Biotin, also known as vitamin B7 or vitamin H, is a water-soluble vitamin that plays a crucial role in the body’s metabolic processes. It serves as a coenzyme for carboxylase enzymes, synthesising fatty acids, generating glucose, and metabolising amino acids. It plays a key role in keeping our hair, skin, and nails healthy. Biotin is also essential for the proper functioning of our nervous system and helps in the production of fatty acids and glucose. When our body does not get enough biotin, it can lead to a deficiency.
Biotin deficiency is rare but can cause various health problems. Some people may not realise that their unexplained symptoms could be linked to a lack of biotin. This deficiency can affect many parts of the body, leading to issues such as hair loss, skin rashes, and digestive problems.
In this blog, we will explore 6 surprising biotin deficiency diseases and conditions you might not know about. Understanding these conditions can help you recognise the importance of biotin in your diet and overall health.
1. What Diseases Cause Biotin Deficiency?
2. What Bodily Conditions Cause Biotin Deficiency?
3. 5 Prominent Biotin Deficiencies
4. Dietitian’s Recommendation
5. The Final Say
6. FAQs
7. References
Here are some diseases and conditions that may result in biotin deficiency:
Here are some genetic disorders that can cause biotin deficiency diseases:
Disorder/ Disease | Description | Symptoms |
Biotinidase Deficiency | An inherited metabolic disorder is when the body lacks biotinidase, an enzyme essential for recycling biotin. |
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Diagnosis: Newborn screening, Enzyme activity assay, Genetic testing Treatment: Lifelong biotin supplementation. | ||
Holocarboxylase Synthetase Deficiency | Genetic disorders affect the enzyme holocarboxylase synthetase, which is necessary for attaching biotin to carboxylases. |
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Diagnosis: Biochemical tests, Genetic testing Treatment: High doses of biotin supplements and early treatment improve outcomes. | ||
Multiple Carboxylase Deficiency | Genetic disorders due to defects in biotin-dependent enzymes impact metabolism. |
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Diagnosis: Biochemical tests and genetic testing. Treatment: High doses of biotin supplements, early intervention is critical. | ||
Biotin-Thiamine-Responsive Basal Ganglia Disease | A rare genetic disorder affecting the brain's basal ganglia, responsive to biotin and thiamine. |
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Diagnosis: Genetic testing, Clinical evaluation. Treatment: Biotin and thiamine supplements; early treatment can prevent neurological symptoms. |
Apart from genetic disorders, later-life malabsorption syndromes can also lead to biotin deficiency diseases:
Disease | Description | Symptoms | Impact & Management | |
Inflammatory Bowel Disease (IBD) | Chronic digestive tract inflammation, including Crohn’s disease and ulcerative colitis. |
| Impact on Biotin
Management Treatment of underlying IBD and biotin supplementation if needed. | |
Celiac Disease | An autoimmune disorder occurs when ingesting gluten, which damages the small intestine. |
| Impact on Biotin Management A gluten-free diet and biotin supplementation if needed. |
It is a condition resulting from the surgical removal of part of the small intestine.
Symptoms | Impact | Management |
Diarrhoea, malnutrition, weight loss, fatigue.
| Reduced absorption surface, leading to nutrient deficiencies, including biotin. | Nutritional support, biotin supplementation. |
Chronic antibiotic use can deplete biotin levels by disrupting gut bacteria that produce this essential nutrient.
Symptoms | Impact | Management |
Skin rashes, hair thinning, neurological issues like depression and lethargy. | Long-term use of antibiotics can disrupt the gut microbiota, reducing biotin production by intestinal bacteria. | Probiotic use, dietary biotin intake, and biotin supplements. |
Late-onset multiple carboxylase deficiency is a rare genetic disorder that impairs the body's ability to utilise biotin, leading to a deficiency.
Description | Symptoms | Diagnosis | Treatment |
A milder form of multiple carboxylase deficiency that presents later in life. | Skin rashes, hair loss, neurological symptoms.
| Genetic testing, enzyme activity assays. | Biotin supplementation. |
Juvenile onset biotinidase deficiency is an inherited condition that prevents the proper recycling of biotin, causing a deficiency in children.
Description | Symptoms | Diagnosis | Treatment |
Milder form of biotinidase deficiency presents in older children or adolescents. | Developmental delays, neurological issues, skin rashes. | Enzyme activity assay, genetic testing. | Biotin supplementation. |
Also Read: Know All About The Best Biotin Tablets For Hair Growth
Some other conditions that are likely to cause biotin deficiency are:
Raw egg whites contain avidin, a protein that binds to biotin and prevents its absorption. When consumed in excess, it may result in biotin deficiency diseases. You can identify its repercussions as skin rashes, hair loss, and neurological symptoms.
An increased requirement for biotin during pregnancy may result in biotin deficiency diseases, as the body fails to fulfil the additional levels. The expecting mother may suffer from skin rashes, hair loss, fatigue, and potential congenital anomalies in the fetus. Adequate dietary biotin intake and prenatal supplements can help pregnant women deal with biotin deficiency.
Alcohol interferes with biotin absorption and utilisation and can cause malnutrition, skin rashes, hair loss, and neurological issues. You must reduce or stop alcohol consumption and take biotin supplementation and nutritional support to dodge biotin deficiency diseases.
Intravenous feeding may lack adequate biotin if not correctly formulated, resulting in skin rashes, hair loss, and neurological issues. Ensure biotin is included in parenteral nutrition formulations and supplements as needed to avoid biotin deficiency diseases.
Drugs like phenytoin, carbamazepine, and valproic acid can decrease biotin levels, causing biotin deficiency in the body, reducing biotin absorption and increasing biotin degradation. In such cases, monitor biotin levels and supplementation if necessary. Isotretinoin is commonly used for severe acne, can reduce biotin levels and result in dry skin and hair loss.
Mitochondrial illnesses might exacerbate biotin-deficient conditions by impairing the metabolic mechanisms necessary for biotin recycling and usage. These illnesses frequently reduce the efficiency with which the mitochondria make energy, which might raise metabolic stress and the need for biotin.
Because biotin is essential for many enzymatic processes related to energy production and metabolism, deficiencies can arise from mitochondrial malfunction that compromises biotin's efficiency and availability.
The body's capacity to maintain appropriate levels of biotin can be compromised by genetic illnesses caused by mutations in genes involved in biotin transport, absorption, or the activity of biotin-dependent enzymes.
Increased demand for biotin or poor biotin utilisation in important biochemical pathways can result from metabolic diseases, such as those that impact carboxylase enzymes that need biotin as a cofactor. These diseases might cause insufficient biotin availability, resulting in symptoms including skin rashes, hair loss, and neurological problems linked to a biotin shortage.
Here are the five prominent biotin deficiencies and diseases:
Also Read: 6 Best Biotin-Rich Foods To Add To Your Diet As Per Dietitian's Recommendation
I recommend increasing biotin-rich foods such as eggs (cooked), nuts, seeds, and leafy greens for biotin deficiency diseases. Incorporate whole grains, liver, and fish to boost biotin intake. Probiotic-rich foods like yoghurt can support gut health, enhancing biotin production.
Biotin supplements may be necessary for people with genetic disorders or malabsorption issues. Pregnant women should ensure adequate biotin through a balanced diet and prenatal vitamins. Avoid consuming raw egg whites, as they contain avidin, which inhibits biotin absorption. Regular monitoring and dietary adjustments are essential for managing biotin deficiency effectively.
Dt. Akshata Gandevikar
Many metabolic functions depend on biotin, and a lack of it can cause a number of health problems. To maintain optimal health, it is vital to comprehend the origins, symptoms, and available treatment choices for biotin deficiency.
People can prevent and manage biotin deficiency by ensuring adequate biotin intake through a balanced diet and addressing underlying conditions. Early diagnosis and treatment are crucial for inherited disorders like biotinidase deficiency and holocarboxylase synthetase deficiency, as timely intervention can significantly improve outcomes.
1. How much biotin do I need daily?
The recommended daily intake for adults is 30 micrograms. Pregnant and breastfeeding women may need slightly more.
2. Can too much biotin be harmful?
Biotin is water-soluble, so excess amounts are excreted in urine. High doses are generally not considered very harmful, but always consult a healthcare provider before supplementing.
3. How can I prevent biotin deficiency?
Prevent biotin deficiency by consuming a balanced diet rich in biotin-containing foods, avoiding raw egg whites, maintaining gut health, and supplementing as needed under medical advice.
4. What are the top biotin deficiency diseases?
Here are some well-known biotin deficiency diseases:
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