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Published on: February 12, 2016
The Contribution of Inflammation to Stroke Recurrence Attenuates at Low LDL-C Levels
Xing Zhang1,2, Wei Lv1,2, Jie Xu1,2
1Department of Neurology, Beijing Tiantan Hospital, Capital Medical University.
Insights
Inflammation increases stroke recurrence risk, but this effect diminishes significantly when low-density lipoprotein cholesterol (LDL-C) is very low. Achieving extremely low LDL-C levels may mitigate inflammation-driven stroke recurrence.
Area of Science:
- Cardiovascular Medicine
- Neurology
- Clinical Research
Background:
- Residual inflammation poses a cardiovascular disease risk even after achieving target low-density lipoprotein cholesterol (LDL-C) levels.
- The impact of inflammation on stroke recurrence at very low LDL-C levels remains unclear.
Purpose of the Study:
- To investigate the role of inflammation in stroke recurrence across different LDL-C levels following ischemic stroke (IS) or transient ischemic attack (TIA).
Main Methods:
- Analysis of 10499 IS/TIA patients from the Third China National Stroke Registry, measuring LDL-C, high-sensitivity C-reactive protein (hsCRP), and interleukin-6 (IL-6).
- Cox regression models were used to assess the association between inflammation markers and recurrent stroke within 1 year, stratified by LDL-C levels.
Main Results:
- Inflammation (hsCRP ≥ 2 mg/L or IL-6 ≥ 1.65 ng/L) was significantly associated with increased recurrent stroke risk when LDL-C was ≥ 55 mg/dL.
- No significant association between inflammation and stroke recurrence was observed when LDL-C was < 55 mg/dL.
Conclusions:
- The contribution of inflammation to stroke recurrence is attenuated at very low LDL-C levels (< 55 mg/dL) in patients with IS/TIA.
- These findings suggest that achieving very low LDL-C may reduce the impact of inflammation on secondary stroke prevention.
Aims:
Residual inflammation risk refers to inflammation that still increases the risk of cardiovascular disease after the level of low-density lipoprotein cholesterol (LDL-C) reached the target (<70 mg/dL). However, whether inflammation is still an important issue even if very low LDL-C levels have been achieved remains unclear. This study aimed to investigate the contribution of inflammation to stroke recurrence on different LDL-C levels following ischemic stroke (IS) or transient ischemic attack (TIA).
Methods:
A total of 10499 IS/TIA patients whose LDL-C and high-sensitivity C-reactive protein (hsCRP) were measured were selected from the Third China National Stroke Registry. The cutoff values were set to 25, 35, 45, 55, 70, and 100 mg/dL for LDL-C, whereas the threshold values of hsCRP and interleukin-6 (IL-6) were 2 mg/L and 1.65 ng/L, respectively. Based on each group of LDL-C, Cox regressions were conducted to investigate the associations between inflammation and recurrent stroke within 1 year.
Results:
The associations between baseline hsCRP levels and stroke recurrence were non-significant in groups with LDL-C <55 mg/dL (P>0.05). After stratification by baseline LDL-C of 55 mg/dL, hsCRP ≥ 2 mg/L (10.9% versus 7.5%, P<0.0001) and IL-6 ≥ 1.65 ng/L (9.8% versus 7.4%, P=0.0002) were found to be related to a high incidence of recurrent IS among patients with LDL-C ≥ 55 mg/dL; however, no associations were observed among patients with LDL-C <55 mg/dL. Compared with low inflammation (both hsCRP <2 mg/L and IL-6 <1.65 ng/L), high inflammation (both hsCRP ≥ 2 mg/L and IL-6 ≥ 1.65 ng/L) was significantly associated with stroke recurrence when LDL-C ≥ 55 mg/dL (adjusted HR 1.38, 95% CI 1.10-1.74), whereas this association was not observed when LDL-C <55 mg/dL (adjusted HR, 0.72; 95% CI, 0.41-1.25).
Conclusion:
For IS/TIA patients, the contribution of inflammation to stroke recurrence seems to be attenuated at a low level of LDL-C.
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