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Polygenic scores link to atherosclerosis and ischemic heart disease in Russian populationsGenetic markers help predict heart disease risk for Russian men and women

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Key Takeaway
Note that polygenic scores link to atherosclerosis and ischemic heart disease in Russian populations.

This meta-analysis review synthesizes data on the link between polygenic scores and atherosclerosis, ischemic heart disease, and myocardial infarction within a Russian population. The study utilized a genetic architecture of lipid metabolism to identify relevant variants. The analysis incorporated 8,732 individuals from a GWAS sample and 3,954 from an additional sample to explore these associations. No specific adverse events or tolerability data were reported in this genetic profiling context.

Total cholesterol and LDL-C variants were found to be associated with variants located in the HMGCR, CERT1, POLK, ANKDD1B, APOC3, BCL3, CBLC, BCAM, NECTIN2, TOMM40, APOE, APOC1, APOC4, and SMARCA4 genes. Additionally, HDL-C variants were associated with variants located in the LPL, ALDH1A2, LIPC, and CETP genes. The direction of these associations was not reported in the source data.

Sex differences in genetic predictors were noted, as men and women differed in their genetic predictors of lipid levels. Variants in the SMARCA4 and LDLR genes were associated with cholesterol levels only in women. The practice relevance of this personalized polygenic profiling approach enables life-long CVD risk assessment. Limitations regarding causality and specific certainty notes were not reported by the authors.

Scientists looked at DNA from thousands of Russian people to find links between genes and heart health. They studied how certain gene changes affect total cholesterol, bad LDL cholesterol, and good HDL cholesterol levels. This helps understand why some people get heart disease while others do not.

The researchers found many gene spots connected to cholesterol. Some of these spots are in genes that the body uses to make or move fats around. Knowing which genes are active helps explain a person's natural risk for atherosclerosis and heart attacks.

Men and women had different genetic patterns for cholesterol. For example, some gene changes only raised cholesterol risk in women. This shows that heart disease risk is not the same for everyone and depends on sex.

Using these genetic profiles allows for better long-term health checks. Doctors can use this information to spot high-risk patients early and start prevention plans sooner.

What this means for you:
Genetic tests show different heart disease risks for men and women in this Russian population.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
ObjectiveElevated cholesterol levels are associated with the risk of the most socially significant cardiovascular diseases, such as atherosclerosis, ischemic heart disease, and myocardial infarction.MethodsIn this study, we sought to study the genetic architecture of lipid metabolism by conducting genome-wide association studies of total cholesterol, LDL-C, and HDL-C levels in a sample of the Russian population (n = 8,732) who were not carriers of variants linked to familial hypercholesterolemia and did not take lipid-regulating agents. Based on the detected associations and machine learning methods, several polygenic score models were constructed for each lipid type, and the link between polygenic scores and atherosclerosis, ischemic heart disease, and myocardial infarction was examined in an additional sample of patients diagnosed with either of these diseases (n = 3,954).ResultsA meta-analysis of the results of the conducted genome-wide association studies showed that total cholesterol and LDL-C were largely associated with the same variants located in the HMGCR, CERT1, POLK, ANKDD1B, APOC3, BCL3, CBLC, BCAM, NECTIN2, TOMM40, APOE, APOC1, APOC4, and SMARCA4 genes, while HDL-C was associated with variants located in the LPL, ALDH1A2, LIPC, and CETP genes. Men and women differed in genetic predictors of lipid levels, with variants in the SMARCA4 and LDLR genes associated with cholesterol levels only in women.ConclusionThe models developed in this study consider age and a modifiable factor, BMI. Therefore, the personalized polygenic profiling approach presented in this study enables life-long CVD risk assessment.
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