Prognostic implications of iron deficiency in patients with atrial fibrillation, with and without chronic heart

Abdullahi Ahmed Mohamed1, Daniel Mølager Christensen2,3, Milan Mohammad4

  • 1Department of Cardiology, Herlev Hospital, Herlev, Denmark abmoh06410@gmail.com.

PubMed

Insights

Iron deficiency (ID) in atrial fibrillation (AF) patients is linked to higher mortality, especially when defined by transferrin saturation (TSAT) or serum iron levels. These criteria are crucial for risk stratification in AF, regardless of heart failure status.

Area of Science:

  • Cardiology
  • Hematology
  • Clinical Research

Background:

  • Iron deficiency (ID) is prevalent in atrial fibrillation (AF) patients.
  • Prognostic implications and diagnostic criteria for ID in AF, particularly with or without heart failure (HF), require clarification.

Purpose of the Study:

  • To assess the associations between different ID definitions and clinical outcomes in AF patients.
  • To determine the prognostic value of various ID diagnostic criteria in AF, considering HF status.

Main Methods:

  • A nationwide cohort study of 10,834 AF patients in Denmark (2008-2019).
  • ID was defined by European Society of Cardiology (ESC) guidelines, ferritin <100 ng/mL, transferrin saturation (TSAT) <20%, and serum iron ≤13 µmol/L.
  • Cox regression models were used to evaluate associations with all-cause mortality, cardiovascular mortality, and hospitalisation, adjusted for confounders.

Main Results:

  • ID prevalence varied significantly (36.2%–62.7%) across definitions.
  • TSAT <20% and serum iron ≤13 µmol/L were associated with increased all-cause and cardiovascular mortality in both HF and non-HF AF patients.
  • ESC guidelines or ferritin <100 ng/mL definitions were not linked to mortality but associated with higher hospitalisation rates in HF patients.

Conclusions:

  • ID definitions based on TSAT <20% or serum iron ≤13 µmol/L are clinically relevant for predicting mortality in AF patients.
  • These specific ID criteria are valuable for risk stratification in AF, irrespective of heart failure presence.
Abstract

Related Concept Videos

Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
1.5K
Imbalances in Cardiac Output01:26

Imbalances in Cardiac Output

The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
1.4K
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
405
Heart Failure Drugs: &#946;-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
324
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
352
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
547