Genetics
A Polynesian-specific SLC22A3 gene variant lowers Lp(a) independent of apo(a) isoform size in 302 Māori and Pacific men (Biosci Rep 2024)
Original title: A Polynesian-specific SLC22A3 variant associates with low plasma lipoprotein(a) concentrations independent of apo(a) isoform size in males
This study investigated a Polynesian-specific SLC22A3 gene coding variant (p.Thr44Met, rs8187715) in 302 healthy Māori and Pacific men, using an apo(a)-size-independent assay to measure plasma Lp(a). Metabolic and blood lipid variables were similar between variant carriers and non-carriers after adjusting for age, ethnicity and BMI, but carriers of the rs8187715 variant had significantly lower median Lp(a) (7.60 nmol/L, interquartile range 5.50-12.10) than non-carriers (10.60 nmol/L, interquartile range 5.40-41.00, P < 0.05). Lp(a) concentration inversely correlated with apo(a) isoform size, and the association between the SLC22A3 variant and lower Lp(a) remained significant even after correcting for apo(a) isoform size, metabolic parameters, and ethnicity. This is the first study to identify this gene variant's association with lower Lp(a), providing evidence to support ethnicity-specific cutoffs for defining elevated Lp(a) in Polynesian populations.
Original abstract
Lipoprotein(a) (Lp(a)) is a low-density lipoprotein (LDL)-like particle in which the apolipoprotein B component is covalently linked to apolipoprotein(a) (apo(a)). Lp(a) is a well-established independent risk factor for cardiovascular diseases. Plasma Lp(a) concentrations vary enormously between individuals and ethnic groups. Several nucleotide polymorphisms in the SLC22A3 gene associate with Lp(a) concentration in people of different ethnicities. We investigated the association of a Polynesian-specific (Māori and Pacific peoples) SLC22A3 gene coding variant p.Thr44Met) with the plasma concentration of Lp(a) in a cohort of 302 healthy Polynesian males. An apo(a)-size independent assay assessed plasma Lp(a) concentrations; all other lipid and apolipoprotein concentrations were measured using standard laboratory techniques. Quantitative real-time polymerase chain reaction was used to determine apo(a) isoforms. The range of metabolic (HbA1c, blood pressure, and blood lipids) and blood lipid variables were similar between the non-carriers and carriers in age, ethnicity and BMI adjusted models. However, rs8187715 SLC22A3 variant was significantly associated with lower Lp(a) concentrations. Median Lp(a) concentration was 10.60 nmol/L (IQR: 5.40-41.00) in non-carrier group, and was 7.60 nmol/L (IQR: 5.50-12.10) in variant carrier group (P<0.05). Lp(a) concentration inversely correlated with apo(a) isoform size. After correction for apo(a) isoform size, metabolic parameters and ethnicity, the association between the SLC22A3 variant and plasma Lp(a) concentration remained. The present study is the first to identify the association of this gene variant and low plasma Lp(a) concentrations. This provides evidence for better guidance on ethnic specific cut-offs when defining 'elevated' and 'normal' plasma Lp(a) concentrations in clinical applications.
Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.