Literature DB >> 16912583

Evidence for an association between mannose-binding lectin 2 (MBL2) gene polymorphisms and pre-term birth.

Olaf A Bodamer1, Georg Mitterer, Wolfgang Maurer, Arnold Pollak, Manfred W Mueller, Wolfgang M Schmidt.   

Abstract

PURPOSE: Human mannose-binding lectin, encoded by the MBL2 gene, is an important component of innate immunity and an important regulator of inflammatory processes. MBL2 gene polymorphisms are associated with an increased risk of neonatal infections and some data suggest a relation between the maternal MBL2 genotype and the risk of premature delivery. In this study, we evaluated whether there is an association between the fetal MBL2 genotype and prematurity.
METHODS: A microarray-based on-chip PCR method was used to simultaneously detect five common MBL2 polymorphisms (codon 52, 54, 57; promoter -550, -221) in 204 DNA samples isolated from archival blood cards. MBL2 genotypes of infants born before the 36th week of pregnancy (N = 102) were compared to a control group of infants born at term after the 37th week (N = 102).
RESULTS: The frequency of the codon 52 polymorphism was significantly higher in the pre-term group compared to the term group (10.8% versus 4.9%, P = 0.04), while the frequency of the codon 54 polymorphism was equal in both groups (11.3% versus 11.8%). Interestingly, carriers of genotypes (O/O) likely conferring deficient MBL plasma levels were more common in the group of premature birth (9.8% versus 2.9%, P = 0.05), while the promoter -550 C/C genotype was underrepresented in the pre-term birth group (24.5% versus 39.2%, P = 0.03).
CONCLUSION: Our data add to the knowledge about genetic predisposition to prematurity and suggest that the fetal MBL2 genotype might be an additional genetic factor contributing to the risk of premature delivery.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16912583     DOI: 10.1097/01.gim.0000232478.43335.19

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  12 in total

1.  Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.

Authors:  Roberto Romero; Digna R Velez Edwards; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Tinnakorn Chaiworapongsa; Brad D Pearce; Lara A Friel; Jacquelaine Bartlett; Madan Kumar Anant; Benjamin A Salisbury; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Scott M Williams; Ramkumar Menon
Journal:  Am J Obstet Gynecol       Date:  2010-05       Impact factor: 8.661

Review 2.  The use of high-dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome.

Authors:  R Romero; J Espinoza; F Gotsch; J P Kusanovic; L A Friel; O Erez; S Mazaki-Tovi; N G Than; S Hassan; G Tromp
Journal:  BJOG       Date:  2006-12       Impact factor: 6.531

3.  California Very Preterm Birth Study: design and characteristics of the population- and biospecimen bank-based nested case-control study.

Authors:  Martin Kharrazi; Michelle Pearl; Juan Yang; Gerald N DeLorenze; Christopher J Bean; William M Callaghan; Althea Grant; Eve Lackritz; Roberto Romero; Glen A Satten; Hyagriv Simhan; Anthony R Torres; Jonna B Westover; Robert Yolken; Dhelia M Williamson
Journal:  Paediatr Perinat Epidemiol       Date:  2012-01-31       Impact factor: 3.980

4.  Innate immune system gene polymorphisms in maternal and child genotype and risk of preterm delivery.

Authors:  Nicole M Jones; Claudia Holzman; Yan Tian; Steven S Witkin; Mehmet Genc; Karen Friderici; Rachel Fisher; Devrim Sezen; Oksana Babula; Katherine A Jernigan; Hwan Chung; Julia Wirth
Journal:  J Matern Fetal Neonatal Med       Date:  2011-06-01

5.  Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study.

Authors:  Ettore Capoluongo; Giovanni Vento; Sandro Rocchetti; Emiliano Giardina; Paola Concolino; Cecilia Sinibaldi; Concetta Santonocito; Valentina Vendettuoli; Milena Tana; Chiara Tirone; Cecilia Zuppi; Costantino Romagnoli; Giuseppe Novelli; Bruno Giardina; Franco Ameglio
Journal:  Intensive Care Med       Date:  2007-07-26       Impact factor: 17.440

Review 6.  Spontaneous preterm birth: advances toward the discovery of genetic predisposition.

Authors:  Jerome F Strauss; Roberto Romero; Nardhy Gomez-Lopez; Hannah Haymond-Thornburg; Bhavi P Modi; Maria E Teves; Laurel N Pearson; Timothy P York; Harvey A Schenkein
Journal:  Am J Obstet Gynecol       Date:  2017-12-14       Impact factor: 8.661

7.  A role for mannose-binding lectin, a component of the innate immune system in pre-eclampsia.

Authors:  Nandor Gabor Than; Roberto Romero; Offer Erez; Juan Pedro Kusanovic; Adi L Tarca; Samuel S Edwin; Jung-Sun Kim; Sonia S Hassan; Jimmy Espinoza; Pooja Mittal; Shali Mazaki-Tovi; Lara Friel; Francesca Gotsch; Edi Vaisbuch; Natalia Camacho; Zoltan Papp
Journal:  Am J Reprod Immunol       Date:  2008-10       Impact factor: 3.886

Review 8.  Factors of the lectin pathway of complement activation and their clinical associations in neonates.

Authors:  Maciej Cedzynski; Anna St Swierzko; David C Kilpatrick
Journal:  J Biomed Biotechnol       Date:  2012-03-22

9.  MBL2 genotypes and their associations with MBL levels and NICU morbidity in a cohort of Greek neonates.

Authors:  Matthaios Speletas; Antonios Gounaris; Eirini Sevdali; Maria Kompoti; Katerina Konstantinidi; Rozeta Sokou; Elena Tsitsami; Anastasios E Germenis
Journal:  J Immunol Res       Date:  2015-03-24       Impact factor: 4.818

10.  Mannose-binding lectin 2 (MBL2) gene polymorphisms do not influence frequency of infections in chronic lymphocytic leukemia patients.

Authors:  Katarina Holanda; Antonio Roberto Lucena-Araujo; Adônis Quintas; Taciana Mendonça; Aleide Lima; Luydson Richardson Vasconcelos; Patrícia Moura; Maria Cavalcanti; Cíntia Machado; Aderson Silva Araújo; Marcos Andre Bezerra
Journal:  Rev Bras Hematol Hemoter       Date:  2014
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.