Copyright: ©Author(s) 2026.
World J Diabetes. Mar 15, 2026; 17(3): 113947
Published online Mar 15, 2026. doi: 10.4239/wjd.v17.i3.113947
Published online Mar 15, 2026. doi: 10.4239/wjd.v17.i3.113947
Figure 2 Mendelian randomization analysis reveals a causal relationship between decreased solute carrier family 30 member 8 expression and higher risk of type 2 diabetes.
A: The quantitative trait loci data from East Asian populations and genome wide association study for type 2 diabetes as the outcome are used for Mendelian randomization analysis; B: The multiple Mendelian randomization methods are implemented using solute carrier family 30 member 8 expression as the exposure and type 2 diabetes as the outcome; C-E: Each instrumental variable’s contribution is assessed to the inverse variance weighted method. GWAS: Genome wide association study; SNP: Single nucleotide polymorphisms; QTL: Quantitative trait loci; SLC30A8: Solute carrier family 30 member 8; MR: Mendelian randomization; LD: Linkage disequilibrium; OR: Odds ratio; CI: Confidence interval.
- Citation: Li N, Li YP, Xu Q, Xu J, Yu YH, Su J, Shen C, Yu JY, Gu HF. SLC30A8 promoter hypermethylation is associated with type 2 diabetes and diabetic kidney disease in a Chinese population. World J Diabetes 2026; 17(3): 113947
- URL: https://www.wjgnet.com/1948-9358/full/v17/i3/113947.htm
- DOI: https://dx.doi.org/10.4239/wjd.v17.i3.113947