Key result
A high systemic immune-inflammation index was an independent risk factor for vulnerable carotid plaques (OR 2.242) and plaque fibrous cap rupture in patients with acute ischemic stroke.
Why the study?
Vulnerable carotid plaque is linked to ischemic stroke, but the relationship between the systemic immune-inflammation index and carotid plaque vulnerability, composition, and stroke severity needed exploration.
Does a high systemic immune-inflammation index (SII) correlate with carotid plaque vulnerability and stroke severity in patients with acute ischemic stroke?
Cohort (n=131)
No
Does a high systemic immune-inflammation index (SII) correlate with carotid plaque vulnerability and stroke severity in patients with acute ischemic stroke?
Odds Ratio: 2.242 (95% CI 1.378–4.024)
Absolute Event Rate: 67.1% vs 44.2%
p-value: p=0.023
Elevated systemic immune-inflammation index (SII) is independently associated with increased carotid plaque vulnerability and greater stroke severity in patients with acute ischemic stroke.
May support SII for plaque risk stratification in acute ischemic stroke; hypothesis-generating and requires prospective validation.
Vulnerable carotid plaque is closely related to the occurrence of Ischemic stroke. Therefore, accurate and rapid identification of the nature of carotid plaques is essential. AS is a chronic immune inflammatory process. Systemic immune-inflammation index (SII) is a novel index of immune inflammation obtained from routine whole blood cell count analysis, which comprehensively reflects the state of inflammation and immune balance in the body. This study sought to explore the relationship between SII level and carotid plaque vulnerability, plaque composition characteristics, and acute ischemic stroke (AIS) severity. A total of 131 patients diagnosed with AIS presenting with a carotid atherosclerotic plaque were enrolled in this study. Using carotid ultrasound (CDU) to assess the carotid-responsible plaque properties, we divided the patients into stable plaques group and vulnerable plaques group, and analyzed the correlation between SII levels and plaque vulnerability. And we further analyzed to evaluate the correlation between high SII levels and plaque characteristics and AIS severity. In addition, Cohen's Kappa statistics was used to detect the consistency of Carotid ultrasound (US) and cervical High-resolution magnetic resonance imaging (HRMRI) in evaluating plaque vulnerability. The findings showed that the vulnerable group had higher levels of SII compared with the stable group. The high SII group had more vulnerable plaques and a high frequency of plaque fibrous cap rupture compared with the low SII group. Logistic analysis showed that a high SII level was an independent risk factor for vulnerable plaques (odds ratio [OR] = 2.242) and plaque fibrous cap rupture (OR=3.462). The results also showed a high consistency between Carotid US and HRMRI methods in the assessment of plaque vulnerability [Cohen's kappa value was 0.89 (95% CI = 0.78–0.97)] and the level of SII was positively associated with NIHSS score ( r = 0.473, P < 0.001). Our study suggests that elevated levels of SII may have adverse effects on the vulnerability of carotid plaques, especially in stroke patients with vulnerable plaques with ruptured fibrous caps, which may aggravate the severity of AIS.
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Zhang et al. (2022) conducted a cohort in Acute ischemic stroke with carotid atherosclerotic plaque (n=131). High systemic immune-inflammation index (SII ≥ 541.27 × 10^9/L) vs. Low systemic immune-inflammation index (SII < 541.27 × 10^9/L) was evaluated on Presence of vulnerable carotid plaque (OR 2.242, 95% CI 1.378-4.024, p=0.023). A high systemic immune-inflammation index was an independent risk factor for vulnerable carotid plaques (OR 2.242) and plaque fibrous cap rupture in patients with acute ischemic stroke.
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