Heart Rate Recovery After Exercise and Its Relation With Neutrophil-To Ratio in Patients With Cardiac Syndrome X

dc.contributor.author Yurtdas, Mustafa
dc.contributor.author Yaylali, Yalin T.
dc.contributor.author Aladag, Nesim
dc.contributor.author Ozdemir, Mahmut
dc.contributor.author Ceylan, Yemlihan
dc.contributor.author Gencaslan, Murat
dc.contributor.author Akbulut, Tayyar
dc.date.accessioned 2025-05-10T17:42:45Z
dc.date.available 2025-05-10T17:42:45Z
dc.date.issued 2014
dc.description Yurtdas, Mustafa/0000-0002-0516-9206; Aladag, Nesim/0000-0003-2346-1152 en_US
dc.description.abstract Objectives The neutrophil-to-lymphocyte ratio (NLR) and the platelet-to-lymphocyte ratio (PLR) are measures of systemic inflammation. Heart rate recovery (HRR) after exercise is influenced by autonomic function. The aim of this study was to ascertain whether HRR and the Duke Treadmill Score (DTS) values are related to NLR and PLR in patients with cardiac syndrome X (CSX). Methods A total of 350 participants were enrolled in the study. Complete blood counts and high-sensitivity C-reactive protein (hsCRP) were obtained. All participants underwent an exercise test. HRR and DTS were calculated after exercise. Abnormal HRR was defined as 12 beats/min or less. Results CSX and coronary artery disease (CAD) groups had higher NLR, PLR, and hsCRP, and lower HRR and DTS values than the control group (for all, P<0.05). In both CSX and CAD groups, HRR was positively correlated with DTS (r=0.468, P<0.001 and r=0.491, P<0.001, respectively) and negatively correlated with NLR (r=-0.519, P<0.001 and r=-0.612, P<0.001, respectively), PLR (r=-0.422, P<0.001 and r=-0.438, P<0.001, respectively), and hsCRP (r=-0.553, P<0.001 and r=-0.521, P<0.001, respectively). NLR and hsCRP were important two predictors of the presence of lower HRR in both CSX [NLR: odds ratio (OR), 0.395; 95% confidence interval (CI), 0.168-0.925; P=0.032 and hsCRP: OR, 0.748; 95% CI, 0.591-0.945; P=0.015], and CAD groups (NLR: OR, 0.115; 95% CI, 0.026-0.501; P=0.004 and hsCRP: OR, 0.637; 95% CI, 0.455-0.892; P=0.009). Conclusion CSX patients have higher NLR and PLR and slower HRR and lower DTS, similar to CAD patients, suggesting that CSX patients may be at a higher risk for developing cardiovascular events in the future. NLR may predict autonomic imbalance assessed by HRR in CSX. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins. en_US
dc.identifier.doi 10.1097/MCA.0000000000000110
dc.identifier.issn 0954-6928
dc.identifier.issn 1473-5830
dc.identifier.uri https://doi.org/10.1097/MCA.0000000000000110
dc.identifier.uri https://hdl.handle.net/20.500.14720/15657
dc.language.iso en en_US
dc.publisher Lippincott Williams & Wilkins en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Atherosclerosis en_US
dc.subject Autonomic Function en_US
dc.subject Exercise en_US
dc.subject Inflammatory Markers en_US
dc.title Heart Rate Recovery After Exercise and Its Relation With Neutrophil-To Ratio in Patients With Cardiac Syndrome X en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Yurtdas, Mustafa/0000-0002-0516-9206
gdc.author.id Aladag, Nesim/0000-0003-2346-1152
gdc.author.wosid Ceylan, Yemlihan/Htn-6576-2023
gdc.author.wosid Yurtdaş, Mustafa/X-7179-2019
gdc.author.wosid Özdemi̇r, Mahmut/Ize-2330-2023
gdc.author.wosid Aladağ, Nesi̇m/Aac-1952-2021
gdc.author.wosid Yaylali, Yalin/Abi-4603-2020
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Yurtdas, Mustafa; Aladag, Nesim; Ozdemir, Mahmut; Ceylan, Yemlihan; Akbulut, Tayyar] Van Reg Training & Res Hosp, Dept Cardiol, TR-65100 Van, Turkey; [Gencaslan, Murat] Istanbul Hosp, Dept Cardiol, Van, Turkey; [Yaylali, Yalin T.] Pamukkale Univ, Sch Med, Dept Cardiol, Denizli, Turkey en_US
gdc.description.endpage 492 en_US
gdc.description.issue 6 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 485 en_US
gdc.description.volume 25 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.pmid 24642808
gdc.identifier.wos WOS:000340560300006
gdc.index.type WoS
gdc.index.type PubMed

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