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Genome-wide association study of medication adherence in chronic diseases in the korean population
Incheol Seo1, Seong-Il Suh1, Min-Ho Suh1
1Department of Microbiology, Keimyung University School of Medicine, Daegu 704-701, Korea.
Insights
Medication adherence, crucial for chronic disease management, shows genetic links. A genome-wide study found suggestive associations near the GCC1 gene, potentially influencing adherence behavior.
Area of Science:
- Genetics
- Pharmacology
- Behavioral Science
Background:
- Medication adherence is vital for managing chronic diseases like hypertension and diabetes, yet non-adherence rates average 50%.
- Understanding the genetic underpinnings of medication adherence can inform strategies to improve patient outcomes.
- Previous research has linked decision-making capabilities to genetic factors in substance abuse.
Purpose of the Study:
- To investigate the genetic basis of medication adherence in patients with chronic diseases.
- To identify single nucleotide polymorphisms (SNPs) associated with medication adherence using a genome-wide association study (GWAS).
Main Methods:
- A genome-wide association study (GWAS) was performed on data from the Korean Association Resource project.
- The study included 235 medication non-adherents and 1,067 medication adherents with hypertension or diabetes, based on self-reported adherence.
- Statistical analyses identified SNPs associated with medication adherence.
Main Results:
- Four SNPs showed suggestive genome-wide associations with medication adherence.
- The most significant SNP, rs6978712, located near the GCC1 gene, was identified (p = 4.87 × 10(-7)).
- Three loci, including rs6978712 and two in strong linkage disequilibrium, showed potential association with adherence behavior, possibly related to decision-making.
Conclusions:
- Genetic factors, particularly those near the GCC1 gene, may play a role in medication adherence behavior.
- Further research is warranted to explore the association between GCC1 gene loci and medication adherence.
- Standardized phenotype criteria for self-reported adherence are needed for future replication studies.
Abstract:
Medication adherence is generally defined as the extent of voluntary cooperation of a patient in taking medicine as prescribed. Adherence to long-term treatment with chronic disease is essential for reducing disease comorbidity and mortality. However, medication non-adherence in chronic disease averages 50%. This study was conducted a genome-wide association study to identify the genetic basis of medication adherence. A total of 235 medication non-adherents and 1,067 medication adherents with hypertension or diabetes were used from the Korean Association Resource project data according to the self-reported treatment status of each chronic disease, respectively. We identified four single nucleotide polymorphisms with suggestive genome-wide association. The most significant single nucleotide polymorphism was rs6978712 (chromosome 7, p = 4.87 × 10(-7)), which is located proximal to the GCC1 gene, which was previously implicated in decision-making capability in drug abusers. Two suggestive single nucleotide polymorphisms were in strong linkage disequilibrium (r(2) > 0.8) with rs6978712. Thus, in the aspect of decision-making in adherence behavior, the association between medication adherence and three loci proximal to the GCC1 gene seems worthy of further research. However, to overcome a few limitations in this study, defining the standardized phenotype criteria for self-reported adherence should be performed before replicating association studies.
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