Platelet-to-lymphocyte ratio and neutrophil-to-lymphocyte ratio as potential makers for digital ulcers and interstitial lung disease in patients with systemic sclerosis: cross-sectional analysis of data from a prospective cohort study.


Journal

Rheumatology international
ISSN: 1437-160X
Titre abrégé: Rheumatol Int
Pays: Germany
ID NLM: 8206885

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 06 04 2020
accepted: 07 05 2020
pubmed: 20 5 2020
medline: 15 4 2021
entrez: 20 5 2020
Statut: ppublish

Résumé

In this study, we aimed to investigate the association of platelet-to-lymphocyte ratio (PLR) and neutrophil-to-lymphocyte ratio (NLR) with clinical manifestations in patients with systemic sclerosis (SSc). We conducted a cross-sectional analysis of data collected from a cohort study of 114 female patients with SSc and of 304 age-matched, healthy, female controls recruited from a tertiary rheumatology center. Patients with digital ulcers (DU) included those with either active or healed ulcers. Interstitial lung disease (ILD) was diagnosed on detection of diffuse ground-glass opacity or pulmonary fibrosis on chest X-ray or on high-resolution computed tomography. Patients with SSc had significantly higher PLR and NLR than ealthy controls. Of 114 patients with SSc, 35 (30.7%) and 54 (47.4%) patients had DU (active: 12, healed: 23) and ILD, respectively. PLR and NLR in SSc patients with concurrent DU or ILD were significantly higher than that in those without these respective complications. The PLR (OR = 1.008, 95% CI 1.002-1.015), but not the NLR, was independently associated with the presence of DU in SSc patients, based on multivariable logistic regression models. Additionally, both PLR (OR = 1.008, 95% CI 1.001-1.014) and NLR (OR = 1.515, 95% CI 1.066-2.155) correlated independently with the presence of ILD. However, both the PLR and NLR showed no significant association with the modified Rodnan skin score, pulmonary arterial hypertension, and gastrointestinal involvement. Our results suggest that PLR and NLR could be considered as potential biomarkers of DU and ILD, in patients with SSc.

Identifiants

pubmed: 32424613
doi: 10.1007/s00296-020-04604-6
pii: 10.1007/s00296-020-04604-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1071-1079

Auteurs

Aran Kim (A)

Division of Rheumatology, Department of Internal Medicine, Pusan National University Hospital, Pusan National University School of Medicine, 179 Gudeok-Ro, Seo-Gu, Busan, 49241, South Korea.
Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea.

Yunkyung Kim (Y)

Division of Rheumatology, Department of Internal Medicine, Kosin University College of Medicine, Busan, South Korea.

Geun-Tae Kim (GT)

Division of Rheumatology, Department of Internal Medicine, Kosin University College of Medicine, Busan, South Korea.

Eunyoung Ahn (E)

Division of Rheumatology, Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, South Korea.

Min Wook So (MW)

Division of Rheumatology, Department of Internal Medicine, Pusan National University Yangsan Hospital, Yangsan, South Korea.

Dong Hyun Sohn (DH)

Department of Microbiology and Immunology, Pusan National University School of Medicine, Yangsan, South Korea.

Seung-Geun Lee (SG)

Division of Rheumatology, Department of Internal Medicine, Pusan National University Hospital, Pusan National University School of Medicine, 179 Gudeok-Ro, Seo-Gu, Busan, 49241, South Korea. sglee@pusan.ac.kr.
Biomedical Research Institute, Pusan National University Hospital, Busan, South Korea. sglee@pusan.ac.kr.

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