Literature DB >> 12478192

Prospective analysis of single nucleotide polymorphisms of the transforming growth factor beta-1 gene in Peyronie's disease.

Ekkehard W Hauck1, Arne Hauptmann, Hans U Schmelz, Gregor Bein, Wolfgang Weidner, Holger Hackstein.   

Abstract

PURPOSE: The detection of increased expression of transforming growth factor beta-1 (TGF-beta1) in Peyronie's disease plaques and the possibility of initiating a Peyronie's disease-like condition by intratunical injection of a synthetic heptopeptide with TGF-beta-like activity in an animal model has provided evidence for the central role of this cytokine in the pathogenesis of this entity. Recently 2 defined single nucleotide polymorphisms in the coding region of the TGF-beta1 gene have been described that are associated with different levels of TGF-beta1 production. Based on these data we prospectively investigated the genetic association of distinct TGF-beta1 genotypes with Peyronie's disease.
MATERIALS AND METHODS: DNA samples from 111 consecutive patients with idiopathic Peyronie's disease and 100 controls were genotyped for the 2 defined dimorphic single nucleotide polymorphisms T869C and G915C in the coding region of the TGF-beta1 gene using allele specific polymerase chain reaction.
RESULTS: We found an increased frequency of the homozygous genotype of the single nucleotide polymorphism G915C in patients with Peyronie's disease compared with healthy controls (89.2% versus 79%, p = 0.04). However, there were no significant differences in allele frequencies of the single nucleotide polymorphism T869C.
CONCLUSIONS: Experimental data from other investigators have shown that TGF-beta1 has an important role in the etiopathology of Peyronie's disease. Our results indicate that the homozygous wild type of the G915C single nucleotide polymorphism in the coding region of the TGF-beta1 gene, which was recently associated with elevated TGF-beta1 production and pulmonary fibrosis, may influence the predisposition to Peyronie's disease. However, it does not represent a major genetic risk factor.

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Year:  2003        PMID: 12478192     DOI: 10.1097/01.ju.0000039347.38539.13

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  7 in total

Review 1.  The Genetic Basis of Peyronie Disease: A Review.

Authors:  Amin S Herati; Alexander W Pastuszak
Journal:  Sex Med Rev       Date:  2016-01-08

2.  Significant familial clustering of Peyronie's disease in close and distant relatives.

Authors:  Kristina L Allen-Brady; Michael B Christensen; Ashlynn D Sandberg; Alexander W Pastuszak
Journal:  Andrology       Date:  2022-07-13       Impact factor: 4.456

3.  Association of genetic variation in the transforming growth factor beta-1 gene with serum levels and risk of colorectal neoplasia.

Authors:  Barbara S Saltzman; Jennifer F Yamamoto; Robert Decker; Lance Yokochi; Andre G Theriault; Thomas M Vogt; Loïc Le Marchand
Journal:  Cancer Res       Date:  2008-02-15       Impact factor: 12.701

Review 4.  The Natural History of Peyronie's Disease.

Authors:  Fabrizio Di Maida; Gianmartin Cito; Luca Lambertini; Francesca Valastro; Girolamo Morelli; Andrea Mari; Marco Carini; Andrea Minervini; Andrea Cocci
Journal:  World J Mens Health       Date:  2020-07-08       Impact factor: 5.400

5.  ABO Blood Type and Risk of Peyronie's Disease in Japanese Males.

Authors:  Yozo Mitsui; Hideyuki Kobayashi; Fumito Yamabe; Koichi Nakajima; Koichi Nagao
Journal:  World J Mens Health       Date:  2022-01-01       Impact factor: 6.494

6.  Experimental investigation of early assessment of corpora cavernosa fibrosis with two-dimensional shear wave elastography.

Authors:  Li Yu; Wan-Ting Rao; Jing-Dong Tang; Jin-Fang Xing
Journal:  Asian J Androl       Date:  2022 Mar-Apr       Impact factor: 3.285

Review 7.  Peyronie's disease: is it genetic or not?

Authors:  J Scott Gabrielsen
Journal:  Transl Androl Urol       Date:  2020-03
  7 in total

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