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Mendelian Randomization Study on hs-CRP and Dyslipidemia in Koreans: Identification of Novel SNP rs76400217
Ximei Huang1, Youngmin Han2, Minjoo Kim1
1Department of Food and Nutrition, College of Life Science and Nano Technology, Hannam University, Daejeon 34054, Republic of Korea.
Insights
High-sensitivity C-reactive protein (hs-CRP) is linked to dyslipidemia, but this study found no causal relationship. The association may stem from other factors, not direct causation, in the Korean population.
Area of Science:
- Biochemistry
- Genetics
- Epidemiology
Background:
- High-sensitivity C-reactive protein (hs-CRP) indicates systemic inflammation.
- hs-CRP is associated with dyslipidemia, but causality is unclear.
Purpose of the Study:
- To investigate the association between hs-CRP and dyslipidemia.
- To explore potential causal links using Mendelian randomization (MR).
Main Methods:
- Nested case-control study with 1174 participants.
- Genome-wide association study (GWAS) identified rs76400217 as an instrumental variable (IV).
- Logistic regression and MR analysis (2SLS method) were employed.
Main Results:
- Logistic regression showed a significant association between hs-CRP and dyslipidemia (OR 2.08).
- This association persisted after adjusting for confounders.
- MR analysis using rs76400217 did not find a statistically significant causal relationship.
Conclusions:
- No evidence of a causal relationship between hs-CRP and dyslipidemia risk in the Korean population.
- The observed association is likely due to confounding factors rather than direct causation.
Abstract:
High-sensitivity C-reactive protein (hs-CRP) is a marker of systemic inflammation and is associated with developing dyslipidemia. However, the causality between hs-CRP and dyslipidemia remains unresolved. This study aimed to investigate the relationship between hs-CRP concentrations and dyslipidemia and to explore the potential causal link using Mendelian randomization (MR) analysis. A nested case-control study was conducted with 1174 participants, and genotype data were analyzed using the Korean Chip. A genome-wide association study (GWAS) identified rs76400217 as a suitable instrumental variable (IV) due to its significant association with hs-CRP (p < 10-8). Logistic regression models, adjusted for confounders, were used to evaluate the association between hs-CRP and dyslipidemia. An MR analysis was performed using a two-stage least squares (2SLS) method, with rs76400217 as the IV to assess causality. Logistic regression showed a significant association between hs-CRP concentrations and dyslipidemia (OR 2.08, 95% CI: 1.81-2.39, p < 0.001). This association remained significant after adjusting for factors such as age, sex, alcohol consumption, and BMI. The MR analysis using rs76400217 as the IV confirmed the strong associations with hs-CRP concentrations (p < 0.001) in all models, but the causality between hs-CRP and dyslipidemia was not statistically significant. Thus, no evidence of a causal relationship between hs-CRP and the risk of dyslipidemia was found in the Korean population. The strong association observed between hs-CRP and dyslipidemia may be due to other contributing factors rather than a direct cause.
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