C反应蛋白与淋巴细胞计数比值可作为甲状腺炎的可靠指标CLEAR‐T研究

IF 0.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
M. Demirkol, G. Aktas
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引用次数: 10

摘要

甲状腺炎症被称为甲状腺炎,与炎症有关。最近的研究发现甲状腺炎与新的炎症和代谢标志物以及C反应蛋白(CRP)之间存在显著关联。CRP/淋巴细胞计数比(CLR)是一种新的炎症标志物,与各种疾病有关,尚未在甲状腺炎中进行研究。我们旨在研究甲状腺炎患者的CRP与淋巴细胞计数的比率,并与健康受试者进行比较。2019年1月至2021年8月期间在我院内科门诊就诊的甲状腺炎患者被纳入回顾性研究。健康志愿者作为对照组。比较甲状腺炎组和对照组的CLR。甲状腺炎组和对照组的中位CLR分别为3.14(0.14%-38)%和0.4(0.03-8.86)%(p  检测甲状腺炎的0.43%分别为92%和58%(AUC:0.88,p < .001,95%CI:0.85-0.92)。CLR与游离T4(FT4)呈显著正相关(r=.18,p < .001)与促甲状腺激素(TSH)水平呈负相关(r=−.52,p=.003)。总之,我们认为高CLR水平可能对甲状腺炎患者产生额外的诊断价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C‐reactive protein to LymphocytE count ratio could be a reliable mArkeR of thyroiditis; the CLEAR‐T study
Inflammation of the thyroid gland is referred to as thyroiditis and is associated with inflammation. Recent studies found significant association between thyroiditis and novel inflammatory and metabolic markers, as well as C‐reactive protein (CRP). CRP/lymphocyte count ratio (CLR) is a novel inflammatory marker that associated with various conditions and has not been studied in thyroiditis, yet. We aimed to investigate CRP to lymphocyte count ratio in patients with thyroiditis and to compare to those in healthy subjects. Patients with thyroiditis that presented to internal medicine outpatient clinics of our institution between January 2019 and August 2021 were enrolled to the retrospective study. Healthy volunteers were enrolled as control group. CLR of the thyroiditis and control groups were compared. Median CLR of the thyroiditis and control groups were 3.14 (0.14%–38)% and 0.4 (0.03–8.86)%, respectively (p < .001). The sensitivity and specificity of CLR > 0.43% in detecting thyroiditis were 92% and 58%, respectively (AUC: 0.88, p < .001, 95% CI: 0.85–0.92).CLR was significantly and positively correlated with free T4 (FT4) (r = .18, p < .001) and inversely correlated with thyroid stimulating hormone (TSH) (r = −.52, p = .003) levels. In conclusion, we suggest that high CLR levels may yield additional diagnostic value in patients with thyroiditis.
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来源期刊
Precision Medical Sciences
Precision Medical Sciences MEDICINE, RESEARCH & EXPERIMENTAL-
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审稿时长
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