دورية أكاديمية

Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations

التفاصيل البيبلوغرافية
العنوان: Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations
المؤلفون: Lam, Vincent Kwok Lim, Ma, Ronald Ching Wan, Lee, Heung Man, Hu, Cheng, Park, Kyong Soo, Furuta, Hiroto, Wang, Ying, Tam, Claudia Ha Ting, Sim, Xueling, Ng, Daniel Peng-Keat, Liu, Jianjun, Wong, Tien-Yin, Tai, E. Shyong, Morris, Andrew P., Tang, Nelson Leung Sang, Woo, Jean, Leung, Ping Chung, Kong, Alice Pik Shan, Ozaki, Risa, Jia, Wei Ping, Lee, Hong Kyu, Nanjo, Kishio, Xu, Gang, Ng, Maggie Chor Yin, So, Wing-Yee, Chan, Juliana Chung Ngor
المصدر: Lam , V K L , Ma , R C W , Lee , H M , Hu , C , Park , K S , Furuta , H , Wang , Y , Tam , C H T , Sim , X , Ng , D P-K , Liu , J , Wong , T-Y , Tai , E S , Morris , A P , Tang , N L S , Woo , J , Leung , P C , Kong , A P S , Ozaki , R , Jia , W P , Lee , ....
سنة النشر: 2013
المجموعة: University of Groningen research database
مصطلحات موضوعية: HUMAN PANCREATIC-ISLETS, ENDOPLASMIC-RETICULUM STRESS, TRANSCRIPTION FACTOR, SUSCEPTIBILITY LOCI, METABOLIC SYNDROME, INSULIN, MELLITUS, OBESITY, HHEX, RISK
الوصف: Type 2 diabetes (T2D) is a complex disease characterized by beta cell dysfunctions. Islet amyloid polypeptide (IAPP) is highly conserved and co-secreted with insulin with over 40% of autopsy cases of T2D showing islet amyloid formation due to IAPP aggregation. Dysregulation in IAPP processing, stabilization and degradation can cause excessive oligomerization with beta cell toxicity. Previous studies examining genetic associations of pathways implicated in IAPP metabolism have yielded conflicting results due to small sample size, insufficient interrogation of gene structure and gene-gene interactions. In this multi-staged study, we screened 89 tag single nucleotide polymorphisms (SNPs) in 6 candidate genes implicated in IAPP metabolism and tested for independent and joint associations with T2D and beta cell dysfunctions. Positive signals in the stage-1 were confirmed by de novo and in silico analysis in a multi-centre unrelated case-control cohort. We examined the association of significant SNPs with quantitative traits in a subset of controls and performed bioinformatics and relevant functional analyses. Amongst the tag SNPs, rs1583645 in carboxypeptidase E (CPE) and rs6583813 in insulin degrading enzyme (IDE) were associated with 1.09 to 1.28 fold increased risk of T2D (P-Meta = 9.4x10(-3) and 0.02 respectively) in a meta-analysis of East Asians. Using genetic risk scores (GRS) with each risk variant scoring 1, subjects with GRS >= 3 (8.2% of the cohort) had 56% higher risk of T2D than those with GRS = 0 (P = 0.01). In a subcohort of control subjects, plasma IAPP increased and beta cell function index declined with GRS (P = 0.008 and 0.03 respectively). Bioinformatics and functional analyses of CPE rs1583645 predicted regulatory elements for chromatin modification and transcription factors, suggesting differential DNA-protein interactions and gene expression. Taken together, these results support the importance of dysregulation of IAPP metabolism in T2D in East Asians.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://research.rug.nl/en/publications/fde77998-8bf7-4340-8784-8ca7b96e260aTest
DOI: 10.1371/journal.pone.0062378
الإتاحة: https://doi.org/10.1371/journal.pone.0062378Test
https://hdl.handle.net/11370/fde77998-8bf7-4340-8784-8ca7b96e260aTest
https://research.rug.nl/en/publications/fde77998-8bf7-4340-8784-8ca7b96e260aTest
https://pure.rug.nl/ws/files/42624314/Genetic_Associations_of_Type_2_Diabetes_with_Islet_Amyloid.PDFTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.97B00F74
قاعدة البيانات: BASE