Key Benefits

• Confirm your vitamin B6 status for healthy nerves, blood, and metabolism.
• Spot deficiency causing tingling, anemia, mouth cracks, skin rash, irritability, or fatigue.
• Flag excess from supplements that may trigger tingling and sensory nerve damage.
• Clarify causes of high homocysteine when paired with vitamin B12 and folate.
• Guide safe use if you take isoniazid, hydralazine, penicillamine, or oral contraceptives.
• Support pregnancy and preconception by confirming levels for fetal development and nausea treatment.
• Track trends if you supplement, follow restrictive diets, or have malabsorption conditions.

What is a Vitamin B6 (Plasma) blood test?

Vitamin B6 (plasma) is the amount of vitamin B6 circulating in your blood. Vitamin B6 is a water‑soluble nutrient you get from food and supplements. After absorption in the small intestine, the liver converts it into its active coenzyme forms, mainly pyridoxal 5′‑phosphate (PLP) and to a lesser extent pyridoxamine phosphate (PMP), derived from the parent compounds pyridoxine, pyridoxal, and pyridoxamine. In the bloodstream, PLP is carried to tissues, representing the readily available pool your body can use.

Vitamin B6’s active form (PLP) is a coenzyme for many enzymes that handle amino acids—building and reshaping proteins, and creating key brain messengers like serotonin, dopamine, and GABA. It supports making heme for hemoglobin in red blood cells, helps the body convert homocysteine into cysteine (transsulfuration), and assists in releasing glucose from glycogen during energy needs (glycogen phosphorylase). Plasma vitamin B6 therefore reflects the body’s immediate supply for protein metabolism, neurotransmitter production, oxygen‑carrying capacity, energy mobilization, and aspects of immune function.

Why is a Vitamin B6 (Plasma) blood test important?

Vitamin B6 (measured in plasma, typically as pyridoxal‑5‑phosphate) is the body’s versatile coenzyme for amino‑acid processing, neurotransmitter production, heme synthesis, glycogen breakdown, and one‑carbon metabolism. This test shows how available B6 is for those reactions across brain, blood, immune, and metabolic systems. On most lab reports, values in the middle of the reference range generally reflect adequate tissue status; values near the bottom suggest limited availability, and very high values usually indicate excess.

When the value is low, the body struggles to make serotonin, dopamine, and GABA, and to build heme and antibodies. People may notice irritability, low mood, poor concentration, peripheral tingling or burning, or a seizure tendency in infants. Fatigue can result from microcytic or sideroblastic anemia; skin and mouth changes (seborrheic rash, glossitis, cheilitis) may appear. Homocysteine can rise, adding cardiovascular strain. Pregnancy, inflammatory states, older age, alcohol use, and certain medicines can depress plasma B6; in pregnancy, low B6 is linked to worse nausea and higher homocysteine.

When the value is high, it is most often from supplements rather than food. Excess B6—especially pyridoxine—can injure sensory nerves, causing numbness, burning, loss of vibration sense, and unsteady gait, sometimes with photosensitivity or rash. Rarely, reduced clearance in liver or kidney disease contributes.

Big picture, B6 status connects neurotransmission, red‑cell and immune health, glucose handling, and vascular biology. It interlocks with folate and B12 around homocysteine, and it is influenced by inflammation and protein status. Keeping B6 in a healthy range supports long‑term neurologic function, hematologic robustness, and cardiovascular resilience.

What insights will I get?

Vitamin B6 (plasma), most often measured as pyridoxal‑5‑phosphate (PLP), reflects the active coenzyme that powers hundreds of enzymes. It is central to amino acid and protein turnover, neurotransmitter formation (serotonin, dopamine, GABA), hemoglobin synthesis, glucose release from glycogen, and one‑carbon metabolism that helps control homocysteine. Adequate PLP supports energy production, cardiovascular integrity, cognition and mood, reproductive health, and immune defense.

Low values usually reflect insufficient intake or absorption, increased demand, or redistribution during inflammation. Physiologically, low PLP limits transamination and decarboxylation reactions, leading to reduced neurotransmitter synthesis (mood changes, irritability, seizures in severe deficiency), impaired heme synthesis (microcytic or sideroblastic anemia, fatigue), less efficient glycogenolysis (low‑energy symptoms), and higher homocysteine (vascular stress). Levels tend to run lower in pregnancy and with estrogen-containing contraceptives, in older adults, with chronic inflammation or low albumin, alcohol use, and with certain medications.

Being in range suggests adequate coenzyme availability for stable protein metabolism, resilient neurochemistry, efficient hemoglobin production, balanced glucose handling, and effective homocysteine control in concert with folate and B12. In the absence of inflammation, values near the mid-portion of a laboratory’s reference interval generally indicate robust status.

High values usually reflect recent supplementation or high intake, or reduced renal clearance of B6 vitamers. Very high circulating B6—especially pyridoxine forms—can be associated with sensory nerve dysfunction, though plasma PLP does not always track toxicity.

Notes: Most labs measure PLP, but some report other B6 forms; assays are light‑sensitive and vary by method. Fasting samples reduce postprandial variation. Inflammation and low albumin lower plasma PLP independent of tissue status. Pregnancy lowers circulating PLP. Renal disease alters B6 vitamer patterns. Recent supplementation transiently elevates results.