Key result
High LPL genetic risk score is linked to lower HDL, higher triglycerides, and increased systolic BP.
Why the study?
Associations between Lipoprotein Lipase gene variations and cardiometabolic disease-related markers remained underexplored in Arab Qatari populations.
Is a high Lipoprotein Lipase genetic risk score associated with adverse cardiometabolic risk indicators in healthy Qatari adults?
Is a high Lipoprotein Lipase genetic risk score associated with adverse cardiometabolic risk indicators in healthy Qatari adults?
A high LPL genetic risk score is associated with unfavorable cardiometabolic markers, such as lower HDL-C, higher triglycerides, and higher systolic blood pressure, in a healthy Qatari population.
Should not yet change practice in healthy adults; extends LPL associations to Qataris but leaves causal and prognostic implications open.
Genetic variations within the Lipoprotein Lipase ( LPL) gene have been shown to influence the risk of cardiometabolic diseases. However, their associations with cardiometabolic disease-related markers remain underexplored in Arab Qatari populations. Hence, we examined the association between a genetic risk score (GRS) based on three LPL single nucleotide polymorphisms (SNPs) and cardiometabolic indicators in a healthy Qatari population. A cross-sectional genetic association study was conducted using data from the Qatar Biobank population-based cohort, involving a sample of metabolically healthy Qatari adults (n = 6,919). The LPL- GRS was computed as the unweighted sum of risk alleles from three LPL SNPs: rs295 (C/A), rs301 (C/T), and rs320 (G/T). Associations between the GRS and metabolic markers were assessed using a generalized linear model, adjusting for age, sex, and body mass index. Individuals with high GRS (>5 risk alleles) showed a significant association with lower fat-free mass index values (β = −0.064, p = 0.029). In addition, a positive association was observed between GRS and fasting insulin levels (β = 0.035, p = 0.016). In addition, high GRS was significantly associated with lower high-density lipoprotein cholesterol (β = −0.025, p = 0.001) and higher triacylglycerol concentrations (β = 0.027, p = 0.0003) and systolic blood pressure (β = 0.007, p = 0.002), respectively. Our study shows that the LPL -GRS is associated with key cardiometabolic risk factors in this self-reported healthy Qatari population. These findings highlight the need for additional research to replicate these findings in independent and ethnically diverse cohorts, as well as the use of longitudinal studies to evaluate the predictive value of the GRS for future metabolic outcomes.
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AlAnazi et al. (2026) studied this question. High LPL genetic risk score (>5 alleles) in healthy Qataris is linked to lower fat-free mass, higher fasting insulin, lower HDL, higher triglycerides, and increased systolic BP.
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