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Published on: September 22, 2020
Cardiac function, inflammatory mediators and mortality in critical limb ischemia
Jamal Barani1, Ingrid Mattiasson, Bengt Lindblad
1University of Lund, Department of Vascular Diseases, Malmö University Hospital, Malmö, Sweden. jamal.barani@skane.se
Insights
Patients with critical limb ischemia (CLI) experience higher cardiac risks. This study found that cardiac rhythm disturbances and ECG changes in CLI patients are linked to inflammation and predict one-year mortality.
Area of Science:
- Cardiology
- Vascular Medicine
- Inflammation Research
Background:
- Critical limb ischemia (CLI) often coexists with coronary heart disease and congestive heart failure.
- Understanding the interplay between cardiac function, inflammation, and outcomes in CLI is crucial.
Purpose of the Study:
- To evaluate cardiac function in relation to inflammatory markers and one-year mortality in patients with CLI.
- To investigate the association between specific cardiac abnormalities and inflammatory mediators.
Main Methods:
- Prospective study of 232 CLI patients.
- Electrocardiogram (ECG), plasma inflammatory markers (ET-1, TNFα, IL-6, neopterin, CD40 ligand, 8-epi-PGF2α), and echocardiography (in 88 patients).
- One-year mortality assessment.
Main Results:
- Ischemic ECG changes were associated with higher endothelin-1, 8-epi-PGF2α, neopterin levels, and increased one-year mortality.
- Atrial fibrillation/flutter correlated with higher IL-6 and neopterin.
- Echocardiographic findings of heart failure correlated with inflammatory markers (IL-6, TNFα, neopterin).
- Lower ejection fraction (<40%) predicted higher one-year mortality.
Conclusions:
- Cardiac rhythm disturbances and ischemic ECG changes in CLI patients are linked to inflammatory mediators.
- These cardiac abnormalities and inflammatory markers predict one-year mortality in CLI.
- Inflammatory markers correlate with echocardiographic evidence of heart failure in CLI patients.
Abstract:
Patients with critical limb ischemia (CLI) have a high frequency of concomitant coronary heart disease and congestive heart failure. The aim of the study was to evaluate cardiac function in relation to inflammatory markers and 1-year mortality rate among patients with CLI. The authors investigated 232 consecutive patients with CLI by means of electrocardiogram (ECG), and measurements of endothelin (ET)-1, tumor necrosis factor alpha (TNF)alpha, interleukin (IL)-6, neopterin, CD40 ligand, and 8-epi-prostaglandin (PG)F2alpha in plasma. Echocardiography (echo) was performed in 88 (38%) patients. One-year mortality rate was assessed after prospective follow-up. One hundred and eighty-six (80%) patients had sinus rhythm (SR), 36 (16%) had atrial fibrillation or flutter (AF), and 10 (4%) pacemaker rhythm. Ischemic ECG changes occurred in 143 (62%) patients. Patients with AF showed higher IL-6 (p = 0.0296) and neopterin (p = 0.0494) concentrations. Patients with ischemic ECG changes showed higher ET-1 (p = 0.0303), 8-epi-PGF2alpha (p = 0.0027), neopterin (p = 0.0004) concentrations and 1-year mortality rate (p = 0.0105). The difference in ET-1 remained in logistic regression (p = 0.0152). Internal diameter of the left ventricle on echo correlated with IL-6 (r = 0.345, p = 0.0017), TNFalpha (r = 0.240, p = 0.0273), and neopterin (r = 0.327, p = 0.0028). Internal diameter of the left atrium correlated with TNFalpha (r = 0.384, p = 0.0092) and neopterin (r = 0.526, p = 0.0004), and ejection fraction (EF) correlated inversely with IL-6 (r = -0.380, p = 0.0015) and neopterin (r = -0.346, p = 0.0038). Patients with EF <40% showed higher (p = 0.0462) 1-year mortality rate than patients with EF >40%. In conclusion, in critical limb ischemia, cardiac rhythm disturbances and ischemic ECG changes were related to inflammatory mediators and predicted 1-year mortality rate. The inflammatory mediators correlated with echocardiographic signs of congestive heart failure.
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