Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0062378
Title: Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations
Authors: 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, H.K.
Nanjo, K.
Xu, G.
Ng, M.C.Y.
So, W.-Y.
Chan, J.C.N.
Issue Date: 11-Jun-2013
Citation: 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, H.K., Nanjo, K., Xu, G., Ng, M.C.Y., So, W.-Y., Chan, J.C.N. (2013-06-11). Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations. PLoS ONE 8 (6) : -. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0062378
Abstract: 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 (PMeta = 9.4×10-3 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. © 2013 Lam et al.
Source Title: PLoS ONE
URI: http://scholarbank.nus.edu.sg/handle/10635/108200
ISSN: 19326203
DOI: 10.1371/journal.pone.0062378
Appears in Collections:Staff Publications
Elements

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
2013-Genetic_Associations_Type_2_Diabetes-published.pdf444.75 kBAdobe PDF

OPEN

PublishedView/Download

SCOPUSTM   
Citations

6
checked on Sep 9, 2019

WEB OF SCIENCETM
Citations

4
checked on Sep 9, 2019

Page view(s)

258
checked on Sep 7, 2019

Download(s)

20
checked on Sep 7, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.