Ticagrelor inhibits platelet aggregation and reduces inflammatory burden more than clopidogrel in patients with stages 4 or 5 chronic kidney disease
No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease (CKD). We conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation...
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Published in | Vascular pharmacology Vol. 148; p. 107143 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.02.2023
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Abstract | No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease (CKD).
We conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls (n = 26) with that of CKD in the ticagrelor-arm.
Average age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] (P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins (n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups.
We report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4–5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. (clinicaltrials.gov # NCT03649711).
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AbstractList | No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4-5 chronic kidney disease (CKD).BACKGROUNDNo study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4-5 chronic kidney disease (CKD).We conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls (n = 26) with that of CKD in the ticagrelor-arm.METHODSWe conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls (n = 26) with that of CKD in the ticagrelor-arm.Average age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] (P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins (n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups.RESULTSAverage age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] (P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins (n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups.We report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4-5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. (clinicaltrials.gov # NCT03649711).CONCLUSIONSWe report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4-5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. (clinicaltrials.gov # NCT03649711). No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease (CKD). We conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls (n = 26) with that of CKD in the ticagrelor-arm. Average age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] (P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins (n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups. We report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4–5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. (clinicaltrials.gov # NCT03649711). [Display omitted] No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4-5 chronic kidney disease (CKD). We conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls (n = 26) with that of CKD in the ticagrelor-arm. Average age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] (P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins (n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups. We report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4-5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. (clinicaltrials.gov # NCT03649711). AbstractBackgroundNo study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease (CKD). MethodsWe conducted a double-blind RCT to compare effects of ticagrelor and clopidogrel in 48 CKD, with the primary outcome of ADP-induced platelet aggregation (WBPA) after 2 weeks of DAPT. In a parallel arm, we compared effects of 2 weeks of ticagrelor plus aspirin on mean changes in WBPA and markers of thromboinflammation among non-CKD controls ( n = 26) with that of CKD in the ticagrelor-arm. ResultsAverage age of CKD was 53.7 years, with 62% women, 54% African American, and 42% with stage 5 CKD. Ticagrelor generated statistically lower WBPA values post treatment [median 0 Ω (IQR 0, 2)] vs. clopidogrel [median 0 Ω (IQR 0, 5)] ( P = 0.002); percent inhibition of WBPA was greater (87 ± 22% vs. 63 ± 50%; P = 0.04; and plasma IL-6 levels were much lower (8.42 ± 1.73 pg/ml vs. 18.48 ± 26.56 pg/ml; P = 0.04). No differences in mean changes in WBPA between CKD-ticagrelor and control groups were observed. Ticagrelor- DAPT reduced levels of IL-1α and IL-1β in CKD-ticagrelor and control groups, attenuated lowering of TNFα and TRAIL levels in CKD-ticagrelor (vs controls), and had global changes in correlation between various cytokines in a subgroup of CKD-ticagrelor subjects not on statins ( n = 10). Peak/trough levels of ticagrelor/metabolite were not different between CKD-ticagrelor and control groups. ConclusionsWe report significant differences in platelet aggregation and anti-inflammatory properties between ticagrelor- and clopidogrel-based DAPT in non-dialysis people with stage 4–5 CKD. These notable inflammatory responses suggest ticagrelor-based DAPT might lower inflammatory burden of asymptomatic patients with stage 4 or 5 CKD. ( clinicaltrials.gov # NCT03649711). |
ArticleNumber | 107143 |
Author | Corken, Adam Ware, Jerry Rahmatallah, Yasir Jain, Nishank Davis, Otis Arulprakash, Narenraj Hedayati, S. Susan Smyth, Susan Mehta, J.L. Arthur, John M. Dai, Junqiang Phadnis, Milind A. |
AuthorAffiliation | g Department of Bioinformatics, University of Arkansas for Medical Sciences, Little Rock, AR a Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR c Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR d Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR f Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS e Department of Neurology, University of Arkansas for Medical Sciences, Little Rock, AR h Department of Medicine, University of Texas Southwestern Medical Center, Dallas, TX b Central Arkansas Veterans Health Care System, Little Rock, AR |
AuthorAffiliation_xml | – name: h Department of Medicine, University of Texas Southwestern Medical Center, Dallas, TX – name: f Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS – name: a Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR – name: c Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR – name: e Department of Neurology, University of Arkansas for Medical Sciences, Little Rock, AR – name: b Central Arkansas Veterans Health Care System, Little Rock, AR – name: d Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR – name: g Department of Bioinformatics, University of Arkansas for Medical Sciences, Little Rock, AR |
Author_xml | – sequence: 1 givenname: Nishank surname: Jain fullname: Jain, Nishank email: njain2@uams.edu organization: Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 2 givenname: Adam surname: Corken fullname: Corken, Adam organization: Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 3 givenname: John M. surname: Arthur fullname: Arthur, John M. organization: Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 4 givenname: Jerry surname: Ware fullname: Ware, Jerry organization: Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 5 givenname: Narenraj surname: Arulprakash fullname: Arulprakash, Narenraj organization: Department of Neurology, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 6 givenname: Junqiang surname: Dai fullname: Dai, Junqiang organization: Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, United States of America – sequence: 7 givenname: Milind A. surname: Phadnis fullname: Phadnis, Milind A. organization: Department of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS, United States of America – sequence: 8 givenname: Otis surname: Davis fullname: Davis, Otis organization: Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 9 givenname: Yasir surname: Rahmatallah fullname: Rahmatallah, Yasir organization: Department of Bioinformatics, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 10 givenname: J.L. surname: Mehta fullname: Mehta, J.L. organization: Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America – sequence: 11 givenname: S. Susan surname: Hedayati fullname: Hedayati, S. Susan organization: Department of Medicine, University of Texas Southwestern Medical Center, Dallas, TX, United States of America – sequence: 12 givenname: Susan surname: Smyth fullname: Smyth, Susan organization: Department of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, United States of America |
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ContentType | Journal Article |
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Keywords | RCT CAD Chronic kidney disease Inflammation PLATO GSNCA ANCOVA SD GFR Clopidogrel Platelets Ticagrelor UACR CKD DAPT LCMS coronary artery disease dual antiplatelet therapy glomerular filtration rate gene sets net correlations analysis randomized controlled trial urine albumin-to-creatinine ratio liquid chromatography mass spectrometry Platelet Inhibition and Patient Outcomes analysis of covariance standard deviation |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Undefined-1 ObjectType-Feature-3 content type line 23 AUTHOR CONTRIBUTIONS JW, JMA, JLM, SSH, and NJ designed the study; AC and NJ carried out experiments; JD and MAP analyzed the data; NA assisted with data entry and performing literature searches; YR performed correlation analysis of cytokines data; NJ drafted and revised the manuscript; and SS provided critical expertise in reviewing and providing meaningful insights for the manuscript. All authors approved the final version of the manuscript. |
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Snippet | No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease (CKD).
We conducted... AbstractBackgroundNo study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4–5 chronic kidney disease... No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4-5 chronic kidney disease (CKD). We conducted... No study has compared pharmacologic properties of ticagrelor and clopidogrel in non-dialysis patients with stage 4-5 chronic kidney disease (CKD).BACKGROUNDNo... |
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StartPage | 107143 |
SubjectTerms | Adenosine Cardiovascular Chronic kidney disease Clopidogrel Clopidogrel - adverse effects Female Humans Inflammation Inflammation - diagnosis Inflammation - drug therapy Male Middle Aged Platelet Aggregation Platelet Aggregation Inhibitors - therapeutic use Platelets Renal Insufficiency, Chronic - diagnosis Renal Insufficiency, Chronic - drug therapy Thrombosis Ticagrelor Ticagrelor - adverse effects Ticlopidine - adverse effects Treatment Outcome |
Title | Ticagrelor inhibits platelet aggregation and reduces inflammatory burden more than clopidogrel in patients with stages 4 or 5 chronic kidney disease |
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