Blood-based biomarkers associated with progressive pulmonary fibrosis in idiopathic inflammatory myositis-associated interstitial lung disease: A retrospective cohort study from a respiratory center.

IF 2.1 Q3 RESPIRATORY SYSTEM
Mayuko Ishiwari, Yuta Kono, Kenichi Kobayashi, Ryota Kikuchi, Mariko Kogami, Takashi Okuma, Shinji Abe
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引用次数: 0

Abstract

Background: Interstitial lung disease (ILD) is a common extramuscular manifestation of idiopathic inflammatory myopathies (IIM). Progressive pulmonary fibrosis (PPF) can develop in a subset of patients with IIM-associated interstitial lung disease (IIM-ILD) and is associated with poor outcomes. This study aimed to evaluate the utility of blood-based biomarkers associated with PPF in patients with IIM-ILD.

Methods: We retrospectively reviewed 54 consecutive patients diagnosed with IIM-ILD between January 2018 and December 2023. Patients were categorized as having PPF or not based on 2022 ATS/ERS/JRS/ALAT guideline criteria within 1 year after the diagnosis of IIM-ILD. Lung-specific macromolecules and systemic inflammatory and nutritional indices were calculated using laboratory data obtained at the initial evaluation. These included Krebs von den Lungen-6 (KL-6), surfactant protein-D, C-reactive protein-to-albumin ratio (CAR), neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-lymphocyte ratio (PLR), systemic immune-inflammation index (SII), systemic inflammation response index (SIRI), aggregate index of systemic inflammation (AISI), fibrosis-4 index, prognostic nutritional index, and geriatric nutritional risk index. Receiver operating characteristic curve analysis was used to determine optimal cutoff values, and logistic regression analyses were performed to identify factors associated with PPF.

Results: Of the 54 patients, 32 were classified as having PPF and 22 as not having PPF. The PPF group showed significantly lower hemoglobin levels and significantly higher platelet counts, neutrophil counts, C-reactive protein, and serum KL-6 levels than the non-PPF group. Several systemic inflammatory indices, including CAR, NLR, MLR, PLR, SII, SIRI, and AISI, were significantly higher in the PPF group. AISI showed the highest discriminative ability among the evaluated biomarkers, with an area under the curve of 0.786 and an optimal cutoff value of 278. In multivariable logistic regression analysis, serum KL-6 ≥626 U/mL and AISI ≥278 were independently associated with PPF, with adjusted odds ratios of 6.480 (95% confidence interval [CI]: 1.440-29.200; p = 0.015) and 9.940 (95% CI: 2.260-43.600; p = 0.002), respectively.

Conclusions: AISI and serum KL-6 may serve as accessible, non-invasive blood-based biomarkers associated with fibrotic progression in patients with IIM-ILD.

与特发性炎性肌炎相关间质性肺病进行性肺纤维化相关的血液生物标志物:一项来自呼吸中心的回顾性队列研究
背景:间质性肺疾病(ILD)是特发性炎性肌病(IIM)常见的肌外表现。进行性肺纤维化(PPF)可发生在iim相关间质性肺疾病(IIM-ILD)的一部分患者中,并与不良预后相关。本研究旨在评估与PPF相关的血液生物标志物在IIM-ILD患者中的应用。方法:我们回顾性分析了2018年1月至2023年12月期间连续诊断为IIM-ILD的54例患者。在IIM-ILD诊断后1年内,根据2022年ATS/ERS/JRS/ALAT指南标准将患者分为是否患有PPF。使用初步评估时获得的实验室数据计算肺特异性大分子和全身炎症和营养指数。这些指标包括Krebs von den lunen -6 (KL-6)、表面活性蛋白- d、c反应蛋白-白蛋白比(CAR)、中性粒细胞-淋巴细胞比(NLR)、单核细胞-淋巴细胞比(MLR)、血小板-淋巴细胞比(PLR)、全身免疫-炎症指数(SII)、全身炎症反应指数(SIRI)、全身炎症聚集指数(AISI)、纤维化-4指数、预后营养指数和老年营养风险指数。采用受试者工作特征曲线分析确定最佳截止值,并采用logistic回归分析确定与PPF相关的因素。结果:54例患者中,32例为PPF, 22例为非PPF。与非PPF组相比,PPF组血红蛋白水平显著降低,血小板计数、中性粒细胞计数、c反应蛋白和血清KL-6水平显著升高。一些全身炎症指数,包括CAR、NLR、MLR、PLR、SII、SIRI和AISI,在PPF组显著升高。在评价的生物标志物中,AISI的判别能力最强,曲线下面积为0.786,最佳截断值为278。在多变量logistic回归分析中,血清KL-6≥626 U/mL和AISI≥278与PPF独立相关,校正比值比分别为6.480(95%可信区间[CI]: 1.440 ~ 29.200, p = 0.015)和9.940 (95% CI: 2.260 ~ 43.600, p = 0.002)。结论:AISI和血清KL-6可作为与IIM-ILD患者纤维化进展相关的易获得的、无创的血液生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
23
审稿时长
>12 weeks
期刊介绍: Multidisciplinary Respiratory Medicine is the official journal of the Italian Respiratory Society - Società Italiana di Pneumologia (IRS/SIP). The journal publishes on all aspects of respiratory medicine and related fields, with a particular focus on interdisciplinary and translational research. The interdisciplinary nature of the journal provides a unique opportunity for researchers, clinicians and healthcare professionals across specialties to collaborate and exchange information. The journal provides a high visibility platform for the publication and dissemination of top quality original scientific articles, reviews and important position papers documenting clinical and experimental advances.
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