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 and Allergy, Nagoya City University Midori Municipal Hospital, 1-77 Shiomigaoka, Midori-Ku, Nagoya, Aichi, 458-0037, Japan.
Respir Investig. 2024 Sep;62(5):889-896. doi: 10.1016/j.resinv.2024.07.019. Epub 2024 Aug 7.
Patients with idiopathic pulmonary fibrosis (IPF) often experience sarcopenia and malnutrition. However, this has not been fully examined through longitudinal surveys. This study investigated whether sarcopenia and malnutrition were associated with 1-year outcomes in IPF.
We evaluated sarcopenia and nutritional status in 64 outpatients with IPF. We assessed the time-to-event for respiratory-related hospitalizations or deaths 12 months after enrollment. Sarcopenia was diagnosed by the criteria of the Asian Working Group for Sarcopenia, 2019. Nutritional status was assessed by serum transthyretin and the Geriatric Nutritional Risk Index (GNRI).
The average age was 73.6 ± 7.9 years, and the percent predicted forced vital capacity (FVC) was 81.9 ± 15.7%. Of the 64 patients, 24 (37.5%) had sarcopenia. The median serum transthyretin level and mean GNRI were 23.8 mg/dL and 102, respectively. Eleven patients (17.2%) experienced respiratory-related hospitalization or death within the first year. Cox regression analysis showed that the % predicted diffusion capacity for carbon monoxide, lowest oxygen saturation in the 6-min walk test, serum transthyretin level, and GNRI were significant predictors of 1-year outcomes. The Kaplan-Meier method, which divided the patients into two groups based on a transthyretin level of 22.6 mg/dL, showed a significant difference (P < 0.001, log-rank test). Sarcopenia and the percent predicted FVC did not predict the 1-year outcomes.
This pilot study represents the first longitudinal survey assessing patients with IPF for sarcopenia and malnutrition. Serum transthyretin levels may predict respiratory-related hospitalization or death within 1 year in patients with IPF.
特发性肺纤维化(IPF)患者常伴有肌肉减少症和营养不良。然而,这尚未通过纵向研究得到充分证实。本研究旨在探讨 IPF 患者的肌肉减少症和营养不良是否与 1 年预后相关。
我们评估了 64 例 IPF 门诊患者的肌肉减少症和营养状况。我们评估了从入组到 12 个月时因呼吸相关住院或死亡的时间事件。根据 2019 年亚洲肌肉减少症工作组的标准诊断肌肉减少症。通过血清转甲状腺素蛋白和老年营养风险指数(GNRI)评估营养状况。
患者平均年龄为 73.6±7.9 岁,预计用力肺活量(FVC)百分比为 81.9±15.7%。64 例患者中,24 例(37.5%)存在肌肉减少症。血清转甲状腺素蛋白水平中位数和平均 GNRI 分别为 23.8mg/dL 和 102。11 例(17.2%)患者在 1 年内发生呼吸相关住院或死亡。Cox 回归分析显示,一氧化碳弥散量预计值、6 分钟步行试验中最低血氧饱和度、血清转甲状腺素蛋白水平和 GNRI 是 1 年预后的显著预测因子。Kaplan-Meier 法根据转甲状腺素蛋白水平(22.6mg/dL)将患者分为两组,结果显示差异具有统计学意义(P<0.001,对数秩检验)。肌肉减少症和预计 FVC 百分比均不能预测 1 年预后。
本研究是首次对 IPF 患者进行肌肉减少症和营养不良的纵向研究。血清转甲状腺素蛋白水平可能预测 IPF 患者 1 年内因呼吸相关住院或死亡的风险。