22.9
%
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22.9
%
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The Transferrin Saturation (TSAT) Calculator determines the percentage of transferrin, the primary iron-transport protein in the blood, that is loaded with iron. Transferrin saturation is calculated by dividing serum iron by the total iron-binding capacity (TIBC) and multiplying by 100. This ratio provides critical information about iron availability for erythropoiesis and cellular functions, complementing ferritin in the comprehensive assessment of iron metabolism disorders.
Transferrin is a glycoprotein produced primarily by the liver that binds and transports iron throughout the body. Each transferrin molecule can bind two atoms of ferric iron. The TIBC measures the maximum amount of iron that transferrin can carry and is an indirect measure of circulating transferrin concentration. Under normal conditions, approximately 20-45% of transferrin binding sites are occupied by iron, representing normal transferrin saturation.
A low TSAT (below 20%) indicates insufficient iron delivery to tissues, including the bone marrow for hemoglobin synthesis. This finding is a hallmark of iron deficiency anemia, where depleted iron stores cannot adequately load transferrin. However, low TSAT also occurs in functional iron deficiency, where iron stores may be adequate but sequestered by inflammation (hepcidin-mediated iron restriction), preventing iron from reaching transferrin. This distinction is clinically critical in patients with chronic kidney disease, heart failure, and inflammatory conditions.
An elevated TSAT (above 45%) raises concern for iron overload conditions. In hereditary hemochromatosis, the most common genetic disorder in Caucasian populations, TSAT is characteristically elevated above 45% and often exceeds 60%. This early elevation of TSAT, occurring before significant organ iron deposition, makes it an effective screening tool. Hemochromatosis screening guidelines from the American Association for the Study of Liver Diseases recommend measuring fasting TSAT as the initial test, with genetic testing for HFE mutations if TSAT exceeds 45%.
The TSAT is influenced by diurnal variation in serum iron levels, with highest levels typically occurring in the morning and lowest in the late afternoon. This variability can cause TSAT to fluctuate by as much as 30% throughout the day, making fasting morning samples the most reliable and reproducible. Recent iron supplementation, transfusions, and dietary iron intake can also acutely affect serum iron and thus TSAT. For accurate interpretation, samples should be drawn fasting and before any iron supplementation.
In clinical practice, TSAT and ferritin are complementary tests that together provide a comprehensive picture of iron metabolism. Ferritin reflects total body iron stores, while TSAT reflects the adequacy of current iron delivery. A patient can have normal ferritin but low TSAT (functional iron deficiency) or low ferritin with initially normal TSAT (early iron depletion before delivery is compromised). Monitoring both values is essential for guiding iron supplementation therapy, particularly in chronic kidney disease where target ranges of TSAT 20-50% and ferritin 200-500 ng/mL guide erythropoiesis-stimulating agent management.
Transferrin saturation is calculated as: TSAT = (Serum Iron / TIBC) x 100. Normal TSAT is 20-45%. Values below 20% indicate iron deficiency or functional iron deficiency with inadequate iron delivery. Values above 45% suggest iron overload, prompting evaluation for hemochromatosis.
TSAT 20-45% is normal. Below 20% indicates insufficient iron for erythropoiesis (iron deficiency or inflammatory iron restriction). Above 45% warrants evaluation for iron overload, especially hereditary hemochromatosis. TSAT above 60% with elevated ferritin strongly suggests iron overload requiring further investigation.
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Results
(80/350) x 100 = 22.9%. Normal transferrin saturation.
Inputs
Results
(30/450) x 100 = 6.7%. Very low TSAT indicating iron deficiency.
TSAT is the percentage of the iron-transport protein transferrin that is carrying iron. It reflects the adequacy of iron supply to tissues and is calculated as serum iron divided by TIBC times 100.
Normal TSAT is 20-45%. Values vary with diurnal rhythm, meals, and recent iron intake. Fasting morning samples provide the most accurate results.
TSAT below 20% means insufficient iron is being delivered to tissues. This occurs in absolute iron deficiency (depleted stores) and functional iron deficiency (iron trapped by inflammation).
TSAT above 45% raises concern for iron overload, particularly hereditary hemochromatosis. TSAT above 60% with elevated ferritin strongly suggests pathological iron accumulation requiring treatment.
Fasting TSAT above 45% is the recommended initial screening test. If confirmed on repeat testing, HFE gene mutation analysis is performed. TSAT rises early in hemochromatosis, before organ damage occurs.
Serum iron follows a diurnal pattern with morning peaks and afternoon troughs. This causes TSAT to fluctuate by up to 30%. Fasting morning samples minimize this variability.
TIBC (Total Iron-Binding Capacity) measures the maximum iron that blood can carry, reflecting transferrin levels. TIBC increases in iron deficiency (body makes more transferrin) and decreases in iron overload and inflammation.
Ferritin reflects iron stores (how much iron is saved). TSAT reflects iron delivery (how much iron is currently being transported). Both are needed for comprehensive iron status assessment.
In chronic kidney disease patients on ESAs, guidelines target TSAT 20-50% and ferritin 200-500 ng/mL. IV iron is given when TSAT < 30% and ferritin < 500 to support erythropoiesis.
Yes. Oral iron taken within hours of blood draw significantly elevates serum iron and TSAT. Patients should stop oral iron 24-48 hours before testing. IV iron can affect results for 1-2 weeks.
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