Literature DB >> 19493606

The V109G polymorphism in the p27 gene is associated with endometriosis.

Cíntia M Camargo-Kosugi1, Ismael D C G da Silva, Hélio Sato, Paulo D'Amora, Cristina V Carvalho, Naiara C Nogueira-de-Souza, Manoel J C B Girão, Eduardo Schor.   

Abstract

OBJECTIVE: To investigate the prevalence of the p27 gene polymorphism in women with endometriosis. STUDY
DESIGN: Transversal case-control study. Genomic DNA was extracted from cells collected from buccal swabs. The p27 V109G polymorphism was investigated using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method in a hospital-based Brazilian population.
RESULTS: We analysed the 104 patients and 109 control subjects. The distribution of genotype and allele frequencies of p27 V109G polymorphism was significantly different between the endometriosis cases and healthy women (p=0.016 and 0.002). Women who had at least one mutated allele presented twofold chances for endometriosis development (OR=1.9; 95% CI, 1.120-3.343).
CONCLUSION: The polymorphic variant at codon 109 of the p27 gene seems to be associated with higher risk of endometriosis development.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19493606     DOI: 10.1016/j.ejogrb.2009.04.027

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  4 in total

1.  Genes Downregulated in Endometriosis Are Located Near the Known Imprinting Genes.

Authors:  Hiroshi Kobayashi; Yumi Higashiura; Natsuki Koike; Juria Akasaka; Chiharu Uekuri; Kana Iwai; Emiko Niiro; Sachiko Morioka; Yuki Yamada
Journal:  Reprod Sci       Date:  2014-03-10       Impact factor: 3.060

2.  Association between p21 Ser31Arg polymorphism and the development of cervical lesion in women infected with high risk HPV.

Authors:  Géssica Lima; Erinaldo Santos; Hildson Angelo; Micheline Oliveira; Sandra Heráclio; Fernanda Leite; Celso de Melo; Sergio Crovella; Maria Maia; Paulo Souza
Journal:  Tumour Biol       Date:  2016-02-17

3.  Germline CDKN1B Loss-of-Function Variants Cause Pediatric Cushing's Disease With or Without an MEN4 Phenotype.

Authors:  Fanny Chasseloup; Nathan Pankratz; John Lane; Fabio R Faucz; Margaret F Keil; Prashant Chittiboina; Denise M Kay; Tara Hussein Tayeb; Constantine A Stratakis; James L Mills; Laura C Hernández-Ramírez
Journal:  J Clin Endocrinol Metab       Date:  2020-06-01       Impact factor: 5.958

4.  Insights into Assessing the Genetics of Endometriosis.

Authors:  Nilufer Rahmioglu; Stacey A Missmer; Grant W Montgomery; Krina T Zondervan
Journal:  Curr Obstet Gynecol Rep       Date:  2012-06-15
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.