Incremental Accuracy of Blood Biomarkers for Predicting Clinical Outcomes After Intracerebral Hemorrhage

被引:13
|
作者
Sagar, Ram [1 ]
Kumar, Amit [1 ]
Verma, Vivek [1 ]
Yadav, Arun Kumar [1 ]
Raj, Ritesh [1 ]
Rawat, Dimple [1 ]
Yadav, Amarnath [1 ]
Srivastava, Achal Kumar [1 ]
Pandit, Awadh Kishor [1 ]
Vivekanandhan, Subiah [2 ]
Gulati, Arti [3 ]
Gupta, Garima [4 ]
Prasad, Kameshwar [1 ]
机构
[1] All India Inst Med Sci, Neurosci Ctr, Dept Neurol, Room 02,6th Floor, New Delhi, India
[2] All India Inst Med Sci, Dept Biochem, Rishikesh, India
[3] All India Inst Med Sci, Clin Epidemiol Unit, New Delhi, India
[4] Minist Sci & Technol, Dept Biotechnol, New Delhi, India
来源
关键词
Intracerebral hemorrhage; Blood-biomarkers; Mortality; Poor-outcome; Net reclassification improvement; Integrated discrimination improvement;
D O I
10.1016/j.jstrokecerebrovasdis.2020.105537
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Intracerebral hemorrhage (ICH) is associated with high mortality, morbidity, and recurrence. Studies have reported the accuracy of several blood biomarkers in predicting clinical outcomes; however, their independent contribution in prediction remains to be established. Aim: To investigate the incremental accuracy in predicting clinical outcomes in patients with ICH in a north Indian population using blood-based biomarkers. Methods: In this study, a total of 250 ICH cases were recruited within 72 hours of onset. Baseline clinical and CT scan measurement were recorded. Homocysteine (HCY), C-reactive protein (CRP), matrix metalloproteinase-9 (MMP9), E-selectin (SELE), and P-selectin (SELP) levels were measured through ELISA. Telephonic follow-up was done by using mRS scale at three months. Results: The mean age of cohort was 54.9 (SD +/- 12.8) years with 64.8% patients being male. A total of 109 (43.6%) deaths were observed over three months follow-up. Area under the receiver operating characteristics curve-(AUROC) for 90day mortality were 0.55 (HCY), 0.62 (CRP), 0.57 (MMP9), 0.60 (SELE) and 0.53 (SELP) and for poor outcome at 90-day (mRS: 3-6) were 0.60 (HCY), 0.62 (CRP), 0.54 (MMP9), 0.67 (SELE) and 0.54 (SELP). In multivariable model including age, ICH volume, IVH and GCS at admission, serum SELE (p = 0.004) significant for poor outcome with improved AUROC (0.86) and HCY (p = 0.04), CRP (p = 0.003) & MMP9 (p = 0.02) for mortality with least Akaike's Information Criterion-(AIC) (1060.5). Conclusions: Our findings suggest that the serum SELE is a significant predictor of poor outcome and HCY, CRP & MMP9 for Mortality in patients with ICH in the north Indian population.
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页数:10
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