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- Title
GALNT2 rs4846914 SNP Is Associated with Obesity, Atherogenic Lipid Traits, and ANGPTL3 Plasma Level.
- Authors
Qaddoumi, Mohammad; Hebbar, Prashantha; Abu-Farha, Mohamed; Al Somaly, Aseelah; Melhem, Motasem; Al-Kayal, Fadi; AlKhairi, Irina; Cherian, Preethi; Alanbaei, Muath; Al-Mulla, Fahd; Abubaker, Jehad; Thanaraj, Thangavel Alphonse
- Abstract
N-Acetylgalactosaminyltransferase 2 (GALNT2) is associated with serum lipid levels, insulin resistance, and adipogenesis. Additionally, angiopoietin-like (ANGPTL) proteins have emerged as regulators of lipoprotein lipase and lipid metabolism. In this study, we evaluated the association between GALNT2 rs4846914 variant, known for its association with lipid levels in European cohorts, with plasma levels of ANGPTL proteins, apolipoproteins, lipids, and obesity traits in individuals of Arab ethnicity. GALNT2 rs4846914 was genotyped in a cohort of 278 Arab individuals from Kuwait. Plasma levels of ANGPTL3 and ANGPTL8 were measured by ELISA and apolipoproteins by Luminex multiplexing assay. Allele-based association tests were performed with Bonferroni-corrected p-value thresholds. The GALNT2 rs4846914_G allele was associated with increased ANGPTL3 (p-values ≤ 0.05) but not with ANGPTL8 plasma levels. The allele was associated significantly with higher BMI and weight (p-values < 0.003), increased ApoC1 levels (p-values ≤ 0.006), and reduced HDL levels (p-values ≤ 0.05). Individuals carrying the GG genotype showed significantly decreased HDL and increased BMI, WC, ApoC1, and TG. Interactions exist between (AG+GG) genotypes and measures of percentage body fat, ApoA1A, ApoC1, and ApoB48-mediated HDL levels. GALNT2 is confirmed further as a potential link connecting lipid metabolism and obesity and has the potential to be a drug target for treating obesity and dyslipidemia.
- Subjects
KUWAIT; LIPID metabolism; FAT; BLOOD lipids; LIPOPROTEIN lipase; SINGLE nucleotide polymorphisms; LIPIDS
- Publication
Genes, 2022, Vol 13, Issue 7, p1201
- ISSN
2073-4425
- Publication type
Article
- DOI
10.3390/genes13071201