Predictive Impact of Hematological and Biochemical Parameters on the Clinical Course of Sarcoidosis.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Tugba Onyilmaz, Serap Argun Baris, Huseyin Kaya, Ayse Zeynep Pehlivan, Hanife Albayrak, Sena Nur Aktoprak, Hasim Boyaci, Ilknur Basyigit
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引用次数: 0

Abstract

Background: Sarcoidosis is a systemic granulomatous disease with a highly variable clinical course, and distinguishing it from other diseases and predicting its prognosis can be challenging. In recent years, hematological and biochemical parameters have been investigated as potential biomarkers for assessing inflammation and predicting disease prognosis. This study aimed to evaluate the prognostic value of the lactate dehydrogenase-to-albumin ratio (LAR), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR) and lymphocyte-to-monocyte ratio (LMR). Methods: This retrospective, single-center study included 369 newly diagnosed patients with sarcoidosis who were admitted between January 2020 and October 2024. Sarcoidosis was diagnosed based on current ERS, ATS, and WASOG guidelines. At the 6-month follow-up, patients' clinical courses were classified as regression, stable, or progression based on clinical, radiological, and pulmonary function tests. The predictive values of various hematological and biochemical parameters were analyzed using statistical methods, including binary logistic regression analysis and ROC analysis. Results: A total of 369 patients were included in the study. At the 6-month follow-up, 63.4% of patients showed regression, 21.4% had a stable course, and 15.2% showed progression. The progression group had a significantly higher LAR (5.26 [4.21-7.76]) compared to the stable/regression group (4.59 [3.82-5.86]) (p = 0.033). Additionally, baseline FVC% (OR, 0.97; p = 0.036) and the presence of dyspnea (OR, 3.08; p = 0.03) were identified as independent risk factors for disease progression. No significant associations were found between NLR, PLR, LMR, and serum ACE levels and the clinical course. The cutoff value of LAR for predicting disease progression was 4.87 (AUC: 0.605), with a sensitivity of 58.8% and specificity of 59.7%. Conclusions: Our study, which is the first to evaluate the prognostic value of LAR in sarcoidosis, identified this parameter as a significant indicator for the clinical course. The finding of significantly higher LAR levels in patients with disease progression suggests its potential as a prognostic biomarker. These results may help guide treatment and follow-up strategies, although further large-scale prospective studies are needed for validation.

Abstract Image

Abstract Image

血液学和生化指标对结节病临床病程的预测作用。
背景:结节病是一种全身性肉芽肿性疾病,具有高度可变的临床病程,将其与其他疾病区分开来并预测其预后是具有挑战性的。近年来,血液学和生化参数已被研究作为评估炎症和预测疾病预后的潜在生物标志物。本研究旨在评价乳酸脱氢酶与白蛋白比值(LAR)、中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)和淋巴细胞与单核细胞比值(LMR)的预后价值。方法:本回顾性单中心研究纳入了2020年1月至2024年10月期间入院的369例新诊断的结节病患者。结节病是根据目前的ERS, ATS和WASOG指南诊断的。在6个月的随访中,根据临床、放射学和肺功能检查,将患者的临床病程分为消退、稳定或进展。采用统计方法,包括二元logistic回归分析和ROC分析,分析血液学和生化指标的预测值。结果:共纳入369例患者。随访6个月,63.4%的患者病情消退,21.4%的患者病程稳定,15.2%的患者病情进展。进展组的LAR(5.26[4.21-7.76])明显高于稳定/回归组(4.59 [3.82-5.86])(p = 0.033)。此外,基线FVC% (OR, 0.97; p = 0.036)和呼吸困难的存在(OR, 3.08; p = 0.03)被确定为疾病进展的独立危险因素。NLR、PLR、LMR和血清ACE水平与临床病程无显著相关性。LAR预测疾病进展的临界值为4.87 (AUC: 0.605),敏感性为58.8%,特异性为59.7%。结论:我们的研究首次评估了LAR在结节病中的预后价值,并将该参数确定为临床病程的重要指标。在疾病进展患者中发现显著较高的LAR水平表明其作为预后生物标志物的潜力。这些结果可能有助于指导治疗和后续策略,尽管需要进一步的大规模前瞻性研究来验证。
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
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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