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中性粒细胞-淋巴细胞比值、血小板-淋巴细胞比值和平均血小板体积在日本银屑病和银屑病关节炎患者中的变化:生物制剂治疗的反应。

Neutrophil-lymphocyte ratio, platelet-lymphocyte ratio and mean platelet volume in Japanese patients with psoriasis and psoriatic arthritis: Response to therapy with biologics.

机构信息

Department of Dermatology, The Jikei University School of Medicine, Tokyo, Japan.

出版信息

J Dermatol. 2017 Oct;44(10):1112-1121. doi: 10.1111/1346-8138.13875. Epub 2017 May 11.


DOI:10.1111/1346-8138.13875
PMID:28493493
Abstract

Recent studies indicate the presence of systemic inflammation in psoriatic patients, and this inflammatory status is significantly associated with a range of comorbidities. The aim of this study was to evaluate the clinical significance of novel inflammatory biomarkers, neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR) and mean platelet volume (MPV) in Japanese patients with plaque-type psoriasis (PsV) and psoriatic arthritis (PsA). One hundred and eighty-six patients with PsV and 50 patients with PsA treated with biologics, including infliximab, adalimumab and ustekinumab, were retrospectively analyzed before and after treatment. At baseline, NLR and PLR, as well as C-reactive protein (CRP), were significantly higher in PsA patients than those in PsV patients, and a significant correlation was found between NLR and PLR. In PsV patients, the NLR-high and PLR-high subgroups exhibited significantly higher Psoriasis Area and Severity Index scores compared with the NLR-low and PLR-low subgroups, respectively, and the NLR-high subgroup also showed higher CRP levels. MPV value was negatively associated with the presence of arthritis, but its association with inflammation was less clear than that of NLR or PLR. After treatment of the patients with biologics for up to 12 months, NLR and PLR decreased promptly in parallel with a decrease of CRP, irrespective of the type of biologics used. Altogether, these results indicate that both NLR and PLR may be useful markers to evaluate systemic inflammation in psoriatic patients. They may serve as simple, convenient and cost-effective biomarkers to monitor the disease course after systemic therapy.

摘要

最近的研究表明,银屑病患者存在系统性炎症,这种炎症状态与多种合并症显著相关。本研究旨在评估新型炎症生物标志物中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)和平均血小板体积(MPV)在日本斑块状银屑病(PsV)和银屑病关节炎(PsA)患者中的临床意义。对 186 例接受生物制剂(包括英夫利昔单抗、阿达木单抗和乌司奴单抗)治疗的 PsV 患者和 50 例 PsA 患者进行回顾性分析。在治疗前和治疗后,分别对基线时的 NLR 和 PLR 以及 C 反应蛋白(CRP)进行分析。结果显示,与 PsV 患者相比,PsA 患者的 NLR 和 PLR 以及 CRP 明显升高,且 NLR 和 PLR 之间存在显著相关性。在 PsV 患者中,与 NLR 低和 PLR 低亚组相比,NLR 高和 PLR 高亚组的银屑病面积和严重程度指数评分分别显著升高,且 NLR 高亚组的 CRP 水平也较高。MPV 值与关节炎的存在呈负相关,但与炎症的相关性不如 NLR 或 PLR 明显。在接受生物制剂治疗长达 12 个月后,无论使用何种生物制剂,NLR 和 PLR 均迅速降低,与 CRP 下降平行。总之,这些结果表明,NLR 和 PLR 可能是评估银屑病患者系统性炎症的有用标志物。它们可以作为一种简单、方便、具有成本效益的生物标志物,用于监测系统性治疗后的疾病进程。

相似文献

[1]
Neutrophil-lymphocyte ratio, platelet-lymphocyte ratio and mean platelet volume in Japanese patients with psoriasis and psoriatic arthritis: Response to therapy with biologics.

J Dermatol. 2017-5-11

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引用本文的文献

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Correlation of lymphocyte-to-monocyte, platelet-to-lymphocyte, and neutrophil-to-lymphocyte ratios with skin-symptom improvement following antimicrobial treatment in palmoplantar pustulosis.

J Pharm Health Care Sci. 2025-8-14

[2]
The Relationship Between Neutrophil-to-Lymphocyte Ratio, Platelet-to-Lymphocyte Ratio, and Systemic Immune-Inflammation Index Markers and Response to Biological Therapy in Patients with Psoriasis.

Int J Mol Sci. 2025-4-19

[3]
Association of the Monocyte-to-High Density Lipoprotein Ratio with the FRS and as a Predictor of Cardiovascular Risk in Individuals with Psoriasis Vulgaris.

Clin Cosmet Investig Dermatol. 2025-5-1

[4]
Effects of biological agents on lipid profile and hemogram parameters in patients with psoriasis.

Arch Dermatol Res. 2025-4-10

[5]
Hematological ratios as an indicator of severity in alopecia areata: A retrospective nationwide study.

PLoS One. 2024-12-2

[6]
Psoriasis treatment and biologic switching: The association with clinical characteristics and laboratory biomarkers over a 13-year retrospective study.

J Dermatol. 2024-12

[7]
Evaluation of the inflammatory parameters as potential biomarkers of systemic inflammation extent and the disease severity in psoriasis patients.

Arch Dermatol Res. 2024-5-24

[8]
Evaluation of inflammatory biomarkers and the ratio of hemoglobin-red cell distribution width in patients with rheumatoid arthritis treated with tumor necrosis factor-alpha inhibitors.

Clin Rheumatol. 2024-6

[9]
Association between systemic immune-inflammation index and psoriasis: a population-based study.

Front Immunol. 2024

[10]
Could Blood Cell-Based Inflammatory Markers Be Used to Monitor Response to Biologic Therapy in Psoriasis?

Sisli Etfal Hastan Tip Bul. 2023-12-20

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