2008
DOI: 10.2337/db08-0250
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Response to Comment on: DiChiara et al. (2007) The Effect of Aspirin Dosing on Platelet Function in Diabetic and Nondiabetic Patients: An Analysis From the Aspirin-Induced Platelet Effect (ASPECT) Study: Diabetes 56:3014–3019, 2007

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Cited by 5 publications
(5 citation statements)
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“…57 More importantly, these dose-dependent effects were more pronounced in patients with diabetes, where treatment with higher doses was found to be effective in inhibiting platelet function. 58 Similar results reporting a low prevalence of aspirin resistance using COX-1-specific assays have been reported. 59 At the same time, further studies have found a correlation between adverse clinical events and aspirin resistance, as measured by PFA-100.…”
Section: Aspirin Resistance Is Assay-specificsupporting
confidence: 74%
“…57 More importantly, these dose-dependent effects were more pronounced in patients with diabetes, where treatment with higher doses was found to be effective in inhibiting platelet function. 58 Similar results reporting a low prevalence of aspirin resistance using COX-1-specific assays have been reported. 59 At the same time, further studies have found a correlation between adverse clinical events and aspirin resistance, as measured by PFA-100.…”
Section: Aspirin Resistance Is Assay-specificsupporting
confidence: 74%
“…These pathological mechanisms are not influenced by antiplatelet drugs, which may explain the lack of a protective effect of aspirin against ASCVD in this study population. Moreover, although patients with diabetes treated with low-dose aspirin exhibit aspirin resistance, higher doses can partially overcome the resistance 28 . Higher doses of aspirin may be necessary to prevent ASCVD in this study population.…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, higher doses (≥325 mg) of aspirin showed a reverse interaction with weight, reducing CV events only at larger body size and increased weights. Further confounding the results of many studies, both obesity and diabetes may affect an individual’s response to aspirin, 22–24 and the enteric-coat of some aspirin formulations, which reduces gastrointestinal protection and impairs consistent absorption of the drug. 25–27…”
Section: Strategies and Evidencementioning
confidence: 99%