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Impaired Activity of Blood Coagulant Factor XIII in Patients with Necrotizing Enterocolitis.


ABSTRACT: Necrotizing enterocolitis (NEC) is the most common gastrointestinal (GI) medical/surgical emergency of the newborn and a leading cause of preterm neonate morbidity and mortality. NEC is a challenge to diagnose since it often shares similar clinical features with neonatal sepsis. In the present study, plasma protein profiling was compared among NEC, sepsis and control cohorts using gel electrophoresis, immunoblot and mass spectrometry. We observed significant impairment in the formation of fibrinogen-? dimers (FGG-dimer) in the plasma of newborns with NEC that could efficiently differentiate NEC and sepsis with a high level of sensitivity and specificity. Interestingly, the impaired FGG-dimer formation could be restored in NEC plasma by the addition of exogenous active factor XIII (FXIII). Enzymatic activity of FXIII was determined to be significantly lower in NEC subject plasma for crosslinking FGG when compared to sepsis. These findings demonstrate a potential novel biomarker and related biologic mechanism for diagnosing NEC, as well as suggest a possible therapeutic strategy.

SUBMITTER: Tao GZ 

PROVIDER: S-EPMC4642514 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

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Impaired Activity of Blood Coagulant Factor XIII in Patients with Necrotizing Enterocolitis.

Tao Guo-Zhong GZ   Liu Bo B   Zhang Rong R   Liu Gigi G   Abdullah Fizan F   Harris Mary Cay MC   Brandt Mary L ML   Ehrenkranz Richard A RA   Bowers Corinna C   Martin Camilia R CR   Moss R Lawrence RL   Sylvester Karl G KG  

Scientific reports 20150817


Necrotizing enterocolitis (NEC) is the most common gastrointestinal (GI) medical/surgical emergency of the newborn and a leading cause of preterm neonate morbidity and mortality. NEC is a challenge to diagnose since it often shares similar clinical features with neonatal sepsis. In the present study, plasma protein profiling was compared among NEC, sepsis and control cohorts using gel electrophoresis, immunoblot and mass spectrometry. We observed significant impairment in the formation of fibrin  ...[more]

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