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Diabetes mellitus is a long-term metabolic condition marked by high blood sugar levels due to issues with insulin production, insulin effectiveness, or a combination of both. It stands as one of the fastest-growing diseases worldwide, projected to afflict 693 million adults by 2045. The escalating prevalence of diabetes and associated health complications (kidney disease, retinopathy, and neuropathy) underscore the imperative to devise predictive models for early diagnosis and intervention. These complications contribute to increased mortality rates, blindness, kidney failure, and an overall diminished quality of life in individuals living with diabetes. While clinical risk factors and glycemic control provide valuable insights, they alone cannot reliably predict the onset of vascular complications. Genetic biomarkers and machine learning techniques have emerged as promising tools for predicting diabetes development risk and associated complications. Despite the emergence of numerous smart AI models for diabetes prediction, there is still a need for a thorough review outlining their progress and challenges. To address this gap, this paper offers a systematic review of the literature on AI-based models for diabetes identification, following the PRISMA extension for scoping reviews guidelines. Our review revealed that multimodal diabetes prediction models outperformed unimodal models. Most studies focused on classical machine learning models, with SNPs being the most used data type, followed by gene expression profiles, while lipidomic and metabolomic data were the least utilized. Moreover, some studies focused on identifying genetic determinants of diabetes complications relied on familial linkage analysis, tailored for robust effect loci. However, these approaches had limitations, including susceptibility to false positives in candidate gene studies and underpowered AI models capabilities due to sample size constraints. The landscape shifted dramatically with the proliferation of genomic datasets, fueled by the emergence of biobanks and the amalgamation of global cohorts. This surge has led to a more than twofold increase in genetic discoveries related to both diabetes and its complications using AI. Our focus here is on these genetic breakthroughs, particularly those empowered by AI models. However, we also highlight the existing gaps in research and underscore the need for further advancements to propel genomic discovery to the next level.
Diabetes mellitus is a long-term metabolic condition marked by high blood sugar levels due to issues with insulin production, insulin effectiveness, or a combination of both. It stands as one of the fastest-growing diseases worldwide, projected to afflict 693 million adults by 2045. The escalating prevalence of diabetes and associated health complications (kidney disease, retinopathy, and neuropathy) underscore the imperative to devise predictive models for early diagnosis and intervention. These complications contribute to increased mortality rates, blindness, kidney failure, and an overall diminished quality of life in individuals living with diabetes. While clinical risk factors and glycemic control provide valuable insights, they alone cannot reliably predict the onset of vascular complications. Genetic biomarkers and machine learning techniques have emerged as promising tools for predicting diabetes development risk and associated complications. Despite the emergence of numerous smart AI models for diabetes prediction, there is still a need for a thorough review outlining their progress and challenges. To address this gap, this paper offers a systematic review of the literature on AI-based models for diabetes identification, following the PRISMA extension for scoping reviews guidelines. Our review revealed that multimodal diabetes prediction models outperformed unimodal models. Most studies focused on classical machine learning models, with SNPs being the most used data type, followed by gene expression profiles, while lipidomic and metabolomic data were the least utilized. Moreover, some studies focused on identifying genetic determinants of diabetes complications relied on familial linkage analysis, tailored for robust effect loci. However, these approaches had limitations, including susceptibility to false positives in candidate gene studies and underpowered AI models capabilities due to sample size constraints. The landscape shifted dramatically with the proliferation of genomic datasets, fueled by the emergence of biobanks and the amalgamation of global cohorts. This surge has led to a more than twofold increase in genetic discoveries related to both diabetes and its complications using AI. Our focus here is on these genetic breakthroughs, particularly those empowered by AI models. However, we also highlight the existing gaps in research and underscore the need for further advancements to propel genomic discovery to the next level.
Background: The triglyceride glucose-body mass index (TyG-BMI) is considered to be an alternative indicator of insulin resistance (IR) with greater clinical value in terms of cardiovascular risk. However, the relationship between TyG-BMI and left ventricular asynchrony, which determines heart function, is unclear. The purpose of this study was to explore the association between the TyG-BMI and left ventricular asynchrony in patients with type 2 diabetes. Methods: This cross-sectional study included 614 patients with type 2 diabetes between September 2021 and June 2023. All patients initially screened with conventional echocardiography underwent subsequent evaluations, including speck-tracking echocardiography and real-time three-dimensional echocardiography. The systolic dyssynchrony index (SDI) was automatically derived from real-time three-dimensional echocardiography in order to assess the degree of left ventricular asynchrony among patients. The TyG-BMI was calculated, and the included patients were stratified according to TyG-BMI quartiles. Results: The analysis of the 614 patients with type 2 diabetes who were ultimately included revealed that the SDI tended to increase as the TyG-BMI increased, with the SDI corresponding to the highest quartile being the highest. According to multiple linear regression analysis, the TyG-BMI is independently related to the SDI. Further exploratory subgroup analysis revealed that the TyG-BMI was more likely to be associated with SDI in patients ≤55 years of age with type 2 diabetes. Conclusions: Our research revealed that the TyG-BMI of patients with type 2 diabetes was positively correlated with the SDI, and this correlation was more obvious in patients with type 2 diabetes who were ≤55 years old.
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