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Published on: August 2, 2018
Hypoxia-inducible factor-1alpha induces the coronary collaterals for coronary artery disease
Song-ming Chen1, Yu-guang Li, Hong-xuan Zhang
1Department of Cardiology, First Affiliated Hospital, Shantou, Guangdong, China. csm@126.com
Insights
Higher levels of hypoxia-inducible factor-1alpha (HIF-1alpha) correlate with increased coronary artery collaterals in patients with ischemic heart disease. This suggests HIF-1alpha may promote collateral formation and aid in predicting disease prognosis.
Area of Science:
- Cardiovascular Biology
- Molecular Medicine
- Ischemic Heart Disease Research
Background:
- Coronary artery collateral variability is significant in ischemic heart disease.
- The role of hypoxia-inducible factor-1alpha (HIF-1alpha) in collateral development is not fully understood.
- HIF-1alpha is a key regulator of oxygen homeostasis.
Purpose of the Study:
- To investigate the expression of HIF-1alpha in patients with coronary artery collaterals.
- To determine the significance of HIF-1alpha expression in relation to collateral development.
- To explore the potential role of HIF-1alpha in promoting coronary collateral formation.
Main Methods:
- Studied 98 patients with significant coronary artery narrowing, including those with and without collaterals, plus 50 controls.
- Assessed collateral extent using the Rentrop scoring system.
- Measured HIF-1alpha protein (immunohistochemistry, Western blot) and mRNA (RT-PCR) in monocytes and lymphocytes.
Main Results:
- HIF-1alpha protein and mRNA expression were significantly higher in patients with coronary collaterals compared to controls and patients without collaterals.
- A strong positive correlation was found between HIF-1alpha expression/transcription levels and the Rentrop collateral score.
- Expression levels were highest in patients with collaterals, intermediate in those without, and lowest in controls.
Conclusions:
- Elevated HIF-1alpha induction is associated with the presence of coronary collaterals.
- HIF-1alpha likely plays a role in promoting coronary collateral formation.
- Monitoring HIF-1alpha expression may help predict the prognosis for patients with coronary artery disease.
Background:
Marked variability exists in coronary artery collaterals in patients with ischemic heart disease. Multiple factors are thought to play a role in collateral development; however, the contribution of hypoxia inducible factor-1alpha (HIF-1alpha), which is a transcriptional activator that functions as a master regulator of oxygen homeostasis, is not completely clear. It could play an important role in modulating collateral development.
Objective:
The objective of this study is to investigate the changes and significance of expression of HIF-1alpha in patients with coronary artery collaterals.
Methods:
Collateral vessels were determined in 98 patients with >or=70% narrowing of at least one coronary artery without earlier revascularization, 42 patients with coronary artery collaterals and 56 patients with no coronary artery collaterals. Extent of collaterals was expressed as scores according to the Rentrop scoring system. Another 50 cases with normal coronary arteries were selected as control. The levels of HIF-1alpha protein expression in monocyte and lymphocyte in the participants were tested by immunohistochemistry (IHC) and western blot; mRNA levels were measured using reverse transcriptase PCR technique.
Results:
Compared with the control with normal coronary artery, the patients had higher expression of HIF-1alpha protein tested by IHC and western blot (52.6+/-10.2 vs. 13.7+/-6.2 by IHC, 50.8+/-4.5 vs. 6.5+/-1.8 by western blot); furthermore, significantly higher HIF-1alpha expression was observed in patients with collaterals compared with patients with no collaterals (81.5+/-11.8 vs. 20.7+/-9.4 by IHC; 87.2+/-6.5 vs. 9.5+/-1.4 by western blot). On the transcriptional levels of HIF-1alpha, the result was the same as the protein, there was significant difference of HIF-1alpha between the three groups. The patients with collaterals were the highest (127.3+/-23.9), followed by patients with no collaterals (35.7+/-12.3), and the control were the lowest (23.5+/-9.3). A highly positive correlation was observed between the expression/transcription of HIF-1alpha and collateral score (P<0.01, IHC: r1=0.78, reverse transcriptase PCR: r2=0.69, western blot: r3=0.84).
Conclusion:
These data suggest that higher inductions of HIF-1alpha are associated with coronary collaterals, thus implying that HIF-1alpha may promote coronary collateral formation. Detection of HIF-1alpha expression might be helpful to predict prognosis of patients with coronary artery disease.
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