Clinical utility of blood neutrophil-lymphocyte ratio in Japanese COPD patients

BMC Pulm Med. 2018 May 2;18(1):65. doi: 10.1186/s12890-018-0639-z.

Abstract

Background: Neutrophil-to-lymphocyte ratio (NLR) is a biomarker of inflammation in chronic obstructive pulmonary disease (COPD) patients. But, a meaningful threshold and the longitudinal changes are unknown. We aimed to investigate the association between NLR and the clinical characteristics of COPD patients and to determine a meaningful threshold and the longitudinal changes for NLR.

Methods: Keio University and its affiliate hospitals conducted an observational COPD cohort study over 3 years. We performed a blood examination and a pulmonary function test. Blood examination was completed at baseline and annually thereafter, at a time when the disease was stable. Two hundred seventy-four patients who had at least 3 blood examinations over 3 years were included.

Results: Baseline NLR was correlated with baseline C-reactive protein (CRP) (r = 0.18, p = 0.003) and SAA (r = 0.34, p < 0.001). We defined an NLR score of 2.7 as the arbitrary cut-off value based on upper quartile points. COPD patients with NLR ≥ 2.7 were older (p = 0.037), had a lower BMI (p = 0.005) and a lower %FEV1 (p = 0.0003) compared to patients with NLR < 2.7. Receiver-operating-characteristic (ROC) curves showed the optimal cutoff for the baseline NLR in the predicting moderate/severe exacerbation to be 2.7, which was same as the upper quartile points. Follow-up analysis over 3 years revealed that the differences in the trends of NLR among the three groups based on the categories of exacerbations (moderate or severe, mild, no exacerbation) were significant (p = 0.006).

Conclusions: NLR is associated with COPD severity and exacerbations. For predicting exacerbations, we estimated the threshold of NLR to be 2.7 at baseline.

Trial registration: Clinical trial registered with the University Hospital Medication Information Network ( UMIN000003470 , April 10, 2010).

Keywords: Acute exacerbation; COPD; Comorbidity; NLR.

Publication types

  • Observational Study

MeSH terms

  • Adult
  • Aged
  • Female
  • Humans
  • Japan / epidemiology
  • Leukocyte Count / methods*
  • Lymphocytes*
  • Male
  • Middle Aged
  • Neutrophils*
  • Patient Acuity
  • Predictive Value of Tests
  • Pulmonary Disease, Chronic Obstructive* / blood
  • Pulmonary Disease, Chronic Obstructive* / diagnosis
  • Pulmonary Disease, Chronic Obstructive* / epidemiology
  • Pulmonary Disease, Chronic Obstructive* / physiopathology
  • Reproducibility of Results
  • Respiratory Function Tests / methods*
  • Severity of Illness Index
  • Symptom Flare Up