| Title : Association of Lipoprotein Lipase (LPL) Variants rs8176337, rs303, and rs304 with Body Mass Index and Total Cholesterol - Al-Bustan_2025_Int.J.Mol.Sci_26_ |
| Author(s) : Al-Bustan SA , Al-Serri AE , Al-Adsani AM , Miranda L , Annice BG , Hamdan H , Alnaqeeb MA |
| Ref : Int J Mol Sci , 26 : , 2025 |
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Abstract :
Several single-nucleotide polymorphisms (SNPs) across the lipoprotein lipase (LPL) gene have been found to be associated with dyslipidemia and obesity. Several InDels and SNPs in exon 1, intron 2, and intron 7 have been reported; however, their association with lipid parameters and body mass index (BMI) remains unclear. Here, we aimed to investigate the relationship among LPL variants, lipid levels, and BMI in a Kuwaiti population. Sanger sequencing was performed on three targeted regions of the LPL gene. Based on the minor allele frequency, Hardy-Weinberg equilibrium, and linkage disequilibrium, five SNPs were selected and genotyped in a cohort of 688 Kuwaiti samples to investigate their association with lipid levels and BMI. A total of 30 variants (6 InDels and 24 SNPs) were identified; of them, 5 SNPs (rs1800590, rs74377536, rs8176337, rs303, and rs304) were selected for their association with BMI and lipid levels. The G-allele of rs8176337 was found to be associated with increased BMI (beta = 1.41; 95% confidence interval = 0.22-2.60; p = 0.02). In addition, an association was observed for rs303 and rs304 with both cholesterol and LDL (p < 0.05). Overall, our results demonstrate an association between LPL variants and lipid levels, and the observed association between rs8176337 and BMI was novel. |
| PubMedSearch : Al-Bustan_2025_Int.J.Mol.Sci_26_ |
| PubMedID: 40806414 |
| Gene_locus related to this paper: human-LPL |
| Gene_locus | human-LPL |
Al-Bustan SA, Al-Serri AE, Al-Adsani AM, Miranda L, Annice BG, Hamdan H, Alnaqeeb MA (2025)
Association of Lipoprotein Lipase (LPL) Variants rs8176337, rs303, and rs304 with Body Mass Index and Total Cholesterol
Int J Mol Sci
26 :
Al-Bustan SA, Al-Serri AE, Al-Adsani AM, Miranda L, Annice BG, Hamdan H, Alnaqeeb MA (2025)
Int J Mol Sci
26 :