Application of genetic risk score for in-stent restenosis of second- and third-generation drug-eluting stents in geriatric patients

BMC Geriatr. 2023 Jul 19;23(1):443. doi: 10.1186/s12877-023-04103-w.

Abstract

Background: The second-and third-generation drug-eluting stents (DESs) in-stent restenosis (ISR) genetic risk score (GRS) model has been previously validated. However, the model has not been validated in geriatric patients. Therefore, we conducted this study to test the feasibility of the DES-ISR GRS model in geriatric patients with coronary artery disease (CAD) in Taiwan.

Methods: We conducted a retrospective, single-center cohort study and included geriatric patients (age ≥ 65 years) with CAD and second-or third-generation DES(s) deployment. Patients undergoing maintenance dialysis were excluded. ISR was defined as ≥ 50% luminal narrowing on the follow-up coronary arteriography. The DES-ISR GRS model included five selected exonic single-nucleotide polymorphisms (SNPs): CAMLG, GALNT2, C11orf84, THOC5, and SAMD11. The GRS was defined as the sum of the five selected SNPs for the risk allele.

Results: We enrolled 298 geriatric patients from January 2010 and December 2019 in this study. After propensity score matching, there were 192 geriatric patients with CAD in the final analysis, of which 32 patients had ISR. Patients were divided into two groups based on their GRS values: low (0-2) and high (≥ 3) GRS. A high GRS was significantly associated with DES-ISR in geriatric patients.

Conclusion: Those geriatric patients with a high GRS had significantly higher second-or third-generation DES ISR rates. The five SNP-derived DES-ISR GRS model could provide genetic information for interventional cardiologists to treat geriatric patients with CAD.

Trial registration: The primary study protocol was registered with clinicaltrials.org. with registration number: NCT03877614; on March 15, 2019. ( http://clinicaltrials.gov/ct2/show/NCT03877614 ).

Keywords: Drug-eluting stent; Genetic risk score; Geriatric patients; In-stent restenosis; Single nucleotide polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cohort Studies
  • Coronary Artery Disease* / diagnostic imaging
  • Coronary Artery Disease* / genetics
  • Coronary Artery Disease* / therapy
  • Coronary Restenosis* / therapy
  • Drug-Eluting Stents*
  • Humans
  • Nuclear Proteins
  • Retrospective Studies
  • Risk Factors
  • Treatment Outcome

Substances

  • THOC5 protein, human
  • Nuclear Proteins

Associated data

  • ClinicalTrials.gov/NCT03877614