Intracerebral
hemorrhage (ICH) could trigger inflammatory responses.
However, the specific role of inflammatory proteins in the pathological
mechanism, complications, and prognosis of ICH remains unclear. In
this study, we investigated the expression of 92 plasma inflammation-related
proteins in patients with ICH (n = 55) and healthy
controls (n = 20) using an Olink inflammation panel
and discussed the relation to the severity of stroke, clinical complications,
30-day mortality, and 90-day outcomes. Our result showed that six
proteins were upregulated in ICH patients compared with healthy controls,
while seventy-four proteins were downregulated. In patients with ICH,
seven proteins were increased in the severe stroke group compared
with the moderate stroke group. In terms of complications, two proteins
were downregulated in patients with pneumonia, while nine proteins
were upregulated in patients with sepsis. Compared with the survival
group, three proteins were upregulated, and one protein was downregulated
in the death group. Compared with the good outcome group, eight proteins
were upregulated, and four proteins were downregulated in the poor
outcome group. In summary, an in-depth exploration of the differential
inflammatory factors in the early stages of ICH could deepen our understanding
of the pathogenesis of ICH, predict patient prognosis, and explore
new treatment strategies.