Why the study?
The association of several InDels and SNPs in LPL exon 1, intron 2, and intron 7 with lipid parameters and body mass index remains unclear.
Are LPL gene variants associated with BMI and lipid levels in a Kuwaiti population?
Are LPL gene variants associated with BMI and lipid levels in a Kuwaiti population?
Specific LPL gene variants are associated with increased BMI and altered lipid profiles in the Kuwaiti population, highlighting genetic contributors to obesity and dyslipidemia.
Answers are grounded in this paper and cite their sources.
Supports LPL variant links to BMI and lipids in Kuwaitis; leaves open clinical utility pending prospective validation.
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 (β = 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.
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Al‐Bustan et al. (2025) studied this question.
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