Literature DB >> 18464276

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients.

Patricia de Carvalho Aguiar1, Patricia Silva Lessa, Clecio Godeiro, Orlando Barsottini, Andre Carvalho Felício, Vanderci Borges, Sonia Maria de Azevedo Silva, Roberta Arb Saba, Henrique Ballalai Ferraz, Carlos A Moreira-Filho, Luiz Augusto F Andrade.   

Abstract

Parkinson's disease (PD) etiology has been attributed both to genetic and environmental factors. In this study, we investigated Brazilian early-onset PD (EOPD) patients for mutations in PARK2 and PARK8, exposure to environmental factors and possible correlations between PARK2 polymorphisms, environmental exposure, and disease age of onset. We enrolled 72 EOPD index patients and 81 healthy volunteers. Both groups were investigated for environmental exposure. EOPD patients were screened for PARK2 and PARK8 mutations. PARK2 coding polymorphisms Ser167Asn and Val380Leu were investigated in both groups. Mutations were present in 18% of the patients and in 32% of those with a positive family history. PARK2 mutations represented 12.5% and PARK8 mutations accounted for 5.5% of the mutations. A novel PARK2 mutation (D53X) was identified in 2 patients. A positive correlation was found between EOPD and well water drinking. In patients exposed to well water, a later age of onset was observed for those who carried at least one PARK2 380Leu allele. PARK2 mutations have an important role in EOPD Brazilian patients and PARK8 might be the second most important disease causing gene in this group. Well water drinking exposure represents a risk factor for EOPD and the PARK2 coding polymorphism Val380Leu might be interacting with environmental factors acting as a disease modifier. (c) 2008 Movement Disorder Society.

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Year:  2008        PMID: 18464276     DOI: 10.1002/mds.22032

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  7 in total

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Journal:  J Hum Genet       Date:  2015-05-28       Impact factor: 3.172

Review 2.  Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

Authors:  Karen Nuytemans; Jessie Theuns; Marc Cruts; Christine Van Broeckhoven
Journal:  Hum Mutat       Date:  2010-07       Impact factor: 4.878

3.  Investigation of Nonmotor Symptoms in First-Degree Relatives of Patients with Different Clinical Types of Parkinson's Disease.

Authors:  Jiang-Bing Liu; Jun-Ling Leng; Ying-Ge Wang; Yu Zhang; Tie-Yu Tang; Li-Hong Tao; Xin-Jiang Zhang; Chun-Feng Liu
Journal:  Parkinsons Dis       Date:  2019-01-02

Review 4.  Review of the epidemiology and variability of LRRK2 non-p.Gly2019Ser pathogenic mutations in Parkinson's disease.

Authors:  Paweł Turski; Iwona Chaberska; Piotr Szukało; Paulina Pyska; Łukasz Milanowski; Stanisław Szlufik; Monika Figura; Dorota Hoffman-Zacharska; Joanna Siuda; Dariusz Koziorowski
Journal:  Front Neurosci       Date:  2022-09-20       Impact factor: 5.152

5.  Genetic analysis of PARK2 and PINK1 genes in Brazilian patients with early-onset Parkinson's disease.

Authors:  Karla Cristina Vasconcelos Moura; Mário Campos Junior; Ana Lúcia Zuma de Rosso; Denise Hack Nicaretta; João Santos Pereira; Delson José Silva; Flávia Lima dos Santos; Fabíola da Costa Rodrigues; Cíntia Barros Santos-Rebouças; Márcia Mattos Gonçalves Pimentel
Journal:  Dis Markers       Date:  2013-08-14       Impact factor: 3.434

6.  MDPD: an integrated genetic information resource for Parkinson's disease.

Authors:  Suisheng Tang; Zhuo Zhang; Gopalakrishnan Kavitha; Eng-King Tan; See Kiong Ng
Journal:  Nucleic Acids Res       Date:  2008-10-23       Impact factor: 16.971

7.  The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.

Authors:  Katarzyna Gaweda-Walerych; Cezary Zekanowski
Journal:  Curr Genomics       Date:  2013-12       Impact factor: 2.236

  7 in total

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