Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jun 3;14(11):e040845.
doi: 10.1161/JAHA.124.040845. Epub 2025 May 22.

Iron Deficiency Is Associated With Impaired Myocardial Reperfusion in ST-Segment-Elevation Myocardial Infarction: Influence of the Definition Used

Affiliations

Iron Deficiency Is Associated With Impaired Myocardial Reperfusion in ST-Segment-Elevation Myocardial Infarction: Influence of the Definition Used

José A Barrabés et al. J Am Heart Assoc. .

Abstract

Background: The role of iron deficiency (ID) in ST-segment-elevation myocardial infarction (STEMI) remains unclear. This study aimed to assess whether ID is associated with impaired myocardial reperfusion in STEMI and whether this association is affected by ID definition.

Methods: We included 942 consecutive patients with STEMI successfully treated with primary percutaneous coronary intervention. ID was defined either as recommended by international guidelines or, alternatively, as ferritin <100 ng/mL, transferrin saturation <20%, or serum iron ≤13 μmol/L. In 595 patients, serum soluble transferrin receptor levels were measured. Impaired myocardial reperfusion was defined as lack of ST-segment resolution ≥50% 60 to 90 minutes after percutaneous coronary intervention.

Results: ID prevalence varied across these definitions. Impaired reperfusion was present in 12.7% of patients without ID and 41.0% of those with ID defined by transferrin saturation <20% (P<0.001). This association was less pronounced for serum iron ≤13 μmol/L, weaker for guideline criteria, and absent for high (≥1.59 mg/L) soluble transferrin receptor levels or low ferritin. Transferrin saturation <20%, but not ferritin-based criteria, was associated with poorer clinical course and left ventricular function and higher in-hospital mortality and remained an independent predictor of impaired reperfusion after adjusting for baseline predictors and anemia.

Conclusions: ID defined by transferrin saturation <20% is strongly related to impaired ST resolution and predicts a worse in-hospital outcome in patients with STEMI treated with primary percutaneous coronary intervention. The association of other ID criteria with myocardial reperfusion or with the clinical course is weaker or absent. The potential preventive or therapeutic strategies targeting ID in STEMI warrant further investigation.

Keywords: acute myocardial infarction; iron deficiency; ischemia; reperfusion; soluble transferrin receptor.

PubMed Disclaimer

Conflict of interest statement

None.

Figures

Figure 1
Figure 1. Study flowchart.
ID indicates iron deficiency; PCI, percutaneous coronary intervention; and STEMI, ST‐segment–elevation myocardial infarction.
Figure 2
Figure 2. Association between iron deficiency, defined by transferrin saturation<20%, and impaired myocardial reperfusion among some relevant subgroups.
P for interaction is shown. STB indicates symptom‐to‐balloon time.

References

    1. Anker SD, Comin Colet J, Filippatos G, Willenheimer R, Dickstein K, Drexler H, Lüscher TF, Bart B, Banasiak W, Niegowska J, et al. Ferric carboxymaltose in patients with heart failure and iron deficiency. N Engl J Med. 2009;361:2436–2448. doi: 10.1056/NEJMoa0908355 - DOI - PubMed
    1. Ponikowski P, Kirwan BA, Anker SD, McDonagh T, Dorobantu M, Drozdz J, Fabien V, Filippatos G, Göhring UM, Keren A, et al. Ferric carboxymaltose for iron deficiency at discharge after acute heart failure: a multicentre, double‐blind, controlled trial. Lancet. 2020;396:1895–1904. doi: 10.1016/S0140-6736(20)32339-4 - DOI - PubMed
    1. Kalra PR, Cleland JGF, Petrie MC, Thomson EA, Kalra PA, Squire IB, Ahmed FZ, Al‐Mohammad A, Cowburn PJ, Foley PWX, et al. Intravenous ferric derisomaltose in patients with heart failure and iron deficiency in the UK (IRONMAN): an investigator‐initiated, prospective, open‐label, blinded‐endpoint trial. Lancet. 2022;400:2199–2209. doi: 10.1016/S0140-6736(22)02083-9 - DOI - PubMed
    1. Mentz RJ, Garg J, Rockhold FW, Butler J, De Pasquale CG, Ezekowitz JA, Lewis GD, O'Meara E, Ponikowski P, Troughton RW, et al. Ferric carboxymaltose in heart failure with iron deficiency. N Engl J Med. 2023;389:975–986. doi: 10.1056/NEJMoa2304968 - DOI - PubMed
    1. Meroño O, Cladellas M, Ribas‐Barquet N, Poveda P, Recasens L, Bazán V, García‐García C, Ivern C, Enjuanes C, Orient S, et al. Iron deficiency is a determinant of functional capacity and health‐related quality of life 30 days after an acute coronary syndrome. Rev Esp Cardiol. 2017;70:363–370. doi: 10.1016/j.rec.2016.10.004 - DOI - PubMed

MeSH terms

LinkOut - more resources