Cargando…

Clinical and Genetic Characteristics of ABCC8 Nonneonatal Diabetes Mellitus: A Systematic Review

OBJECTIVES: Diabetes mellitus (DM) is a major chronic metabolic disease in the world, and the prevalence has been increasing rapidly in recent years. The channel of K(ATP) plays an important role in the regulation of insulin secretion. The variants in ABCC8 gene encoding the SUR1 subunit of K(ATP) c...

Descripción completa

Detalles Bibliográficos
Autores principales:	Li, Meng, Han, Xueyao, Ji, Linong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2021
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497126/ https://www.ncbi.nlm.nih.gov/pubmed/34631896 http://dx.doi.org/10.1155/2021/9479268

Ejemplares similares

Clinical Characteristics of Young Type 2 Diabetes Patients with Atherosclerosis
por: Yang, Wenjia, et al.
Publicado: (2016)

Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
por: Kapoor, R. R., et al.
Publicado: (2011)

Transient neonatal diabetes mellitus caused by a de novo ABCC8 gene mutation
por: Kong, Jung Hyun, et al.
Publicado: (2011)

Transient Neonatal Diabetes Mellitus in a Very Preterm Infant due to ABCC8 Mutation
por: Piccini, Barbara, et al.
Publicado: (2018)

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

A novel de novo mutation at the ABCC8 gene in a newborn with transient diabetes mellitus
por: Bolu, Semih, et al.
Publicado: (2020)

Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations
por: Riveline, Jean-Pierre, et al.
Publicado: (2012)

A Variation in the ABCC8 Gene Is Associated with Type 2 Diabetes Mellitus and Repaglinide Efficacy in Chinese Type 2 Diabetes Mellitus Patients
por: Zhou, Xueyan, et al.
Publicado: (2019)

Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation
por: Saito-Hakoda, Akiko, et al.
Publicado: (2012)

Efficacy and Safety of Initial Combination Therapy in Treatment-Naïve Type 2 Diabetes Patients: A Systematic Review and Meta-analysis
por: Cai, Xiaoling, et al.
Publicado: (2018)

The genetic and clinical characteristics of WFS1 related diabetes in Chinese early onset type 2 diabetes
por: Li, Yating, et al.
Publicado: (2023)

Neonatal hyperinsulinism with an ABCC8 mutation: A case report
por: Liu, Meng-Tong, et al.
Publicado: (2023)

Genetics and Clinical Characteristics of PPARγ Variant-Induced Diabetes in a Chinese Han Population
por: Gong, Siqian, et al.
Publicado: (2021)

Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population
por: Tran, Nam Quang, et al.
Publicado: (2022)

ABCC8-Related Monogenic Diabetes Presenting Like Type 1 Diabetes in an Adolescent
por: Grier, Alexandra E., et al.
Publicado: (2023)

Non-Insulin Antidiabetes Treatment in Type 1 Diabetes Mellitus: A Systematic Review and Meta-Analysis
por: Cai, Xiaoling, et al.
Publicado: (2021)

ABCC8-Related Maturity-Onset Diabetes of the Young (MODY12): Clinical Features and Treatment Perspective
por: Ovsyannikova, Alla K., et al.
Publicado: (2016)

SUN-270 Heterozygous Mutation in ABCC8 in a Pedigree with Congenital Hyperinsulinism, Multiple Macrosomic Stillbirths, and Adult-Onset Diabetes Mellitus
por: Ludwig, Karissa, et al.
Publicado: (2019)

Neonatal Hypoglycaemia due to ABCC8 Gene Mutation
por: Kumar, Ashok, et al.
Publicado: (2020)

Association study of the ABCC8 gene variants with type 2 diabetes in south Indians
por: Venkatesan, Radha, et al.
Publicado: (2014)

A case of transient neonatal diabetes due to a novel mutation in ABCC8
por: Takagi, Masaki, et al.
Publicado: (2016)

An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression
por: Flanagan, Sarah E., et al.
Publicado: (2017)

Case Report: A Novel ABCC8 Variant in a Chinese Pedigree of Maturity-Onset Diabetes of the Young
por: Tang, Chaoyan, et al.
Publicado: (2021)

Analysis of Insulin Doses of Chinese Type 2 Diabetic Patients with Intensive Insulin Treatment
por: Cai, Xiaoling, et al.
Publicado: (2012)

A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide
por: Takeda, Ryojun, et al.
Publicado: (2015)

Targeted gene panel analysis of Japanese patients with maturity‐onset diabetes of the young‐like diabetes mellitus: Roles of inactivating variants in the ABCC8 and insulin resistance genes
por: Yorifuji, Tohru, et al.
Publicado: (2022)

Correspondence to ‘Neonatal hypoglycaemia due to ABCC8 gene mutation’
por: Maralihalli, Mahesh
Publicado: (2021)

Case report: Congenital hyperinsulinemia with ABCC8 gene mutations
por: Zhang, Jin, et al.
Publicado: (2022)

Comparisons of the Efficacy of Alpha Glucosidase Inhibitors on Type 2 Diabetes Patients between Asian and Caucasian
por: Cai, Xiaoling, et al.
Publicado: (2013)

Clinical characteristics and ABCC2 genotype in Dubin-Johnson syndrome: A case report and review of the literature
por: Wu, Huan, et al.
Publicado: (2021)

Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in Type 2 Diabetes in a Chinese population
por: Han, Xueyao, et al.
Publicado: (2010)

Promoter DNA Methylation Regulates Murine SUR1 (Abcc8) and SUR2 (Abcc9) Expression in HL-1 Cardiomyocytes
por: Fatima, Naheed, et al.
Publicado: (2012)

ABCC9 Is Downregulated and Prone to Microsatellite Instability on ABCC9tetra in Canine Breast Cancer
por: Hao, Pan, et al.
Publicado: (2022)

Serum leptin, resistin, and adiponectin levels in obese and non-obese patients with newly diagnosed type 2 diabetes mellitus: A population-based study
por: Liu, Wei, et al.
Publicado: (2020)

Clinical Case Report of Non-Diabetic Hypoglycemia Due to a Combination of Germline Mutations in the MEN1 and ABCC8 Genes
por: Yukina, Marina, et al.
Publicado: (2023)

Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo‐optico‐neuropathy (SMON)
por: Matsumoto, Hideki, et al.
Publicado: (2021)

Rs4074134 Near BDNF Gene Is Associated with Type 2 Diabetes Mellitus in Chinese Han Population Independently of Body Mass Index
por: Han, Xueyao, et al.
Publicado: (2013)

Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism
por: Chandran, Suresh, et al.
Publicado: (2013)

Diazoxide-unresponsive congenital hyperinsulinism associated with ABCC8 nonsense mutation
por: Hussain, Suhaimi, et al.
Publicado: (2015)

Genome-edited zebrafish model of ABCC8 loss-of-function disease
por: Ikle, Jennifer M., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_ifqc8if0ullu48c2rhm35vp6u3