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Updated: Jan 22, 2026

Genetically-encoded Molecular Probes to Study G Protein-coupled Receptors
Published on: September 13, 2013
Gender difference and genetic variance in lipoprotein receptor-related protein 1 is associated with mortality
Urban Alehagen1, Dick Wågsäter2
1Division of Cardiovascular Medicine, Faculty of Medicine and Health Sciences, Linköping University, SE-581 85 Linköping, Sweden.
Insights
Genetic variations in the lipoprotein receptor-related protein 1 (LRP1) gene are linked to cardiovascular disease risk. Specific LRP1 genotypes significantly increase mortality risk in elderly women, highlighting potential gender-specific cardiovascular prevention strategies.
Area of Science:
- Genetics
- Cardiology
- Epidemiology
Background:
- Cardiovascular diseases (CVDs) pose a significant health burden.
- Genetic associations, particularly single nucleotide polymorphisms (SNPs), are implicated in CVDs.
- Lipoprotein receptor-related protein 1 (LRP1) has been linked to coronary artery disease.
Purpose of the Study:
- To investigate the association between LRP1 gene genotypes and all-cause and cardiovascular mortality.
- To explore potential gender-specific differences in this association.
Main Methods:
- A cohort of 489 elderly community-living individuals was studied.
- Participants underwent clinical examination, echocardiography, and blood sampling for LRP1 (rs1466535) SNP analysis (T/T, C/T, C/C genotypes).
- Follow-up was conducted for 6.7 years, recording all-cause and cardiovascular deaths.
Main Results:
- A total of 116 (24%) all-cause deaths and 75 (15%) cardiovascular deaths occurred.
- In females, LRP1 T/T or C/T genotypes were associated with a 5.6-fold increased risk of cardiovascular mortality and a 2.8-fold increased risk of all-cause mortality compared to the C/C genotype.
- No significant genotype-related mortality differences were observed in the male population.
Conclusions:
- Significant gender differences exist in mortality risk associated with LRP1 genotypes.
- Females with LRP1 T/T or C/T genotypes face a substantially higher risk of all-cause and cardiovascular mortality.
- These findings suggest the need for individualized cardiovascular prevention and treatment strategies, though further research is warranted due to the study's small size.
Abstract:
Cardiovascular diseases are an important health resource problem and studies have shown a genetic association between single nucleotide polymorphisms (SNPs) and cardiovascular diseases. According to the literature, lipoprotein receptor-related protein 1 (LRP1) is associated with coronary artery disease. The aim of the present study was to evaluate a possible association between different genotypes of LRP1 and all-cause and cardiovascular mortality from a gender perspective. In the present study, 489 elderly community-living people were invited to participate. Clinical examination, echocardiography and blood sampling including SNP analyses of LRP1 (rs1466535) were performed, including the T/T, C/T and C/C genotypes, and the participants were followed for 6.7 years. During the follow-up period, 116 (24%) all-cause and 75 (15%) cardiovascular deaths were registered. In the female population, the LRP1 of the T/T or C/T genotype exhibited a 5.6-fold increased risk of cardiovascular mortality and a 2.8-fold increased risk of all-cause mortality compared with the C/C genotype. No such genotype differences could be seen in the male population. Gender differences could be seen regarding the risk of mortality in the different genotypes. Females with the LRP1 T/T or C/T genotypes exhibited a significantly increased risk of both all-cause and cardiovascular mortality compared with the C/C genotypes. Therefore, more individualized cardiovascular prevention and treatment should be prioritized. However, since this was a small study, the observations should only be regarded as hypothesis-generating.
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