Literature DB >> 19571582

Polymorphisms in the Renin-Angiotensin system and outcome of very-low-birthweight infants.

J Spiegler1, A Gilhaus, I R Konig, E Kattner, M Vochem, H Kuster, J Moller, D Muller, A Kribs, H Segerer, C Wieg, W Nikischin, A von der Wense, C Gebauer, E Herting, W Gopel.   

Abstract

BACKGROUND: The insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE-ins/del) and the angiotensin II type 1 receptor 1166A/C polymorphism (ATR1166A/C) were reported to be associated with several unfavorable outcome parameters in preterm infants like bronchopulmonary dysplasia, persistent ductus arteriosus and impaired insulin sensitivity.
OBJECTIVE: To confirm the above-mentioned associations in a large cohort of very-low-birthweight (VLBW) infants.
METHOD: Clinical data of VLBW infants were prospectively recorded. The ACE-ins/del polymorphism and the ATR1166A/C polymorphism were determined by polymerase chain reaction in 1,209 and 1,168 infants, respectively.
RESULTS: There was no significant association between ACE-ins/del or ATR1166A/C genotype and outcome parameters (death, intraventricular hemorrhage, sepsis, bronchopulmonary dysplasia, ventilation, supplemental oxygen at discharge, postnatal treatment with insulin, surgery for intestinal perforation/necrotizing enterocolitis/retinopathy of prematurity/persistent ductus arteriosus.
CONCLUSION: Both known functional polymorphisms of the renin-angiotensin system do not seem to be associated with the outcome of VLBW infants. Copyright 2009 S. Karger AG, Basel.

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Mesh:

Year:  2009        PMID: 19571582     DOI: 10.1159/000226602

Source DB:  PubMed          Journal:  Neonatology        ISSN: 1661-7800            Impact factor:   4.035


  6 in total

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Review 2.  Targeting inflammation to prevent bronchopulmonary dysplasia: can new insights be translated into therapies?

Authors:  Clyde J Wright; Haresh Kirpalani
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Review 3.  Retinopathy of prematurity: contribution of inflammatory and genetic factors.

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Review 4.  Genetic susceptibility to advanced retinopathy of prematurity (ROP).

Authors:  Barkur S Shastry
Journal:  J Biomed Sci       Date:  2010-08-25       Impact factor: 8.410

5.  Genetic Contributions to the Development of Complications in Preterm Newborns.

Authors:  Chiara Poggi; Betti Giusti; Elena Gozzini; Alice Sereni; Ilaria Romagnuolo; Ada Kura; Elisabetta Pasquini; Rosanna Abbate; Carlo Dani
Journal:  PLoS One       Date:  2015-07-14       Impact factor: 3.240

6.  Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.

Authors:  Tamas Jilling; Namasivayam Ambalavanan; C Michael Cotten; Colin A Martin; Akhil Maheshwari; Kurt Schibler; Joshua Levy; Grier P Page
Journal:  Pediatr Res       Date:  2018-05-16       Impact factor: 3.756

  6 in total

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