Department of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8601, Japan.
Department of Respiratory Medicine, Nagoya City University East Medical Center, Nagoya, Japan.
BMC Pulm Med. 2022 May 23;22(1):203. doi: 10.1186/s12890-022-02000-3.
The serum creatinine/cystatin C (Cr/CysC) ratio has attracted attention as a marker for sarcopenia, but has not been studied in patients with idiopathic pulmonary fibrosis (IPF). This study aimed to confirm the utility of the serum Cr/CysC ratio in predicting sarcopenia and investigate its clinical relevance.
This cross-sectional pilot study prospectively enrolled patients with stable IPF. IPF was diagnosed through multidisciplinary discussions according to the 2018 international guidelines, and sarcopenia was diagnosed according to the 2019 consensus report of the Asian Working Group for Sarcopenia. Patient-reported outcomes (PROs) were evaluated using the modified Medical Research Council (mMRC) dyspnea scale, chronic obstructive pulmonary disease assessment test (CAT), and King's Brief Interstitial Lung Disease (K-BILD) questionnaire. The associations between serum Cr/CysC ratio and the presence of sarcopenia and other clinical parameters, including PROs scores, were examined.
The study enrolled 49 Japanese patients with IPF with a mean age of 73.0 ± 7.7 years and a mean percentage of predicted forced vital capacity of 80.4 ± 15.5%. Sarcopenia was diagnosed in 18 patients (36.7%), and the serum Cr/CysC ratio was 0.86 [0.76-0.94] (median [interquartile range]). The receiver operating characteristic curve analyses for the detection of sarcopenia according to the serum Cr/CysC showed that the area under the curve, optimal cutoff value, specificity, and sensitivity were 0.85, 0.88, 0.65, and 0.94, respectively. Sarcopenia was identified in 13% of patients with a high serum Cr/CysC ratio (≥ 0.88) and 60% of patients with a low serum Cr/CysC ratio (< 0.88) (P < 0.001). Multiple linear regression analysis showed that the serum Cr/CysC ratio was an independent predictive marker of worse PROs evaluated using mMRC (P < 0.05), CAT (P < 0.05), and K-BILD (P < 0.05).
This study showed that the serum Cr/CysC ratio may be a surrogate marker of sarcopenia in patients with IPF. Furthermore, it is important to pay attention to the serum Cr/CysC ratio because a lower serum Cr/CysC ratio is associated with worse PROs. Further studies are required to validate these observations to determine whether the Cr/CysC ratio can be used to detect sarcopenia in patients with IPF.
血清肌酐/胱抑素 C(Cr/CysC)比值作为肌少症的标志物受到关注,但尚未在特发性肺纤维化(IPF)患者中进行研究。本研究旨在证实血清 Cr/CysC 比值在预测肌少症中的效用,并探讨其临床相关性。
本横断面前瞻性研究纳入了稳定期 IPF 患者。根据 2018 年国际指南,通过多学科讨论诊断 IPF,根据 2019 年亚洲肌少症工作组共识报告诊断肌少症。使用改良的医学研究委员会(mMRC)呼吸困难量表、慢性阻塞性肺疾病评估测试(CAT)和 King's 简短间质性肺病(K-BILD)问卷评估患者报告的结局(PROs)。检测血清 Cr/CysC 比值与肌少症及其他临床参数(包括 PROs 评分)之间的相关性。
该研究纳入了 49 名日本 IPF 患者,平均年龄 73.0±7.7 岁,预计用力肺活量的平均百分比为 80.4±15.5%。18 名患者(36.7%)诊断为肌少症,血清 Cr/CysC 比值为 0.86[0.76-0.94](中位数[四分位距])。根据血清 Cr/CysC 检测肌少症的受试者工作特征曲线分析显示,曲线下面积、最佳截断值、特异性和敏感性分别为 0.85、0.88、0.65 和 0.94。高血清 Cr/CysC 比值(≥0.88)患者中肌少症的检出率为 13%,低血清 Cr/CysC 比值(<0.88)患者中肌少症的检出率为 60%(P<0.001)。多元线性回归分析显示,血清 Cr/CysC 比值是 mMRC(P<0.05)、CAT(P<0.05)和 K-BILD(P<0.05)评估的 PROs 较差的独立预测标志物。
本研究表明,血清 Cr/CysC 比值可能是 IPF 患者肌少症的替代标志物。此外,需要注意血清 Cr/CysC 比值,因为较低的血清 Cr/CysC 比值与较差的 PROs 相关。需要进一步的研究来验证这些观察结果,以确定 Cr/CysC 比值是否可用于检测 IPF 患者的肌少症。