Jeffery U, Ruterbories L, Hanel R, LeVine D N
Department of Veterinary Microbiology and Preventative Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA.
Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC.
J Vet Intern Med. 2017 Sep;31(5):1441-1450. doi: 10.1111/jvim.14808. Epub 2017 Aug 20.
Immune-mediated hemolytic anemia (IMHA) in dogs has a high risk of thrombosis and is associated with marked neutrophilia and necrosis. Cell death and release of neutrophil extracellular traps contribute to increased serum concentrations of cell-free DNA, and in human autoimmune disease reduced DNase activity further increases cell-free DNA. Free DNA in blood has prothrombotic properties and could contribute to hypercoagulability in IMHA.
Cell-free DNA is elevated and DNase activity reduced in dogs with IMHA compared to healthy dogs.
Dogs presenting to two referral hospitals with IMHA (n = 28) and healthy controls (n = 20).
Prospective observational study. Blood was collected and death and thrombotic events occurring in the first 14 days after hospitalization recorded. DNA was extracted from plasma with a commercial kit and quantified by PicoGreen fluorescence. DNase activity of serum was measured by radial diffusion assay.
Cell-free DNA was significantly higher in cases (median: 45 ng/mL, range: 10-2334 ng/mL) than controls (26 ng/mL, range 1-151 ng/mL, P = 0.0084). DNase activity was not different between cases and controls (P = 0.36). Four cases died and there were five suspected or confirmed thrombotic events. Cell-free DNA concentration was associated with death (odds ratio for upper quartile versus lower 3 quartiles: 15; 95% confidence interval 1.62-201; P = 0.03) but not thrombosis (P = 0.57).
Cell-free DNA is elevated in dogs with IMHA and likely reflects increased release rather than impaired degradation of DNA. Cell-free DNA concentration is potentially associated with death and might be a prognostic indicator, but this requires confirmation in a larger population.
犬免疫介导性溶血性贫血(IMHA)具有较高的血栓形成风险,且与明显的中性粒细胞增多及坏死有关。细胞死亡及中性粒细胞胞外诱捕网的释放会导致血清中游离DNA浓度升高,而在人类自身免疫性疾病中,脱氧核糖核酸酶(DNase)活性降低会进一步增加游离DNA。血液中的游离DNA具有促血栓形成特性,可能导致IMHA患者出现高凝状态。
与健康犬相比,IMHA犬的游离DNA水平升高,DNase活性降低。
两所转诊医院收治的患有IMHA的犬(n = 28)及健康对照犬(n = 20)。
前瞻性观察性研究。采集血液,并记录住院后前14天内发生的死亡及血栓形成事件。使用商业试剂盒从血浆中提取DNA,并通过PicoGreen荧光法进行定量。采用放射扩散法测定血清中的DNase活性。
病例组的游离DNA水平(中位数:45 ng/mL,范围:10 - 2334 ng/mL)显著高于对照组(26 ng/mL,范围1 - 151 ng/mL,P = 0.0084)。病例组与对照组的DNase活性无差异(P = 0.36)。4例犬死亡,发生了5起疑似或确诊的血栓形成事件。游离DNA浓度与死亡相关(上四分位数与下三个四分位数相比的比值比:15;95%置信区间1.62 - 201;P = 0.03),但与血栓形成无关(P = 0.57)。
IMHA犬的游离DNA水平升高,这可能反映了DNA释放增加而非降解受损。游离DNA浓度可能与死亡相关,或许可作为一项预后指标,但这需要在更大规模的群体中得到证实。