RETRACTED: eNOS Gene Polymorphisms in Perinatal Hypoxic-Ischemic Encephalopathy (Retracted article. See vol. 53, pg. 345, 2019)

被引:3
作者
Cho, Min [3 ]
Hyun, Kwang-Sun [3 ]
Chung, David Chanwook [1 ]
Choi, In-Young [2 ]
Kim, Myeung Ju [2 ,3 ]
Chang, Young Pyo [1 ]
机构
[1] Dankook Univ, Dept Pediat, Coll Med, Cheonan 330714, South Korea
[2] Dankook Univ, Dept Anat, Coll Med, Cheonan 330714, South Korea
[3] Dankook Univ, Inst Med Sci, Coll Med, Cheonan 330714, South Korea
关键词
Nitric oxide; Endothelial NOS (eNOS); Genetic polymorphism; Hypoxic-ischemic encephalopathy; Newborn; Infant; Persistent pulmonary hypertension of the newborn (PPHN); NITRIC-OXIDE SYNTHASE; NOS3; GENE; ASSOCIATION; STROKE; RISK; RETINOPATHY; HAPLOTYPES; DISEASE; ARTERY; BRAIN;
D O I
10.4132/KoreanJPathol.2009.43.4.306
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background : In perinatal hypoxic-ischemic encephalopathy (HIE), cerebral blood flow is impaired and the activity of nitric oxide systhase (NOS) is markedly increased. For the association with the development of a stroke, the endothelial NOS (eNOS) polymorphisms are well-known. Methods: Three clinically relevant polymorphisms of the eNOS gene were determined in 37 term/near-term infants with perinatal HIE (HIE group) and 54 normal term newborn infants without any perinatal problems (control group) using a polymerase chain reaction with or with out restriction fragment enzyme digestion. The differences in the genotype, allele, and haplotype frequencies were evaluated between the groups. Results : The analysis of the allele frequencies showed that the G allele of Glu298Asp was more frequent in the HIE group than in the controls. The comparisons between the controls and each subgroups with complications that occurred with HIE showed that the TC genotype and C allele of T-786C were more common in patients with persistent pulmonary hypertension of the newborn (PPHN) than in the controls. The frequency of the A b T haplotype was lower in the HIE patients than in the controls. Conclusions : The G allele of Glu298Asp was associated with perinatal HIE, while the TC genotype and C allele of T-786C were associated with PPHN.
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收藏
页码:306 / 311
页数:6
相关论文
共 30 条
  • [1] Endothelial influences on cerebrovascular tone
    Andresen, J
    Shafi, NI
    Bryan, RM
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 2006, 100 (01) : 318 - 327
  • [2] Neuroprotective properties of nitric oxide
    Chiueh, CC
    [J]. NEUROPROTECTIVE AGENTS: FOURTH INTERNATIONAL CONFERENCE, 1999, 890 : 301 - 311
  • [3] Nitric oxide synthase: Role in the genesis of vascular disease
    Cooke, JP
    Dzau, VJ
    [J]. ANNUAL REVIEW OF MEDICINE, 1997, 48 : 489 - 509
  • [4] Endothelial nitric oxide synthase genotype and haplotype are not associated with diabetic retinopathy in diabetes type 2 patients
    de Syllos, Roger W. C.
    Sandrim, Valeria C.
    Lisboa, Hugo R. K.
    Tres, Glaucia S.
    Tanus-Santos, Jose E.
    [J]. NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2006, 15 (04): : 417 - 422
  • [5] Association between the Glu298Asp polymorphism in the endothelial constitutive nitric oxide synthase gene and brain infarction
    Elbaz, A
    Poirier, O
    Moulin, T
    Chédru, F
    Cambien, F
    Amarenco, P
    [J]. STROKE, 2000, 31 (07) : 1634 - 1639
  • [6] The intron 4c allele of the NOS3 gene is associated with ischemic stroke in African Americans
    Grewal, R. P.
    Dutra, A. V. C.
    Liao, Yi C.
    Juo, Ss H.
    Papamitsakis, N. I. H.
    [J]. BMC MEDICAL GENETICS, 2007, 8
  • [7] Peroxynitrite: reactive, invasive and enigmatic
    Groves, JT
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (02) : 226 - 235
  • [8] GRYGLEWSKI RJ, 1995, ANN NY ACAD SCI, V748, P194
  • [9] Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease
    Hassan, A
    Gormley, K
    O'Sullivan, M
    Knight, J
    Sham, P
    Vallance, P
    Bamford, J
    Markus, H
    [J]. STROKE, 2004, 35 (03) : 654 - 659
  • [10] Increase in nitric oxide in the hypoxic-ischemic neonatal rat brain and suppression by 7-nitroindazole and aminoguanidine
    Higuchi, Y
    Hattori, H
    Kume, T
    Tsuji, M
    Akaike, A
    Furusho, K
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 342 (01) : 47 - 49