a>].<\/p>\n Similarly, large doses of vitamin B5<\/a> (pantothenic acid<\/a>) have the potential to compete with vitamin B7 for absorption by the SMVT [R<\/a>, R<\/a>].<\/p>\n Prolonged use of antibiotics like tetracycline and sulfonamides can reduce biotin levels because they kill biotin-producing bacteria in the intestines [R<\/a>].<\/p>\n Furthermore, some anticonvulsants such as primidone and carbamazepine inhibit vitamin B7 absorption. Chronic anticonvulsant use can also increase vitamin B7 breakdown [R<\/a>].<\/p>\n Raw egg whites contain the protein avidin, which binds biotin tightly and inhibits its absorption [R<\/a>].<\/p>\n Smoking accelerates biotin breakdown, especially in women, resulting in marginal biotin deficiency [<\/a>Pharmacokinetics<\/strong><\/span><\/h3>\n
<\/a>Health Benefits of Biotin<\/strong><\/span><\/h2>\n
<\/a>Effective for:<\/strong><\/span><\/h3>\n
<\/a>1) Energy Metabolism<\/strong><\/span><\/h3>\n
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<\/a>2) Brain Function <\/strong><\/span><\/h3>\n
<\/a>3) Immune System Function<\/strong><\/span><\/h3>\n
<\/a>Possibly Effective for:<\/strong><\/span><\/h3>\n
<\/a>1) Type 2 Diabetes<\/strong><\/span><\/h3>\n
<\/a>2) Lowering the Risk of Heart Disease<\/strong><\/span><\/h3>\n
<\/a>3) Skin, Hair, and Nail Health<\/strong><\/span><\/h3>\n
<\/a>Insufficient Evidence for:<\/strong><\/span><\/h3>\n
<\/a>1) Preventing Birth Defects<\/strong><\/span><\/h3>\n
<\/a>2) Preventing DNA Damage<\/strong><\/span><\/h3>\n
<\/a>Animal and Cell Research (Lack of Evidence)<\/strong><\/span><\/h3>\n
<\/a>Inflammatory and Allergic Disorders<\/strong><\/span><\/h3>\n
<\/a>Genetics of Biotin<\/strong><\/span><\/h2>\n
<\/a>BTD Gene – The Enzyme that Recycles Biotin<\/strong><\/span><\/h3>\n
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<\/a>SLC5A6 Gene – The Transporter that Transport Biotin Into the Cells<\/strong><\/span><\/h3>\n
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<\/a>HLCS Gene – The Enzyme that Attaches Biotin to Other Proteins<\/strong><\/span><\/h3>\n
<\/a>Side Effects & Precautions<\/strong><\/span><\/h2>\n
<\/a>Contraindications<\/strong><\/span><\/h3>\n
<\/a>Nutrient\/Drug interactions<\/strong><\/span><\/h3>\n