Mentzer index

MCV ÷ red cell count — iron deficiency vs thalassaemia trait in microcytosis

Sources last checked: 2026-11-03

Mentzer index

MCV ÷ red cell count — iron deficiency vs thalassaemia trait in microcytosis

Fill in every field to see the result.

A screening index, not a diagnosis. Combined iron deficiency and thalassaemia trait, α-thalassaemia, pregnancy, children and anaemia of chronic disease all blur the cut-off; it is only meaningful in microcytosis.

Source: Mentzer WC Jr. Differentiation of iron deficiency from thalassaemia trait. Lancet 1973;1(7808):882.Open

Interpretation

< 13 — favours thalassaemia traitMentzer (1973): an index below 13 points towards thalassaemia trait, in which the red cell count is relatively preserved despite small cells. Confirmation needs haemoglobin analysis (HbA₂/HbF) and iron studies.
≥ 13 — favours iron deficiencyMentzer (1973): an index above 13 points towards iron deficiency. Validation studies show substantial overlap, so ferritin and, where appropriate, haemoglobin analysis still decide.

What is the Mentzer index?

The Mentzer index divides the mean corpuscular volume by the red cell count. William Mentzer proposed it in a 1973 letter to the Lancet as a quick way to separate iron deficiency from thalassaemia trait in microcytic anaemia: in thalassaemia trait the red cell count is relatively high, so the index is low.

When to use it

  • Microcytosis (low MCV) on a routine blood count, as a first orientation
  • Deciding which confirmatory test to request first (ferritin vs haemoglobin analysis)
  • Teaching the red cell indices in microcytic anaemia

When not to use it

  • Normocytic or macrocytic anaemia
  • As a substitute for ferritin or haemoglobin electrophoresis/HPLC
  • When iron deficiency and thalassaemia trait may coexist, which is common in high-prevalence populations

How it is calculated

Mentzer index = MCV (fL) / RBC (× 10¹²/L)

Clinical pearls and limitations

  • A screening index, not a diagnosis. Combined iron deficiency and thalassaemia trait, α-thalassaemia, pregnancy, children and anaemia of chronic disease all blur the cut-off; it is only meaningful in microcytosis.
  • Below 13 favours thalassaemia trait, above 13 iron deficiency; values close to 13 are uninformative.
  • Iron deficiency can lower HbA₂ and mask β-thalassaemia trait — repeat haemoglobin analysis after iron repletion if suspicion remains.
  • Validation studies show variable performance, especially in children and in α-thalassaemia.
  • Relevant for premarital and antenatal screening programmes in Turkey and in Mediterranean-origin populations in Germany and Austria.

Frequently asked questions

How is the Mentzer index calculated?

MCV in fL divided by the red cell count in 10¹²/L (the same number as 10⁶/µL).

What does a Mentzer index below 13 mean?

It favours thalassaemia trait over iron deficiency; confirmation needs haemoglobin analysis and iron studies.

Is the Mentzer index reliable?

It is a quick screen with modest accuracy; studies report sensitivities and specificities ranging widely, so it does not replace ferritin and HbA₂.

Evidence and guidelines

  1. Primary source: Mentzer WC Jr. Differentiation of iron deficiency from thalassaemia trait. Lancet 1973;1(7808):882.
  2. AlQarni AM et al. Diagnostic test performance of the Mentzer index in evaluating Saudi children with microcytosis. Front Med 2024;11:1361805 (sensitivity 74 %, specificity 63 % for β-thalassaemia trait).

Have a follow-up question?

Medelix answers clinical questions from current guidelines and studies — every statement with its source.

Related calculators

Embed this calculatorFree to use on your website, intranet or teaching page. Copy the code below.
<iframe src="https://medelix.ai/en/embed/mentzer-index" title="Mentzer index – Medelix" width="100%" height="620" style="border:0;max-width:720px" loading="lazy"></iframe> <p><a href="https://medelix.ai/en/calculators/mentzer-index">Mentzer index calculator by Medelix</a></p>

For healthcare professionals and medical students. These tools support, and do not replace, clinical judgement. Always check results against the original source and your local protocols.