Circulating Inflammatory Biomarkers in Early Prediction of Stroke-Associated Infections

被引:3
|
作者
Hasse, Isabel M. C. [1 ]
Grosse, Gerrit M. [1 ]
Schuppner, Ramona [1 ]
Van Gemmeren, Till [1 ]
Gabriel, Maria M. [1 ]
Weissenborn, Karin [1 ]
Lichtinghagen, Ralf [2 ]
Worthmann, Hans [1 ]
机构
[1] Hannover Med Sch, Dept Neurol, D-30625 Hannover, Germany
[2] Hannover Med Sch, Inst Clin Chem, D-30625 Hannover, Germany
关键词
CRP; IL-6; LBP; IL-10; infection; inflammation; pneumonia; stroke; outcome; ACUTE ISCHEMIC-STROKE; RISK; COMPLICATIONS; ANTIBIOTICS; PNEUMONIA; DIAGNOSIS; MONOCYTES; SYSTEM;
D O I
10.3390/ijms232213747
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
(1) Background: Patients with acute ischaemic stroke (AIS) are at high risk for stroke-associated infections (SAIs). We hypothesised that increased concentrations of systemic inflammation markers predict SAIs and unfavourable outcomes; (2) Methods: In 223 patients with AIS, blood samples were taken at <= 24 h, 3 d and 7d after a stroke, to determine IL-6, IL-10, CRP and LBP. The outcome was assessed using the modified Rankin Scale at 90 d. Patients were thoroughly examined regarding the development of SAIs; (3) Results: 47 patients developed SAIs, including 15 lower respiratory tract infections (LRTIs). IL-6 and LBP at 24 h differed, between patients with and without SAIs (IL-6: p < 0.001; LBP: p = 0.042). However, these associations could not be confirmed after adjustment for age, white blood cell count, reduced consciousness and NIHSS. When considering the subgroup of LRTIs, in patients who presented early (<= 12 h after stroke, n = 139), IL-6 was independently associated with LRTIs (OR: 1.073, 95% CI: 1.002-1.148). The ROC-analysis for prediction of LRTIs showed an AUC of 0.918 for the combination of IL-6 and clinical factors; (4) Conclusions: Blood biomarkers were not predictive for total SAIs. At early stages, IL-6 was independently associated with outcome-relevant LRTIs. Further studies need to clarify the use of biochemical markers to identify patients prone to SAIs.
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页数:12
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