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Heparin-binding protein in lower airway samples as a biomarker for pneumonia
被引:18
|作者:
Paulsson, Magnus
[1
,2
,3
]
Thelaus, Louise
[2
]
Riesbeck, Kristian
[3
]
Qvarfordt, Ingemar
[4
]
Smith, Margaretha E.
[4
]
Linden, Anders
[5
,6
]
Linder, Adam
[1
,2
]
机构:
[1] Skane Univ Hosp, Dept Infect Dis, Lund, Sweden
[2] Lund Univ, Fac Med, Dept Clin Sci, Div Infect Med, BMC B14, SE-22185 Lund, Sweden
[3] Lund Univ, Fac Med, Dept Translat Med, Clin Microbiol, Malmo, Sweden
[4] Univ Gothenburg, Sahlgrenska Acad, Inst Med, Dept Internal Med & Clin Nutr, Gothenburg, Sweden
[5] Karolinska Inst, Unit Lung & Airway Res, Inst Environm Med, Stockholm, Sweden
[6] Karolinska Univ Hosp, Karolinska Severe COPD Ctr, Dept Resp Med & Allergy, Stockholm, Sweden
基金:
瑞典研究理事会;
关键词:
Pneumonia;
Critical Care;
Neutrophil Biology;
Assisted Ventilation;
Biomarkers;
Bronchoalveolar lavage;
D O I:
10.1186/s12931-021-01764-2
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Objectives Ventilator-associated pneumonia (VAP) is difficult to diagnose using clinical criteria and no biomarkers have yet been proved to be sufficiently accurate. The use of the neutrophil-derived Heparin-binding protein (HBP) as a biomarker for pneumonia was investigated in this exploratory case-control study in two intensive care units at a tertiary referral hospital. Methods Patients with clinical signs of pneumonia were recruited and bronchoalveolar lavage fluid (BALF) or bronchial wash (BW) samples were collected. Mechanically ventilated and lung healthy subjects were recruited as controls. HBP was measured with enzyme-linked immunosorbent assay. Results BALF was collected from 14 patients with pneumonia and 14 healthy controls. Median HBP in BALF pneumonia samples was 14,690 ng/ml and controls 16.2 ng/ml (p < 0.0001). BW was collected from 10 pneumonia patients and 10 mechanically ventilated controls. Median HBP in BW pneumonia was 9002 ng/ml and controls 7.6 ng/ml (p < 0.0001). Conclusions These data indicate that HBP concentrations is significantly higher in lower airway samples from patients with pneumonia than control subjects and is a potentially useful biomarker for diagnosis of VAP.
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