Hyperhomocysteinemia and MTHFR Polymorphisms as Antenatal Risk Factors of White Matter Abnormalities in Two Cohorts of Late Preterm and Full Term Newborns

Higher total homocysteine (tHcy) levels, and C677T and A1298C methylenetetrahydrofolate (MTHFR) polymorphisms, have been reported in preterm or full term newborns with neonatal encephalopathy following perinatal hypoxic-ischemic insult. This study investigated the causal role of tHcy and MTHFR polym...

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Veröffentlicht in:Oxidative medicine and cellular longevity 2015-01, Vol.2015 (2015), p.1-8
Hauptverfasser: D’Angelo, Gabriella, Mamì, Carmelo, Di Rosa, Gabriella, Caccamo, Daniela, Alibrandi, Angela, Bonsignore, Maria, Cardile, Giovanna, Giaimo, Elisa, Salpietro, Vincenzo, Nicotera, Antonio, Marseglia, Lucia, Manti, Sara
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Sprache:eng
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Zusammenfassung:Higher total homocysteine (tHcy) levels, and C677T and A1298C methylenetetrahydrofolate (MTHFR) polymorphisms, have been reported in preterm or full term newborns with neonatal encephalopathy following perinatal hypoxic-ischemic insult. This study investigated the causal role of tHcy and MTHFR polymorphisms together with other acquired risk factors on the occurrence of brain white matter abnormalities (WMA) detected by cranial ultrasound scans (cUS) in a population of late preterm and full term infants. A total of 171 newborns (81 M, 47.4%), 45 (26.3%) born
ISSN:1942-0900
1942-0994
1942-0994
DOI:10.1155/2015/543134