Cross-Ancestry DNA Methylation Marks of Insulin Resistance in Pregnancy: An Integrative Epigenome-Wide Association Study

• Published in: Diabetes (New York, N.Y.) Vol. 72; no. 3; pp. 415 - 426
• Main Authors: Fragoso-Bargas, Nicolas, Elliott, Hannah R, Lee-Ødegård, Sindre, Opsahl, Julia O, Sletner, Line, Jenum, Anne Karen, Drevon, Christian A, Qvigstad, Elisabeth, Moen, Gunn-Helen, Birkeland, Kåre I, Prasad, Rashmi B, Sommer, Christine
• Format: Journal Article
• Language: English
• Published: United States American Diabetes Association 01.03.2023
• Subjects: Basic Medicine; CpG Islands; DNA Methylation; Epigenesis, Genetic; Epigenetics; Epigenome; Female; Genetics/Genomes/Proteomics/Metabolomics; Genome-Wide Association Study; Humans; Insulin; Insulin resistance; Insulin Resistance - genetics; Leukocytes; Medical and Health Sciences; Medical Genetics; Medicin och hälsovetenskap; Medicinsk genetik; Medicinska och farmaceutiska grundvetenskaper; Peripheral blood; Phenotypes; Pregnancy; Quantitative trait loci
• ISSN: 0012-1797; 1939-327X; 1939-327X
• DOI: 10.2337/db22-0504

Although there are some epigenome-wide association studies (EWAS) of insulin resistance, for most of them authors did not replicate their findings, and most are focused on populations of European ancestry, limiting the generalizability. In the Epigenetics in Pregnancy (EPIPREG; n = 294 Europeans and 162 South Asians) study, we conducted an EWAS of insulin resistance in maternal peripheral blood leukocytes, with replication in the Born in Bradford (n = 879; n = 430 Europeans and 449 South Asians), Methyl Epigenome Network Association (MENA) (n = 320), and Botnia (n = 56) cohorts. In EPIPREG, we identified six CpG sites inversely associated with insulin resistance across ancestry, of which five were replicated in independent cohorts (cg02988288, cg19693031, and cg26974062 in TXNIP; cg06690548 in SLC7A11; and cg04861640 in ZSCAN26). From methylation quantitative trait loci analysis in EPIPREG, we identified gene variants related to all five replicated cross-ancestry CpG sites, which were associated with several cardiometabolic phenotypes. Mediation analyses suggested that the gene variants regulate insulin resistance through DNA methylation. To conclude, our cross-ancestry EWAS identified five CpG sites related to lower insulin resistance.