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Dryad

Data from: Association and function analysis of genetic variants and the risk of gestational diabetes mellitus in a southern Chinese population

Abstract

This dataset include 538 gestational diabetes mellitus (GDM) patients and 626 healthy pregnancies’ baseline information obtained from unique questionnaires and medical records, and the genetic loci were genotyped by the Sequenom MassARRAY platform. The clinical indicators and genetic variants that are statistically associated with GDM were used to construct a nomogram model. The nomogram model is formulated as a standard of scoring based on the regression coefficient (β) of indicators. Each level of the indicators will be given a specific score and the scores of each factor are added up to get the total point, which can be used to predict the probability of GDM occurrence.  Subjects’ baseline data involve systolic blood pressure (SBP, mmHg), diastolic blood pressure (DBP, mmHg), fasting plasma glucose (FPG, mmol/L), oral glucose tolerance test 1h plasma glucose (1hPG, mmol/L), oral glucose tolerance test 2h plasma glucose (2hPG, mmol/L), glycated hemoglobin (HbA1c, %), triglyceride (TG, mmol/L), total cholesterol (TC, mmol/L), high-density lipoprotein cholesterol (HDL-c, mmol/L), low-density lipoprotein cholesterol (LDL-c, mmol/L). The data of genetic polymorphism include rs4134819 C>T, rs720918 A>G, rs2034410 T>C, rs11109509 A>G, and rs12524768 G>A and their corresponding dominant and recessive genetic model.