Literature DB >> 28965242

Uteroglobin gene polymorphism (G38A) may be a risk factor in childhood idiopathic nephrotic syndrome.

Beltinge Demircioglu Kılıc1,2, Mithat Buyukcelik3, Sibel Oguzkan Balcı4, Sacide Pehlivan5, Seval Kul6, Nilgun Col7, Ayse Balat3.   

Abstract

BACKGROUND: Uteroglobin (UG) is a multifunctional protein with anti-inflammatory properties. The aim of this study was to first evaluate the role of UG gene G38A polymorphism in childhood idiopathic nephrotic syndrome (INS), and determine whether this variation may be related to the occurrence of INS or a steroid response.
METHODS: One hundred and thirty-six children diagnosed with INS in Gaziantep University, Department of Pediatric Nephrology, and 70 healthy volunteers were included. Children with INS were divided into two groups: steroid-sensitive (n = 84), and steroid-resistant (n = 52). Samples were examined using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) enzyme method.
RESULTS: The distributions of AA, GG, and AG genotypes of UG gene G38A (G/A) were 16.9%, 44.9%, and 38.2% in the all-INS group, whereas they were 14.3%, 48.8%, and 36.9% in the steroid-sensitive INS (SSINS) group compared with 21.1%, 38.5%, and 40.4% in steroid-resistant INS (SRINS), and 5.7%, 41.4%, and 52.9% in controls. The risk of INS was increased almost 4-fold in children with the AA genotype (p = 0.016). The risk of having SSINS was increased 3.5-fold (p = 0.042) whereas the risk of SRINS was increased 4.8-fold in the same genotype (p = 0.014).
CONCLUSIONS: The uteroglobin gene may play an important role in the development of INS, and the AA genotype of UG gene G38A polymorphism was found more frequently in those children. Further studies evaluating all polymorphisms in larger patient groups are needed to exactly determine the effect of UG gene on the development of INS and steroid response in children.

Entities:  

Keywords:  Children; G38A polymorphism; Nephrotic syndrome; Uteroglobin gene

Mesh:

Substances:

Year:  2017        PMID: 28965242     DOI: 10.1007/s00467-017-3800-7

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  31 in total

1.  The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents.

Authors: 
Journal:  Pediatrics       Date:  2004-08       Impact factor: 7.124

2.  Association of uteroglobin G38A polymorphism with IgA nephropathy: a meta-analysis.

Authors:  Du Yong; Wu QingQing; Liang Hua; Li Xiu Yang; Zou QingLing; Hu Ying; Qin QiaoJing; Shen HanChao
Journal:  Am J Kidney Dis       Date:  2006-07       Impact factor: 8.860

Review 3.  Insight into the physiological function(s) of uteroglobin by gene-knockout and antisense-transgenic approaches.

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Journal:  Ann N Y Acad Sci       Date:  2000       Impact factor: 5.691

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Journal:  Am J Med       Date:  1986-08-25       Impact factor: 4.965

5.  Association between the clara cell secretory protein (CC16) G38A polymorphism and the progression of IgA nephropathy.

Authors:  C S Lim; S M Kim; Y K Oh; Y S Kim; D W Chae; J S Han; S Kim; J S Lee; H J Yoon
Journal:  Clin Nephrol       Date:  2007-02       Impact factor: 0.975

6.  "Blastokinin": inducer and regulator of blastocyst development in the rabbit uterus.

Authors:  R S Krishnan; J C Daniel
Journal:  Science       Date:  1967-10-27       Impact factor: 47.728

Review 7.  Uteroglobin: physiological role in normal glomerular function uncovered by targeted disruption of the uteroglobin gene in mice.

Authors:  A B Mukherjee; G C Kundu; A K Mandal; N Pattabiraman; C J Yuan; Z Zhang
Journal:  Am J Kidney Dis       Date:  1998-12       Impact factor: 8.860

Review 8.  Uteroglobin: a steroid-inducible immunomodulatory protein that founded the Secretoglobin superfamily.

Authors:  Anil B Mukherjee; Zhongjian Zhang; Beverly S Chilton
Journal:  Endocr Rev       Date:  2007-10-04       Impact factor: 19.871

9.  [Uteroglobin G38A polymorphism is associated with the progression of IgA nephropathy in Chinese patients].

Authors:  Ji-cheng Lü; Hong Zhang; Yu-qing Chen; Gang Liu; Hai-yan Wang
Journal:  Zhonghua Nei Ke Za Zhi       Date:  2004-01

10.  The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children.

Authors: 
Journal:  J Pediatr       Date:  1981-04       Impact factor: 4.406

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