دورية أكاديمية

Loci for insulin processing and secretion provide insight into type 2 diabetes risk.

التفاصيل البيبلوغرافية
العنوان: Loci for insulin processing and secretion provide insight into type 2 diabetes risk.
المؤلفون: Broadaway, K Alaine, Yin, Xianyong, Williamson, Alice, Parsons, Victoria A, Wilson, Emma P, Moxley, Anne H, Vadlamudi, Swarooparani, Varshney, Arushi, Jackson, Anne U, Ahuja, Vasudha, Bornstein, Stefan R, Corbin, Laura J, Delgado, Graciela E, Dwivedi, Om P, Fernandes Silva, Lilian, Frayling, Timothy M, Grallert, Harald, Gustafsson, Stefan, Hakaste, Liisa, Hammar, Ulf, Herder, Christian, Herrmann, Sandra, Højlund, Kurt, Hughes, David A, Kleber, Marcus E, Lindgren, Cecilia M, Liu, Ching-Ti, Luan, Jian'an, Malmberg, Anni, Moissl, Angela P, Morris, Andrew P, Perakakis, Nikolaos, Peters, Annette, Petrie, John R, Roden, Michael, Schwarz, Peter EH, Sharma, Sapna, Silveira, Angela, Strawbridge, Rona J, Tuomi, Tiinamaija, Wood, Andrew R, Wu, Peitao, Zethelius, Björn, Baldassarre, Damiano, Eriksson, Johan G, Fall, Tove, Florez, Jose C, Fritsche, Andreas, Gigante, Bruna, Hamsten, Anders, Kajantie, Eero, Laakso, Markku, Lahti, Jari, Lawlor, Deborah A, Lind, Lars, März, Winfried, Meigs, James B, Sundström, Johan, Timpson, Nicholas J, Wagner, Robert, Walker, Mark, Wareham, Nicholas J, Watkins, Hugh, Barroso, Inês, O'Rahilly, Stephen, Grarup, Niels, Parker, Stephen Cj, Boehnke, Michael, Langenberg, Claudia, Wheeler, Eleanor, Mohlke, Karen L
بيانات النشر: Elsevier BV
office of The School of Clinical Medicine
//dx.doi.org/10.1016/j.ajhg.2023.01.002
Am J Hum Genet
سنة النشر: 2023
المجموعة: Apollo - University of Cambridge Repository
مصطلحات موضوعية: GWAS, colocalization, conditional, eQTL, enhancer, fine-mapping, meta-analysis, proinsulin, signal, type 2 diabetes, Humans, Diabetes Mellitus, Type 2, Genome-Wide Association Study, Insulin, Glucose, Transcription Factors, Homeodomain Proteins
الوصف: Insulin secretion is critical for glucose homeostasis, and increased levels of the precursor proinsulin relative to insulin indicate pancreatic islet beta-cell stress and insufficient insulin secretory capacity in the setting of insulin resistance. We conducted meta-analyses of genome-wide association results for fasting proinsulin from 16 European-ancestry studies in 45,861 individuals. We found 36 independent signals at 30 loci (p value < 5 × 10-8), which validated 12 previously reported loci for proinsulin and ten additional loci previously identified for another glycemic trait. Half of the alleles associated with higher proinsulin showed higher rather than lower effects on glucose levels, corresponding to different mechanisms. Proinsulin loci included genes that affect prohormone convertases, beta-cell dysfunction, vesicle trafficking, beta-cell transcriptional regulation, and lysosomes/autophagy processes. We colocalized 11 proinsulin signals with islet expression quantitative trait locus (eQTL) data, suggesting candidate genes, including ARSG, WIPI1, SLC7A14, and SIX3. The NKX6-3/ANK1 proinsulin signal colocalized with a T2D signal and an adipose ANK1 eQTL signal but not the islet NKX6-3 eQTL. Signals were enriched for islet enhancers, and we showed a plausible islet regulatory mechanism for the lead signal in the MADD locus. These results show how detailed genetic studies of an intermediate phenotype can elucidate mechanisms that may predispose one to disease.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://www.repository.cam.ac.uk/handle/1810/354046Test; https://doi.org/10.17863/CAM.100055Test
DOI: 10.17863/CAM.100055
الإتاحة: https://doi.org/10.17863/CAM.100055Test
https://www.repository.cam.ac.uk/handle/1810/354046Test
حقوق: Attribution 4.0 International ; https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.11B4C17F
قاعدة البيانات: BASE