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May 29, 2015Cardiovascular Diabetology26 citationsOpen Access

Diabetes mellitus and platelet reactivity in patients under prasugrel or ticagrelor treatment: an observational study

DADimitrios AlexopoulosCVChrysoula VogiatziKSKaterina Stavrou

Key Result

Ticagrelor treatment was associated with a 58% decrease in platelet reactivity compared to prasugrel, while insulin-treated diabetes mellitus was associated with a 30% increase compared to non-diabetic patients.

Study Design

Type

Cross-Sectional (n=777)

Multicenter

No

Structured PICO

Does ticagrelor compared to prasugrel reduce platelet reactivity in patients with acute coronary syndrome undergoing PCI, and how does diabetes mellitus status affect this?

P
Population
777 consecutive patients with acute coronary syndrome undergoing percutaneous coronary intervention, discharged on prasugrel or ticagrelor, with platelet function assessed at one month.
E
Exposure
Ticagrelor 90 mg oral twice daily
C
Comparator
Prasugrel 10 mg oral once daily
O
Outcome
Platelet reactivity assessed using the VerifyNow P2Y12 function assay (in PRU) at one month post interventionsurrogate

Ticagrelor provides stronger and more consistent platelet inhibition than prasugrel in ACS patients post-PCI, independent of diabetes status, whereas prasugrel's efficacy is attenuated in insulin-treated diabetic patients.

Main Result

Effect estimate: 58% decrease in PR (ticagrelor vs prasugrel)

p-value: p=<0.001

Limitations

  • Cross-sectional study of independent groups (nonrandomized)
  • HbA1C levels were not measured
  • Genetic variants of the insulin receptor substrate were not analyzed
  • Narrow dynamic range of the VerifyNow assay
  • Nonrandomized cross-sectional design
  • HbA1C levels not measured
  • Genetic variants of the insulin receptor substrate not analyzed
  • Small sample size

Abstract

BACKGROUND: The influence of diabetes mellitus (DM) on platelet reactivity (PR) in prasugrel or ticagrelor treated patients is not well studied. METHODS: In an observational study involving 777 patients with acute coronary syndrome undergoing percutaneous coronary intervention treated by either prasugrel 10 mg od (n = 315) or ticagrelor 90 mg bid (n = 462), platelet function was assessed using the VerifyNow P2Y12 function assay (in PRU) at one month post intrvention. RESULTS: In the overall population, ticagrelor and insulin-treated DM affected PR, with a decrease in log by 0.88 (corresponding to a 58 % decrease in PR) compared to prasugrel-treated patients (p < 0.001), and an increase in log by 0.26 (corresponding to a 30 % increase in PR) compared to non-diabetic patients (p = 0.01), respectively. PR in prasugrel-treated patients differed significantly by DM status: 70.0 (36.3-113.0) in non-diabetic vs 69.0 (44.5-115.3) in non insulin-treated diabetic vs 122.0 (69.0-161.0) in insulin-treated diabetic patients, p for trend = 0.01. No differences were observed in ticagrelor-treated patients. By multivariate analysis, in prasugrel-treated patients insulin-treated DM was the only factor predicting PR, with log of PR increased by 0.42 (corresponding to a 52 % increase in PR) compared to non-diabetic patients (p = 0.001). No factor was found to affect PR in ticagrelor-treated patients. CONCLUSIONS: Patients with insulin-treated DM treated with prasugrel post PCI have higher PR, than patients without DM or non insulin-treated diabetic patients treated with this drug. Ticagrelor treated patients have overall lower PR than patients on prasugrel, independent of DM status or insulin treatment. TRIAL REGISTRATION: Clinical Trials Gov. NCT01774955.

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Cite This Study

Alexopoulos et al. (2015) conducted a cross-sectional in Acute coronary syndrome (n=777). Ticagrelor and insulin-treated diabetes mellitus vs. Prasugrel and non-diabetic status was evaluated on Platelet reactivity (PRU) at 1 month (58% decrease in PR (ticagrelor vs prasugrel), p=<0.001). Ticagrelor treatment was associated with a 58% decrease in platelet reactivity compared to prasugrel, while insulin-treated diabetes mellitus was associated with a 30% increase compared to non-diabetic patients.

synapsesocial.com/papers/6a884dfe2c11edba2ecf1e8bhttps://doi.org/10.1186/s12933-015-0232-1
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