Novel loci for triglyceride/HDL-C ratio longitudinal change among subjects without T2D
2024

Genetic Factors Influencing Triglyceride/HDL-C Ratio Changes

Sample size: 1384 publication 10 minutes Evidence: high

Author Information

Author(s): Wang Lihua, Wang Siyu, Anema Jason A., Moghaddam Vaha A., Lu Yanli, Lin Shiow, Daw E. Warwick, Kuipers Allison L., Miljkovic Iva, Brent Michael, Patti Gary J., Thygarajan Bharat, Zmuda Joseph M., Province Michael A., An Ping

Primary Institution: Washington University School of Medicine

Hypothesis

What are the genetic variants that regulate the longitudinal change of triglyceride/HDL-C ratio in nondiabetic individuals?

Conclusion

The study identified novel genetic variants associated with changes in triglyceride/HDL-C ratio, providing insights into insulin resistance mechanisms.

Supporting Evidence

  • The study identified a significant locus at the LPL gene associated with triglyceride/HDL-C ratio changes.
  • Two novel variants were found that explain a significant portion of the genetic linkage for triglyceride/HDL-C ratio.
  • Replication in the Framingham Heart Study showed modest effects of the identified loci on triglyceride/HDL-C ratio changes.

Takeaway

Researchers found new genes that can help predict changes in fat levels in the blood, which can show if someone is at risk for diabetes.

Methodology

The study used genome-wide association study (GWAS) and genome-wide linkage scan (GWLS) to analyze genetic data from a family-based cohort.

Potential Biases

Selection bias may exist due to the study's focus on exceptionally long-lived families.

Limitations

The study's findings may not be generalizable beyond European descent, and lifestyle factors influencing insulin resistance were not accounted for.

Participant Demographics

Participants were predominantly of European descent, with a mean age of 61.9 years and 59.3% female.

Statistical Information

P-Value

1.58e-9

Statistical Significance

p<5e-8

Digital Object Identifier (DOI)

10.1016/j.jlr.2024.100702

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