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Updated: Feb 5, 2026

Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis
Published on: October 17, 2018
Circulating monocyte subsets and heart failure prognosis
Elena Elchinova1,2,3, Iris Teubel4, Santiago Roura5,6
1Heart Failure Unit and Cardiology Service, Germans Trias i Pujol University Hospital, Badalona, Spain.
Insights
The absolute count of intermediate monocytes, not their percentage, predicts worse outcomes in heart failure (HF) patients. Higher intermediate monocyte cell counts indicate increased risk for death and composite endpoints in ambulatory HF.
Area of Science:
- Immunology
- Cardiology
- Clinical Research
Background:
- Monocytes are crucial immune cells involved in tissue repair.
- Heart failure (HF) prognosis can be influenced by immune cell dynamics.
- Understanding monocyte subset roles is vital for HF patient management.
Purpose of the Study:
- To investigate the prognostic significance of monocyte subsets in ambulatory heart failure patients.
- To determine whether monocyte percentage or absolute count is a better predictor of adverse outcomes in HF.
- To identify specific monocyte subsets associated with mortality and hospitalization in HF.
Main Methods:
- Classification of monocyte subsets: classical (CD14++/CD16-), intermediate (CD14++/CD16+), and non-classical (CD14+/CD16++).
- Assessment of percentage distribution and absolute cell counts for each subset.
- Multivariable Cox regression analyses to evaluate associations with all-cause death, HF hospitalization, and composite endpoints in 400 HF patients.
Main Results:
- Monocyte subsets as percentages were not independently associated with any endpoints.
- Absolute cell count of the intermediate monocyte subset showed independent association with increased all-cause death (HR 1.25) and composite endpoints (HR 1.20).
- Follow-up of 2.6 years revealed significant differences in outcomes based on intermediate monocyte counts.
Conclusions:
- Absolute monocyte counts, specifically for the intermediate subset, are superior to percentages for prognostic stratification in ambulatory HF patients.
- The intermediate monocyte subset serves as a valuable biomarker for increased risk of mortality and composite events in HF.
- This finding aids in refining risk assessment and potentially guiding therapeutic strategies for HF management.
Abstract:
Monocytes are a heterogeneous population of effector cells with key roles in tissue integrity restoration and maintenance. Here, we explore the association of monocyte subsets and prognosis in patients with ambulatory heart failure (HF). Monocyte subsets were classified as classical (CD14++/CD16-), intermediate (CD14++/CD16+), or non-classical (CD14+/CD16++). Percentage distribution and absolute cell count were assessed in each subset, and multivariable Cox regression analyses were performed with all-cause death, HF-related hospitalization, and the composite end-point of both as dependent variables. 400 patients were consecutively included (72.8% male, age 69.4±12.2 years, 45.5% from ischemic aetiology, left ventricle ejection fraction (LVEF) 41.6% ±14.5, New York Heart Association (NYHA) class II 62.8% and III 30.8%). During a mean follow-up of 2.6±0.9 years, 107 patients died, 99 had a HF-related hospitalization and 160 suffered the composite end-point of all-cause death or HF-related hospitalization. Monocyte subsets assessed in percentages were not independently associated to any of the end-points. When considering number of cells/μL, intermediate subset was independently associated with an increase of all-cause death (HR 1.25 [95% CI 1,02-1.52], p = 0.03), and the composite end-point HR 1.20 [95% CI 1,03-1.40], p = 0.02). The presented findings show that absolute cell count of monocyte subsets was preferred over monocyte percentage for prognosis stratification for outpatients with HF. The intermediate monocyte subset provides information on increased risk of all-cause death and the composite end-point.
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