Neutrophil to Lymphocyte Ratio and Long-Term Cardiovascular Outcomes in Coronary Artery Disease Patients with Low High-Sensitivity C-Reactive Protein Level.


Journal

International heart journal
ISSN: 1349-3299
Titre abrégé: Int Heart J
Pays: Japan
ID NLM: 101244240

Informations de publication

Date de publication:
30 May 2020
Historique:
pubmed: 19 5 2020
medline: 6 6 2020
entrez: 19 5 2020
Statut: ppublish

Résumé

Although an elevated neutrophil to lymphocyte ratio (NLR) has been associated with the adverse outcomes of coronary artery disease (CAD), less is known about its prognostic value among patients with low high-sensitivity C-reactive protein (hs-CRP) levels. We enrolled 2,591 consecutive patients with stable CAD who underwent elective percutaneous coronary intervention (PCI) and had available data on preprocedural hs-CRP and NLR between 2000 and 2016. Of these patients, 1,951 with low-grade hs-CRP levels (< 2.0 mg/L) were divided into quartiles based on the NLR values. The primary endpoint was a composite of cardiovascular death, nonfatal myocardial infarction, and nonfatal stroke after the index PCI. Clinical follow-up data were obtained up to 5 years. The median NLR was 1.9 (interquartile range: 1.5-2.5). During the follow-up, 102 events occurred (5.2%), with a cumulative incidence that was significantly higher in the highest NLR group than in the other groups (log-rank, P = 0.02). After adjusting for the other cardiovascular risk factors, the risk for the primary endpoint was significantly higher for the highest than in the lowest NLR group (HR 1.97, 95% CI 1.09-3.54, P = 0.02). Increasing NLR as a continuous variable was associated with the incidence of adverse cardiovascular events (HR 1.85 per log 1 NLR increase, 95% CI 1.19-2.88, P = 0.007). In conclusion, the adverse long-term clinical outcomes of CAD patients with low-grade hs-CRP levels has been independently predicted by increased NLR level. NLR could be useful for risk stratification of CAD patients with increased inflammatory marker levels.

Identifiants

pubmed: 32418963
doi: 10.1536/ihj.19-543
doi:

Substances chimiques

C-Reactive Protein 9007-41-4

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

447-453

Auteurs

Hideki Wada (H)

Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital.

Tomotaka Dohi (T)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Katsumi Miyauchi (K)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Ryota Nishio (R)

Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital.

Mitsuhiro Takeuchi (M)

Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital.

Norihito Takahashi (N)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Hirohisa Endo (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Manabu Ogita (M)

Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital.

Hiroshi Iwata (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Takatoshi Kasai (T)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Shinya Okazaki (S)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Kikuo Isoda (K)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

Satoru Suwa (S)

Department of Cardiovascular Medicine, Juntendo University Shizuoka Hospital.

Hiroyuki Daida (H)

Department of Cardiovascular Medicine, Juntendo University Graduate School of Medicine.

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Classifications MeSH