Type 2 Diabetes risk alleles in Peptidyl-glycine Alpha-amidating Monooxygenase influence GLP-1 levels and response to GLP-1 Receptor Agonists

التفاصيل البيبلوغرافية
العنوان: Type 2 Diabetes risk alleles in Peptidyl-glycine Alpha-amidating Monooxygenase influence GLP-1 levels and response to GLP-1 Receptor Agonists
المؤلفون: Umapathysivam, Mahesh M, Araldi, Elisa, Hastoy, Benoit, Dawed, Adem Y, Vatandaslar, Hasan, Sengupta, Shahana, Kaufmann, Adrian, Thomsen, Søren, Hartmann, Bolette, Jonsson, Anna E, Kabakci, Hasan, Thaman, Swaraj, Grarup, Niels, Have, Christian T, Færch, Kristine, Gjesing, Anette P, Nawaz, Sameena, Cheeseman, Jane, Neville, Matthew J, Pedersen, Oluf, Walker, Mark, Jennison, Christopher, Hattersley, Andrew T, Hansen, Torben, Karpe, Fredrik, Holst, Jens J, Jones, Angus G, Ristow, Michael, McCarthy, Mark I, Pearson, Ewan R, Stoffel, Markus, Gloyn, Anna L
المصدر: Umapathysivam , M M , Araldi , E , Hastoy , B , Dawed , A Y , Vatandaslar , H , Sengupta , S , Kaufmann , A , Thomsen , S , Hartmann , B , Jonsson , A E , Kabakci , H , Thaman , S , Grarup , N , Have , C T , Færch , K , Gjesing , A P , Nawaz , S , Cheeseman , J , Neville , M J , Pedersen , O , Walker , M , Jennison , C , Hattersley , A T , ....
بيانات النشر: medRxiv
سنة النشر: 2023
المجموعة: University of Copenhagen: Research / Forskning ved Københavns Universitet
الوصف: UNLABELLED: Patients with type 2 diabetes vary in their response to currently available therapeutic agents (including GLP-1 receptor agonists) leading to suboptimal glycemic control and increased risk of complications. We show that human carriers of hypomorphic T2D-risk alleles in the gene encoding peptidyl-glycine alpha-amidating monooxygenase (PAM), as well as Pam- knockout mice, display increased resistance to GLP-1 in vivo . Pam inactivation in mice leads to reduced gastric GLP-1R expression and faster gastric emptying: this persists during GLP-1R agonist treatment and is rescued when GLP-1R activity is antagonized, indicating resistance to GLP-1's gastric slowing properties. Meta-analysis of human data from studies examining GLP-1R agonist response (including RCTs) reveals a relative loss of 44% and 20% of glucose lowering (measured by glycated hemoglobin) in individuals with hypomorphic PAM alleles p.S539W and p.D536G treated with GLP-1R agonist. Genetic variation in PAM has effects on incretin signaling that alters response to medication used commonly for treatment of T2D. (Funded by the Wellcome, Medical Research Council, European Union, NIHR Oxford Biomedical Research Centre, United Kingdom, Registered on ClinicalTrials.gov, NCT02723110 .). SUMMARY PARAGRAPH: Type 2 diabetes (T2D) is a leading cause of morbidity and mortality globally 1 . Current management of T2D patients focuses on lowering glycemic exposure and reducing complications with lifestyle and pharmacological interventions 2 . Despite the availability of multiple medications to lower glycated hemoglobin (HbA1c), only 53% of individuals with T2D reach the glycemic target (HbA1c <7%) 3, 4 . There is potential to improve medication selection through "precision medicine" where patient specific factors (e.g. genetic markers) are used to indicate whether a patient is more or less likely to respond to a medication. Here we show that human carriers of hypomorphic T2D-risk alleles in the gene encoding peptidyl-glycine alpha-amidating monooxygenase ...
نوع الوثيقة: report
وصف الملف: application/pdf
اللغة: English
DOI: 10.1101/2023.04.07.23288197
الإتاحة: https://doi.org/10.1101/2023.04.07.23288197Test
https://curis.ku.dk/portal/da/publications/type-2-diabetes-risk-alleles-in-peptidylglycine-alphaamidating-monooxygenase-influence-glp1-levels-and-response-to-glp1-receptor-agonistsTest(039f97f5-5faa-4fc8-8068-724551948168).html
https://curis.ku.dk/ws/files/350979933/2023.04.07.23288197v1.full.pdfTest
حقوق: info:eu-repo/semantics/restrictedAccess
رقم الانضمام: edsbas.1738E3C9
قاعدة البيانات: BASE