Dynamic Change of Fecal Calprotectin in Very Low Birth Weight Infants during the First Month of Life
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作者:
Yang, Qing
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Wake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USAWake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
Yang, Qing
[1
,2
]
Smith, P. Brian
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Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USAWake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
Smith, P. Brian
[2
]
Goldberg, Ronald N.
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Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USAWake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
Goldberg, Ronald N.
[2
]
Cotten, C. Michael
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Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USAWake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
Cotten, C. Michael
[2
]
机构:
[1] Wake Forest Univ Hlth Sci, Dept Pediat, Div Neonatol, Winston Salem, NC 27157 USA
[2] Duke Univ, Med Ctr, Dept Pediat, Div Neonatol, Durham, NC 27710 USA
Background: Calprotectin is a cytosolic component of neutrophils. Fecal calprotectin (FC) level is a useful marker for exacerbation of inflammatory bowel disease in children. FC may be a useful marker for necrotizing enterocolitis (NEC). Objective: To determine normal baseline levels of FC and observe dynamic changes of FC levels over the first postnatal month in very low birth weight (VLBW) infants. Methods: FC levels of 14 VLBW infants (gestational age 23-30 weeks, birth weight <= 1,500 g) were serially measured in the first postnatal month. Demographics, feeding regimens, antibiotic use, laboratory and x-ray results, and maternal information were recorded. We assessed how FC levels changed over time, varied with nutritional source and differed between sick versus well infants. Results: FC levels were not related to gestational age or feedings regimen. FC levels tended to decrease with increasing age (p = 0.121) and feeding volumes (p = 0.179). FC levels differed between 'well' and 'sick' infants (122.8 +/- 98.9 vs. 380.4 +/- 246.3 mu g/g stool, p 0.001). FC >350 mu g/g stool was noted with signs of gastrointestinal injury, such as bloody stool and bowel perforation. FC levels decreased after initiation of treatments in sick infants who recovered. Conclusions: FC levels may be a marker for early diagnosis and resolution of gastrointestinal illnesses in VLBW infants. Its utility for early diagnosis and assessment of resolution of NEC should be studied in a larger cohort of VLBW infants. Copyright (C) 2008 S. Karger AG, Basel
机构:
Department of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FLDepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
Sola M.C.
Del Vecchio A.
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Department of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FLDepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
Del Vecchio A.
Edwards T.J.
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Department of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FLDepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
Edwards T.J.
Suttner D.
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Children's Medical Group, San Diego Children's Hospital, San Diego, CADepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
Suttner D.
Hutson A.D.
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Department of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FLDepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
Hutson A.D.
Christensen R.D.
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Department of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FLDepartment of Pediatrics, General Clinical Research Center, University of Florida College of Medicine, Gainesville, FL
机构:
Univ Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Miranda Goncalves, Daniela de Melo
Wandalsen, Gustavo Falbo
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Univ Fed Sao Paulo, Div Allergy Clin Immunol & Rheumatol, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Wandalsen, Gustavo Falbo
Scavacini, Ana Silvia
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Univ Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Scavacini, Ana Silvia
Lanza, Fernanda Cordoba
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Univ Fed Sao Paulo, Div Allergy Clin Immunol & Rheumatol, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Lanza, Fernanda Cordoba
Goulart, Ana Lucia
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Univ Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Goulart, Ana Lucia
Sole, Dirceu
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Univ Fed Sao Paulo, Div Allergy Clin Immunol & Rheumatol, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil
Sole, Dirceu
Nunes dos Santos, Amelia Miyashiro
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Univ Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Neonatal Div Med, Dept Pediat, Sao Paulo, SP, Brazil