Last reviewed: May 12, 2026 Last updated: May 12, 2026

Written by: Jay Hastings , CEO of PlexusDx

Jay Hastings is the CEO of PlexusDx, a precision health company focused on genetic testing, blood biomarker insights, and personalized wellness recommendations. He has more than 20 years of experience across healthcare innovation, genomics, laboratory operations, healthcare investing, and strategic finance. His work has included scaling healthcare startups, leading CLIA lab integrations, and helping expand consumer access to precision health tools.

Medically reviewed by: Jayden Lee, PharmD, EMBA

Jayden Lee, PharmD, EMBA, is the PlexusDx Medical Science Liaison with a PharmD and MBA specializing in pharmacogenomics and clinical product development, with a proven ability to bridge the gap between genomic research and practical patient outcomes. Dr. Lee has more than 10 years of professional experience in clinical pharmacy, academia, and research.

This article is part of the PlexusDx Education Hub — your resource for evidence-based guidance on diet & genetics. Browse all Diet & Genetics education

Biotin, also known as vitamin B7, is a water-soluble nutrient the body relies on to convert food into energy and to maintain healthy skin, hair, and nails. Deficiency is uncommon, but when it happens the effects can be real — and how efficiently your body recycles biotin depends partly on your genes. Understanding both the nutrition and the genetics helps you keep levels where they should be.

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What Biotin Does in the Body

Biotin acts as an essential cofactor for a family of enzymes called carboxylases, which drive key steps in metabolizing fats, carbohydrates, and protein. Pyruvate carboxylase supports glucose production, acetyl-CoA carboxylase helps build fatty acids, and other carboxylases process amino acids. Without enough functional biotin, these pathways slow down.

This metabolic role is why biotin is linked to energy, and why its deficiency shows up in fast-turnover tissues like skin and hair.

Signs and Risk Factors for Biotin Deficiency

Symptoms of low biotin can include thinning hair, a scaly red rash around the eyes and nose, brittle nails, and, in more advanced cases, neurological effects such as tingling. Certain groups face higher risk: pregnant women, heavy alcohol users, smokers, and people with conditions affecting nutrient absorption such as inflammatory bowel disease.

Prolonged consumption of raw egg whites, which contain avidin that binds biotin, can also deplete levels over time.

The Genes That Shape Biotin Status

Your body constantly recycles biotin, and the gene BTD is central to that process. BTD encodes biotinidase, the enzyme that frees biotin from dietary proteins and reclaims it from the body's own proteins. The BTD variant rs13078881-C has been reported to reduce enzyme activity by as much as half, suggesting carriers may need more dietary biotin to meet the same demand.

Two other genes complete the picture: HLCS (holocarboxylase synthetase), which attaches biotin to carboxylase enzymes, and SLC5A6, which transports biotin into cells. Rare variants in these genes cause inherited biotin-processing disorders, while more common variants simply nudge a person's baseline requirement.

How Much Biotin You Actually Need

The general adequate intake for adults is about 30 micrograms per day, readily met by a varied diet. Biotin is abundant in eggs, salmon, beef liver, pork, sunflower seeds, sweet potatoes, and almonds. For most people, food alone is enough; those with higher requirements or absorption issues sometimes use supplements, and low-biotin symptoms often resolve quickly once intake improves.

Because genetic variants like those in BTD can raise individual demand, two people eating similar diets may have different needs — which is where genetic context can help.

What Pathway-Level Genetic Insight Reveals

The PlexusDx Precision Peptide Genetic Test analyzes 14 pathways, 49 peptides, 150+ genetic insights, including variants in nutrient-metabolism pathways where genes such as BTD and HLCS operate. It reports how your genes may influence these pathways at the biological level — not a diagnosis of deficiency, and not a prescription for any supplement.

PlexusDx tells you about your biology; it does not tell you what to put in your body. Genetics is a guide, not a guarantee. Decisions about supplementation should be made with a qualified healthcare provider.

Frequently Asked Questions

What are the main benefits of biotin?

Biotin acts as a cofactor for carboxylase enzymes that metabolize fats, carbohydrates, and protein into usable energy. It also supports healthy skin, hair, and nails, which is why deficiency often shows up in those tissues first. Most people meet their needs through a varied diet.

How can I prevent biotin deficiency?

Eating biotin-rich foods such as eggs, salmon, liver, sunflower seeds, and nuts usually meets the roughly 30-microgram daily adequate intake. People at higher risk, including pregnant women and those with absorption issues, should discuss their needs with a provider before starting supplements.

Does the BTD gene affect biotin needs?

Yes. BTD encodes biotinidase, which recycles biotin in the body. The BTD variant rs13078881-C can lower enzyme activity substantially, suggesting carriers may require more dietary biotin. This is a tendency in a nutrient pathway, not a deficiency diagnosis, and is best interpreted with a provider.

Can a genetic test tell me if I am biotin deficient?

No. A genetic test describes tendencies in nutrient-metabolism pathways, not your current biotin status. The PlexusDx Precision Peptide Genetic Test offers pathway-level context about genes like BTD. Confirming an actual deficiency requires blood testing and evaluation by a qualified provider.

Curious whether your genes raise your biotin needs? Explore the Precision Peptide Genetic Test for pathway-level insight you can bring to your provider before changing your diet or supplements.

This article is part of the PlexusDx Education Hub. Browse all Diet & Genetics education

The Precision Peptide Genetic Test analyzes how your genes influence peptide-related biological pathways. It does not recommend, prescribe, or determine which peptides you should use. Consult a qualified healthcare provider before beginning any peptide protocol.

Medical and Editorial Standards

Medical review process: This article was reviewed for medical accuracy, scientific clarity, evidence alignment, and appropriate discussion of genetics, medications, supplements, biomarkers, and health-related claims.

Sources and evidence: PlexusDx educational content is developed using peer-reviewed research, clinical literature, reputable medical references, and, where applicable, public health or regulatory guidance. References are included at the end of the article when scientific, medical, or health-related claims are discussed.

Commercial transparency: PlexusDx offers genetic testing, blood biomarker testing, personalized supplement recommendations, and related precision wellness services. Product mentions are intended to help readers understand available options and should not be interpreted as medical advice.

Important disclaimer: PlexusDx educational content is for informational purposes only and should not be used as a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making decisions about medications, supplements, genetic testing, lab testing, or health-related care.

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