Cargando…

Pro198Leu missense polymorphism of the glutathione peroxidase 1 gene might be a common genetic predisposition of distal symmetric polyneuropathy and macrovascular disease in Japanese type 2 diabetic patients

Aims/Introduction: We have previously reported that the Pro198Leu missense polymorphism in the glutathione peroxidase 1 (GPx‐1) gene was associated with frequent macrovascular disease (MVD). Our goal was to examine whether the GPx‐1 genotype is associated with diabetic neuropathy. Materials and Met...

Descripción completa

Detalles Bibliográficos
Autores principales:	Matsuno, Shohei, Sasaki, Hideyuki, Yamasaki, Hiroshi, Yamaoka, Hiroyuki, Ogawa, Kenichi, Nakatani, Muneki, Hamanishi, Tohru, Doi, Asako, Nakano, Yoshio, Wakasaki, Hisao, Furuta, Hiroto, Nishi, Masahiro, Akamizu, Takashi, Nanjo, Kishio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Blackwell Publishing Ltd 2011
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014907/ https://www.ncbi.nlm.nih.gov/pubmed/24843532 http://dx.doi.org/10.1111/j.2040-1124.2011.00127.x

Ejemplares similares

Numbness and paresthesia in bilateral toes and soles, and disproportional sweating restricted to face and trunk are suitable symptoms useful for the diagnosis of diabetic symmetric polyneuropathy
por: Nakatani, Muneki, et al.
Publicado: (2011)

Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional “seiza” style
por: Kishimoto, Shohei, et al.
Publicado: (2020)

Increased arterial stiffness is closely associated with hyperglycemia and improved by glycemic control in diabetic patients
por: Ibata, Junko, et al.
Publicado: (2013)

Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus
por: Takagi, Tomoyuki, et al.
Publicado: (2013)

Clinical polyneuropathy does not increase with prediabetes or metabolic syndrome in the Japanese general population
por: Kurisu, Seigo, et al.
Publicado: (2019)

Truncal Pruritus of Unknown Origin May Be a Symptom of Diabetic Polyneuropathy
por: Yamaoka, Hiroyuki, et al.
Publicado: (2010)

Pro198Leu Polymorphism in the Glutathione Peroxidase 1 Gene Contributes to Diabetic Peripheral Neuropathy in Type 2 Diabetes Patients
por: Buraczynska, Monika, et al.
Publicado: (2016)

Association of glutathione peroxidase-1 (GPx-1) rs1050450 Pro198Leu and Pro197Leu polymorphisms with cardiovascular risk: a meta-analysis of observational studies
por: Zhang, Jun-Xia, et al.
Publicado: (2014)

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6‐year clinical course
por: Uraki, Shinsuke, et al.
Publicado: (2019)

Difference in normal limit values of nerve conduction parameters between Westerners and Japanese people might need to be considered when diagnosing diabetic polyneuropathy using a Point‐of‐Care Sural Nerve Conduction Device (NC‐stat®/DPNCheck™)
por: Hirayasu, Kazuhiro, et al.
Publicado: (2018)

Lack of association between glutathione peroxidase1 (GPx1) activity, Pro198Leu polymorphism and stenosis of coronary arteries: A population-based prediction
por: Najafi, Mohammad, et al.
Publicado: (2014)

Interaction of Polymorphisms of Resistin Gene Promoter -420C/G, Glutathione Peroxidase -1 Gene Pro198Leu and Cigarette Smoking in Nonalcoholic Fatty Liver Disease
por: Zhang, Chao-Xian, et al.
Publicado: (2015)

Case control feasibility study assessing the association between severity of coronary artery disease with Glutathione Peroxidase-1 (GPX-1) and GPX-1 polymorphism (Pro198Leu)
por: Wickremasinghe, Dinushka, et al.
Publicado: (2016)

Resistance to Thyroid Hormone Complicated with Type 2 Diabetes and Cardiomyopathy in a Patient with a TRβ Mutation
por: Wakasaki, Hisao, et al.
Publicado: (2016)

Clinical Utility of the Meal Tolerance Test in the Care of Patients with Type 2 Diabetes Mellitus
por: Wakasaki, Hisao, et al.
Publicado: (2020)

Association between glutathione peroxidase 1 codon 198 variant and the occurrence of breast cancer in Rwanda
por: Habyarimana, Thierry, et al.
Publicado: (2018)

Effect of anti‐oxidants, Ricetrienol and α‐tocopherol, on adipocytokine abnormalities and fatty liver in Otsuka Long‐Evans Tokushima Fatty diabetic rats
por: Tatsumi, Kunihiro, et al.
Publicado: (2010)

Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young‐onset diabetes with exome sequencing
por: Matsutani, Norihiko, et al.
Publicado: (2019)

From Six Gene Polymorphisms of the Antioxidant System, Only GPX Pro198Leu and GSTP1 Ile105Val Modulate the Risk of Acute Myeloid Leukemia
por: Bănescu, Claudia, et al.
Publicado: (2016)

Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
por: Bhattacharjee, Ashima, et al.
Publicado: (2008)

Insulin gene mutations and diabetes
por: Nishi, Masahiro, et al.
Publicado: (2011)

Alpha decay of $^{198}$Rn
por: Calaprice, F P, et al.
Publicado: (1984)

Macrovascular Complications in Patients with Diabetes and Prediabetes
por: Huang, Dou, et al.
Publicado: (2017)

Endothelium in Coronary Macrovascular and Microvascular Diseases
por: Godo, Shigeo, et al.
Publicado: (2021)

Effect of the Hydration Shell on the Carbonyl Vibration in the Ala-Leu-Ala-Leu Peptide
por: Hassan, Irtaza, et al.
Publicado: (2021)

Contribution of glutathione peroxidase 1 (Pro200Leu) single nucleotide polymorphism and serum homocysteine levels in the risk of acute myocardial infarction in Egyptians
por: Ismail, Lamia K., et al.
Publicado: (2022)

Identification of a variant associated with early‐onset diabetes in the intron of the insulin gene with exome sequencing
por: Matsuno, Shohei, et al.
Publicado: (2018)

Residual macrovascular risk in 2013: what have we learned?
por: Fruchart, Jean-Charles, et al.
Publicado: (2014)

Health Tract, No. 198: Balm of Gilead
Publicado: (1865)

Heart in Diabetes: Not Only a Macrovascular Disease
por: Stratmann, Bernd, et al.
Publicado: (2011)

Type 2 Diabetes Mellitus and Macrovascular Complications
por: Shan, Peng-Fei, et al.
Publicado: (2017)

Genetics of macrovascular complications in type 2 diabetes
por: Tonyan, Ziravard N, et al.
Publicado: (2021)

Hypersecretion of ACTH and PRL from pituitary adenoma in MEN1, adequately managed by medical therapy
por: Uraki, Shinsuke, et al.
Publicado: (2017)

Measurements of Serum Mac-2-Binding Protein Glycosylation Isomer and Shear Wave Velocity in Health Checkups Are Useful in Screening for Non-Alcoholic Steatohepatitis
por: Tamai, Hideyuki, et al.
Publicado: (2021)

Future U.S. supply of Mo-99 production through fission based LEU/LEU technology
por: Welsh, James, et al.
Publicado: (2015)

De novo TRPV4 Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathy
por: Ragamin, Aviel, et al.
Publicado: (2022)

NGF (−198C > T, Ala35Val) and p75(NTR) (Ser205Leu) gene mutations are associated with liver function in different histopathological profiles of the patients with chronic viral hepatitis in the Brazilian Amazon
por: Pereira, Leonn Mendes Soares, et al.
Publicado: (2020)

LeuRS can leucylate type I and type II tRNA(Leu)s in Streptomyces coelicolor
por: Fan, Jia-Yi, et al.
Publicado: (2019)

The charge radii of $^{198}$Pt - $^{183}$Pt
por: Hilberath, T, et al.
Publicado: (1989)

Au-198m as novel PAC probe
por: Correia, Guilherme, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_b3la4noc646jka8n2lmkjj8rka