| Literature DB >> 32928870 |
Mohamed A Elhadad1,2,3, Christian Jonasson4,5, Cornelia Huth2,6, Rory Wilson7,2, Christian Gieger7,2,6, Pamela Matias7,2,3, Harald Grallert7,2,6, Johannes Graumann8,9, Valerie Gailus-Durner10, Wolfgang Rathmann6,11, Christine von Toerne12, Stefanie M Hauck12, Wolfgang Koenig3,13,14, Moritz F Sinner3,15, Tudor I Oprea16,17,18, Karsten Suhre19, Barbara Thorand2,6, Kristian Hveem4,5, Annette Peters2,3,6,20, Melanie Waldenberger1,2,3.
Abstract
With an estimated prevalence of 463 million affected, type 2 diabetes represents a major challenge to health care systems worldwide. Analyzing the plasma proteomes of individuals with type 2 diabetes may illuminate hitherto unknown functional mechanisms underlying disease pathology. We assessed the associations between type 2 diabetes and >1,000 plasma proteins in the Cooperative Health Research in the Region of Augsburg (KORA) F4 cohort (n = 993, 110 cases), with subsequent replication in the third wave of the Nord-Trøndelag Health Study (HUNT3) cohort (n = 940, 149 cases). We computed logistic regression models adjusted for age, sex, BMI, smoking status, and hypertension. Additionally, we investigated associations with incident type 2 diabetes and performed two-sample bidirectional Mendelian randomization (MR) analysis to prioritize our results. Association analysis of prevalent type 2 diabetes revealed 24 replicated proteins, of which 8 are novel. Proteins showing association with incident type 2 diabetes were aminoacylase-1, growth hormone receptor, and insulin-like growth factor-binding protein 2. Aminoacylase-1 was associated with both prevalent and incident type 2 diabetes. MR analysis yielded nominally significant causal effects of type 2 diabetes on cathepsin Z and rennin, both known to have roles in the pathophysiological pathways of cardiovascular disease, and of sex hormone-binding globulin on type 2 diabetes. In conclusion, our high-throughput proteomics study replicated previously reported type 2 diabetes-protein associations and identified new candidate proteins possibly involved in the pathogenesis of type 2 diabetes.Entities:
Year: 2020 PMID: 32928870 PMCID: PMC7679779 DOI: 10.2337/db20-0296
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461