Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes

• Published in: International journal of molecular sciences 2023-01, Vol.24 (2), p.984
• Main Authors: Timasheva, Yanina, Balkhiyarova, Zhanna, Avzaletdinova, Diana, Rassoleeva, Irina, Morugova, Tatiana V, Korytina, Gulnaz, Prokopenko, Inga, Kochetova, Olga
• Format: Article
• Language: English
• Subjects: Age; CCL20 protein; CCR5 protein; Chemokines; Diabetes; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2 - genetics; Genetic diversity; Genetic factors; genetic predictors; Genetic Predisposition to Disease; Genome-Wide Association Study; Glucose; Glucose metabolism; Humans; Hyperglycemia; Insulin resistance; Metabolism; Molecular modelling; Monocyte chemoattractant protein 1; polygenic scores; Polymorphism, Single Nucleotide; Reclassification; Regression analysis; Risk analysis; Risk Factors; Sex; Single-nucleotide polymorphism; type 2 diabetes
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24020984

We tested associations between 13 established genetic variants and type 2 diabetes (T2D) in 1371 study participants from the Volga-Ural region of the Eurasian continent, and evaluated the predictive ability of the model containing polygenic scores for the variants associated with T2D in our dataset, alone and in combination with other risk factors such as age and sex. Using logistic regression analysis, we found associations with T2D for the rs6749704 (OR = 1.68, P = 3.40 × 10 ), rs333 (OR = 1.99, P = 0.033), rs17366743 (OR = 3.17, P = 2.64 × 10 ) rs114758349 (OR = 1.77, P = 9.37 × 10 ), and rs1024611 (OR = 1.38, P = 0.033) polymorphisms. We showed that the most informative prognostic model included weighted polygenic scores for these five loci, and non-genetic factors such as age and sex (AUC 85.8%, 95%CI 83.7-87.8%). Compared to the model containing only non-genetic parameters, adding the polygenic score for the five T2D-associated loci showed improved net reclassification (NRI = 37.62%, 1.39 × 10 ). Inclusion of all 13 tested SNPs to the model with age and sex did not improve the predictive ability compared to the model containing five T2D-associated variants (NRI = -17.86, = 0.093). The five variants associated with T2D in people from the Volga-Ural region are linked to inflammation ( ) and glucose metabolism regulation ( ). Further studies in independent groups of T2D patients should validate the prognostic value of the model and elucidate the molecular mechanisms of the disease development.