Faculty of Science, Charles University in Prague, 128 43 Prague 2, Czech Republic; Institute of Microbiology of The Czech Academy of Sciences, v.v.i., 142 20 Prague 4, Czech Republic.
Department of Pediatric Surgery, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, 150 06 Prague 5, Czech Republic.
J Immunol Res. 2016;2016:5727312. doi: 10.1155/2016/5727312. Epub 2016 Mar 24.
Necrotizing enterocolitis (NEC) is severe disease of gastrointestinal tract, yet its early symptoms are nonspecific, easily interchangeable with sepsis. Therefore, reliable biomarkers for early diagnostics are needed in clinical practice. Here, we analyzed if markers of gut mucosa damage, caspase cleaved cytokeratin 18 (ccCK18) and intestinal fatty acid-binding protein (I-FABP), could be used for differential diagnostics of NEC at early stage of disease. We collected paired serum (at enrollment and week later) and urine (collected for two days in 6 h intervals) samples from 42 patients with suspected NEC. These patients were later divided into NEC (n = 24), including 13 after gastrointestinal surgery, and sepsis (n = 18) groups using standard criteria. Healthy infants (n = 12), without any previous gut surgery, served as controls. Both biomarkers were measured by a commercial ELISA assay. There were no statistically significant differences in serum ccCK18 between NEC and sepsis but NEC patients had significantly higher levels of serum and urinary I-FABP than either sepsis patients or healthy infants. Urinary I-FABP has high sensitivity (81%) and specificity (100%) and can even distinguish NEC from sepsis in patients after surgery. Urinary I-FABP can be used to distinguish NEC from neonatal sepsis, including postoperative one, better than abdominal X-ray.
坏死性小肠结肠炎(NEC)是一种严重的胃肠道疾病,但它的早期症状不具有特异性,容易与败血症混淆。因此,临床上需要可靠的生物标志物来进行早期诊断。在这里,我们分析了肠黏膜损伤标志物半胱氨酸蛋白酶切割细胞角蛋白 18(ccCK18)和肠脂肪酸结合蛋白(I-FABP)是否可用于疾病早期对 NEC 进行鉴别诊断。我们收集了 42 名疑似 NEC 患者的配对血清(入组时和一周后)和尿液(在 6 小时间隔内收集两天)样本。这些患者后来根据标准标准分为 NEC(n = 24),包括 13 名胃肠手术后患者和败血症(n = 18)组。无任何先前肠道手术的健康婴儿(n = 12)作为对照组。两种生物标志物均通过商业 ELISA 测定法进行测量。NEC 和败血症患者之间的血清 ccCK18 无统计学差异,但 NEC 患者的血清和尿液 I-FABP 水平明显高于败血症患者或健康婴儿。尿 I-FABP 具有高灵敏度(81%)和特异性(100%),甚至可以区分手术后患者的 NEC 和败血症。尿 I-FABP 可用于区分 NEC 和新生儿败血症,包括术后败血症,优于腹部 X 射线。