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Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. | LitMetric

AI Article Synopsis

  • - The study investigates the genetic factors linked to changes in fasting glucose levels over time in nearly 13,807 non-diabetic individuals of European descent, aiming to understand elements that could lead to Type 2 diabetes (T2D).
  • - Researchers found no strong genetic associations (defined as genome-wide significance) with fasting glucose changes, suggesting that any genetic influences are likely to be minimal.
  • - Several genetic loci previously connected to T2D and glucose levels showed nominal associations, and the data collected will serve as a resource for future research on genetic links to T2D and other metabolic traits.

Article Abstract

Type 2 diabetes (T2D) affects the health of millions of people worldwide. The identification of genetic determinants associated with changes in glycemia over time might illuminate biological features that precede the development of T2D. Here we conducted a genome-wide association study of longitudinal fasting glucose changes in up to 13,807 non-diabetic individuals of European descent from nine cohorts. Fasting glucose change over time was defined as the slope of the line defined by multiple fasting glucose measurements obtained over up to 14 years of observation. We tested for associations of genetic variants with inverse-normal transformed fasting glucose change over time adjusting for age at baseline, sex, and principal components of genetic variation. We found no genome-wide significant association (P < 5 × 10) with fasting glucose change over time. Seven loci previously associated with T2D, fasting glucose or HbA1c were nominally (P < 0.05) associated with fasting glucose change over time. Limited power influences unambiguous interpretation, but these data suggest that genetic effects on fasting glucose change over time are likely to be small. A public version of the data provides a genomic resource to combine with future studies to evaluate shared genetic links with T2D and other metabolic risk traits.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602949PMC
http://dx.doi.org/10.1038/s41598-019-45823-7DOI Listing

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