IS -94INS/DELATTG POLYMORPHISM IN THE NUCLEAR FACTOR KAPPA-B1 GENE (NFKB1) ASSOCIATED WITH NECROTIZING ENTEROCOLITIS?
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作者:
Ferdinando, Danielle Lopes Teixeira
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Fac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, BrazilFac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, Brazil
Ferdinando, Danielle Lopes Teixeira
[1
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Fraga, Fernanda Del Campo Braojos
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Fac Med Sao Jose do Rio Preto, Image Unit, Sao Jose Do Rio Preto, SP, BrazilFac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, Brazil
Fraga, Fernanda Del Campo Braojos
[2
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Piatto, Vania Belintani
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Fac Med Sao Jose do Rio Preto, Anat Unit, Sao Jose Do Rio Preto, SP, BrazilFac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, Brazil
Piatto, Vania Belintani
[3
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Souza, Antonio Soares
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Fac Med Sao Jose do Rio Preto, Image Unit, Sao Jose Do Rio Preto, SP, BrazilFac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, Brazil
Souza, Antonio Soares
[2
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机构:
[1] Fac Med Sao Jose do Rio Preto, Pediat & Pediat Surg, Sao Jose Do Rio Preto, SP, Brazil
[2] Fac Med Sao Jose do Rio Preto, Image Unit, Sao Jose Do Rio Preto, SP, Brazil
[3] Fac Med Sao Jose do Rio Preto, Anat Unit, Sao Jose Do Rio Preto, SP, Brazil
来源:
ABCD-ARQUIVOS BRASILEIROS DE CIRURGIA DIGESTIVA-BRAZILIAN ARCHIVES OF DIGESTIVE SURGERY
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2022年
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35卷
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01期
<bold>Background: </bold>Abnormalities in the different stages of the intestinal maturation process cause metabolic and molecular changes. Among the genetic alterations associated with necrotizing enterocolitis, the -94ins/delATTG polymorphism in NFKB1 gene leads to unregulated activation of the NFKB protein due to an increase in the inherent pro-inflammatory state of the premature intestine.<bold>Aims: </bold>To determine the prevalence of the -94ins/delATTG polymorphism in NFKB1 gene in neonates with and without necrotizing enterocolitis.<bold>Methods: </bold>This is a case-control study, in which 25 neonates were evaluated as the case group and 50 neonates as the control group, of both genders. DNA was extracted from peripheral blood leukocytes, and the site encompassing the polymorphism was amplified by molecular techniques (polymerase chain reaction/polymorphism in restriction fragment length).<bold>Results: </bold>Necrotizing enterocolitis was diagnosed in 25 (33%) neonates and, of these, 3 (12%) died. Male gender was more prevalent in both groups (p=0.1613): cases (52%) and controls (62%). Moderate and extreme preterm newborns were predominant in both groups: cases (80%) and controls (88%) (p=0.3036). Low birth weight and extremely low birth weight newborns were the most prevalent in cases (78%), and very low birth weight and extremely low birth weight were the most prevalent in controls (81%) (p=0.1073). Clinical treatment was successful in 72%, and hospital discharge was achieved in 88% of newborns with NEC. The -94ins/delATTG polymorphism in NFKB1 gene was not identified in all the 150 alleles analyzed (100%).<bold>Conclusions: </bold>The absence of the -94ins/delATTG polymorphism in NFKB1 gene in newborns with and without necrotizing enterocolitis does not rule out the possibility of alterations in this and/or in other genes in newborns with this condition, which reinforces the need for further research
机构:
Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Wang, J. F.
Bian, J. J.
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Bian, J. J.
Wan, X. J.
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Wan, X. J.
Zhu, K. M.
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Zhu, K. M.
Sun, Z. Z.
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Sun, Z. Z.
Lu, A. D.
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
Second Mil Med Univ, Changhai Hosp, Intens Care Unit, Shanghai, Peoples R ChinaSecond Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai, Peoples R China
机构:
Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Suzairi, Mohd Shafi'i Mohd
Tan, Shing Cheng
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Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Tan, Shing Cheng
Aizat, Abdul Aziz Ahmad
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Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Aizat, Abdul Aziz Ahmad
Aminudin, Mustapha Mohd
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Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Aminudin, Mustapha Mohd
Nurfatimah, Mohd Shahpudin Siti
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Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Nurfatimah, Mohd Shahpudin Siti
Andee, Zakaria Dzulkarnaen
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Univ Sains Malaysia, Dept Surg, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia
Andee, Zakaria Dzulkarnaen
Ankathil, Ravindran
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Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, MalaysiaUniv Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kubang Kerian 16150, Kelantan, Malaysia