Back to Search Start Over

Deciphering the Plasma Proteome of Type 2 Diabetes.

Deciphering the Plasma Proteome of Type 2 Diabetes.

Authors :
Elhadad, Mohamed A.
Jonasson, Christian
Huth, Cornelia
Wilson, Rory
Gieger, Christian
Matias, Pamela
Grallert, Harald
Graumann, Johannes
Gailus-Durner, Valerie
Rathmann, Wolfgang
von Toerne, Christine
Hauck, Stefanie M.
Koenig, Wolfgang
Sinner, Moritz F.
Oprea, Tudor I.
Suhre, Karsten
Thorand, Barbara
Hveem, Kristian
Peters, Annette
Waldenberger, Melanie
Source :
Diabetes; Dec2020, Vol. 69 Issue 12, p2766-2778, 13p
Publication Year :
2020

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121797
Volume :
69
Issue :
12
Database :
Complementary Index
Journal :
Diabetes
Publication Type :
Academic Journal
Accession number :
152364106
Full Text :
https://doi.org/10.2337/db20-0296