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Plasma high-mobility group box 1 levels predict mortality after ST-segment elevation myocardial infarction
Morten V Sørensen1, Sune Pedersen, Rasmus Møgelvang
1Medical Research Laboratories, Clinical Institute, Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Denmark.
Insights
High-mobility group box 1 (HMGB1) levels are elevated in ST-segment elevation myocardial infarction (STEMI) patients. Higher HMGB1 is linked to increased mortality risk following percutaneous coronary intervention.
Area of Science:
- Cardiology
- Biomarkers
- Myocardial Infarction Research
Background:
- Ischemic/reperfusion injury can compromise reperfusion effectiveness in STEMI.
- High-mobility group box 1 (HMGB1) is released by necrotic cells and implicated in myocardial injury.
- HMGB1's role in myocardial ischemic/reperfusion injury warrants further investigation.
Purpose of the Study:
- To evaluate the association between plasma HMGB1 levels and patient outcomes.
- To determine if HMGB1 can serve as a prognostic biomarker in STEMI patients.
- To assess HMGB1 levels in STEMI patients treated with primary percutaneous coronary intervention.
Main Methods:
- 141 STEMI patients with LAD occlusion treated with PCI were included.
- Plasma HMGB1 levels were measured using enzyme-linked immunosorbent assay at admission.
- 42 healthy individuals served as control subjects for comparison.
Main Results:
- STEMI patients exhibited higher baseline HMGB1 levels than controls.
- Higher HMGB1 levels were observed in STEMI patients who died during follow-up.
- A doubling of HMGB1 concentrations independently increased mortality risk by 75% (HR 1.75).
Conclusions:
- Plasma HMGB1 levels are elevated in STEMI patients compared to healthy individuals.
- Elevated HMGB1 is independently associated with increased 10-month mortality in STEMI patients post-PCI.
- Plasma HMGB1 shows potential as a novel prognostic biomarker for STEMI.
Objectives:
We evaluated the potential association between plasma high-mobility group box 1 (HMGB1) levels and outcome in patients with ST-segment elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention.
Background:
The positive effect of reperfusion after STEMI may be compromised by ischemic/reperfusion injury. HMGB1 is released by necrotic cells and, in pre-clinical studies, has been implicated to play a role in myocardial ischemic/reperfusion injury.
Methods:
The study included 141 STEMI patients, with acute occlusion of the left anterior descending coronary artery successfully treated with percutaneous coronary intervention. Plasma HMGB1 levels were measured by enzyme-linked immunoadsorbent assay at admission. Forty-two healthy individuals served as control subjects.
Results:
After a median of 10 months of follow-up, 13 STEMI patients died. There were no significant differences with regard to baseline variables between the group of patients who survived and those who died. Baseline HMGB1 levels were increased in STEMI patients when compared with control subjects. Furthermore, the STEMI patients who died had higher HMGB1 levels than those who survived. After adjusting for age, sex, troponin I, and creatine kinase-myocardial band, we found that a doubling of HMGB1 concentrations increased the risk of mortality by 75% (hazard ratio: 1.75; 95% confidence interval: 1.1 to 2.8).
Conclusions:
Plasma HMGB1 levels are elevated in STEMI patients compared with healthy control subjects. Furthermore, after a follow-up period of 10 months, plasma HMGB1 levels are shown to be independently associated with increased mortality in STEMI patients treated with PCI. These data suggest that plasma HMGB1 may be used as a new prognostic biomarker in STEMI patients.
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